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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Cyp4f14
cytochrome P450, family 4, subfamily f, polypeptide 14
MGI:1927669
10 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Cyp4f14tm1b(EUCOMM)Hmgu/Cyp4f14tm1b(EUCOMM)Hmgu
C57BL/6N-Cyp4f14tm1b(EUCOMM)Hmgu/Ieg
abnormal lens morphology J:211773
abnormal retina blood vessel morphology J:211773
abnormal retina morphology J:211773
abnormal retina vasculature morphology J:211773
cataract J:211773
persistence of hyaloid vascular system J:211773
Cyp4f14tm1Rspk/Cyp4f14tm1Rspk
involves: 129S/SvEv * C57BL/6J
abnormal enzyme/coenzyme activity J:188849
abnormal enzyme/coenzyme level J:188849
abnormal feces composition J:188849
abnormal urine homeostasis J:188849

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
11/19/2024
MGI 6.24
The Jackson Laboratory