GSX1
GS homeobox 1
Also known as: Gsh-1, GSH1, GSX1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H4S2
- Gene
- GSX1
- Ensembl
- ENSG00000169840
- Chromosome
- 13
- Canonical length
- 264 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm,Golgi apparatus,Cytosol
OverviewNCBI Gene
Enables sequence-specific double-stranded DNA binding activity. Acts upstream of or within positive regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
264 residues, UniProt reviewed canonical sequence.
>Q9H4S2|GSX1
1 MPRSFLVDSL VLREAGEKKA PEGSPPPLFP YAVPPPHALH GLSPGACHAR KAGLLCVCPL
61 CVTASQLHGP PGPPALPLLK ASFPPFGSQY CHAPLGRQHS AVSPGVAHGP AAAAAAAALY
121 QTSYPLPDPR QFHCISVDSS SNQLPSSKRM RTAFTSTQLL ELEREFASNM YLSRLRRIEI
181 ATYLNLSEKQ VKIWFQNRRV KHKKEGKGSN HRGGGGGGAG GGGSAPQGCK CASLSSAKCS
241 EDDDELPMSP SSSGKDDRDL TVTPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GSX1 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)
- 0.65
- Highest tissue expression
- 2.4 nTPM
Expression across tissuesHPA
Tissue
- hypothalamus: 2.4 nTPM
- basal ganglia: 0.3 nTPM
- cerebral cortex: 0.3 nTPM
- amygdala: 0.2 nTPM
- hippocampal formation: 0.2 nTPM
- midbrain: 0.1 nTPM
Single-cell type
- oligodendrocyte progenitor cells: 0.5 nCPM
- other brain neurons: 0.5 nCPM
- adipocytes: 0 nCPM
- adrenal cortex cells: 0 nCPM
- adrenal medulla cells: 0 nCPM
- alveolar cells type 1: 0 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
- hypothalamus: 16 nTPM
- thalamus: 0.8 nTPM
- basal ganglia: 0.7 nTPM
- medulla oblongata: 0.5 nTPM
- amygdala: 0.4 nTPM
- cerebral cortex: 0.3 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)
- 1.13
- gnomAD pLI
- 0.04
- gnomAD missense Z
- 0.5
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- adenohypophysis development
- brain development
- central nervous system development
- hypothalamus development
- neuron differentiation
- neuron fate commitment
- positive regulation of transcription by RNA polymerase II
- spinal cord association neuron differentiation
- transcription by RNA polymerase II
Molecular functions
- DNA-binding transcription activator activity, RNA polymerase II-specific
- DNA-binding transcription factor activity, RNA polymerase II-specific
- RNA polymerase II cis-regulatory region sequence-specific DNA binding
- sequence-specific DNA binding
- sequence-specific double-stranded DNA binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GSX1 as an antibody target. Whether an autoantibody or antibody against GSX1 could matter depends on whether native GSX1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GSX1 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 GSX1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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