Gene Gene information from NCBI Gene database.
Entrez ID 414149
Gene name Acyl-CoA binding domain containing 7
Gene symbol ACBD7
Synonyms (NCBI Gene)
bA455B2.2
Chromosome 10
Chromosome location 10p13
miRNA miRNA information provided by mirtarbase database.
618
miRTarBase ID miRNA Experiments Reference
MIRT693651 hsa-miR-34b-3p HITS-CLIP 23313552
MIRT693650 hsa-miR-3123 HITS-CLIP 23313552
MIRT693649 hsa-miR-3929 HITS-CLIP 23313552
MIRT693648 hsa-miR-4419b HITS-CLIP 23313552
MIRT693647 hsa-miR-4478 HITS-CLIP 23313552
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
5
GO ID Ontology Definition Evidence Reference
GO:0000062 Function Fatty-acyl-CoA binding IBA
GO:0000062 Function Fatty-acyl-CoA binding IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0006631 Process Fatty acid metabolic process IBA
GO:0008289 Function Lipid 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.
Q8N6N7
Protein name Acyl-CoA-binding domain-containing protein 7
Protein function Binds medium- and long-chain acyl-CoA esters.
PDB 3EPY
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00887 ACBP 4 84 Acyl CoA binding protein Domain
Sequence
Sequence length 88
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Mitochondrial Fatty Acid Beta-Oxidation
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
OBESITY GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations