DCDC2

doublecortin domain containing 2

Associated Studies

Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes

2022 | Karczewski et al.

Phenotype: ME/CFS

Details

HGNC: HGNC:18141
GeneCards: DCDC2
NCBI: 51473
Ensembl: ENSG00000146038
UniProt: Q9UHG0
OMIM: 605755
UCSC: uc003ndx.4
VEGA: OTTHUMG00000016275
ENA: AB032980
Alias Symbols: RU2, KIAA1154, DCDC2A, NPHP19
Previous Symbols: DFNB66
Alias Names: "nephronophthisis 19"
Previous Names: "deafness, autosomal recessive 66"