Variant ID | 16766 |
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Entrez Gene ID | 1272 |
Gene | CNTN1 (GeneCards) |
Location | hg19 12:41222536-41222536
hg38 12:40828734-40828734 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000012.11:g.41222536 G>A (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 | 133851895 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | 0.248 |
CADD Raw score (version 1.3) | 0.295278 (Deleterious) |
FATHMM raw prediction score | 0.17638 (Tolerated) |
Deleterious probability by DeFine | 0.8193 (Deleterious) |
Entrez Gene ID | 1272 (NCBI Gene) |
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Official Gene Symbol | CNTN1 (GeneCards) |
Number of variants in CNTN1 in this database | 6 (view all the variants) |
Full name | contactin 1 |
Band | 12q12 |
Other IDs | Vega: OTTHUMG00000169362 OMIM: 600016 HGNC: HGNC:2171 Ensembl: ENSG00000018236 |
Other names | F3, GP135, MYPCN |
Summary | The protein encoded by this gene is a member of the immunoglobulin superfamily. It is a glycosylphosphatidylinositol (GPI)-anchored neuronal membrane protein that functions as a cell adhesion molecule. It may play a role in the formation of axon connections in the developing nervous system. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011] |
Individual ID | 29217584.14 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217584 |
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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; |