Identity
HGNC
LOCATION
16q12.2
LOCUSID
ALIAS
IRX-3,IRX7,IRXB3
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 79190
MIM: 606196
HGNC: 14675
Ensembl: ENSG00000159387
Variants:
dbSNP: 79190
ClinVar: 79190
TCGA: ENSG00000159387
COSMIC: IRX6
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000159387 | ENST00000290552 | P78412 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 33891002 | 2021 | A duplication on chromosome 16q12 affecting the IRXB gene cluster is associated with autosomal dominant cone dystrophy with early tritanopic color vision defect. | 2 |
| 33891002 | 2021 | A duplication on chromosome 16q12 affecting the IRXB gene cluster is associated with autosomal dominant cone dystrophy with early tritanopic color vision defect. | 2 |
| 30063927 | 2019 | Single Nucleotide Polymorphisms of HAAO and IRX6 Genes as Risk Factors for Hypospadias. | 4 |
| 30063927 | 2019 | Single Nucleotide Polymorphisms of HAAO and IRX6 Genes as Risk Factors for Hypospadias. | 4 |
Citation
Dessen P
IRX6 (iroquois homeobox 6)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/64666/irx6-(iroquois-homeobox-6)
