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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Krt17
keratin 17
MGI:96691
12 phenotypes from 1 allele in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Krt17tm1Cou/Krt17tm1Cou
B6.129S2(D2)-Krt1-17tm1Cou
alopecia J:82089
Krt17tm1Cou/Krt17tm1Cou
involves: 129S2/SvPas
normal integument phenotype J:82089
Krt17tm1Cou/Krt17tm1Cou
involves: 129S2/SvPas * C57BL/6 * DBA/2
abnormal hair cycle J:82089
abnormal hair follicle matrix region morphology J:82089
abnormal hair follicle melanin granule morphology J:82089
abnormal hair follicle morphology J:82089
abnormal hair medulla J:82089
abnormal hair shaft morphology J:82089
absent vibrissae J:82089
alopecia J:82089
brittle hair J:82089
hair follicle degeneration J:82089
increased hair follicle apoptosis J:82089

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
06/30/2020
MGI 6.15
The Jackson Laboratory