HOXA9
Homeobox protein Hox-A9
Also known as: HOX1, HOX1G, HXA9_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P31269
- Gene
- HOXA9
- Ensembl
- ENSG00000078399
- Chromosome
- 7
- Canonical length
- 272 aa
- Protein class
- Cancer-related genes, Disease related genes, Plasma proteins, Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. This gene is highly similar to the abdominal-B (Abd-B) gene of Drosophila. A specific translocation event which causes a fusion between this gene and the NUP98 gene has been associated with myeloid leukemogenesis. Read-through transcription exists between this gene and the upstream homeobox A10 (HOXA10) gene.[provided by RefSeq, Mar 2011]
Canonical amino-acid sequenceUniProt
272 residues, UniProt reviewed canonical sequence.
>P31269|HOXA9
1 MATTGALGNY YVDSFLLGAD AADELSVGRY APGTLGQPPR QAATLAEHPD FSPCSFQSKA
61 TVFGASWNPV HAAGANAVPA AVYHHHHHHP YVHPQAPVAA AAPDGRYMRS WLEPTPGALS
121 FAGLPSSRPY GIKPEPLSAR RGDCPTLDTH TLSLTDYACG SPPVDREKQP SEGAFSENNA
181 ENESGGDKPP IDPNNPAANW LHARSTRKKR CPYTKHQTLE LEKEFLFNMY LTRDRRYEVA
241 RLLNLTERQV KIWFQNRRMK MKKINKDRAK DELocalizationUniProt · AlphaFold · HPA
Whether an antibody against HOXA9 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)
- 0.66
- Highest tissue expression
- 27 nTPM
Expression across tissuesHPA
Tissue
- kidney: 27 nTPM
- skin: 24 nTPM
- colon: 21 nTPM
- fallopian tube: 20 nTPM
- endometrium: 17 nTPM
- skeletal muscle: 15 nTPM
Single-cell type
- hematopoietic stem cells: 51 nCPM
- prostatic club cells: 38 nCPM
- epididymal principal cells: 37 nCPM
- basal prostatic cells: 36 nCPM
- prostatic hillock cells: 35 nCPM
- podocytes: 30 nCPM
Immune cell
- NK-cell: 12 nTPM
- basophil: 6.7 nTPM
- myeloid DC: 5.6 nTPM
- plasmacytoid DC: 1.8 nTPM
- gdT-cell: 1.3 nTPM
- naive B-cell: 0.9 nTPM
Brain region
- medulla oblongata: 0.5 nTPM
- white matter: 0.5 nTPM
- spinal cord: 0.4 nTPM
- pons: 0.2 nTPM
- amygdala: 0.1 nTPM
- basal ganglia: 0.1 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)
- 1.62
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.06
- DepMap mean gene effect
- -0.15
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- anterior/posterior pattern specification
- definitive hemopoiesis
- DNA-templated transcription
- embryonic forelimb morphogenesis
- embryonic skeletal system morphogenesis
- endothelial cell activation
- male gonad development
- mammary gland development
- negative regulation of myeloid cell differentiation
- prostate gland development
- proximal/distal pattern formation
- regulation of transcription by RNA polymerase II
- response to testosterone
- single fertilization
- spermatogenesis
- uterus development
Molecular functions
- DNA-binding transcription activator activity, RNA polymerase II-specific
- DNA-binding transcription factor activity
- DNA-binding transcription factor activity, RNA polymerase II-specific
- enzyme binding
- RNA polymerase II cis-regulatory region sequence-specific DNA binding
- sequence-specific double-stranded DNA binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of HOXA9 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads HOXA9 as an antibody target. Whether an autoantibody or antibody against HOXA9 could matter depends on whether native HOXA9 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HOXA9 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 HOXA9 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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