Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
7781
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 30 member 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC30A3
Synonyms (NCBI Gene) Gene synonyms aliases
ZNT3
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2p23.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT607465 hsa-miR-8485 HITS-CLIP 23824327
MIRT634030 hsa-miR-548aa HITS-CLIP 23824327
MIRT634029 hsa-miR-548ap-3p HITS-CLIP 23824327
MIRT634028 hsa-miR-548t-3p HITS-CLIP 23824327
MIRT607465 hsa-miR-8485 HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005385 Function Zinc ion transmembrane transporter activity IBA 21873635
GO:0005515 Function Protein binding IPI 25416956, 25657003, 26728129, 32296183
GO:0005737 Component Cytoplasm IDA 17349999
GO:0005765 Component Lysosomal membrane IEA
GO:0005768 Component Endosome TAS 8962159
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602878 11014 ENSG00000115194
Protein
UniProt ID Q99726
Protein name Probable proton-coupled zinc antiporter SLC30A3 (Solute carrier family 30 member 3) (Zinc transporter 3) (ZnT-3)
Protein function Probable proton-coupled zinc ion antiporter mediating the import of zinc from cytoplasm into synaptic vesicles and participating to cellular zinc ion homeostasis in the brain. {ECO:0000269|PubMed:17349999, ECO:0000269|PubMed:19521526, ECO:000026
PDB 8XN1
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01545 Cation_efflux 76 293 Cation efflux family Family
Sequence
MEPSPAAGGLETTRLVSPRDRGGAGGSLRLKSLFTEPSEPLPEESKPVEMPFHHCHRDPL
PPPGLTPERLHARRQLYAACAVCFVFMAGEVVGGYLAHSLAIMTDAAHLLADVGSMMGSL
FSLWLSTRPATRTMTFGWHRSETLGALASVVSLWMVTGILLYLAFVRLLHSDYHIEGGAM
LLTASIAVCANLLMAFVLHQAGPPHSHGSRGAEYAPLEEGPEEPLPLGNTSVRAAFVHVL
GDLLQSFGVLAASILIYFKPQYKAADPISTFLFSICALGSTAPTLRDVLRILM
EGTPRNV
GFEPVRDTLLSVPGVRATHELHLWALTLTYHVASAHLAIDSTADPEAVLAEASSRLYSRF
GFSSCTLQVEQYQPEMAQCLRCQEPPQA
Sequence length 388
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Atrial fibrillation Atrial Fibrillation rs120074192, rs121908590, rs121908593, rs121434558, rs587776851, rs387906612, rs387906613, rs387906614, rs387906615, rs199472687, rs199472705, rs199473324, rs587777336, rs587777339, rs587777557
View all (6 more)
27790247
Diabetes Diabetes rs80356611 27790247
Diabetes mellitus Diabetes Mellitus rs587776515, rs61730328, rs606231121, rs606231122, rs79020217, rs77625743, rs78378398, rs606231123, rs1362648752, rs104893649, rs80356624, rs80356616, rs80356625, rs80356611, rs104894237
View all (293 more)
27790247
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
23849395
Unknown
Disease term Disease name Evidence References Source
Coronary heart disease Coronary heart disease 27790247 ClinVar
Heart failure Heart failure 27790247 ClinVar
Alzheimer disease Alzheimer disease GWAS
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Inhibit 22640423
Amyotrophic lateral sclerosis 1 Inhibit 32599739
Depressive Disorder Major Inhibit 27661418
Neoplasms Associate 39596116
Zinc Deficiency Neonatal due to Low Breast Milk Zinc Associate 25657003