Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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55799
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Calcium voltage-gated channel auxiliary subunit alpha2delta 3 |
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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CACNA2D3 |
Synonyms (NCBI Gene)
Gene synonyms aliases
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HSA272268 |
Chromosome
Chromosome number
|
3 |
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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3p21.1-p14.3 |
Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a member of the alpha-2/delta subunit family, a protein in the voltage-dependent calcium channel complex. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization and consist of a complex of alpha-1, a |
UniProt ID |
Q8IZS8
|
Protein name |
Voltage-dependent calcium channel subunit alpha-2/delta-3 (Voltage-gated calcium channel subunit alpha-2/delta-3) [Cleaved into: Voltage-dependent calcium channel subunit alpha-2-3; Voltage-dependent calcium channel subunit delta-3] |
Protein function |
The alpha-2/delta subunit of voltage-dependent calcium channels regulates calcium current density and activation/inactivation kinetics of the calcium channel. Acts as a regulatory subunit for P/Q-type calcium channel (CACNA1A), N-type (CACNA1B), |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF08399
|
VWA_N |
113 → 229 |
VWA N-terminal |
Family |
PF13768
|
VWA_3 |
255 → 419 |
von Willebrand factor type A domain |
Domain |
PF08473
|
VGCC_alpha2 |
643 → 1068 |
Neuronal voltage-dependent calcium channel alpha 2acd |
Family |
|
Tissue specificity |
TISSUE SPECIFICITY: Only detected in brain. Not present in lung, testis, aorta, spleen, jejunum, ventricular muscle and kidney (at protein level). According to PubMed:11687876, it is brain-specific, while according to PubMed:11245980, it is widely express |
Sequence |
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Sequence length |
1091 |
Interactions |
View interactions
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Causal |
Disease term |
Disease name |
dbSNP ID |
References |
Leukemia |
Leukemia, Myelocytic, Acute |
rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 |
27903959 |
Neurodevelopmental disorders |
Neurodevelopmental Disorders |
rs869312846, rs869312840, rs869312848, rs869312849, rs869312845, rs886041956, rs1064795110, rs1555762734, rs1555764992, rs1568512728, rs1568532361, rs1595472741, rs1595472764, rs1595476797, rs1016320330, rs1595127294, rs1600392059 View all (2 more) |
28191889 |
Prostate cancer |
Prostate carcinoma |
rs121909139, rs121909140, rs121909141, rs121909142, rs121909143, rs606231169, rs606231170, rs137852584, rs137852578, rs137852580, rs137852581, rs137852582 |
31095341 |
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Unknown |
Disease term |
Disease name |
Evidence |
References |
Source |
Gout |
Gout |
|
|
GWAS |
Diabetes |
Diabetes |
|
|
GWAS |
Insomnia |
Insomnia |
|
|
GWAS |
Takayasu Arteritis |
Takayasu Arteritis |
|
|
GWAS |
Glioblastoma |
Glioblastoma |
CRISPR screening of E3 ubiquitin ligases reveals Ring Finger Protein 185 as a novel tumor suppressor in glioblastoma repressed by promoter hypermethylation and miR-587 |
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GWAS, CBGDA |
Parkinson disease |
Parkinson disease |
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GWAS |
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