Variant ID | 26581 |
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Entrez Gene ID | 2131 |
Gene | EXT1 (GeneCards) |
Location | hg19 8:119134332-119134332
hg38 8:118122093-118122093 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000008.10:g.119134332 G>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 | 146364022 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.1762 |
CADD Raw score (version 1.3) | -0.338409 (Deleterious) |
FATHMM raw prediction score | 0.12782 (Tolerated) |
Deleterious probability by DeFine | 0.6514 (Deleterious) |
Entrez Gene ID | 2131 (NCBI Gene) |
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Official Gene Symbol | EXT1 (GeneCards) |
Number of variants in EXT1 in this database | 6 (view all the variants) |
Full name | exostosin glycosyltransferase 1 |
Band | 8q24.11 |
Other IDs | Vega: OTTHUMG00000059718 OMIM: 608177 HGNC: HGNC:3512 Ensembl: ENSG00000182197 |
Other names | EXT, LGS, TTV, LGCR, TRPS2 |
Summary | This gene encodes an endoplasmic reticulum-resident type II transmembrane glycosyltransferase involved in the chain elongation step of heparan sulfate biosynthesis. Mutations in this gene cause the type I form of multiple exostoses. [provided by RefSeq, Jul 2008] |
Individual ID | 29217587.02 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |