KLF3
Krueppel-like factor 3
Also known as: BKLF, KLF3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P57682
- Gene
- KLF3
- Ensembl
- ENSG00000109787
- Chromosome
- 4
- Canonical length
- 345 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
345 residues, UniProt reviewed canonical sequence.
>P57682|KLF3
1 MLMFDPVPVK QEAMDPVSVS YPSNYMESMK PNKYGVIYST PLPEKFFQTP EGLSHGIQME
61 PVDLTVNKRS SPPSAGNSPS SLKFPSSHRR ASPGLSMPSS SPPIKKYSPP SPGVQPFGVP
121 LSMPPVMAAA LSRHGIRSPG ILPVIQPVVV QPVPFMYTSH LQQPLMVSLS EEMENSSSSM
181 QVPVIESYEK PISQKKIKIE PGIEPQRTDY YPEEMSPPLM NSVSPPQALL QENHPSVIVQ
241 PGKRPLPVES PDTQRKRRIH RCDYDGCNKV YTKSSHLKAH RRTHTGEKPY KCTWEGCTWK
301 FARSDELTRH FRKHTGIKPF QCPDCDRSFS RSDHLALHRK RHMLVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against KLF3 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)
- 0.64
- Highest tissue expression
- 90 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 90 nTPM
- skin: 59 nTPM
- esophagus: 50 nTPM
- rectum: 45 nTPM
- stomach: 44 nTPM
- colon: 42 nTPM
Single-cell type
- esophageal apical cells: 977 nCPM
- esophageal suprabasal cells: 416 nCPM
- platelets: 344 nCPM
- colonocytes: 338 nCPM
- goblet cells: 324 nCPM
- respiratory secretory cells: 313 nCPM
Immune cell
- eosinophil: 17 nTPM
- neutrophil: 14 nTPM
- non-classical monocyte: 13 nTPM
- basophil: 11 nTPM
- naive CD4 T-cell: 9.7 nTPM
- T-reg: 8.4 nTPM
Brain region
- white matter: 46 nTPM
- medulla oblongata: 44 nTPM
- basal ganglia: 40 nTPM
- midbrain: 40 nTPM
- thalamus: 37 nTPM
- cerebellum: 37 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)
- 0.43
- gnomAD pLI
- 0.83
- gnomAD missense Z
- 1.56
- DepMap mean gene effect
- 0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular response to endothelin
- hemopoiesis
- negative regulation of transcription by RNA polymerase II
- regulation of transcription by RNA polymerase II
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
- sequence-specific double-stranded DNA binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of KLF3 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 KLF3 as an antibody target. Whether an autoantibody or antibody against KLF3 could matter depends on whether native KLF3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KLF3 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 KLF3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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