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
Number of entries/variants: 1
Publications / Origin
- 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)
Disclaimer: The information on this website is provided as an information resource only
and must not to be used as a substitute for professional diagnosis and treatment.
The ITHANET Portal and IthaGenes are not responsible or liable for any advice, course of treatment,
diagnosis or any other information, services or products that an individual obtains through this website.