Variant ID | 8241 |
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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) |
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 | 180915260 |
MAF in gnomAD genome (version 2.0.1) | 0.00003229 |
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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) |
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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 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; |