Kelch-like protein 7

KLHL7
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	3II7
Identifiers
Aliases	KLHL7, KLHL6, SBBI26, kelch like family member 7, CISS3, PERCHING
External IDs	OMIM: 611119; MGI: 1196453; HomoloGene: 10317; GeneCards: KLHL7; OMA:KLHL7 - orthologs
Gene location (Human)
Chr.	Chromosome 7 (human)
End	23,177,914 bp
Gene location (Mouse)
Chr.	Chromosome 5 (mouse)
End	24,365,790 bp
RNA expression pattern
	Top expressed in
	oocyte; ; secondary oocyte; ; right ventricle; ; sperm; ; ganglionic eminence; ; left testis; ; right testis; ; lateral nuclear group of thalamus; ; ventricular zone; ; myocardium of left ventricle;
	Top expressed in
	ganglionic eminence; ; medial ganglionic eminence; ; ventricular zone; ; superior cervical ganglion; ; islet of Langerhans; ; ventromedial nucleus; ; Epithelium of choroid plexus; ; sternocleidomastoid muscle; ; nucleus accumbens; ; myocardium of ventricle;
	More reference expression data
	; ;
	More reference expression data
Gene ontology
Molecular function	protein binding; protein homodimerization activity; identical protein binding; ubiquitin-protein transferase activity;
Cellular component	plasma membrane; nucleolus; nucleoplasm; nucleus; Cul3-RING ubiquitin ligase complex; cytoplasm; cytosol; perinuclear region of cytoplasm;
Biological process	protein ubiquitination;
	Sources:Amigo / QuickGO
Orthologs
	55975
	52323
	ENSG00000122550
	ENSMUSG00000028986
	Q8IXQ5
	Q8BUL5
	NM_001031710; NM_001172428; NM_018846
	NM_001161800; NM_026448
	NP_001026880; NP_001165899; NP_061334
	NP_001155272; NP_080724
	Wikidata
View/Edit Human	View/Edit Mouse

Kelch-like protein 7 is a protein that in humans is encoded by the KLHL7 gene.^[5]^[6]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000122550 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000028986 – 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.
^ Friedman JS, Ray JW, Waseem N, Johnson K, Brooks MJ, Hugosson T, Breuer D, Branham KE, Krauth DS, Bowne SJ, Sullivan LS, Ponjavic V, Granse L, Khanna R, Trager EH, Gieser LM, Hughbanks-Wheaton D, Cojocaru RI, Ghiasvand NM, Chakarova CF, Abrahamson M, Goring HH, Webster AR, Birch DG, Abecasis GR, Fann Y, Bhattacharya SS, Daiger SP, Heckenlively JR, Andreasson S, Swaroop A (Jun 2009). "Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa". Am J Hum Genet. 84 (6): 792–800. doi:10.1016/j.ajhg.2009.05.007. PMC 2694974. PMID 19520207.
^ "Entrez Gene: KLHL7 kelch-like 7 (Drosophila)".

External links

GeneReviews/NCBI/NIH/UW entry on Retinitis Pigmentosa Overview

This article on a gene on human chromosome 7 is a stub. You can help Wikipedia by expanding it.

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000122550 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000028986 – 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.

[pmid19520207-5] Friedman JS, Ray JW, Waseem N, Johnson K, Brooks MJ, Hugosson T, Breuer D, Branham KE, Krauth DS, Bowne SJ, Sullivan LS, Ponjavic V, Granse L, Khanna R, Trager EH, Gieser LM, Hughbanks-Wheaton D, Cojocaru RI, Ghiasvand NM, Chakarova CF, Abrahamson M, Goring HH, Webster AR, Birch DG, Abecasis GR, Fann Y, Bhattacharya SS, Daiger SP, Heckenlively JR, Andreasson S, Swaroop A (Jun 2009). "Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa". Am J Hum Genet. 84 (6): 792–800. doi:10.1016/j.ajhg.2009.05.007. PMC 2694974. PMID 19520207.

[entrez-6] "Entrez Gene: KLHL7 kelch-like 7 (Drosophila)".

[1]

[2]

[3]

[4]

[5]

[6]

References

Further reading

External links