GeneID: 395


Names

Common Name: LOC107985792-KLHL29 Type: Intergenic Region
Chromosome: 2 (NC_000002.12) Locus: N/A
HUGO Symbol: N/A Full Name: N/A
Exons: N/A Introns: N/A

Description:
LOC107985792 is reported as a protein-coding uncharacterized gene [XM_017005441.1]. KLHL29 (kelch like family member 29) is member of the KLHL family of proteins containing a BTB/POZ domain, a BACK domain and five-to-six Kelch motifs. A variant located in the LOC107985792-KLHL29 intergenic region associated with F-cell levels in sickle cell disease.

Synonyms: N/A

Comments:
N/A

External Links

Publications / Origin

  1. Bhatnagar P, Purvis S, Barron-Casella E, DeBaun MR, Casella JF, Arking DE, Keefer JR, Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients., J. Hum. Genet. , 56(4), 316-23, 2011
Created on 2020-10-06 12:36:53, Last reviewed on 2020-10-06 13:34:39 (Show full history)


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