Variant ID | 16407 |
---|---|
Entrez Gene ID | 23085 |
Gene | ERC1 (GeneCards) |
Location | hg19 12:1423362-1423362
hg38 12:1314196-1314196 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000012.11:g.1423362 C>A (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 | 133851895 |
MAF in gnomAD genome (version 2.0.1) | 0 |
---|---|
EIGEN score | -0.4652 |
CADD Raw score (version 1.3) | -0.470368 (Deleterious) |
FATHMM raw prediction score | 0.08644 (Tolerated) |
Deleterious probability by DeFine | 0.2996 (Neutral) |
Entrez Gene ID | 23085 (NCBI Gene) |
---|---|
Official Gene Symbol | ERC1 (GeneCards) |
Number of variants in ERC1 in this database | 3 (view all the variants) |
Full name | ELKS/RAB6-interacting/CAST family member 1 |
Band | 12p13.33 |
Other IDs | OMIM: 607127 HGNC: HGNC:17072 Ensembl: ENSG00000082805 |
Other names | ELKS, Cast2, ERC-1, RAB6IP2 |
Summary | The protein encoded by this gene is a member of a family of RIM-binding proteins. RIMs are active zone proteins that regulate neurotransmitter release. This gene has been found fused to the receptor-type tyrosine kinase gene RET by gene rearrangement due to the translocation t(10;12)(q11;p13) in thyroid papillary carcinoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014] |
Individual ID | 29217584.09 (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; |