Variant ID | 31366 |
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Entrez Gene ID | 9817 |
Gene | KEAP1 (GeneCards) |
Location | hg19 19:10610316-10610317
hg38 19:10499640-10499641 |
Disease | Asymptomatic |
Method | NGS gene panel |
Mutation(HGVS format) | NC_000019.9:g.10610316 CC>TT (Genome Assembly: hg19) |
Exon or Intron | Exon |
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Position in protein | 132 |
Amino acid changes in protein | V > I |
Position in cDNA | 393 |
Changes in cDNA | G > A |
mRNA accession | NA |
mRNA length | NA |
Reference length | 59128983 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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Deleterious probability by DeFine | 0.9704 (Deleterious) |
Entrez Gene ID | 9817 (NCBI Gene) |
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Official Gene Symbol | KEAP1 (GeneCards) |
Number of variants in KEAP1 in this database | 11 (view all the variants) |
Full name | kelch like ECH associated protein 1 |
Band | 19p13.2 |
Other IDs | Vega: OTTHUMG00000180579 OMIM: 606016 HGNC: HGNC:23177 Ensembl: ENSG00000079999 |
Other names | INrf2, KLHL19 |
Summary | This gene encodes a protein containing KELCH-1 like domains, as well as a BTB/POZ domain. Kelch-like ECH-associated protein 1 interacts with NF-E2-related factor 2 in a redox-sensitive manner and the dissociation of the proteins in the cytoplasm is followed by transportation of NF-E2-related factor 2 to the nucleus. This interaction results in the expression of the catalytic subunit of gamma-glutamylcysteine synthetase. Two alternatively spliced transcript variants encoding the same isoform have been found for this gene. [provided by RefSeq, Jul 2008] |
Individual ID | 25999502.02 (view all the variants in this individual) |
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Pubmed ID | 25999502 |
Whose mosaic mutation | Normal |
Origin of mosaic mutation in patients | de novo |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 25999502 |
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Title | High burden and pervasive positive selection of somatic mutations in normal human skin |
Journal | Science |
Publication date | 2015.05 |
Disease | Asymptomatic |
Number of cases | Male cases: 1; Female cases: 3; |