IRX6 - iroquois homeobox 6 Gene

Also Known as IRX7; IRX-3; IRXB3

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 79190

About IRX6

Cytogenetic location: 16q12.2 Genomic coordinates (GRCh38): 16:55,324,203-55,330,756 (from NCBI)

This gene has 2 transcripts (splice variants), 194 orthologues and 6 paralogues. Biased expression in fat (RPKM 7.9), heart (RPKM 3.1) and 5 other tissues.

Summary

Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific; DNA-binding transcription repressor activity, RNA polymerase II-specific; and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in cell development; neuron differentiation; and regulation of transcription, DNA-templated. Predicted to act upstream of or within detection of visible light; negative regulation of transcription, DNA-templated; and retina morphogenesis in camera-type eye. Predicted to be part of chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

IRX6 Products (1)

mRNA Protein Name
NM_024335.3 NP_077311.2 iroquois-class homeodomain protein IRX-6
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

IRX6 Protein Structure

Homeobox_KN

Homeobox_KN: Homeobox KN domain (164 - 203)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 446 a.a.
Protein Preferred Names Protein Names

iroquois-class homeodomain protein IRX-6

  • homeodomain protein IRXB3

IRX6 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
IRX6 P78412 KRTAP19-7 Homo sapiens Q3SYF9 32296183
Intra
IRX6 P78412 KRTAP19-7 Homo sapiens Q3SYF9 32296183
Intra
IRX6 P78412 KRTAP19-7 Homo sapiens Q3SYF9 32296183
Intra
IRX6 P78412 NFKBID Homo sapiens Q8NI38 32296183
Intra
IRX6 P78412 NFKBID Homo sapiens Q8NI38 32296183
Intra
IRX6 P78412 NFKBID Homo sapiens Q8NI38 32296183
Intra
IRX6 P78412 TLE5 Homo sapiens Q08117-2 32296183
Intra
IRX6 P78412 TLE5 Homo sapiens Q08117-2 32296183
Intra
IRX6 P78412 TLE5 Homo sapiens Q08117-2 32296183
Intra
IRX6 P78412 TBX19 Homo sapiens O60806 32296183
Intra
IRX6 P78412 TBX19 Homo sapiens O60806 32296183
Intra
IRX6 P78412 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
IRX6 P78412 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
IRX6 P78412 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
IRX6 P78412 PFDN5 Homo sapiens Q99471 32296183
Intra
IRX6 P78412 PFDN5 Homo sapiens Q99471 32296183
Intra
IRX6 P78412 PFDN5 Homo sapiens Q99471 32296183
Intra
IRX6 P78412 GLRX3 Homo sapiens O76003 32296183
Intra
IRX6 P78412 GLRX3 Homo sapiens O76003 32296183
Intra
IRX6 P78412 TRIB3 Homo sapiens Q96RU7 32296183
Intra
IRX6 P78412 TRIB3 Homo sapiens Q96RU7 32296183
Intra
IRX6 P78412 TRIB3 Homo sapiens Q96RU7 32296183
Intra
IRX6 P78412 MYL2 Homo sapiens P10916 32296183
Intra
IRX6 P78412 MYL2 Homo sapiens P10916 32296183
Intra
IRX6 P78412 HOXA1 Homo sapiens P49639 32296183
Intra
IRX6 P78412 HOXA1 Homo sapiens P49639 32296183
Intra
IRX6 P78412 CRX Homo sapiens O43186 32296183
Intra
IRX6 P78412 CRX Homo sapiens O43186 32296183
Intra
IRX6 P78412 ARID5A Homo sapiens Q03989 32296183
Intra
IRX6 P78412 ARID5A Homo sapiens Q03989 32296183
Intra
IRX6 P78412 ARID5A Homo sapiens Q03989 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Transient Refractive Change
Aniseikonia
Lateral Displacement Of Eye
  • Lateral Displacement Of Globe

Cycloplegia
  • Ciliary Muscle Paresis

  • Cycloplegic Paralysis Of Accommodation

  • Paresis Of Accommodation

  • Visual Accommodation Paralysis

  • Accommodation Paralysis

  • Intrinsic Paralysis Of Eye Muscle

  • Cycloplegic

Brugada Syndrome
  • Sudden Unexpected Nocturnal Death Syndrome

  • Sudden Unexplained Nocturnal Death Syndrome

  • Bangungut

  • Brugada Type Idiopathic Ventricular Fibrillation

  • Pokkuri Death Syndrome

  • Sunds

  • Idiopathic Ventricular Fibrillation, Brugada Type

  • Sudden Unexplained Death

  • Dream Disease

  • Right Bundle Branch Block, St Segment Elevation, And Sudden Death Syndrome

  • Sudden Unexplained Death Syndrome

  • Suds

  • Sunds - [Sudden Unexplained Nocturnal Death Syndrome]

Eye Accommodation Disease
Cone Dystrophy
  • Retinal Cone Dystrophy

  • Dystrophy, Cone

  • Cone Dystrophy 3

Pulmonary Immaturity
  • Primary Atelectasis Of Newborn

  • Primary Atelectasis, In Perinatal Period

  • Primary Failure To Expand Terminal Respiratory Units

  • Immature Lungs

  • Primary Atelectasis

  • Pulmonary Immaturity Nos

  • Lung Lobe Hypoplasia, Associated With Short Gestation

  • Lung Nonexpansion

  • Premature Lungs

  • Pulmonary Hypoplasia Associated With Short Gestation

  • Failure Of Expansion Of Terminal Respiratory Units

  • Primary Atelectasis Of Fetus Or Newborn

  • Primary Atelectasis In Perinatal Period

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris IRX6 VGNC VGNC:42103
Mus musculus IRX6 MGD MGI:1927642
Macaca mulatta IRX6 VGNC VGNC:73598
Rattus norvegicus IRX6 RGD RGD:1564830
Felis catus IRX6 VGNC VGNC:62973
Bos taurus IRX6 VGNC VGNC:30290
Others IRX6 NCBI