Gene Gene information from NCBI Gene database.
Entrez ID 79877
Gene name Dephospho-CoA kinase domain containing
Gene symbol DCAKD
Synonyms (NCBI Gene)
-
Chromosome 17
Chromosome location 17q21.31
miRNA miRNA information provided by mirtarbase database.
176
miRTarBase ID miRNA Experiments Reference
MIRT018751 hsa-miR-335-5p Microarray 18185580
MIRT024049 hsa-miR-1-3p Proteomics;Microarray 18668037
MIRT607535 hsa-miR-6867-5p HITS-CLIP 24906430
MIRT607534 hsa-miR-574-5p HITS-CLIP 24906430
MIRT526602 hsa-miR-4802-3p PAR-CLIP 22012620
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
11
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0004140 Function Dephospho-CoA kinase activity EXP 11923312
GO:0004140 Function Dephospho-CoA kinase activity IBA
GO:0004140 Function Dephospho-CoA kinase activity IEA
GO:0005524 Function ATP binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8WVC6
Protein name Dephospho-CoA kinase domain-containing protein
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01121 CoaE 2 183 Dephospho-CoA kinase Domain
Sequence
Sequence length 231
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CRANIOFACIAL MICROSOMIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HYPERTENSION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
INSOMNIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Huntington Disease Huntington disease Pubtator 33049985 Associate
★☆☆☆☆
Found in Text Mining only
Parkinson Disease Parkinson disease Pubtator 32066731 Associate
★☆☆☆☆
Found in Text Mining only