Fam151b Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fam151b
family with sequence similarity 151, member B
MGI:1921192

10 phenotypes from 1 allele in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fam151b^{tm1b(EUCOMM)Hmgu}/Fam151b^{tm1b(EUCOMM)Hmgu} C57BL/6N-Fam151b^{tm1b(EUCOMM)Hmgu}/H	abnormal retina morphology	J:211773
	increased neutrophil cell number	J:211773
Fam151b^{tm1b(EUCOMM)Hmgu}/Fam151b^{tm1b(EUCOMM)Hmgu} involves: C57BL/6J * C57BL/6N * C57BL/6NTac	abnormal retina pigmentation	J:284934
	decreased a-wave amplitude	J:284934
	decreased photoreceptor outer segment number	J:284934
	photoreceptor outer segment degeneration	J:284934
	retina cone cell degeneration	J:284934
	retina rod cell degeneration	J:284934
	short photoreceptor outer segment	J:284934
	normal vision/eye phenotype	J:284934

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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