Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
51076
Gene name Gene Name - the full gene name approved by the HGNC.
CutC copper transporter
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CUTC
Synonyms (NCBI Gene) Gene synonyms aliases
CGI-32
Chromosome Chromosome number
10
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10q24.2
Summary Summary of gene provided in NCBI Entrez Gene.
Members of the CUT family of copper transporters are associated with copper homeostasis and are involved in the uptake, storage, delivery, and efflux of copper (Gupta et al., 1995 [PubMed 7635807]; Li et al., 2005 [PubMed 16182249]).[supplied by OMIM, Mar
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT916775 hsa-miR-134 CLIP-seq
MIRT916776 hsa-miR-200b CLIP-seq
MIRT916777 hsa-miR-200c CLIP-seq
MIRT916778 hsa-miR-219-2-3p CLIP-seq
MIRT916779 hsa-miR-2964a-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005507 Function Copper ion binding IBA
GO:0005507 Function Copper ion binding IDA 19878721
GO:0005507 Function Copper ion binding NAS 16182249
GO:0005515 Function Protein binding IPI 25416956, 29748336, 31515488, 32296183, 35271311
GO:0005634 Component Nucleus HDA 21630459
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
610101 24271 ENSG00000119929
Protein
UniProt ID Q9NTM9
Protein name Copper homeostasis protein cutC homolog
Protein function May play a role in copper homeostasis. Can bind one Cu(1+) per subunit.
PDB 3IWP
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03932 CutC 26 227 CutC family Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. {ECO:0000269|PubMed:16182249}.
Sequence
Sequence length 273
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Insomnia Insomnia N/A N/A GWAS