Fgf20 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fgf20
fibroblast growth factor 20
MGI:1891346

16 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Fgf20^tm1.1Dor/Fgf20^tm1.1Dor involves: 129X1/SvJ * C57BL/6J	abnormal auchene hair morphology	J:193958
	abnormal awl hair morphology	J:193958
	abnormal cochlear hair cell development	J:184501
	abnormal cochlear hair cell morphology	J:184501
	abnormal cochlear inner hair cell morphology	J:184501
	abnormal hair follicle development	J:193958
	abnormal organ of Corti morphology	J:184501
	abnormal pillar cell morphology	J:184501
	abnormal zigzag hair morphology	J:193958
	absent guard hair	J:193958
	deafness	J:184501
	decreased cochlear hair cell number	J:184501
	decreased cochlear outer hair cell number	J:184501
	decreased organ of Corti supporting cell number	J:184501
	normal hearing/vestibular/ear phenotype	J:184501
	increased or absent threshold for auditory brainstem response	J:184501

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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