Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
26505
Gene name Gene Name - the full gene name approved by the HGNC.
Cyclin and CBS domain divalent metal cation transport mediator 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CNNM3
Synonyms (NCBI Gene) Gene synonyms aliases
ACDP3, SLC70A3
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q11.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT020730 hsa-miR-155-5p Proteomics 18668040
MIRT027933 hsa-miR-96-5p Sequencing 20371350
MIRT052005 hsa-let-7b-5p CLASH 23622248
MIRT692307 hsa-miR-3156-5p HITS-CLIP 23313552
MIRT692306 hsa-miR-1285-5p HITS-CLIP 23313552
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 16189514, 19060904, 21516116, 25416956, 32296183
GO:0005886 Component Plasma membrane IBA 21873635
GO:0006810 Process Transport IBA 21873635
GO:0006811 Process Ion transport IEA
GO:0016020 Component Membrane HDA 19946888
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
607804 104 ENSG00000168763
Protein
UniProt ID Q8NE01
Protein name Metal transporter CNNM3 (Ancient conserved domain-containing protein 3) (Cyclin-M3)
Protein function Probable metal transporter.
PDB 5K22 , 5K23 , 5K25 , 5TSR , 6DFD , 6MN6 , 6WUR
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00571 CBS 382 446 CBS domain Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed. Expressed at higher level in heart and spleen. {ECO:0000269|PubMed:12657465}.
Sequence
MAAAVAAAGRLGWLFAALCLGNAAGEAAPGPRVLGFCLEEDGAAGAGWVRGGAARDTPDA
TFLLRLFGPGFANSSWSWVAPEGAGCREEAASPAGEWRALLRLRLRAEAVRPHSALLAVR
VEPGGGAAEEAAPPWALGLGAAGLLALAALARGLQLSALALAPAEVQVLRESGSEAERAA
ARRLEPARRWAGCALGALLLLASLAQAALAVLLYRAAGQRAVPAVLGSAGLVFLVGEVVP
AAVSGRWTLALAPRALGLSRLAVLLTLPVALPVGQLLELAARPGRLRERVLELARGGGDP
YSDLSKGVLRCRTVEDVLTPLEDCFMLDASTVLDFGVLASIMQSGHTRIPVYEEERSNIV
DMLYLKDLAFVDPEDCTPLSTITRFYNHPLHFVFNDTKLDAVLEEFKRGKSHLAIVQKVN
NEGEGDPFYEVLGLVTLEDVIEEIIR
SEILDESEDYRDTVVKRKPASLMAPLKRKEEFSL
FKVSDDEYKVTISPQLLLATQRFLSREVDVFSPLRISEKVLLHLLKHPSVNQEVRFDESN
RLATHHYLYQRSQPVDYFILILQGRVEVEIGKEGLKFENGAFTYYGVSALTVPSSVHQSP
VSSLQPIRHDLQPDPGDGTHSSAYCPDYTVRALSDLQLIKVTRLQYLNALLATRAQNLPQ
SPENTDLQVIPGSQTRLLGEKTTTAAGSSHSRPGVPVEGSPGRNPGV
Sequence length 707
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
26198764
Unknown
Disease term Disease name Evidence References Source
Bipolar Disorder Bipolar Disorder GWAS
Associations from Text Mining
Disease Name Relationship Type References
Neoplasms Associate 26371886