Gene: CWF19L1

Alternate names for this Gene: C19L1|SCAR17|hDrn1

Gene Summary: This gene encodes a member of the CWF19 protein family. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia-17 and mild cognitive disability. Alternative splicing results in multiple transcript variants.

Gene is located in Chromosome: 10

Location in Chromosome : 10q24.31

Description of this Gene: CWF19 like cell cycle control factor 1

Type of Gene: protein-coding

rs12784396 in CWF19L1 gene and High density lipoprotein measurement PMID 29507422 2018 A large electronic-health-record-based genome-wide study of serum lipids.

rs12784396 in CWF19L1 gene and Serum total cholesterol measurement PMID 29507422 2018 A large electronic-health-record-based genome-wide study of serum lipids.