Overview

Variant ID 17135
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)

Other information

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 115169878

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
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)
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 #1

Individual ID 29217584.03 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217584

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;