Cfap97d1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cfap97d1
CFAP97 domain containing 1
MGI:1922687

8 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cfap97d1^em1Osb/Cfap97d1^em1Osb involves: C57BL/6NJcl * DBA/2NJcl	abnormal sperm axoneme morphology	J:294173
	asthenozoospermia	J:294173
	impaired sperm penetration of zona pellucida	J:294173
	reduced male fertility	J:294173
	reproductive system phenotype	J:294173
Cfap97d1^{tm1a(KOMP)Wtsi}/Cfap97d1^{tm1a(KOMP)Wtsi} involves: 129S/SvEv * C57BL/6N	asthenozoospermia	J:294173
	impaired sperm penetration of zona pellucida	J:294173
	reduced male fertility	J:294173
	normal reproductive system phenotype	J:294173
Cfap97d1^{tm1b(KOMP)Wtsi}/Cfap97d1^{tm1b(KOMP)Wtsi} C57BL/6N-Cfap97d1^{tm1b(KOMP)Wtsi}/BayMmucd	abnormal retina blood vessel morphology	J:211773
	decreased prepulse inhibition	J:211773

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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