| 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: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
| MP:0000049 | abnormal middle ear morphology | "malformation or malfunction of any components of the tympanic cavity or its ossicles" [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: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
| MP:0000088 | short mandible | "reduced length of the lower bony framework of the mouth where the inferior teeth are held" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
| MP:0000098 | abnormal vomer bone morphology | "missing triangular flat bone of the nasal septum" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Gsctm1Pgr/Gsctm1Pgr
Genetic Background: either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
| MP:0000100 | abnormal ethmoidal bone morphology | "defect in the midline facial bone that encloses the nasal cavity" [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: Gsctm1Pgr/Gsctm1Pgr
Genetic Background: either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
| MP:0000107 | abnormal frontal bone morphology | "malformed bone forming the forehead and part of the eye orbit" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:17489] |
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Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
| 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: Gsctm1Pgr/Gsctm1Pgr
Genetic Background: either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
| MP:0000150 | abnormal rib morphology | "malformed bones forming the bony wall of the chest" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:50311] |
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Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: B6.129S7-Gsctm1Bhr
Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: 129S7/SvEvBrd-Gsctm1Bhr
|
| MP:0000154 | rib fusion | "appearance of one or more ribs as a single structure" [J:62022, J:62023] |
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Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
Allelic Composition: Gsctm1Pgr/Gsctm1Pgr
Genetic Background: either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
| MP:0000267 | abnormal cardiac development | "aberrant formation or incomplete differentiation of the heart" [MGI:cls, J:53370] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
|
| MP:0000269 | abnormal looping morphogenesis | "atypical bending of the primitive heart tube during early development" [J:27443] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
|
| MP:0000428 | abnormal craniofacial morphology | "anomalous structure or development of the face and/or cranium" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Foxa2tm1Jrt/Foxa2tm1Jrt,Gsctm1Bhr/Gsc+
Genetic Background: involves: 129/Sv * C57BL/6 * CD-1
Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: B6.129S7-Gsctm1Bhr
Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: 129S7/SvEvBrd-Gsctm1Bhr
|
| MP:0000433 | microcephaly | "an abnormally small head" [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: Dkk1tm1Lmgd/Dkk1+,Gsctm2Bhr/Gsctm2Bhr
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
|
| MP:0000454 | abnormal jaw morphology | "malformation of the bony framework of the mouth where the teeth are held" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Foxa2tm1Jrt/Foxa2tm1Jrt,Gsctm1Bhr/Gsc+
Genetic Background: involves: 129/Sv * C57BL/6 * CD-1
|
| 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] |
Show
Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
| 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] |
Show
Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
| 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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| MP:0000480 | increased number of ribs | "greater than normal numbers of the pairs of bony structures that make up the body wall" [MeSH:National Library of Medicine - Medical Subject Headings, 2003] |
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Allelic Composition: Gsctm1Pgr/Gsctm1Pgr
Genetic Background: either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
| MP:0000559 | abnormal femur morphology | "structural anomaly of the long bone of the thigh" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Lpin1fld-2J/Lpin1fld-2J
Genetic Background: C3H/HeJ-Lpin1fld-2J/J
|
| MP:0000956 | reduced spinal cord size | "smaller appearance of the spinal cord" [J:35802] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
|
| 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: Dkk1tm1Lmgd/Dkk1+,Gsctm2Bhr/Gsctm2Bhr
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
|
| MP:0001436 | abnormal suckling behavior | "reduced ability or inability to exert suction by the mouth, or atypical suckling pattern" [J:16461] |
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Allelic Composition: Foxa2tm1Jrt/Foxa2tm1Jrt,Gsctm1Bhr/Gsc+
Genetic Background: involves: 129/Sv * C57BL/6 * CD-1
|
| MP:0001672 | abnormal embryogenesis/ development | "anomaly in the establishment of the characteristic configuration of the embryonic body" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
Allelic Composition: Foxa2tm1Jrt/Foxa2tm1Jrt,Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129/Sv * C57BL/6 * CD-1
Allelic Composition: Foxa2tm1Jrt/Foxa2tm1Jrt,Gsctm1Bhr/Gsc+
Genetic Background: involves: 129/Sv * C57BL/6 * CD-1
Allelic Composition: Dkk1tm1Lmgd/Dkk1+,Gsctm2Bhr/Gsctm2Bhr
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
|
| MP:0001698 | reduced embryo size | "smaller proportions of embryo compared to littermates" [J:61790] |
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Allelic Composition: Foxa2tm1Jrt/Foxa2tm1Jrt,Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129/Sv * C57BL/6 * CD-1
Allelic Composition: Foxa2tm1Jrt/Foxa2tm1Jrt,Gsctm1Bhr/Gsc+
Genetic Background: involves: 129/Sv * C57BL/6 * CD-1
|
| MP:0001704 | abnormal dorsal-ventral axis patterning | "anomaly in the development or formation of the axis that runs from the front to the back surface of the body" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
|
| MP:0001730 | embryonic growth arrest | "the cessation of development beyond a particular stage" [J:17509] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
|
| MP:0001951 | abnormal breathing | "irregular or atypical breathing pattern " [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:17489] |
Show
Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
| 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] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
|
| MP:0002152 | abnormal brain morphology | "anomalous structure of or abnormal development of the brain, one of the two components of the central nervous system and the center of thought and emotion; controls coordination, bodily activities and the interpretation of information from the senses (sight, hearing, smell, etc.)" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, http://cancerweb.ncl.ac.uk] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
|
| MP:0002233 | abnormal nose morphology | "any structural anomaly of the organ that is specialized for smell and is part of the respiratory system " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
| MP:0002234 | abnormal pharynx morphology | "structural anomaly in the passage between the mouth and the posterior nares and the larynx and esophagus" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
|
| MP:0002237 | abnormal nasal cavity morphology | "any structural anomaly of the portion of the respiratory tract that extends from the nares to the pharynx; the nasal cavity is lined with ciliated mucosa" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
| MP:0002238 | abnormal nasal mucosa morphology | "any structural anomaly of the mucous membrane that lines the nasal cavity" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
| MP:0002239 | abnormal nasal septum morphology | "any structural anomaly of the structure that separates the two nasal cavities " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
| MP:0002825 | abnormal notochord | "malformation or absence of the axial fibrocellular cord in embryos around which develops the vertebral primordia" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
|
| 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: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
|
| MP:0002932 | abnormal joint | "defect in the articulation point of two or more bones" [RGD:Rat Genome Database submission, MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Gsctm1Pgr/Gsctm1Pgr
Genetic Background: either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
| MP:0003110 | absent malleal processus brevis | |
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Allelic Composition: Gsctm1Pgr/Gsctm1Pgr,Msx1tm1Rilm/Msx1tm1Rilm
Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ
|
| MP:0003138 | absent tympanic ring | "missing the bony ring at the ear canal to which the tympanic membrane is attached" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator, J:46972] |
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Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
| MP:0003232 | abnormal forebrain development | "anomaly in the formation or patterning of the anterior primitive cerebral vesicle; most rostral of three primary vesicles of the embryonic neural tube" [J:93081, smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
|
| 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] |
Show
Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
| MP:0003425 | abnormal optic vesicle formation | "anomalous formation of the hollow outgrowth from the lateral aspects of the embryonic forebrain from which the retina and optic nerve develop" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:94391] |
Show
Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
|
| MP:0003717 | pallor | "an unnatural paleness to the skin, generally attributable to anemia" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
| MP:0003984 | embryonic growth retardation | "slow or limited development before birth" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
|
| MP:0004234 | abnormal masticatory muscle morphology | "any structural anomaly of any of the muscles responsible for the movement of the jaws during mastication, including the masseter, temporal, and medial and lateral pterygoid muscles" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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| MP:0004448 | abnormal presphenoid bone morphology | "any structural anomaly of the anterior part of the body of the sphenoid bone in front of the basisphenoid; it is usually a separate bone in the young or fetus, but becomes a part of the sphenoid in the adult" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
Show
Allelic Composition: Gsctm1Pgr/Gsctm1Pgr
Genetic Background: either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
| MP:0004450 | presphenoid bone hypoplasia | "underdevelopment or reduced size, usually due to a reduced number of cells, of the anterior part of the body of the sphenoid bone in front of the basisphenoid; it is usually a separate bone in the young or fetus, but becomes a part of the sphenoid in the adult" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
Show
Allelic Composition: Gsctm1Pgr/Gsctm1Pgr
Genetic Background: either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
| MP:0004452 | abnormal pterygoid process morphology | "any structural anomaly of the process projecting downward from either side of the sphenoid bone, in vertebrates divided into two plates, an inner and an outer (sometimes called the lateral and medial); the posterior nares pass through the space, called the pterygoid fossa, between the processes" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
Show
Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
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| MP:0004456 | small pterygoid bone | "reduced size of 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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| MP:0004459 | small alisphenoid bone | "reduced size of either of the broad curved wing like expanses on each side of the sphenoid bone in adults; may exist independently in the young" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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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"] |
Show
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| MP:0004554 | small pharynx | "reduced size/diameter of the passage between the mouth and the posterior nares and the larynx and esophagus" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
|
| 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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| MP:0004615 | cervical vertebral transformation | "homeotic transformation of any cervical vertebrae to adopt the fate of another vertebrae" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Gsctm1Pgr/Gsctm1Pgr
Genetic Background: either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
| MP:0004627 | abnormal trochanter morphology | "any structural anomaly of the bony prominences near the upper extremity of the femur; there are two in human (greater and lesser trochanters) and three in many other mammalian species (greater, lesser and third); these normally serve as attachment points for hip and thigh muscles" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
Show
Allelic Composition: Gsctm1Pgr/Gsctm1Pgr
Genetic Background: either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
| 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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| MP:0004784 | abnormal anterior cardinal vein morphology | "any structural anomaly of the two paired veins draining the cephalic part of the body" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
Show
Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
|
| MP:0004787 | abnormal dorsal aorta morphology | "any structural anomaly of the paired arterial structures of the embryo that supplies each developing somite via efferent segmental arteries; the dorsal aortae articulate with the umbilical arteries, which return mixed blood to the villi of the chorion for reoxygenation" [ISBN:0-914294-08-3 "Gray s Anatomy"] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
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| MP:0004873 | absent turbinates | "absence of the small curved bones that extend horizontally along the lateral wall of the nasal passage" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
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| MP:0005249 | abnormal palatine bone morphology | "structural anomaly of the anteriorly located rigid section of the palate" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
Show
Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
| MP:0005296 | abnormal humerus morphology | "malformation of the bone of the forelimb that articulates with the scapula above and the radius and ulna below" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: Gsctm1Pgr/Gsctm1Pgr
Genetic Background: either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
| 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] |
Show
Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
Allelic Composition: Gsctm1Pgr/Gsctm1Pgr,Msx1tm1Rilm/Msx1tm1Rilm
Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ
|
| MP:0006018 | abnormal tympanic membrane morphology | "any structural alterations in the thin, tense membrane forming the greater part of the lateral wall of the tympanic cavity and separating it from the external acoustic meatus; the tympanic membrane consitutes the boundary between the external and middle ear." [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator, smb:Susan M Bello, Mouse Genome Informatics Curator, J:46639:] |
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| MP:0006019 | absent tympanic membrane | "missing drum membrane that forms the greater part of the lateral wall of the tympanic cavity" [smb:Susan M Bello, Mouse Genome Informatics Curator, anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator] |
Show
Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
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| MP:0006020 | reduced size of tympanic ring | "smaller than average tympanic ring" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator, smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Gsctm1Pgr/Gsctm1Pgr,Msx1tm1Rilm/Msx1tm1Rilm
Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ
|
| MP:0006033 | abnormal external auditory canal | "malformation of the canal that connects the outer and middle ear" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:57313] |
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Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
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| MP:0006294 | absent optic vesicle | "absence of the hollow outgrowth from the lateral aspects of the embryonic forebrain from which the retina and optic nerve develop" [J:94391, MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
|
| MP:0006337 | abnormal first branchial arch morphology | "anomaly in the structure of the first arch which contributes to development of mastication muscles, maxilla, mandible, incus, malleus, Meckel s cartilage, trigeminal nerve, and maxillary artery" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
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| MP:0006338 | abnormal second branchial arch morphology | "anomaly in the structure of the second arch which contributes to the development of the stapes, styloid process, hyoid bone, stylohyoid ligament, muscles of facial expression, stapedius muscle, stylohyoid muscle, and lining of the palatine tonsils" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
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| MP:0006341 | small first branchial arch | "reduced size of the first branchial arch" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
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| MP:0006344 | small second branchial arch | "reduced size of the second branchial arch" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
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| MP:0008148 | abnormal rib-sternum attachment | "any anomaly in the in the normal joining of the ribs to the sternum" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
Allelic Composition: Gsctm1Pgr/Gsctm1Pgr
Genetic Background: either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
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| MP:0008376 | small manubrium | "reduced size of the handle of the malleus" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
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| MP:0008378 | small malleal processus brevis | "reduced size of the projection extending from the base of the manubrium of the malleus which contacts the upper part of the tympanic membrane" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
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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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| MP:0009703 | decreased birth body size | "reduction in average body size at birth compared to controls" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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| MP:0009707 | absent external auditory canal | "absence of the canal that connects the outer and middle ear" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Gsctm1Pgr/Gsctm1Pgr,Msx1tm1Rilm/Msx1tm1Rilm
Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ
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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: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
Allelic Composition: Gsctm1Pgr/Gsctm1Pgr
Genetic Background: either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
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| MP:0010355 | abnormal first branchial arch artery morphology | "any structural anomaly of the vessels formed within the first pair of branchial arches in embryogenesis" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
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| MP:0010549 | absent dorsal mesocardium | "absence of the part of the mesocardium that lies dorsal to the embryonic heart; the dorsal mesocardium gives rise to the transverse sinus of the pericardium in the adult" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
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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: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * 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: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
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| MP:0011732 | decreased somite size | "reduced size of any of the segmental masses along the notochord of the developing embryo" [MGI:smb] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
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| MP:0012069 | abnormal horizontal basal cell morphology | "any structural anomaly of the flat or angular epithelial cell with condensed nuclei and darkly staining cytoplasm containing numerous intermediate filaments inserted into desmosomes contacting surrounding supporting cells, that lie in contact with the basal lamina of olfactory epithelium" [CL:0002184] |
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| MP:0012138 | decreased forebrain size | "size reduction or truncation of the anterior of the three primary divisions of the developing chordate brain or the corresponding part of the adult brain (in vertebrates, includes especially the cerebral hemispheres, the thalamus, and the hypothalamus and especially in higher vertebrates is the main control center for sensory and associative information processing, visceral functions, and voluntary motor functions)" [GO:0048853] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
Allelic Composition: Dkk1tm1Lmgd/Dkk1+,Gsctm2Bhr/Gsc+
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Allelic Composition: Dkk1tm1Lmgd/Dkk1+,Gsctm2Bhr/Gsctm2Bhr
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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| MP:0012263 | decreased hindbrain size | "size reduction or truncation of the part of the brain developed from the posterior of the three primary brain vesicles of the embryonic neural tube from which the metencephalon and myelencephalon are derived" [MGI:anna] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
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| MP:0012703 | decreased embryonic neuroepithelium thickness | "reduced width of the epithelial cell layer that lines the neural tube and develops into the nervous system and into the neural crest cells" [MGI:anna] |
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Allelic Composition: Wnt3atm1Amc/Wnt3atm1Amc
Genetic Background: involves: 129S1/Sv
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| MP:0030059 | absent ethmoturbinates | "absence of the conchae of the ethmoid bone which normally occupy the caudal part of the nasal fossae and form the lateral and superior portions of the turbinate bones in mammals" [MGI:anna] |
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| MP:0030154 | abnormal tympanic cavity morphology | "any structural anomaly of the small, air-filled, mucosa-lined cavity that is located in the petrous portion of the temporal bone and houses the auditory ossicles and intratympanic muscles (tensor tympani and stapedius) as well as the chorda tympani and the tympanic plexus of nerves; it is split into two parts: the tympanic cavity proper (the space directly internal to the tympanic membrane) and the epitympanic recess or attic (the space superior to the tympanic membrane)" [] |
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Allelic Composition: Gsctm1Pgr/Gsctm1Pgr,Msx1tm1Rilm/Msx1tm1Rilm
Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ
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| MP:0030187 | abnormal epitympanic recess morphology | "any structural anomaly of the upper portion of the tympanic cavity located above the tympanic membrane; it contains the head of the malleus and the body of the incus" [https://radiopaedia.org/articles/middle-ear, https://www.drugs.com/dict/epitympanum.html] |
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| MP:0030208 | abnormal intrinsic tongue muscle morphology | "any structural anomaly of any of the four paired muscles that originate and insert within the tongue, running along its length; these muscles alter the shape of the tongue by lengthening and shortening it, curling and uncurling its apex and edges, and flattening and rounding its surface; they include the superior longitudinal muscle, the inferior longitudinal muscle, the vertical muscle, and the transverse muscle" [https://en.wikipedia.org/wiki/Tongue, https://www.imaios.com/en/e-Anatomy/Anatomical-Parts/Muscles-of-tongue, MGI:anna] |
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| MP:0030209 | abnormal extrinsic tongue muscle morphology | "any structural anomaly of any of the four paired muscles that originate outside of and insert into the tongue and act to alter the position of the tongue, allowing for protrusion, retraction, and side-to-side movement; these muscles include the genioglossus, the hyoglossus (often including the chondroglossus), the styloglossus, and the palatoglossus" [https://en.wikipedia.org/wiki/Tongue, https://www.imaios.com/en/e-Anatomy/Anatomical-Parts/Muscles-of-tongue, MGI:anna] |
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Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
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| MP:0030210 | abnormal genioglossus muscle morphology | "any structural anomaly of the paired, fan-shaped extrinsic tongue muscle which forms the majority of the body of the tongue, arises from the mental spine of the mandible and inserts into the hyoid bone and the bottom of the tongue; its action protracts and depresses the tongue" [https://en.wikipedia.org/wiki/Genioglossus, MGI:anna] |
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Allelic Composition: Gsctm1Bhr/Gsctm1Bhr
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
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| MP:0030266 | small vomer bone | "reduced size of the triangular flat bone of the nasal septum" [MGI:anna] |
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Allelic Composition: Gsctm1Pgr/Gsctm1Pgr
Genetic Background: either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
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| MP:0030283 | small mandibular coronoid process | "reduced size of the thin, flattened, triangular eminence that arises from the upper surface of the mandibular ramus (perpendicular portion)" [MGI:anna] |
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| MP:0030305 | small cribriform plate | "reduced size of the sieve-like structure located between the anterior cranial fossa and the nasal cavity; it is a part of the ethmoid bone and supports the olfactory bulb, which lies in the olfactory fossa" [MGI:anna] |
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Allelic Composition: Gsctm1Pgr/Gsctm1Pgr
Genetic Background: either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
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