Fgf20 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fgf20
fibroblast growth factor 20
MGI:1891346

51 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fgf20^{em1(IMPC)Ccpcz}/Fgf20^{em1(IMPC)Ccpcz} C57BL/6NCrl-Fgf20^{em1(IMPC)Ccpcz}/Ccpcz	abnormal autopod morphology	J:211773
	abnormal bone structure	J:211773
	abnormal digit morphology	J:211773
	abnormal heart morphology	J:211773
	abnormal kidney morphology	J:211773
	abnormal liver morphology	J:211773
	abnormal lymph node morphology	J:211773
	abnormal nail morphology	J:211773
	abnormal seminal vesicle morphology	J:211773
	abnormal skin morphology	J:211773
	abnormal spleen morphology	J:211773
	abnormal startle reflex	J:211773
	abnormal stomach morphology	J:211773
	abnormal thoracic cage shape	J:211773
	abnormal thymus morphology	J:211773
	abnormal tooth morphology	J:211773
	abnormal uterus morphology	J:211773
	abnormal vertebrae morphology	J:211773
	abnormal vertebral arch morphology	J:211773
	cornea opacity	J:211773
	decreased kidney weight	J:211773
	decreased prepulse inhibition	J:211773
	decreased startle reflex	J:211773
	enlarged heart	J:211773
	enlarged lymph nodes	J:211773
	enlarged spleen	J:211773
	enlarged stomach	J:211773
	enlarged thymus	J:211773
	fusion of vertebral arches	J:211773
	increased blood urea nitrogen level	J:211773
	increased circulating cholesterol level	J:211773
	increased circulating HDL cholesterol level	J:211773
	increased circulating total protein level	J:211773
	small kidney	J:211773
	vertebral fusion	J:211773
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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