IRX2
Iroquois-class homeodomain protein IRX-2
Also known as: IRX2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BZI1
- Gene
- IRX2
- Ensembl
- ENSG00000170561
- Chromosome
- 5
- Canonical length
- 471 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm,Nucleoli
OverviewNCBI Gene
IRX2 is a member of the Iroquois homeobox gene family. Members of this family appear to play multiple roles during pattern formation of vertebrate embryos.[supplied by OMIM, Apr 2004]
Canonical amino-acid sequenceUniProt
471 residues, UniProt reviewed canonical sequence.
>Q9BZI1|IRX2
1 MSYPQGYLYQ APGSLALYSC PAYGASALAA PRSEELARSA SGSAFSPYPG SAAFTAQAAT
61 GFGSPLQYSA DAAAAAAGFP SYMGAPYDAH TTGMTGAISY HPYGSAAYPY QLNDPAYRKN
121 ATRDATATLK AWLNEHRKNP YPTKGEKIML AIITKMTLTQ VSTWFANARR RLKKENKMTW
181 APRNKSEDED EDEGDATRSK DESPDKAQEG TETSAEDEGI SLHVDSLTDH SCSAESDGEK
241 LPCRAGDPLC ESGSECKDKY DDLEDDEDDD EEGERGLAPP KPVTSSPLTG LEAPLLSPPP
301 EAAPRGGRKT PQGSRTSPGA PPPASKPKLW SLAEIATSDL KQPSLGPGCG PPGLPAAAAP
361 ASTGAPPGGS PYPASPLLGR PLYYTSPFYG NYTNYGNLNA ALQGQGLLRY NSAAAAPGEA
421 LHTAPKAASD AGKAGAHPLE SHYRSPGGGY EPKKDASEGC TVVGGGVQPY LLocalizationUniProt · AlphaFold · HPA
Whether an antibody against IRX2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.69
- Highest tissue expression
- 27 nTPM
Expression across tissuesHPA
Tissue
- salivary gland: 27 nTPM
- skin: 25 nTPM
- breast: 23 nTPM
- lung: 17 nTPM
- kidney: 15 nTPM
- stomach: 14 nTPM
Single-cell type
- breast lactating cells: 798 nCPM
- alveolar cells type 1: 253 nCPM
- breast myoepithelial cells: 216 nCPM
- pancreatic islet cells: 194 nCPM
- gastric chief cells: 174 nCPM
- basal keratinocytes: 155 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- pons: 47 nTPM
- medulla oblongata: 29 nTPM
- midbrain: 17 nTPM
- cerebellum: 10 nTPM
- thalamus: 10 nTPM
- spinal cord: 8.9 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.78
- gnomAD pLI
- 0.02
- gnomAD missense Z
- 0.56
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell development
- negative regulation of transcription by RNA polymerase II
- neuron differentiation
- proximal/distal pattern formation involved in metanephric nephron development
- regulation of transcription by RNA polymerase II
- specification of loop of Henle identity
Molecular functions
- DNA-binding transcription factor activity, RNA polymerase II-specific
- DNA-binding transcription repressor activity, RNA polymerase II-specific
- RNA polymerase II cis-regulatory region sequence-specific DNA binding
- sequence-specific DNA binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads IRX2 as an antibody target. Whether an autoantibody or antibody against IRX2 could matter depends on whether native IRX2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
IRX2 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label IRX2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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