| Variant ID | 12941 |
|---|---|
| Entrez Gene ID | 169522 |
| Gene | KCNV2 (GeneCards) |
| Location | hg19 9:2792025-2792025
hg38 9:2792025-2792025 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000009.11:g.2792025 C>T (Genome Assembly: GRCh37) |
| Exon or Intron | NA |
|---|---|
| Position in protein | NA |
| Amino acid changes in protein | NA > NA |
| Position in cDNA | NA |
| Changes in cDNA | NA > NA |
| mRNA accession | NA |
| mRNA length | NA |
| Reference length | 141213431 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.2916 |
| CADD Raw score (version 1.3) | 0.074424 (Deleterious) |
| FATHMM raw prediction score | 0.09368 (Tolerated) |
| Deleterious probability by DeFine | 0.0811 (Neutral) |
| Entrez Gene ID | 169522 (NCBI Gene) |
|---|---|
| Official Gene Symbol | KCNV2 (GeneCards) |
| Number of variants in KCNV2 in this database | 2 (view all the variants) |
| Full name | potassium voltage-gated channel modifier subfamily V member 2 |
| Band | 9p24.2 |
| Other IDs | Vega: OTTHUMG00000019449 OMIM: 607604 HGNC: HGNC:19698 Ensembl: ENSG00000168263 |
| Other names | Kv8.2, RCD3B, KV11.1 |
| Summary | Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium voltage-gated channel subfamily V. This member is identified as a 'silent subunit', and it does not form homomultimers, but forms heteromultimers with several other subfamily members. Through obligatory heteromerization, it exerts a function-altering effect on other potassium channel subunits. This protein is strongly expressed in pancreas and has a weaker expression in several other tissues. [provided by RefSeq, Jul 2008] |
| Individual ID | 29217584.03 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217584 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |
| Pubmed ID | 29217584 |
|---|---|
| Title | Aging and neurodegeneration are associated with increased mutations in single human neurons. |
| Journal | Science |
| Publication date | 2018.02 |
| Disease | Cockayne syndrome Xeroderma Pigmentosum |
| Number of cases | Male cases: 3; Female cases: 6; cases of unknown sex: 15; |