Variant ID | 9839 |
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Entrez Gene ID | 3617 |
Gene | IMPG1 (GeneCards) |
Location | hg19 6:77950992-77950992
hg38 6:77241275-77241275 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000006.11:g.77950992 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 | 171115067 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.396 |
CADD Raw score (version 1.3) | -0.404897 (Deleterious) |
FATHMM raw prediction score | 0.08089 (Tolerated) |
Deleterious probability by DeFine | 0.2568 (Neutral) |
Entrez Gene ID | 3617 (NCBI Gene) |
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Official Gene Symbol | IMPG1 (GeneCards) |
Number of variants in IMPG1 in this database | 24 (view all the variants) |
Full name | interphotoreceptor matrix proteoglycan 1 |
Band | 6q14.1 |
Other IDs | Vega: OTTHUMG00000015063 OMIM: 602870 HGNC: HGNC:6055 Ensembl: ENSG00000112706 |
Other names | VMD4, GP147, SPACR, IPM150 |
Summary | This gene encodes a protein that is a major component of the retinal interphotoreceptor matrix. The encoded protein is a proteoglycan that is thought to play a role in maintaining viability of photoreceptor cells and in adhesion of the neural retina to the retinal pigment epithelium. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013] |
Individual ID | 29217584.13 (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; |