KRT39

KRT39
Identifiers
Aliases	KRT39, CK-39, K39, KA35, keratin 39
External IDs	OMIM: 616678; MGI: 3588208; HomoloGene: 19078; GeneCards: KRT39; OMA:KRT39 - orthologs
Gene location (Human)
Chr.	Chromosome 17 (human)
End	40,966,948 bp
Gene location (Mouse)
Chr.	Chromosome 11 (mouse)
End	99,412,164 bp
RNA expression pattern
	Top expressed in
	testicle; ; skin of abdomen; ; gallbladder; ; skin of leg; ; mucosa of transverse colon; ; olfactory zone of nasal mucosa; ; islet of Langerhans; ; placenta; ; duodenum; ; right lung;
	Top expressed in
	lip; ; skin of abdomen; ; skin of back; ; hair follicle; ; tail of embryo; ; dermis; ; skin of external ear; ; spermatid; ; pituitary gland; ; triceps brachii muscle;
	More reference expression data
	n/a
Gene ontology
Molecular function	structural molecule activity;
Cellular component	intermediate filament; cytosol;
Biological process	keratinization; cornification;
	Sources:Amigo / QuickGO
Orthologs
	390792
	237934
	ENSG00000196859; ENSG00000262164
	ENSMUSG00000064165
	Q6A163
	Q6IFX4
	NM_213656
	NM_213730
	NP_998821
	NP_998895
	Wikidata
View/Edit Human	View/Edit Mouse

KRT39 is a keratin gene.^[5] The encoded protein is a type I keratin.

References

This article on a gene on human chromosome 17 is a stub. You can help Wikipedia by expanding it.