KRT24

KRT24
Identifiers
Aliases	KRT24, K24, KA24, keratin 24
External IDs	OMIM: 607742; MGI: 1922956; HomoloGene: 10379; GeneCards: KRT24; OMA:KRT24 - orthologs
Gene location (Human)
Chr.	Chromosome 17 (human)
End	40,703,752 bp
Gene location (Mouse)
Chr.	Chromosome 11 (mouse)
End	99,176,088 bp
RNA expression pattern
	Top expressed in
	amniotic fluid; ; gonad; ; tail of epididymis; ; mucosa of pharynx; ; buccal mucosa cell; ; corpus epididymis; ; mucosa of esophagus; ; periodontal fiber; ; nasal epithelium; ; testicle;
	Top expressed in
	skin of external ear; ; lip; ; interventricular septum; ; molar; ; skin of back; ; soleus muscle; ; knee joint; ; triceps brachii muscle; ; ciliary body; ; endothelial cell of lymphatic vessel;
	More reference expression data
	n/a
Gene ontology
Molecular function	structural molecule activity; molecular function;
Cellular component	extracellular exosome; intermediate filament; cytosol;
Biological process	keratinization; cornification; biological process;
	Sources:Amigo / QuickGO
Orthologs
	192666
	75706
	ENSG00000167916
	ENSMUSG00000020913
	Q2M2I5
	A1L317
	NM_019016
	NM_029393
	NP_061889
	NP_083669
	Wikidata
View/Edit Human	View/Edit Mouse

KRT24 is a keratin gene that also influences cellular responses to apoptotic signals. It produces a cytokeratin-like protein of 525 amino acids.^[5]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000167916 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000020913 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Sprecher E, Itin P, Whittock NV, McGrath JA, Meyer R, DiGiovanna JJ, et al. (September 2002). "Refined mapping of Naegeli-Franceschetti- Jadassohn syndrome to a 6 cM interval on chromosome 17q11.2-q21 and investigation of candidate genes". The Journal of Investigative Dermatology. 119 (3): 692–698. doi:10.1046/j.1523-1747.2002.01855.x. PMID 12230514.

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

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000167916 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000020913 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[5] Sprecher E, Itin P, Whittock NV, McGrath JA, Meyer R, DiGiovanna JJ, et al. (September 2002). "Refined mapping of Naegeli-Franceschetti- Jadassohn syndrome to a 6 cM interval on chromosome 17q11.2-q21 and investigation of candidate genes". The Journal of Investigative Dermatology. 119 (3): 692–698. doi:10.1046/j.1523-1747.2002.01855.x. PMID 12230514.

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