Overview

Variant ID 8241
Entrez Gene ID 79192
Gene IRX1 (GeneCards)
Location hg19 5:4426041-4426041
hg38 5:4425928-4425928
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000005.9:g.4426041 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 180915260

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0.00003229
EIGEN score -0.3754
CADD Raw score (version 1.3) -0.258294 (Deleterious)
FATHMM raw prediction score 0.09058 (Tolerated)
Deleterious probability by DeFine 0.6165 (Deleterious)
Entrez Gene ID 79192 (NCBI Gene)
Official Gene Symbol IRX1 (GeneCards)
Number of variants in IRX1 in this database 15 (view all the variants)
Full name iroquois homeobox 1
Band 5p15.33
Other IDs Vega: OTTHUMG00000161632
OMIM: 606197
HGNC: HGNC:14358
Ensembl: ENSG00000170549
Other names IRX-5, IRXA1
Summary This gene encodes a member of the Iroquois homeobox protein family. Homeobox genes in this family are involved in pattern formation in the embryo. The gene product has been identified as a tumor suppressor in gastric (PMID: 21602894, 20440264) and head and neck cancers (PMID: 18559491). A pseudogene of this gene is located on chromosome 13. [provided by RefSeq, Dec 2011]

Individual #1

Individual ID 29217584.13 (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;