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

KLHL7
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesKLHL7, KLHL6, SBBI26, kelch like family member 7, CISS3, PERCHING
External IDsOMIM: 611119; MGI: 1196453; HomoloGene: 10317; GeneCards: KLHL7; OMA:KLHL7 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001031710
NM_001172428
NM_018846

NM_001161800
NM_026448

RefSeq (protein)

NP_001026880
NP_001165899
NP_061334

NP_001155272
NP_080724

Location (UCSC)Chr 7: 23.11 – 23.18 MbChr 5: 24.31 – 24.37 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse


References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000122550Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000028986Ensembl, 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. ^ 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.
  6. ^ "Entrez Gene: KLHL7 kelch-like 7 (Drosophila)".

Further reading

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