IRX6 (iroquois homeobox 6)

2014-11-01  

Identity

HGNC
LOCATION
16q12.2
LOCUSID
ALIAS
IRX-3,IRX7,IRXB3
FUSION GENES

Other Information

Locus ID:

NCBI: 79190
MIM: 606196
HGNC: 14675
Ensembl: ENSG00000159387

Variants:

dbSNP: 79190
ClinVar: 79190
TCGA: ENSG00000159387
COSMIC: IRX6

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000159387ENST00000290552P78412

Expression (GTEx)

0
5
10
15

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
338910022021A duplication on chromosome 16q12 affecting the IRXB gene cluster is associated with autosomal dominant cone dystrophy with early tritanopic color vision defect.2
338910022021A duplication on chromosome 16q12 affecting the IRXB gene cluster is associated with autosomal dominant cone dystrophy with early tritanopic color vision defect.2
300639272019Single Nucleotide Polymorphisms of HAAO and IRX6 Genes as Risk Factors for Hypospadias.4
300639272019Single 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)