GeneID: 409
Names
| Common Name: | ZCCHC2-RN7SL705P | Type: | Intergenic Region |
|---|---|---|---|
| Chromosome: | 18 (NC_000018.10) | Locus: | N/A |
| HUGO Symbol: | N/A | Full Name: | N/A |
| Exons: | N/A | Introns: | N/A |
Description:
ZCCHC2 (zinc finger CCHC-type containing 2) is a protein-coding gene. RN7SL705P (RNA, 7SL, cytoplasmic 705, pseudogene) is a pseudogene. A variant located in the ZCCHC2-RN7SL705P intergenic region associated with F-cell levels in sickle cell disease.
Synonyms: N/A
Comments:
N/A
Number of entries/variants: 1
Sequence Viewer
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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 PubMed
Created on 2020-10-15 13:55:15,
Last reviewed on (Show full history)
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