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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Ssr1
signal sequence receptor, alpha
MGI:105082
32 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Ssr1em1(IMPC)Mbp/Ssr1+
C57BL/6N-Ssr1em1(IMPC)Mbp/MbpMmucd
abnormal kidney morphology J:211773
abnormal liver morphology J:211773
abnormal placenta morphology J:211773
abnormal skin morphology J:211773
abnormal testis morphology J:211773
abnormal vitreous body morphology J:211773
cataract J:211773
microphthalmia J:211773
persistence of hyaloid vascular system J:211773
small kidney J:211773
small liver J:211773
Ssr1em1(IMPC)Mbp/Ssr1em1(IMPC)Mbp
C57BL/6N-Ssr1em1(IMPC)Mbp/MbpMmucd
abnormal blood vessel morphology J:211773
abnormal placenta morphology J:211773
abnormal placenta size J:211773
abnormal placenta vasculature J:211773
edema J:211773
embryonic growth retardation J:211773
preweaning lethality, complete penetrance J:211773
Ssr1Gt(ble-lacZl)16Brr/Ssr1Gt(ble-lacZl)16Brr
involves: 129S2/SvPas
abnormal cardiac epithelial to mesenchymal transition J:115006
abnormal heart development J:115006
abnormal heart ventricle morphology J:115006
abnormal interventricular septum morphology J:115006
abnormal semilunar valve morphology J:115006
abnormal truncus arteriosus septation J:115006
aorticopulmonary septal defect J:115006
decreased fetal size J:115006
dilated heart left ventricle J:115006
dilated heart right ventricle J:115006
double outlet right ventricle J:115006
edema J:115006
enlarged heart J:115006
failure of conotruncal ridge closure J:115006
neonatal lethality, complete penetrance J:115006
persistent truncus arteriosus J:115006

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory