Variant ID | 24938 |
---|---|
Entrez Gene ID | 3667 |
Gene | IRS1 (GeneCards) |
Location | hg19 2:227668049-227668049
hg38 2:226803333-226803333 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000002.11:g.227668049 T>A (Genome Assembly: GRCh37) |
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 | 243199373 |
MAF in gnomAD genome (version 2.0.1) | 0.0909 |
---|---|
SNP ID (dbSNP ID version 137) | rs62190996 |
EIGEN score | -0.64 |
CADD Raw score (version 1.3) | -0.457062 (Deleterious) |
FATHMM raw prediction score | 0.09104 (Tolerated) |
Deleterious probability by DeFine | 0.0557 (Neutral) |
Entrez Gene ID | 3667 (NCBI Gene) |
---|---|
Official Gene Symbol | IRS1 (GeneCards) |
Number of variants in IRS1 in this database | 3 (view all the variants) |
Full name | insulin receptor substrate 1 |
Band | 2q36.3 |
Other IDs | Vega: OTTHUMG00000133179 OMIM: 147545 HGNC: HGNC:6125 Ensembl: ENSG00000169047 |
Other names | HIRS-1 |
Summary | This gene encodes a protein which is phosphorylated by insulin receptor tyrosine kinase. Mutations in this gene are associated with type II diabetes and susceptibility to insulin resistance. [provided by RefSeq, Nov 2009] |
Individual ID | 29217587.03 (view all the variants in this individual) |
---|---|
Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |