Variant ID | 25299 |
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Entrez Gene ID | 8618 |
Gene | CADPS (GeneCards) |
Location | hg19 3:62875307-62875307
hg38 3:62889632-62889632 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000003.11:g.62875307 A>C (Genome Assembly: GRCh37) |
Exon or Intron | NA |
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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 | 198022430 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | 0.061 |
CADD Raw score (version 1.3) | -0.205091 (Deleterious) |
FATHMM raw prediction score | 0.21993 (Tolerated) |
Deleterious probability by DeFine | 0.5132 (Deleterious) |
Entrez Gene ID | 8618 (NCBI Gene) |
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Official Gene Symbol | CADPS (GeneCards) |
Number of variants in CADPS in this database | 12 (view all the variants) |
Full name | calcium dependent secretion activator |
Band | 3p14.2 |
Other IDs | Vega: OTTHUMG00000158651 OMIM: 604667 HGNC: HGNC:1426 Ensembl: ENSG00000163618 |
Other names | CAPS, CAPS1, CADPS1, UNC-31 |
Summary | This gene encodes a novel neural/endocrine-specific cytosolic and peripheral membrane protein required for the Ca2+-regulated exocytosis of secretory vesicles. The protein acts at a stage in exocytosis that follows ATP-dependent priming, which involves the essential synthesis of phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2). Alternative splicing has been observed at this locus and three variants, encoding distinct isoforms, are described. [provided by RefSeq, Aug 2008] |
Individual ID | 29217587.03 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |