MP:0000377 | abnormal hair follicle | "malformed invagination of the epidermis from which the hair shaft develops" [J:65031] |
Show
Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA
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MP:0000379 | reduced hair follicle number | "fewer number of the epidermal invaginations from which the hair shaft develops" [J:15108] |
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Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
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MP:0000382 | underdeveloped hair follicles | "arrest of or retarded differentiation of the epidermal invaginations from which the hair shaft develops" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61790] |
Show
Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
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MP:0000414 | alopecia | "absence of hair or loss of hair; not usually in reference to primary genetic hairlessness but may be due to dietary, stress, secondary to immune condition" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:30772, J:33796] |
Show
Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
Allelic Composition: St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA
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MP:0000443 | abnormal snout morphology | "anomalous structure or development of the anterior facial part of the muzzle" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
Show
Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
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MP:0000479 | abnormal intestinal cell | "anomalous structure or development of the cells comprising the intestine" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
Show
Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA
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MP:0000489 | abnormal large intestine morphology | "structural or developmental anomalies of the intestinum crassum " [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA
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MP:0000495 | abnormal colon morphology | "malformation of the portion of the large intestine between the cecum and the rectum" [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: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0 Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)
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MP:0000507 | absent digestive secretion | "missing the production and/or release of a physiologically active substance (usually but not exclusively in liquid form) from a cell or a gland of the digestive system" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, tc:Teresa Chu , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0 Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)
Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA
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MP:0000623 | reduced salivation | "decrease flow, secretion, or amount of saliva" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
Show
Allelic Composition: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0 Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)
Allelic Composition: St14tm3Bug/St14tm3Bug Genetic Background: involves: 129S6/SvEvTac
Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss
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MP:0000764 | abnormal tongue epithelium morphology | "malformation of the epithelial layer of the tongue" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:tc] |
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Allelic Composition: Abca3tm1Holz/Abca3tm1Holz Genetic Background: involves: 129S6/SvEvTac * C57BL/6
Allelic Composition: St14Gt(XM184)Byg/St14Gt(XM184)Byg Genetic Background: involves: 129P2/OlaHsd * 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] |
Show
Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14+ Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: F2rl1tm1Cgh/F2rl1tm1Cgh,Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14+ Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae
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MP:0001190 | reddish skin | "skin has a more intense ruddy appearance than normal, often due to capillary congestion" [J:65038] |
Show
Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14Gt(XM184)Byg/St14Gt(XM184)Byg Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss
Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss
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MP:0001192 | scaly skin | "skin covered with shedding scales or flakes" [J:65146] |
Show
Allelic Composition: St14tm2Bug/St14tm2Bug Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA
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MP:0001196 | shiny skin | "skin with a glossy or glistening appearance" [J:56641] |
Show
Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
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MP:0001211 | wrinkled skin | "irregular folds and/or indentations on the skin" [J:19212] |
Show
Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14Gt(XM184)Byg/St14Gt(XM184)Byg Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss
Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss
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MP:0001216 | abnormal epidermal layer morphology | "anomalous structure or development of the superficial epithelial portion of the skin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: Spint1tm1Bug/Spint1tm1Bug Genetic Background: involves: 129S6/SvEvTac * NIH Black Swiss
Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss
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MP:0001218 | thin epidermis | "reduced thickness of the superficial epithelial portion of the skin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61790] |
Show
Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14Gt(XM184)Byg/St14Gt(XM184)Byg Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss
Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss
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MP:0001219 | thickened epidermis | "increase in the width of the epidermal cell layer in the skin" [J:65146] |
Show
Allelic Composition: St14tm2Bug/St14tm2Bug Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd
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MP:0001239 | abnormal granular layer morphology | "structural or developmental anomaly of the layer of flattened cells containing basophilic granules of keratohyalin and lying just above the stratum spinosum (spiny layer) of the epidermis" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: St14tm2Bug/St14tm2Bug Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd
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MP:0001240 | abnormal cornified layer morphology | "structural or developmental anomaly of the outer layer of the epidermis, consisting of several layers of flat keratinized non-nucleated cells" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
Allelic Composition: St14tm2Bug/St14tm2Bug Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: St14Gt(XM184)Byg/St14Gt(XM184)Byg Genetic Background: involves: 129P2/OlaHsd * Black Swiss
Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14Gt(XM184)Byg/St14Gt(XM184)Byg Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss
Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss
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MP:0001242 | hyperkeratosis | "increased depth of the corneal layer of the epidermis; thickening of the horny layer of the epidermis" [J:1133] |
Show
Allelic Composition: St14tm2Bug/St14tm2Bug Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA
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MP:0001258 | decreased body length | "decreased crown to tail distance compared to controls" [cwg:Carroll W. Goldsmith, Mouse Genome Informatics Curator] |
Show
Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
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MP:0001262 | decreased body weight | "lower than normal average weight " [J:61295] |
Show
Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
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MP:0001263 | weight loss | "progressive reduction of body weight below normal average for age" [J:45400] |
Show
Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA
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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] |
Show
Allelic Composition: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0 Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)
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MP:0001284 | absent vibrissae | "missing whiskers" [J:18378] |
Show
Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14Gt(XM184)Byg/St14Gt(XM184)Byg Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss
Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss
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MP:0001429 | dehydration | "excessive water loss from the body or from an organ or bodily part" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:50053] |
Show
Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
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MP:0001665 | chronic diarrhea | "prolonged diarrhea" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0 Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)
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MP:0001711 | abnormal placenta | |
Show
Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd
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MP:0001716 | abnormal placental labyrinth | "malformed structure where embryonic blood vessels are surrounded by trophoblast cells and maternal blood" [J:23171] |
Show
Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14+ Genetic Background: involves: 129P2/OlaHsd
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MP:0001874 | acanthosis | "diffuse hyperplasia of the spinous layer of the skin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
Show
Allelic Composition: St14tm2Bug/St14tm2Bug Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd
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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] |
Show
Allelic Composition: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0 Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)
Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA
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MP:0002151 | abnormal neural tube morphology/development | "anomalous structure of or development of the embryonic neural tube resulting in structural anomaly" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd
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MP:0002656 | abnormal keratinocyte differentiation | "developmental anomaly of the cells of the epidermis that produce keratin in the process of differentiating into the dead and fully keratinized cells of the stratum corneum
" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: St14tm2Bug/St14tm2Bug Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd
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MP:0002731 | megacolon | "extreme dilation of the colon" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:40722] |
Show
Allelic Composition: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0 Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)
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MP:0002796 | impaired skin barrier function | "impaired ability of the skin to regulate water loss; frequently leads to dehydration" [J:56641] |
Show
Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
Allelic Composition: St14tm2Bug/St14tm2Bug Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: St14Gt(RST485)Byg/St14+ Genetic Background: involves: 129P2/OlaHsd * Black Swiss
Allelic Composition: St14Gt(XM184)Byg/St14+ Genetic Background: involves: 129P2/OlaHsd * Black Swiss
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MP:0002816 | colitis | "local accumulation of fluid, plasma proteins, and leukocytes in the colon region of the large intestine" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
Show
Allelic Composition: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0 Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)
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MP:0003009 | abnormal cytokine secretion | "impairment or increase of the cellular release of any of the non-antibody proteins made by inflammatory leukocytes and some non-leukocytic cells that affect the behavior of other cells " [Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7, smb:Susan M. Bello , Mouse Genome Informatics Curator] |
Show
Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss
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MP:0003051 | curly tail | "a loop or corkscrew-like curl in the tail" [csmith:Cynthia L. Smith, Mouse Genome Informatics Curator] |
Show
Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14+ Genetic Background: involves: 129P2/OlaHsd
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MP:0003054 | spina bifida | "common congenital midline defect of fusion of the vertebral arch" [MeSH:National Library of Medicine - Medical Subject Headings, 2003] |
Show
Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14+ Genetic Background: involves: 129P2/OlaHsd
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MP:0003288 | intestinal edema | "an accumulation of an excessive amount of serous fluid in the intestine or intestinal cells " [ncbi:Matthew Mailman, NCBI request] |
Show
Allelic Composition: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0 Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)
Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA
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MP:0003403 | absent placental labyrinth | "malformed structure where embryonic blood vessels are surrounded by trophoblast cells and maternal blood" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator, J:73417] |
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Allelic Composition: Spint1tm1Bug/Spint1tm1Bug Genetic Background: involves: 129S6/SvEvTac
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MP:0003725 | increased autoantibody level | "elevated level of antibodies to self-antigens present in the sera; often indicative of autoimmune disease" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, acv:Alicia Valenzuela, Genetic Resources Curator] |
Show
Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss
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MP:0003743 | abnormal facial morphology | "anomalous structure or development of the face" [ncbi:Matthew Mailman, NCBI request] |
Show
Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA
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MP:0003756 | abnormal hard palate | "abnormality in the anterior part of the palate that is supported by and includes the palatal extensions of the maxillary and palatine bones " [ncbi:Matthew Mailman, NCBI request] |
Show
Allelic Composition: Abca3tm1Holz/Abca3tm1Holz Genetic Background: involves: 129S6/SvEvTac * C57BL/6
Allelic Composition: St14Gt(XM184)Byg/St14Gt(XM184)Byg Genetic Background: involves: 129P2/OlaHsd * Black Swiss
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MP:0003809 | abnormal hair shaft morphology | "irregular or unusual structure of the cuticle, and/or cortex and/or medulla of a hair" [llw2:Linda Washburn , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
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MP:0003853 | dry skin | "skin characterized by the lack of natural or normal moisture" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator] |
Show
Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14Gt(XM184)Byg/St14Gt(XM184)Byg Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss
Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss
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MP:0004794 | increased anti-nuclear antigen antibody level | "elevated level of antibodies to nuclear antigens present in the sera" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss
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MP:0004842 | abnormal large intestine crypts of Lieberkuhn morphology | "any structural anomaly in the tubular intestinal glands found in the mucosal membranes of the large intestine" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
Show
Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA
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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"] |
Show
Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss
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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: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
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MP:0005150 | cachexia | "general weight loss and wasting occurring in the course of chronic disease" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA
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MP:0005310 | abnormal salivary gland physiology | "anomalous function of any of the glands in the mouth that secrete saliva" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: St14tm3Bug/St14tm3Bug Genetic Background: involves: 129S6/SvEvTac
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MP:0008075 | decreased CD4-positive T cell number | "reduced 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: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss
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MP:0008079 | decreased CD8-positive T cell number | "reduction in the 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: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss
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MP:0008722 | abnormal chemokine secretion | "anomaly in the production or cellular release of any of the class of pro-inflammatory cytokines that attract and activate leukocytes" [MESH:D12.644.276.374.200] |
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss
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MP:0008879 | submandibular gland inflammation | "local accumulation of fluid, plasma proteins, and leukocytes in either of the large major salivary glands situated beneath the mandible" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss
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MP:0008880 | lacrimal gland inflammation | "local accumulation of fluid, plasma proteins, and leukocytes in the glands that secrete tears" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss
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MP:0008882 | abnormal enterocyte physiology | "any functional anomaly of the epithelial cells that have an apical plasma membrane folded into microvilli to provide ample surface for the absorption of nutrients from the intestinal lumen" [CL:0000584, MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA
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MP:0008883 | abnormal enterocyte proliferation | "anomaly in the ability of the enterocyte cell population to undergo expansion by cell division" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0 Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)
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MP:0009541 | increased thymocyte apoptosis | "increase in the number of immature T cells located in the thymus that are undergoing programmed cell death" [CL:0000893, MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
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MP:0009546 | absent gastric milk in neonates | "failure of nursing offspring to ingest milk as indicated by stomach content" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
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Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
Allelic Composition: St14Gt(XM184)Byg/St14Gt(XM184)Byg Genetic Background: involves: 129P2/OlaHsd * Black Swiss
Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14Gt(XM184)Byg/St14Gt(XM184)Byg Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss
Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss
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MP:0009595 | enlarged corneocyte envelope | "increased size of the electron-dense layer of highly transglutaminase cross-linked protein that is deposited on the inner surface of the plasma membrane of corneocytes in the outermost layers of the epidermis" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: St14tm2Bug/St14tm2Bug Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd
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MP:0009596 | abnormal stratum corneum lipid matrix formation | "altered lipid composition or intercellular lipid matrix assembly in the stratum corneum, usually resulting in loss of epidermal barrier function; normally, the intercorneocyte lipid matrix consists of a complex lipid mixture of ceramides, cholesterol and long-chain saturated fatty acids that self-assembles into an ordered multilayer structure known as lipid lamellae" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: St14tm2Bug/St14tm2Bug Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd
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MP:0009597 | impaired stratum corneum desquamation | "dysregulated shedding of the outermost layer of corneocytes, affecting the integrity and thickness of the stratum corneum; may result in xerotic and ichthyotic conditions" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: St14tm2Bug/St14tm2Bug Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd
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MP:0009931 | abnormal skin appearance | "skin that looks different from the usual state" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
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Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
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MP:0009932 | skin fibrosis | "invasion of fibrous connective tissue into the skin, often resulting from inflammation or injury" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA
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MP:0010168 | increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number | "a greater number of the CD4-positive, CD25-positive T cell subset which regulates overall immune responses as well as the responses of other T cell subsets through direct cell-cell contact and cytokine release" [ISBN:0781735149] |
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss
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MP:0010169 | decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number | "a reduction in the number of the CD4-positive, CD25-positive T cell subset which regulates overall immune responses as well as the responses of other T cell subsets through direct cell-cell contact and cytokine release" [ISBN:0781735149] |
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss
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MP:0010234 | abnormal vibrissa follicle morphology | "any structural anomaly of one of the tubular invaginations of the epidermis enclosing the hair roots and from which grow the vibrissae located on the muzzle and face of many species" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
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Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
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MP:0010844 | increased effector memory CD4-positive, alpha-beta T cell number | "increased number of CD4-positive, alpha-beta memory T cells with the phenotype CCR7-negative, CD127-positive, CD45RO-positive, and CD25-negative" [CL:0000905, GO_REF:0000031, GOC:add, GOC:pam, GOC:tfm] |
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss
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MP:0010850 | increased effector memory CD8-positive, alpha-beta T cell number | "increased number of CD8-positive, alpha beta memory T cells with the phenotype CCR7-negative, CD127-positive, CD45RO-positive, and CD25-negative" [CL:0000913, GO_REF:0000031, GOC:add, GOC:pam, PMID:20146720] |
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss
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MP:0011085 | complete postnatal lethality | "premature death anytime between the neonatal period and weaning age of all organisms of a given genotype in a population (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith] |
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Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
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MP:0011087 | complete neonatal lethality | "death of all organisms of a given genotype in a population within the neonatal period after birth (Mus: P0)" [MGI:csmith] |
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Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
Allelic Composition: St14Gt(XM184)Byg/St14Gt(XM184)Byg Genetic Background: involves: 129P2/OlaHsd * Black Swiss
Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14Gt(XM184)Byg/St14Gt(XM184)Byg Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss
Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14tm1Bug Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss
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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: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14+ Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac
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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: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14+ Genetic Background: involves: 129P2/OlaHsd
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MP:0011100 | complete preweaning lethality | "death of all organisms of a given genotype in a population between fertilization and weaning age (Mus: approximately 3-4 weeks of age)" [MGI:csmith] |
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Allelic Composition: Rad9atm1.1(KOMP)Wtsi/Rad9atm1.1(KOMP)Wtsi Genetic Background: C57BL/6N-Rad9atm1.1(KOMP)Wtsi/Bay
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MP:0011105 | partial embryonic lethality between implantation and placentation | "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms between the point of implantation and the initiation of placentation (Mus: E4.5 to less than E9)" [MGI:csmith] |
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Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14+ Genetic Background: involves: 129P2/OlaHsd
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MP:0011108 | partial embryonic lethality during organogenesis | "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms between embryo turning and the completion of organogenesis (Mus: E9 to less than E14)" [MGI:csmith] |
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Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14+ Genetic Background: involves: 129P2/OlaHsd
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MP:0020220 | decreased tear production | "decreased production of the amount of fluid produced in the eye" [GOC:NV] |
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0 Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss
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MP:0030570 | abnormal piliary canal morphology | "any structural anomaly of the tubular connection that is found between the epidermal surface and the most distal part of the hair follicle inner root sheath and contains the hair shaft" [PMID:19211055, UBERON:0035610] |
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Allelic Composition: Becn1tm1Blev/Becn1+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
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