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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Cyp7b1
cytochrome P450, family 7, subfamily b, polypeptide 1
MGI:104978
12 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Cyp7b1tm1b(EUCOMM)Wtsi/Cyp7b1tm1b(EUCOMM)Wtsi
C57BL/6N-Cyp7b1tm1b(EUCOMM)Wtsi/Bay
decreased total retina thickness J:211773
impaired glucose tolerance J:211773
Cyp7b1tm1Lth/Cyp7b1tm1Lth
involves: 129P2/OlaHsd * C57BL/6
abnormal estrous cycle J:96829
abnormal mammary gland development J:96829
abnormal uterus development J:96829
absent estrous cycle J:96829
early sexual maturation J:96829
premature ovarian failure J:96829
uterus atrophy J:96829
Cyp7b1tm1Rus/Cyp7b1tm1Rus
involves: 129S/SvEv * C57BL/6J
abnormal cholesterol homeostasis J:62587, J:62589
decreased IgA level J:170807
normal homeostasis/metabolism phenotype J:62587

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
04/30/2024
MGI 6.23
The Jackson Laboratory