Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
26507
Gene name Gene Name - the full gene name approved by the HGNC.
Cyclin and CBS domain divalent metal cation transport mediator 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CNNM1
Synonyms (NCBI Gene) Gene synonyms aliases
ACDP1, CLP-1, SLC70A1
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.
This gene encodes a member of the ancient conserved domain protein family. The encoded protein may bind copper. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT899915 hsa-miR-1237 CLIP-seq
MIRT899916 hsa-miR-1245 CLIP-seq
MIRT899917 hsa-miR-1248 CLIP-seq
MIRT899918 hsa-miR-125a-5p CLIP-seq
MIRT899919 hsa-miR-125b CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 28330616, 32296183
GO:0005886 Component Plasma membrane IBA 21873635
GO:0006810 Process Transport IBA 21873635
GO:0006811 Process Ion transport IEA
GO:0016021 Component Integral component of membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
607802 102 ENSG00000119946
Protein
UniProt ID Q9NRU3
Protein name Metal transporter CNNM1 (Ancient conserved domain-containing protein 1) (Cyclin-M1)
Protein function Probable metal transporter.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01595 DUF21 227 414 Cyclin M transmembrane N-terminal domain Domain
PF00571 CBS 498 562 CBS domain Domain
Tissue specificity TISSUE SPECIFICITY: Restricted to brain and testis. {ECO:0000269|PubMed:12657465}.
Sequence
MAAAAAAAAAVGVRLRDCCSRGAVLLLFFSLSPRPPAAAAWLLGLRPEDTAGGRVSLEGG
TLRAAEGTSFLLRVYFQPGPPATAAPVPSPTLNSGENGTGDWAPRLVFIEEPPGGGGVAP
SAVPTRPPGPQRCREQSDWASDVEVLGPLRPGGVAGSALVQVRVRELRKGEAERGGAGGG
GKLFSLCAWDGRAWHHHGAAGGFLLRVRPRLYGPGGDLLPPAWLRALGALLLLALSALFS
GLRLSLLSLDPVELRVLRNSGSAAEQEQARRVQAVRGRGTHLLCTLLLGQAGANAALAGW
LYTSLPPGFGGTGEDYSEEGIHFPWLPALVCTGAVFLGAEICPYSVCSRHGLAIASHSVC
LTRLLMAAAFPVCYPLGRLLDWALRQEISTFYTREKLLETLRAADPYSDLVKEE
LNIIQG
ALELRTKVVEEVLTPLGDCFMLRSDAVLDFATVSEILRSGYTRIPVYEGDQRHNIVDILF
VKDLAFVDPDDCTPLLTVTRFYNRPLHCVFNDTRLDTVLEEFKKGKSHLAIVQRVNNEGE
GDPFYEVMGIVTLEDIIEEIIK
SEILDETDLYTDNRKKQRVPQRERKRHDFSLFKLSDTE
MRVKISPQLLLATHRFMATEVEPFKSLYLSEKILLRLLKHPNVIQELKFDEKNKKAPEHY
LYQRNRPVDYFVLLLQGKVEVEVGKEGLRFENGAFTYYGVPAIMTTACSDNDVRKVGSLA
GSSVFLNRSPSRCSGLNRSESPNRERSDFGGSNTQLYSSSNNLYMPDYSVHILSDVQFVK
ITRQQYQNALTACHMDSSPQSPDMEAFTDGDSTKAPTTRGTPQTPKDDPAITLLNNRNSL
PCSRSDGLRSPSEVVYLRMEELAFTQEEMTDFEEHSTQQLTLSPAAVPTRAASDSECCNI
NLDTETSPCSSDFEENVGKKLLRTLSGQKRKRSPEGERTSEDNSNLTPLIT
Sequence length 951
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Melanoma melanoma rs121913315, rs121913323, rs137853080, rs137853081, rs121909232, rs121913388, rs104894094, rs104894095, rs104894097, rs104894098, rs104894099, rs104894109, rs137854599, rs11547328, rs104894340
View all (64 more)
16778180
Associations from Text Mining
Disease Name Relationship Type References
Diabetes Mellitus Type 2 Inhibit 25733456
Diabetes Mellitus Type 2 Associate 25733456
Epilepsy Associate 37192718
Glioma Associate 37192718
Infertility Male Associate 36446526
Urofacial syndrome Associate 15498024, 21393841