Gene Gene information from NCBI Gene database.
Entrez ID 1318
Gene name Solute carrier family 31 member 2
Gene symbol SLC31A2
Synonyms (NCBI Gene)
COPT2CTR2hCTR2
Chromosome 9
Chromosome location 9q32
miRNA miRNA information provided by mirtarbase database.
55
miRTarBase ID miRNA Experiments Reference
MIRT022361 hsa-miR-124-3p Microarray 18668037
MIRT1359900 hsa-miR-4529-5p CLIP-seq
MIRT2106557 hsa-miR-3074-5p CLIP-seq
MIRT2106558 hsa-miR-515-3p CLIP-seq
MIRT2106559 hsa-miR-519e CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
25
GO ID Ontology Definition Evidence Reference
GO:0005375 Function Copper ion transmembrane transporter activity IDA 17617060, 17944601
GO:0005375 Function Copper ion transmembrane transporter activity IEA
GO:0005375 Function Copper ion transmembrane transporter activity TAS 9207117
GO:0005515 Function Protein binding IPI 32296183
GO:0005764 Component Lysosome IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
603088 11017 ENSG00000136867
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O15432
Protein name Protein SLC31A2 (Copper transporter 2) (hCTR2) (Solute carrier family 31 member 2)
Protein function Does not function as a copper(1+) importer in vivo (By similarity). However, in vitro functions as a low-affinity copper(1+) importer (PubMed:17617060, PubMed:17944601). Regulator of SLC31A1 which facilitates the cleavage of the SLC31A1 ecto-dom
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04145 Ctr 1 136 Ctr copper transporter family Family
Tissue specificity TISSUE SPECIFICITY: Ubiquitous with high expression in placenta and heart. {ECO:0000269|PubMed:17944601, ECO:0000269|PubMed:9207117}.
Sequence
Sequence length 143
Interactions View interactions
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
BREAST CARCINOMA 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
Atherosclerosis Atherosclerosis Pubtator 37324184 Associate
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Breast neoplasm Pubtator 38263039 Associate
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 33146201, 38538282 Associate
★☆☆☆☆
Found in Text Mining only
Carcinoma, Ovarian Epithelial Ovarian Epithelial carcinoma BEFREE 21570711
★☆☆☆☆
Found in Text Mining only
Hepatolenticular Degeneration Hepatolenticular Degeneration BEFREE 10425268
★☆☆☆☆
Found in Text Mining only
Hepatolenticular Degeneration Hepatolenticular degeneration Pubtator 35357466 Associate
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of ovary Ovarian cancer BEFREE 21570711
★☆☆☆☆
Found in Text Mining only
Malignant Neoplasms Malignant Neoplasm BEFREE 24522273
★☆☆☆☆
Found in Text Mining only
Medullary carcinoma of thyroid Megalencephaly, Polymicrogyria, Polydactyly, Hydrocephalus Syndrome BEFREE 9510122
★☆☆☆☆
Found in Text Mining only
Multiple Myeloma Multiple myeloma BEFREE 17714780
★☆☆☆☆
Found in Text Mining only