KLF9
Krueppel-like factor 9
Also known as: BTEB1, KLF9_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q13886
- Gene
- KLF9
- Ensembl
- ENSG00000119138
- Chromosome
- 9
- Canonical length
- 244 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm,Plasma membrane,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is a transcription factor that binds to GC box elements located in the promoter. Binding of the encoded protein to a single GC box inhibits mRNA expression while binding to tandemly repeated GC box elements activates transcription. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
244 residues, UniProt reviewed canonical sequence.
>Q13886|KLF9
1 MSAAAYMDFV AAQCLVSISN RAAVPEHGVA PDAERLRLPE REVTKEHGDP GDTWKDYCTL
61 VTIAKSLLDL NKYRPIQTPS VCSDSLESPD EDMGSDSDVT TESGSSPSHS PEERQDPGSA
121 PSPLSLLHPG VAAKGKHASE KRHKCPYSGC GKVYGKSSHL KAHYRVHTGE RPFPCTWPDC
181 LKKFSRSDEL TRHYRTHTGE KQFRCPLCEK RFMRSDHLTK HARRHTEFHP SMIKRSKKAL
241 ANALLocalizationUniProt · AlphaFold · HPA
Whether an antibody against KLF9 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)
- 0.53
- Highest tissue expression
- 115 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 115 nTPM
- blood vessel: 101 nTPM
- tongue: 88 nTPM
- liver: 85 nTPM
- adipose tissue: 77 nTPM
- lung: 67 nTPM
Single-cell type
- schwann cells: 580 nCPM
- thymic myoid cells: 479 nCPM
- platelets: 423 nCPM
- pericytes: 367 nCPM
- fibroblasts: 360 nCPM
- vascular smooth muscle cells: 340 nCPM
Immune cell
- memory B-cell: 1 nTPM
- basophil: 0.7 nTPM
- naive CD4 T-cell: 0.7 nTPM
- MAIT T-cell: 0.6 nTPM
- naive B-cell: 0.6 nTPM
- T-reg: 0.6 nTPM
Brain region
- cerebellum: 66 nTPM
- cerebral cortex: 51 nTPM
- thalamus: 51 nTPM
- medulla oblongata: 50 nTPM
- basal ganglia: 50 nTPM
- midbrain: 49 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)
- 0.42
- gnomAD pLI
- 0.89
- gnomAD missense Z
- 2.27
- DepMap mean gene effect
- -0.08
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- circadian rhythm
- negative regulation of keratinocyte proliferation
- regulation of transcription by RNA polymerase II
- cellular response to cortisol stimulus
Molecular functions
- DNA-binding transcription factor activity
- DNA-binding transcription factor activity, RNA polymerase II-specific
- RNA polymerase II cis-regulatory region sequence-specific DNA binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of KLF9 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 KLF9 as an antibody target. Whether an autoantibody or antibody against KLF9 could matter depends on whether native KLF9 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KLF9 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 KLF9 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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