KRT27

KRT27
Identifiers
Aliases	KRT27, KRT25C, K25IRS3, keratin 27
External IDs	OMIM: 616676; MGI: 1339999; HomoloGene: 7805; GeneCards: KRT27; OMA:KRT27 - orthologs
Gene location (Human)
Chr.	Chromosome 17 (human)
End	40,782,550 bp
Gene location (Mouse)
Chr.	Chromosome 11 (mouse)
End	99,241,930 bp
RNA expression pattern
	Top expressed in
	skin of arm; ; testicle; ; skin of hip; ; skin of leg; ; skin of abdomen; ; nipple; ; right lung; ; right coronary artery; ; mucosa of transverse colon; ; gallbladder;
	Top expressed in
	hair follicle; ; lip; ; lumbar spinal ganglion; ; skin of back; ; skin of abdomen; ; embryo; ; lower jaw; ; Meckel's cartilage; ; skin of external ear; ; sexually immature organism;
	More reference expression data
	n/a
Gene ontology
Molecular function	structural molecule activity; molecular function;
Cellular component	cytoplasm; extracellular exosome; intermediate filament; cytosol;
Biological process	hair follicle morphogenesis; keratinization; cornification; biological process;
	Sources:Amigo / QuickGO
Orthologs
	342574
	16675
	ENSG00000171446
	ENSMUSG00000017588
	Q7Z3Y8
	Q9Z320
	NM_181537
	NM_010666
	NP_853515
	NP_034796
	Wikidata
View/Edit Human	View/Edit Mouse

Keratin, type I cytoskeletal 27 is a keratin belonging to the Type I family of intermediate filament proteins. In humans, in it encoded by a gene with symbol KRT27.