Kdf1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Kdf1
keratinocyte differentiation factor 1
MGI:1916323

20 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Kdf1^shd/Kdf1^shd involves: C3HeB/FeJ * C57BL/6J	abnormal ear development	J:203995
	abnormal esophageal epithelium morphology	J:203995
	abnormal hindlimb morphology	J:203995
	abnormal keratinocyte differentiation	J:203995
	abnormal nose morphology	J:203995
	abnormal reproductive system morphology	J:203995
	abnormal tail morphology	J:203995
	abnormal tongue epithelium morphology	J:203995
	absent epidermis stratum corneum	J:203995
	cleft palate	J:203995
	impaired skin barrier function	J:203995
	increased keratinocyte proliferation	J:203995
	neonatal lethality, complete penetrance	J:203995
	oral atresia	J:203995
	palatal shelf fusion with tongue or mandible	J:203995
	short forelimb	J:203995
	short limbs	J:203995
	short snout	J:203995
	thick epidermis	J:203995
	tight skin	J:203995
Kdf1^shd/Kdf1^{tm1a(EUCOMM)Wtsi} involves: C3HeB/FeJ * C57BL/6J * C57BL/6N	abnormal keratinocyte differentiation	J:203995
	impaired skin barrier function	J:203995
Kdf1^{tm1a(EUCOMM)Wtsi}/Kdf1^{tm1a(EUCOMM)Wtsi} involves: C57BL/6N	abnormal keratinocyte differentiation	J:203995
	impaired skin barrier function	J:203995

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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