MP:0000029 | abnormal malleus morphology | "structural anomaly in the largest of the three auditory ossicles, which resembles a club or hammer " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Tg(ACTB-Edn1)1398Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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MP:0000030 | abnormal tympanic ring morphology | "malformed bony ring at the ear canal to which the tympanic membrane is attached" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:23837] |
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Allelic Composition: Tg(ACTB-Edn1)1398Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
Allelic Composition: Tg(ACTB-Edn1)1416Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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MP:0000040 | absent middle ear ossicles | "missing small bones of the tympanic cavity" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:1776] |
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Allelic Composition: Hand1tm2Eno/Hand1tm4Abfi,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S6/SvEvTac * C3H * C57BL/6
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MP:0000091 | short premaxilla | "reduced length of the anterior and interior portion of the maxilla" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:53370] |
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Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0000103 | nasal bone hypoplasia | "reduced cell number in the bone which forms the nasal bridge" [J:53370] |
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Allelic Composition: Foxn1tm3(cre)Nrm/Foxn1+,Gt(ROSA)26Sortm1(Tbx1)Rche/Gt(ROSA)26Sor+ Genetic Background: involves: C57BL/6 * C57BL/6NHsd
Allelic Composition: Hand1tm4Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0000108 | midline facial cleft | "incomplete merging or fusion of the tissues normally uniting to form the face" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840] |
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Allelic Composition: Foxn1tm3(cre)Nrm/Foxn1+,Gt(ROSA)26Sortm1(Tbx1)Rche/Gt(ROSA)26Sor+ Genetic Background: involves: C57BL/6 * C57BL/6NHsd
Allelic Composition: Hand1tm2Eno/Hand1tm4Abfi,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S6/SvEvTac * C3H * C57BL/6
Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
Allelic Composition: Hand1tm4Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
Allelic Composition: Tg(ACTB-Edn1)721Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
Allelic Composition: Tg(ACTB-Edn1)1416Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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MP:0000111 | cleft palate | "congenital fissure of the tissues normally uniting to form the palate" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840] |
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Allelic Composition: Pvalbtm1(cre)Arbr/Pvalb+,Slc12a6tm2.1Dlp/Slc12a6tm2.1Dlp Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J
Allelic Composition: Tg(ACTB-Edn1)1398Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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MP:0000163 | abnormal cartilage morphology | "anomalous structure or development of the nonvascular, resilient, flexible connective tissue found primarily in joints, walls of the throax, and tubular structures, but which also comprises most of the skeleton in early fetal life " [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: E2f3tm3Lees/E2f3tm3Lees Genetic Background: either: 129S/Sv-E2f3tm3Lees or (involves: 129S4/SvJae * C57BL/6)
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MP:0000166 | abnormal chondrocyte morphology | "anomalous structure, organization, or differentiation of nondividing cartilage cells" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:40203] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd,E2f3tm2Lees/E2f3tm2Lees Genetic Background: involves: 129S2/SvPas * 129S4/SvJae * C57BL/6
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MP:0000313 | abnormal cell death | "anomalous cessation of function at the cellular level" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Rbl1tm1Htr/Rbl1tm1Htr,Tg(Chx10-EGFP/cre,-ALPP)2Clc/? Genetic Background: involves: 129 * C57BL/6 * FVB/N * NMRI * SJL
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MP:0000352 | decreased cell proliferation | "less than the normal growth and reproduction of similar cells" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: E2f3tm1.1Gle/E2f3tm1.1Gle Genetic Background: 129-E2f3tm1.1Gle
Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f2tm1Zubi/E2f2tm1Zubi,E2f3tm3.1Gle/E2f3tm3.1Gle Genetic Background: involves: 129 * FVB/N * NIH Black Swiss
Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm2.1Gle/E2f3tm2.1Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
Allelic Composition: E2f1tm1Njd/E2f1tm1Njd,E2f3tm2Lees/E2f3tm2Lees Genetic Background: involves: 129S2/SvPas * 129S4/SvJae * C57BL/6
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MP:0000455 | abnormal maxilla morphology | "malformation of the upper bony framework of the mouth where the superior teeth are held" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Hand1tm2Eno/Hand1tm4Abfi,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S6/SvEvTac * C3H * C57BL/6
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MP:0000458 | abnormal mandible morphology | "malformation of the lower bony framework of the mouth where the inferior teeth are held" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Pvalbtm1(cre)Arbr/Pvalb+,Slc12a6tm2.1Dlp/Slc12a6tm2.1Dlp Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J
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MP:0000460 | mandible hypoplasia | "arrested growth or atrophy of the lower bony framework of the mouth where the inferior teeth are held" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, tc:Teresa Chu , Mouse Genome Informatics Curator, J:54637] |
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Allelic Composition: Foxn1tm3(cre)Nrm/Foxn1+,Gt(ROSA)26Sortm1(Tbx1)Rche/Gt(ROSA)26Sor+ Genetic Background: involves: C57BL/6 * C57BL/6NHsd
Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0000613 | abnormal salivary gland morphology | "malformed saliva-secreting glands of the oral cavity" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:63764] |
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Allelic Composition: Axin1tm4Cos/Axin1tm4Cos,Ctnnb1tm2.1Kem/Ctnnb1+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * FVB/N
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MP:0000623 | reduced salivation | "decrease flow, secretion, or amount of saliva" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Erbb2tm2Mul/Erbb2tm2Mul Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/c
Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: NOD.Cg-E2f1tm1Meg
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MP:0000681 | abnormal thyroid gland morphology | "anomalous structure of the endocrine gland located in the front and to the sides of the upper part of the trachea and which secretes thyroid hormone and calcitonin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: E2f1tm1Njd/E2f1+,Rb1tm1Tyj/Rb1+ Genetic Background: either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)
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MP:0000709 | enlarged thymus | "increased size of thymus" [J:50053] |
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Allelic Composition: Erbb2tm2Mul/Erbb2tm2Mul Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/c
Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: NOD.Cg-E2f1tm1Meg
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MP:0000714 | increased thymocyte number | "greater than expected number of precursors to T cells" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Erbb2tm2Mul/Erbb2tm2Mul Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/c
Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: NOD.Cg-E2f1tm1Meg
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MP:0000762 | abnormal tongue morphology | "anomalous structure or development of the mobile mass of muscular tissue and surrounding epithelial tissue occupying the cavity of the mouth and forming part of the floor" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Foxn1tm3(cre)Nrm/Foxn1+,Gt(ROSA)26Sortm1(Tbx1)Rche/Gt(ROSA)26Sor+ Genetic Background: involves: C57BL/6 * C57BL/6NHsd
Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
Allelic Composition: Hand1tm4Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0000771 | abnormal brain size | "deviation from the average range of brain size for a given strain" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm2.1Gle/E2f3tm2.1Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
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MP:0000914 | exencephaly | "neurocranial defects resulting in exposure or extrusion of the brain" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840] |
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Allelic Composition: Phactr4humdy/Phactr4humdy Genetic Background: C.B6-Phactr4humdy
Allelic Composition: E2f1tm1Meg/E2f1+,Phactr4humdy/Phactr4humdy Genetic Background: involves: 129S4/SvJae * C57BL/6J
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MP:0001152 | Leydig cell hyperplasia | "increased number of interstitial cells of the seminiferous tubules that secrete testosterone" [J:45065] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0001154 | seminiferous tubule degeneration | "a retrogressive impairment of function or destruction of the tubules in the testes where spermatogenesis occurs" [J:50844] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0001203 | skin irradiation sensitivity | "increased incidence of aberrant or damaged cells due to irradiation induced genotoxic damage" [J:65162] |
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Allelic Composition: Rag1tm1Jsek/Rag1tm1Jsek,Trp53tm1Tyj/Trp53tm1Tyj Genetic Background: involves: 129S2/SvPas * 129S6/SvEvTac
Allelic Composition: E2f1tm1Njd/E2f1tm1Njd,Trp53tm1Brd/Trp53tm1Brd Genetic Background: involves: 129S2/SvPas * 129S7/SvEvBrd * SKH1
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MP:0001262 | decreased body weight | "lower than normal average weight " [J:61295] |
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Allelic Composition: Erbb2tm2Mul/Erbb2tm2Mul Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/c
Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f2tm1Zubi/E2f2tm1Zubi,E2f3tm3.1Gle/E2f3tm3.1Gle Genetic Background: involves: 129 * FVB/N * NIH Black Swiss
Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm2.1Gle/E2f3tm2.1Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm3.1Gle/E2f3tm3.1Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
Allelic Composition: E2f1tm1Njd/E2f1tm1Njd,E2f3tm2Lees/E2f3tm2Lees Genetic Background: involves: 129S2/SvPas * 129S4/SvJae * C57BL/6
Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0001265 | reduced body size | "smaller than average body weight, height and/or length of an organism compared to controls" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:23170] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f2tm1Zubi/E2f2tm1Zubi,E2f3tm3.1Gle/E2f3tm3.1Gle Genetic Background: involves: 129 * FVB/N * NIH Black Swiss
Allelic Composition: E2f1tm1Njd/E2f1tm1Njd,Klhl40tm1.1Itl/Klhl40tm1.1Itl Genetic Background: involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6N
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MP:0001272 | increased metastatic potential | |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0001286 | abnormal eye development | "malformation or arrest of differentiation of the visual organ" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:49840] |
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Allelic Composition: Wt1tm1Nhsn/Wt1+ Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0001325 | abnormal retina morphology | "structural or developmental anomaly of the thin layer of neural tissue lining the back of the eyeball which contains visual receptors " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,Rbl1tm1Htr/Rbl1tm1Htr,Tg(Pax6-cre,GFP)2Pgr/? Genetic Background: involves: 129 * C57BL/6 * FVB/N * NMRI
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MP:0001505 | hunched posture | "stooped low with the limbs pulled in close to the body and arched back" [J:67231, J:30404] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,Rb1tm1Tyj/Rb1tm1Tyj,Tg(Rb1)1Blg/0 Genetic Background: involves: 129S2/SvPas * 129S4/SvJae
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MP:0001560 | abnormal circulating insulin level | "anomalous blood concentration of this polypeptide hormone, secreted by beta cells of the pancreas, that promotes glucose utilization, protein synthesis, and the formation and storage of neutral lipids" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0001783 | decreased white fat amount | "reduced quantity of fat-storing cells/tissue" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm2.1Gle/E2f3tm2.1Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
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MP:0001870 | salivary gland inflammation | "local accumulation of fluid, plasma proteins, and leukocytes in the salivary gland" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: NOD.Cg-E2f1tm1Meg
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MP:0001925 | male infertility | "inability of male to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm2.1Gle/E2f3tm2.1Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
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MP:0001926 | female infertility | "inability of female to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:34193] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm2.1Gle/E2f3tm2.1Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
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MP:0001940 | testicular hypoplasia | "decreased cell number in the testicles" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm2.1Gle/E2f3tm2.1Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
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MP:0001944 | abnormal pancreas morphology | "malformation of the organ that secretes pancreatic juice into the duodenum and secretes glucagon and insulin into the bloodstream" [il:Ira Lu , Mouse Genome Informatics Curator] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0002020 | increased tumor incidence | "greater than average number of tumors, usually a specific type" [MGI:cls, J:34193] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
Allelic Composition: E2f1tm1Njd/E2f1+,Rb1tm1Tyj/Rb1+ Genetic Background: either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)
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MP:0002024 | T cell derived lymphoma | "group of heterogeneous lymphoid tumors representing malignant transformations of T-lymphocytes" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Erbb2tm2Mul/Erbb2tm2Mul Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/c
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MP:0002027 | lung adenocarcinoma | "malignant neoplasm of epithelial cells in the lung" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:18542] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0002058 | neonatal lethality | "death of animal within one day after birth" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Foxn1tm3(cre)Nrm/Foxn1+,Gt(ROSA)26Sortm1(Tbx1)Rche/Gt(ROSA)26Sor+ Genetic Background: involves: C57BL/6 * C57BL/6NHsd
Allelic Composition: Hand1tm2Eno/Hand1tm4Abfi,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S6/SvEvTac * C3H * C57BL/6
Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
Allelic Composition: Hand1tm4Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0002081 | perinatal lethality | "death anytime between E18.5 and postnatal day 1 " [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: E2f3tm1.1Gle/E2f3tm1.1Gle Genetic Background: 129-E2f3tm1.1Gle
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MP:0002083 | premature death | "death after 3 weeks of age, but before normal life span" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Erbb2tm2Mul/Erbb2tm2Mul Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/c
Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm2.1Gle/E2f3tm2.1Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
Allelic Composition: E2f1tm1Njd/E2f1+,Rb1tm1Tyj/Rb1+ Genetic Background: either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)
Allelic Composition: E2f1tm1Njd/E2f1tm1Njd,Rb1tm1Tyj/Rb1+ Genetic Background: either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)
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MP:0002106 | abnormal muscle physiology | "anomolous function of the muscle, not due to an anatomical defect" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Rb1tm1Tyj/Rb1tm1Tyj,Tg(Rb1)1Blg/0 Genetic Background: involves: 129S2/SvPas
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MP:0002163 | abnormal gland morphology | "abnormal development of any glandular tissue resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Axin1tm4Cos/Axin1tm4Cos,Ctnnb1tm2.1Kem/Ctnnb1+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * FVB/N
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MP:0002169 | no phenotype detected | "normal, viable and fertile appearance and behavior; indistinguishable from controls" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm5(E2f1)Gle/E2f3tm5(E2f1)Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm4Gle/E2f3tm4Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
Allelic Composition: E2f1tm1Njd/E2f1tm1Njd,E2f3tm3Lees/E2f3tm3Lees Genetic Background: involves: 129S2/SvPas * 129S4/SvJae * C57BL/6
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MP:0002408 | abnormal double-positive T cell | "anomalous development or number of the subset of T cells found in the thymus that express both CD4 and CD8" [Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Erbb2tm2Mul/Erbb2tm2Mul Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/c
Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: NOD.Cg-E2f1tm1Meg
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MP:0002432 | abnormal CD4+ T cell morphology/development | "anomalous structure, differentiation, or number of the subset of T lymphocytes that carry the CD4 marker, recognize intravesicular peptides bound to MHC class-II molecules, and turn on antibody production" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: NOD.Cg-E2f1tm1Meg
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MP:0002644 | decreased circulating triglyceride level | "lower than normal concentration of triacylglycerols in the blood" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm2.1Gle/E2f3tm2.1Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
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MP:0002679 | abnormal corpora lutea | "malformed or absent yellow endocrine body formed in the ovary after follicle rupture" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm2.1Gle/E2f3tm2.1Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
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MP:0002727 | decreased circulating insulin level | "less than normal levels of insulin in the blood" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, dlb:Donna Burkart , Mouse Genome Informatics Curator] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0002884 | abnormal branchial arches | "malformation or anomaly in the transient structures of the embryo that develop into regions of the head, neck and ears" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Foxn1tm3(cre)Nrm/Foxn1+,Gt(ROSA)26Sortm1(Tbx1)Rche/Gt(ROSA)26Sor+ Genetic Background: involves: C57BL/6 * C57BL/6NHsd
Allelic Composition: Hand1tm2Eno/Hand1tm4Abfi,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S6/SvEvTac * C3H * C57BL/6
Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
Allelic Composition: Hand1tm4Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0002891 | increased insulin sensitivity | "greater ability to clear glucose from the bloodstream when given insulin than normal; can result in hypoglycemia" [RGD:Rat Genome Database submission] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0002947 | hemangioma | "proliferation of blood vessels leading to a mass that resembles a neoplasm" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:87544] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd,Rb1tm1Tyj/Rb1+ Genetic Background: either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)
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MP:0003055 | abnormal epiphyseal plate morphology | "malformed or absent cartilagenous center of ossification on the long bones permitting growth of the bone in both directions during development" [MeSH:National Library of Medicine - Medical Subject Headings, 2003] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd,E2f3tm2Lees/E2f3tm2Lees Genetic Background: involves: 129S2/SvPas * 129S4/SvJae * C57BL/6
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MP:0003059 | decreased insulin secretion | "less than normal release of this hormone secreted by beta cells of the pancreas, that promotes glucose utilization, protein synthesis, and the formation and storage of neutral lipids " [MeSH:National Library of Medicine - Medical Subject Headings, 2003, RGD:Rat Genome Database submission] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0003077 | abnormal cell cycle | "failure to progress or abnormal progression through the stages of of the cell cycle" [smb:Susan M. Bello, Mouse Genome Informatics Curator, J:91266] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: NOD.Cg-E2f1tm1Meg
Allelic Composition: E2f1tm1Njd/E2f1tm1Njd,E2f3tm2Lees/E2f3tm2Lees Genetic Background: involves: 129S2/SvPas * 129S4/SvJae * C57BL/6
Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,Rb1tm1Tyj/Rb1tm1Tyj,Tg(Rb1)1Blg/0 Genetic Background: involves: 129S2/SvPas * 129S4/SvJae
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MP:0003084 | abnormal skeletal muscle fiber morphology | "anomalous structure of the skeletal muscle fibers, the large multinucleated cells that make up the skeletal muscles" [smb:Susan M. Bello, Mouse Genome Informatics Curator, Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,Rb1tm1Tyj/Rb1tm1Tyj,Tg(Rb1)1Blg/0 Genetic Background: involves: 129S2/SvPas * 129S4/SvJae
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MP:0003205 | testicular atrophy | "wasting of the male reproductive glands resulting in reduced size" [RGD:Rat Genome Database submission] |
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Allelic Composition: Erbb2tm2Mul/Erbb2tm2Mul Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/c
Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
Allelic Composition: E2f1tm1Njd/E2f1tm1Njd,E2f3tm1Lees/E2f3+ Genetic Background: involves: 129S2/SvPas
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MP:0003235 | abnormal alisphenoid bone morphology | "malformation in either of the broad curved winglike expanses on each side of the sphenoid bone" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:93183, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
Allelic Composition: Hand1tm4Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0003452 | abnormal parotid gland morphology | "malformation of either of the largest of the major salivary glands situated below and in front of each ear and opening into the parotid duct" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:94478] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0003496 | thyroid adenoma | "appearance of benign neoplasms in the thyroid gland" [ncbi:Matthew Mailman, NCBI request] |
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Allelic Composition: E2f1tm1Njd/E2f1+,Rb1tm1Tyj/Rb1+ Genetic Background: either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)
Allelic Composition: E2f1tm1Njd/E2f1tm1Njd,Rb1tm1Tyj/Rb1+ Genetic Background: either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)
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MP:0003734 | abnormal inner plexiform layer morphology | "malformation/anomalous structure of the retinal cell layer where bipolar and amacrine cell axons synapse with ganglion cell dendrites
" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,Rbl1tm1Htr/Rbl1tm1Htr,Tg(Pax6-cre,GFP)2Pgr/? Genetic Background: involves: 129 * C57BL/6 * FVB/N * NMRI
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MP:0003793 | abnormal submandibular gland morphology | "any structural malformation of either of the large major salivary glands situated beneath the mandible" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0003843 | abnormal sagittal suture morphology | "malformation of the articulation between the parietal bones" [smb:Susan M Bello, Mouse Genome Informatics Curator, Taber s Cyclopedic Medical Dictionary:19th edition: ISBN N 0-8036-0655-99] |
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Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0003869 | ectopic cartilage | "positional abnormality of cartilage" [smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Tg(ACTB-Edn1)1416Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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MP:0003935 | abnormal craniofacial development | "anomaly in the process of forming the face and/or cranium" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Foxn1tm3(cre)Nrm/Foxn1+,Gt(ROSA)26Sortm1(Tbx1)Rche/Gt(ROSA)26Sor+ Genetic Background: involves: C57BL/6 * C57BL/6NHsd
Allelic Composition: Hand1tm2Eno/Hand1tm4Abfi,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S6/SvEvTac * C3H * C57BL/6
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MP:0004022 | abnormal cone electrophysiology | "anomaly in the function of light adapted vision mediated by the cones" [smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,Rbl1tm1Htr/Rbl1tm1Htr,Tg(Pax6-cre,GFP)2Pgr/? Genetic Background: involves: 129 * C57BL/6 * FVB/N * NMRI
Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: involves: 129 * C57BL/6 * FVB/N * NMRI
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MP:0004025 | polyploidy | "more than two chromosome sets are present" [llw2:Linda Washburn , Mouse Genome Informatics Curator] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,Rb1tm1Tyj/Rb1tm1Tyj,Tg(Rb1)1Blg/0 Genetic Background: involves: 129S2/SvPas * 129S4/SvJae
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MP:0004031 | insulitis | "a histologic change in the islets of Langerhans characterized by edema and the infiltration of small numbers of white blood cells" [rbabiuk:Randall Babiuk, Mouse Genome Informatics Curator] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: NOD.Cg-E2f1tm1Meg
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MP:0004385 | interparietal bone hypoplasia | "underdevelopment or reduced size, usually due to a reduced number of cells, in the bone of the cranium that lies above and anterior to the occipital bone in some mammals" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0004423 | abnormal squamosal bone morphology | "any structural anomaly of the thin, platelike part of the temporal bone" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Tg(ACTB-Edn1)721Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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MP:0004455 | pterygoid bone hypoplasia | "underdevelopment or reduced size, usually due to a reduced number of cells, in the bone region which corresponds to the inner plate of the pterygoid process of the mammalian skull" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0004461 | basisphenoid bone hypoplasia | "underdevelopment or reduced size, usually due to reduced cell number, in part of the base of the cranium between the basioccipital and the presphenoid, which usually ossifies separately in the embryo or in the young, and becomes a part of the sphenoid in the adult; in many animals it persists as a separate bone between the basioccipital bone and the presphenoidal bone" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Foxn1tm3(cre)Nrm/Foxn1+,Gt(ROSA)26Sortm1(Tbx1)Rche/Gt(ROSA)26Sor+ Genetic Background: involves: C57BL/6 * C57BL/6NHsd
Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
Allelic Composition: Tg(ACTB-Edn1)721Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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MP:0004467 | absent zygomatic bone | "absence of the quadrilateral bone that forms the prominence of the cheek" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Tg(ACTB-Edn1)721Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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MP:0004473 | absent nasal bone | "absence of either of two rectangular bone plates forming the bridge of the nose" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0004475 | palatine bone hypoplasia | "underdevelopment or reduced size, usually due to a reduced number of cells, in either of two irregularly shaped bones that form the back of the hard palate and helps to form the nasal cavity and the floor of the orbits" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Tg(ACTB-Edn1)1398Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
Allelic Composition: Tg(ACTB-Edn1)1416Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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MP:0004476 | absent palatine bone | "absence of either of two irregularly shaped bones that form the back of the hard palate and helps to form the nasal cavity and the floor of the orbits" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Tg(ACTB-Edn1)721Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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MP:0004501 | increased incidence of UV-induced tumors | "higher than normal frequency of tumor incidence induced by exposure to ultraviolet light" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Emilin1tm1Gmb/Emilin1tm1Gmb Genetic Background: involves: 129S1/Sv * 129X1/SvJ
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MP:0004592 | small mandible | "reduced size of the lower bony framework of the mouth where the inferior teeth are held" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Hand1tm4Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0004596 | abnormal mandibular angle morphology | "any structural anomaly of the portion of the mandible where the body of the mandible (horizontal portion) and the rami (perpendicular portions) meet; these normally unite nearly at right angles" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Tg(ACTB-Edn1)1398Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
Allelic Composition: Tg(ACTB-Edn1)1416Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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MP:0004701 | decreased circulating insulin-like growth factor I level | "reduced blood concentration of this polypeptide hormone with growth-regulating, insulin-like, and mitogenic activities" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm2.1Gle/E2f3tm2.1Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
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MP:0004726 | abnormal nasal capsule morphology | "any structural abnormality in the cartilage around the developing nasal cavity of the embryo" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Foxn1tm3(cre)Nrm/Foxn1+,Gt(ROSA)26Sortm1(Tbx1)Rche/Gt(ROSA)26Sor+ Genetic Background: involves: C57BL/6 * C57BL/6NHsd
Allelic Composition: Hand1tm2Eno/Hand1tm4Abfi,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S6/SvEvTac * C3H * C57BL/6
Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
Allelic Composition: Hand1tm4Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0004803 | increased susceptibility to autoimmune diabetes | "greater likelihood that an organism will develop inflammatory pancreatic disease resulting from the body attacking and destroying the insulin-producing beta islet cells of the pancreas" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: NOD.Cg-E2f1tm1Meg
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MP:0004852 | decreased testis weight | "reduced average weight of the male reproductive glands" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0004869 | frontal bone hypoplasia | "underdevelopment or reduced size, usually due to a reduced number of cells, in the bone which forms the forehead and roof of the eye orbit" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0004871 | premaxilla hypoplasia | "underdevelopment or reduced size, usually due to a reduced number of cells, in the anterior and interior portion of the maxilla" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Hand1tm4Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0004872 | absent nasal septum | "absence of the structure that separates the two nasal cavities" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Foxn1tm3(cre)Nrm/Foxn1+,Gt(ROSA)26Sortm1(Tbx1)Rche/Gt(ROSA)26Sor+ Genetic Background: involves: C57BL/6 * C57BL/6NHsd
Allelic Composition: Hand1tm2Eno/Hand1tm4Abfi,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S6/SvEvTac * C3H * C57BL/6
Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
Allelic Composition: Hand1tm4Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0004898 | uterine hemorrhage | "presence of bleeding in the uterus; often in response to failed pregnancy" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd,Rb1tm1Tyj/Rb1+ Genetic Background: either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)
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MP:0004899 | absent squamosal bone | "absence of the thin, plate-like part of the temporal bone" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0004912 | absent mandibular coronoid process | "absence of the thin, flattened, triangular eminence that arises from the upper surface of the mandibular ramus (perpendicular portion)" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Tg(ACTB-Edn1)1398Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
Allelic Composition: Tg(ACTB-Edn1)1416Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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MP:0004915 | abnormal Reichert s cartilage | "any structural abnormality of the cartilage found in the mesenchyme of the second pharyngeal arch in the embryo from which develop the stapes, styloid process, lesser horn and upper part of the body of the hyoid bone; its proximal end gives rise to the stylohyoid ligament" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0004955 | increased thymus weight | "greater than average weight of the primary lymphoid organ that is required for maturation of T cells" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Erbb2tm2Mul/Erbb2tm2Mul Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/c
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MP:0004974 | decreased regulatory T cell number | "reduced number of the specialized subpopulation of T cells that act to suppress activation of the immune system and thus maintain immune system homeostasis and prevent pathological self-reactivity" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: NOD.Cg-E2f1tm1Meg
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MP:0005010 | abnormal CD8+ T cell morphology/development | "anomalous structure, formation, or numbers of the regulatory subset of T lymphocytes that are involved in MHC class I restricted interactions" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: NOD.Cg-E2f1tm1Meg
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MP:0005015 | increased T cell number | "greater than normal T cell numbers" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: NOD.Cg-E2f1tm1Meg
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MP:0005092 | decreased double-positive T cell count | "less than the expected number of the subset of T cells found in the thymus that express both CD4 and CD8" [Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: NOD.Cg-E2f1tm1Meg
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MP:0005095 | decreased T cell proliferation | "reduced clonal expansion of naive T cells in response to stimuli" [Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7] |
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Allelic Composition: Rbl1tm1Htr/Rbl1tm1Htr,Tg(Chx10-EGFP/cre,-ALPP)2Clc/? Genetic Background: involves: 129 * C57BL/6 * FVB/N * NMRI * SJL
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MP:0005106 | abnormal incus morphology | "structural anomaly of the middle of the three auditory ossicles" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:83132] |
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Allelic Composition: Tg(ACTB-Edn1)1398Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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MP:0005120 | decreased circulating growth hormone level | "less than the expected blood concentration of the hormone that promotes body growth, fat mobilization, and inhibition of glucose utilization" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm2.1Gle/E2f3tm2.1Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
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MP:0005158 | ovary hypoplasia | "underdeveloped ovaries, usually due to reduced cell number" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:78931] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm2.1Gle/E2f3tm2.1Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
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MP:0005215 | abnormal islet of Langerhans morphology | "anomalous morphology of these structures that are scattered throughout the pancreas and comprise its endocrine portion; within each islet there are three cell types: alpha, beta, and delta " [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: NOD.Cg-E2f1tm1Meg
Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0005217 | abnormal pancreatic beta cell morphology | "malformation of the cells of the pancreas that secrete insulin" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0005220 | abnormal exocrine pancreas morphology | "malformation of the acinar gland portion of the pancreas that secretes digestive enzymes " [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0005240 | abnormal amacrine cell morphology | "anomalous structure of the interneurons of the retina" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,Rbl1tm1Htr/Rbl1tm1Htr,Tg(Pax6-cre,GFP)2Pgr/? Genetic Background: involves: 129 * C57BL/6 * FVB/N * NMRI
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MP:0005270 | abnormal zygomatic bone morphology | "anomalous structure of the bone that forms the prominence of the cheek" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Tg(ACTB-Edn1)1398Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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MP:0005293 | impaired glucose tolerance | "less than the normal response to oral consumption or intravenous injection of specified amounts of glucose and indicative of insulin resistance; measured by determining whole blood or plasma sugar level in a fasting state before and after taking glucose at specified intervals" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0005498 | hyporesponsive to tactile stimuli | "reduced reflex action normally induced by touch or pain" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,Rb1tm1Tyj/Rb1tm1Tyj,Tg(Rb1)1Blg/0 Genetic Background: involves: 129S2/SvPas * 129S4/SvJae
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MP:0005560 | decreased circulating glucose level | "less than the normal concentration in the blood of this major monosaccharide of the body; it is an important energy source" [RGD:Rat Genome Database submission, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0005587 | abnormal Meckel s cartilage morphology | "structural anomaly of this cartilage bar in the mandibular arch that forms a temporary supporting structure in the embryonic mandible; gives rise to middle ear bones and sphenomandibular and anterior malleolar ligaments" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:17694] |
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Allelic Composition: Tg(ACTB-Edn1)721Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
Allelic Composition: Tg(ACTB-Edn1)1416Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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MP:0005668 | decreased circulating leptin level | "less than the normal blood concentration of the peptide hormone secreted by white adipocytes and believed to regulate food intake and energy balance" [MeSH:National Library of Medicine - Medical Subject Headings, 2003, J:34751] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm2.1Gle/E2f3tm2.1Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
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MP:0006043 | decreased apoptosis | "less than normal cell death" [RGD:Rat Genome Database submission, smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Erbb2tm2Mul/Erbb2tm2Mul Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/c
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MP:0006071 | abnormal retinal progenitor morphology | "anomoly in the proliferation or differentiation of the cells that give rise to the various cells of the retina" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:92622:] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,Rbl1tm1Htr/Rbl1tm1Htr,Tg(Pax6-cre,GFP)2Pgr/? Genetic Background: involves: 129 * C57BL/6 * FVB/N * NMRI
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MP:0006073 | abnormal retinal bipolar cell morphology | "anomalous structure of the cells that transmit signals from the photoreceptors to retinal amacrine and ganglion cells" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:92623:] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,Rbl1tm1Htr/Rbl1tm1Htr,Tg(Pax6-cre,GFP)2Pgr/? Genetic Background: involves: 129 * C57BL/6 * FVB/N * NMRI
Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: involves: 129 * C57BL/6 * FVB/N * NMRI
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MP:0006309 | decreased retinal ganglion cell number | "reduced number of ganglion neurons located in the innermost nuclear layer of the retina of that receive visual information from photoreceptors via various intermediate cells such as bipolar cells, amacrine cells, and horizontal cells; axons from these cells form the optic nerve and connect mainly to the lateral geniculate nucleus (LGN) and to the suprachiasmatic nucleus in the brain" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,Rbl1tm1Htr/Rbl1tm1Htr,Tg(Pax6-cre,GFP)2Pgr/? Genetic Background: involves: 129 * C57BL/6 * FVB/N * NMRI
Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: involves: 129 * C57BL/6 * FVB/N * NMRI
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MP:0006382 | abnormal lung epithelium morphology | "any structural anomaly of the epithelial layer of the lung" [MGI:rbabiuk "Randall Babiuk, Mouse Genome Informatics Curator", MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm2.1Gle/E2f3tm2.1Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
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MP:0006395 | abnormal epiphyseal plate morphology | "any structural anomaly of the cartilaginous center of ossification on the bones permitting growth of the bone in both directions during development" [MESH:A02.835.232.251.352] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm2.1Gle/E2f3tm2.1Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
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MP:0008074 | increased CD4-positive T cell number | "greater number of the subset of T lymphocytes that carry the CD4 marker, recognize intravesicular peptides bound to MHC class-II molecules, and turn on antibody production" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Erbb2tm2Mul/Erbb2tm2Mul Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/c
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MP:0008078 | increased CD8-positive T cell number | "greater number of the regulatory subset of T lymphocytes that are involved in MHC class I restricted interactions" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Erbb2tm2Mul/Erbb2tm2Mul Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/c
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MP:0008288 | abnormal adrenal cortex morphology | "any structural anomaly of the thick outer layer of the adrenal gland that produces and secretes steroid hormones such as corticosterone, estrone and aldosterone" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm2.1Gle/E2f3tm2.1Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
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MP:0008301 | adrenal medulla hyperplasia | "overdevelopment or increased size of the inner portion of the adrenal gland that consists mainly of chromaffin cells, usually due to an increase in the number of cells" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd,Rb1tm1Tyj/Rb1+ Genetic Background: either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)
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MP:0008382 | gonial bone hypoplasia | "underdevelopment or reduced size of the investing bone that lies on the surface of the malleus, usually due to reduced cell number" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Tg(ACTB-Edn1)1398Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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MP:0008489 | postnatal slow weight gain | "the weight gain over a span of postnatal developmental time is slower than controls, with or without ever attaining a similar weight to controls as adults" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd,E2f3tm1Lees/E2f3+ Genetic Background: involves: 129S2/SvPas
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MP:0008515 | thin retinal outer nuclear layer | "reduced thickness of the retinal layer that contains the nuclei and cell bodies of rods and cones" [MGI:monikat "Monika Tomczuk, Mouse Genome Informatics Curator"] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,Rbl1tm1Htr/Rbl1tm1Htr,Tg(Pax6-cre,GFP)2Pgr/? Genetic Background: involves: 129 * C57BL/6 * FVB/N * NMRI
Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: involves: 129 * C57BL/6 * FVB/N * NMRI
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MP:0008566 | increased interferon-gamma secretion | "increase in the production or release of the major interferon produced by mitogenically or antigenically stimulated lymphocytes that is involved in immunoregulation" [MESH:D12.644.276.374.440.893] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: NOD.Cg-E2f1tm1Meg
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MP:0008699 | increased interleukin-4 secretion | "increase in the production or release of a soluble factor produced by activated T-cells that induces the expression of MHC class II genes and FC receptors on B-cells and causes their proliferation and differentiation; it also acts on T-cells, mast cells and several other hematopoietic lineage cells" [MESH:D12.644.276.374.465.504] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg Genetic Background: NOD.Cg-E2f1tm1Meg
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MP:0008716 | lung non-small cell carcinoma | "a heterogeneous aggregate of at least three distinct histological types of lung cancer" [MESH:C04.557.470.200.300] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0008770 | decreased survivor rate | "a smaller percentage of organisms than expected survive to adulthood and have a lifespan similar to controls" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,E2f3tm2.1Gle/E2f3tm2.1Gle Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss
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MP:0009109 | decreased pancreas weight | "reduction in the average weight of the organ that secretes pancreatic juice into the duodenum and secretes glucagon and insulin into the bloodstream" [MESH:A03.734, MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0009168 | decreased pancreatic islet number | "reduction in the number of the clusters of hormone-producing cells that are scattered throughout the pancreas" [MA:0000127, MESH:A03.734.414] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0009172 | small pancreatic islets | "decrease in the size of the clusters of hormone-producing cells that are scattered throughout the pancreas" [MA:0000127, MESH:A03.734.414] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0009321 | histiocytic sarcoma | |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0009655 | abnormal secondary palate development | "any anomaly in the formation of the part of the palate that is formed during embryonic development when palatal projections from the inner part of the maxillary processes emerge, extend and elevate into a horizontal position above the tongue" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator", PMID:16942766] |
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Allelic Composition: Foxn1tm3(cre)Nrm/Foxn1+,Gt(ROSA)26Sortm1(Tbx1)Rche/Gt(ROSA)26Sor+ Genetic Background: involves: C57BL/6 * C57BL/6NHsd
Allelic Composition: Hand1tm2Eno/Hand1tm4Abfi,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S6/SvEvTac * C3H * C57BL/6
Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0009796 | abnormal base-excision repair | "any anomaly in the process whereby an altered base is removed by a DNA glycosylase enzyme, followed by excision of the resulting sugar phosphate; the small gap left in the DNA helix is filled in by the sequential action of DNA polymerase and DNA ligase" [GO:0006284] |
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Allelic Composition: Ntn1tm1.2Tek/Ntn1tm1.2Tek Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6 * SJL
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MP:0009887 | abnormal palatal shelf fusion at midline | "any anomaly in the process in which the palatal shelves grow toward the midline and adhere along the medial edge epithelia, forming the midline epithelial seam which disappears in later stages" [PMID:16942766] |
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Allelic Composition: Foxn1tm3(cre)Nrm/Foxn1+,Gt(ROSA)26Sortm1(Tbx1)Rche/Gt(ROSA)26Sor+ Genetic Background: involves: C57BL/6 * C57BL/6NHsd
Allelic Composition: Hand1tm2Eno/Hand1tm4Abfi,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S6/SvEvTac * C3H * C57BL/6
Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
Allelic Composition: Hand1tm4Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0009895 | decreased palatine shelf size | "reduced size of the bony projection of the palatine bone that normally fuses with maxillary shelf to form secondary (hard) palate" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Hand1tm2Eno/Hand1tm4Abfi,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S6/SvEvTac * C3H * C57BL/6
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MP:0009897 | decreased maxillary shelf size | "reduced size of the bony projection of the maxilla that normally fuses with palatine shelf to form secondary (hard) palate" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Hand1tm2Eno/Hand1tm4Abfi,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S6/SvEvTac * C3H * C57BL/6
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MP:0010025 | decreased total body fat amount | "less than the normal total amount of connective tissue composed of fat cells within the entire body" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0010029 | abnormal basicranium morphology | "any structural anomaly of the sloping floor of the cranial cavity that is comprised of parts of the ethmoidal, occipital and sphenoid bones" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0010287 | increased reproductive system tumor incidence | "greater than the expected number of tumors originating in the reproductive system in a given population in a given time period" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0010320 | increased pituitary gland tumor incidence | "greater than the expected number of neoplams in the pituitary gland occurring in a specific population in a given time period" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd,Rb1tm1Tyj/Rb1+ Genetic Background: either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)
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MP:0010326 | malleus hypoplasia | "underdevelopment or reduced size, usually due to a reduced number of cells, of the largest of the three auditory ossicles, which resembles a club or hammer" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Tg(ACTB-Edn1)1416Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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MP:0010940 | abnormal maxillary prominence morphology | |
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Allelic Composition: Foxn1tm3(cre)Nrm/Foxn1+,Gt(ROSA)26Sortm1(Tbx1)Rche/Gt(ROSA)26Sor+ Genetic Background: involves: C57BL/6 * C57BL/6NHsd
Allelic Composition: Hand1tm2Eno/Hand1tm4Abfi,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S6/SvEvTac * C3H * C57BL/6
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MP:0010948 | abnormal double-strand DNA break repair | "any annomaly in the process of repair of double-strand breaks in DNA via homologous and nonhomologous mechanisms to reform a continuous DNA helix" [GO:0006302] |
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Allelic Composition: Ntn1tm1.2Tek/Ntn1tm1.2Tek Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6 * SJL
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MP:0011086 | partial postnatal lethality | "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms anytime between the neonatal period and weaning age (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith] |
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Allelic Composition: E2f1tm1Meg/E2f1tm1Meg,Rb1tm2.1Fad/Rb1tm2.1Fad Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0011088 | partial neonatal lethality | "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms within the neonatal period after birth (Mus: P0)" [MGI:csmith] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd,E2f3tm2Lees/E2f3tm2Lees Genetic Background: involves: 129S2/SvPas * 129S4/SvJae * C57BL/6
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MP:0011091 | complete prenatal lethality | "death of all organisms of a given genotype in a population between fertilization and birth (Mus: approximately E18.5)" [MGI:csmith] |
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Allelic Composition: Muttm1Cpv/Muttm1Cpv Genetic Background: involves: 129S/SvEv * C57BL/6 * FVB/N
Allelic Composition: E2f1tm1Njd/E2f1+,Rb1tm1Tyj/Rb1tm1Tyj Genetic Background: either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)
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MP:0011098 | complete embryonic lethality during organogenesis | "death of all organisms of a given genotype in a population between embryo turning and the completion of organogenesis (Mus: E9 to less than E14)" [MGI:csmith] |
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Allelic Composition: E2f1tm1Njd/E2f1+,E2f3tm1Lees/E2f3tm1Lees Genetic Background: involves: 129S2/SvPas
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MP:0011099 | complete lethality throughout fetal growth and development | "death of all organisms of a given genotype in a population between the completion of organogenesis and birth (Mus: E14 to approximately E18.5)" [MGI:csmith] |
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Allelic Composition: E2f1tm1Njd/E2f1+,E2f3tm1Lees/E2f3tm1Lees Genetic Background: involves: 129S2/SvPas
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MP:0011168 | abnormal fat cell differentiation | "abnormal or arrest of differentiation of fat-storing cells found mostly in the abdominal cavity and subcutaneous tissue of mammals" [CL:0000449, MGI:csmith] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0012431 | increased lymphoma incidence | "greater than the expected number of neoplasms characterized by a proliferation of malignant lymphocytes in lymphoid tissue in a specific population in a given time period" [http://orcid.org/0000-0001-5208-3432, MGI:csmith] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0013440 | abnormal exorbital lacrimal gland morphology | "any structural anomaly of the large exorbital (extra-orbital) lacrimal glands that are located subcutaneously at the anteroventral base of the ear adjacent to the parotid gland" [ISBN:0123813611, MGI:Anna] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0013933 | short Meckel s cartilage | |
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Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0014166 | ectopic cranial bone | "the appearance of an extra bone structure at an atypical location in or near the cranium" [MGI:csmith] |
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Allelic Composition: Tg(ACTB-Edn1)1398Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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MP:0030016 | increased adipocyte glucose uptake | "increased ability of adipocytes to take in glucose" [MGI:anna] |
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Allelic Composition: E2f1tm1Njd/E2f1tm1Njd Genetic Background: involves: 129S2/SvPas * C57BL/6
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MP:0030112 | zygomatic bone hypoplasia | "underdevelopment or reduced size, usually due to a reduced number of cells, of the quadrilateral bone that forms the prominence of the cheek" [MGI:anna] |
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Allelic Composition: Hand1tm3Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
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MP:0030122 | temporal bone squamous part hypoplasia | "underdevelopment or reduced size, usually due to a reduced number of cells, of the anterosuperior portion of the temporal bone that is thin, scale-like, and translucent and forms part of the lateral wall of the cranial vault" [MGI:anna] |
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Allelic Composition: Hand1tm2Eno/Hand1tm4Abfi,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S6/SvEvTac * C3H * C57BL/6
Allelic Composition: Hand1tm4Abfi/Hand1+,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: C3H * C57BL/6
Allelic Composition: Tg(ACTB-Edn1)1398Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
Allelic Composition: Tg(ACTB-Edn1)1416Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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MP:0030124 | middle ear ossicle hypoplasia | "underdevelopment or reduced size of the three bones of the middle ear, usually due to reduced cell number" [MGI:anna] |
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Allelic Composition: Hand1tm2Eno/Hand1tm4Abfi,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S6/SvEvTac * C3H * C57BL/6
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MP:0030300 | upper jaw to lower jaw transformation | "homeotic transformation of upper jaw (maxillary) elements into lower jaw-like (mandibular) structures" [MGI:anna, PMID:25725491] |
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Allelic Composition: Tg(ACTB-Edn1)721Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
Allelic Composition: Tg(ACTB-Edn1)1398Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
Allelic Composition: Tg(ACTB-Edn1)1416Clou/0,E2f1Tg(Wnt1-cre)2Sor/E2f1+ Genetic Background: involves: 129S4/SvJae * C3H * C57BL/6
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