Overview

Variant ID 13310
Entrez Gene ID 3717
Gene JAK2 (GeneCards)
Location hg19 9:5121158-5121158
hg38 9:5121158-5121158
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000009.11:g.5121158 C>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 141213431

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.2351
CADD Raw score (version 1.3) 0.203124 (Deleterious)
FATHMM raw prediction score 0.08896 (Tolerated)
Deleterious probability by DeFine 0.1332 (Neutral)
Entrez Gene ID 3717 (NCBI Gene)
Official Gene Symbol JAK2 (GeneCards)
Number of variants in JAK2 in this database 15 (view all the variants)
Full name Janus kinase 2
Band 9p24.1
Other IDs Vega: OTTHUMG00000019490
OMIM: 147796
HGNC: HGNC:6192
Ensembl: ENSG00000096968
Other names JTK10, THCYT3
Summary This gene product is a protein tyrosine kinase involved in a specific subset of cytokine receptor signaling pathways. It has been found to be constituitively associated with the prolactin receptor and is required for responses to gamma interferon. Mice that do not express an active protein for this gene exhibit embryonic lethality associated with the absence of definitive erythropoiesis. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217584.10 (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;