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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Ctsh
cathepsin H
MGI:107285
10 phenotypes from 2 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Ctshtm1b(KOMP)Wtsi/Ctshtm1b(KOMP)Wtsi
C57BL/6N-Ctshtm1b(KOMP)Wtsi/Bay
abnormal retina inner nuclear layer morphology J:211773
abnormal retina outer nuclear layer morphology J:211773
decreased total retina thickness J:211773
increased bone mineral content J:211773
increased bone mineral density J:211773
Ctshtm1Thre/Ctshtm1Thre
B6N.129P2-Ctshtm1Thre
abnormal respiratory system physiology J:178096
decreased surfactant secretion J:178096
normal growth/size/body region phenotype J:178096
normal reproductive system phenotype J:178096
Ctshtm1Thre/Ctshtm1Thre
involves: 129P2/OlaHsd
abnormal eye morphology J:206689

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
04/16/2024
MGI 6.23
The Jackson Laboratory