Variant ID | 17135 |
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Entrez Gene ID | 10082 |
Gene | GPC6 (GeneCards) |
Location | hg19 13:94944045-94944045
hg38 13:94291791-94291791 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000013.10:g.94944045 A>T (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 | 115169878 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | 0.0625 |
CADD Raw score (version 1.3) | -0.238222 (Deleterious) |
FATHMM raw prediction score | 0.14367 (Tolerated) |
Deleterious probability by DeFine | 0.7491 (Deleterious) |
Entrez Gene ID | 10082 (NCBI Gene) |
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Official Gene Symbol | GPC6 (GeneCards) |
Number of variants in GPC6 in this database | 15 (view all the variants) |
Full name | glypican 6 |
Band | 13q31.3-q32.1 |
Other IDs | Vega: OTTHUMG00000017205 OMIM: 604404 HGNC: HGNC:4454 Ensembl: ENSG00000183098 |
Other names | OMIMD1 |
Summary | The glypicans comprise a family of glycosylphosphatidylinositol-anchored heparan sulfate proteoglycans, and they have been implicated in the control of cell growth and cell division. The glypican encoded by this gene is a putative cell surface coreceptor for growth factors, extracellular matrix proteins, proteases and anti-proteases. Mutations in this gene are associated with omodysplasia 1. [provided by RefSeq, Nov 2016] |
Individual ID | 29217584.03 (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; |