KLF17
Krueppel-like factor 17
Also known as: FLJ40160, KLF17_HUMAN, Zfp393, ZNF393
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5JT82
- Gene
- KLF17
- Ensembl
- ENSG00000171872
- Chromosome
- 1
- Canonical length
- 389 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
OverviewNCBI Gene
Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II. Predicted to act upstream of or within gamete generation. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
389 residues, UniProt reviewed canonical sequence.
>Q5JT82|KLF17
1 MYGRPQAEME QEAGELSRWQ AAHQAAQDNE NSAPILNMSS SSGSSGVHTS WNQGLPSIQH
61 FPHSAEMLGS PLVSVEAPGQ NVNEGGPQFS MPLPERGMSY CPQATLTPSR MIYCQRMSPP
121 QQEMTIFSGP QLMPVGEPNI PRVARPFGGN LRMPPNGLPV SASTGIPIMS HTGNPPVPYP
181 GLSTVPSDET LLGPTVPSTE AQAVLPSMAQ MLPPQDAHDL GMPPAESQSL LVLGSQDSLV
241 SQPDSQEGPF LPEQPGPAPQ TVEKNSRPQE GTGRRGSSEA RPYCCNYENC GKAYTKRSHL
301 VSHQRKHTGE RPYSCNWESC SWSFFRSDEL RRHMRVHTRY RPYKCDQCSR EFMRSDHLKQ
361 HQKTHRPGPS DPQANNNNGE QDSPPAAGPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against KLF17 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)
- 0.62
- Highest tissue expression
- 8 nTPM
Expression across tissuesHPA
Tissue
- testis: 8 nTPM
- smooth muscle: 1.1 nTPM
- urinary bladder: 1.1 nTPM
- endometrium: 0.7 nTPM
- adrenal gland: 0.5 nTPM
- esophagus: 0.5 nTPM
Single-cell type
- early spermatids: 249 nCPM
- late spermatids: 62 nCPM
- late primary spermatocytes: 60 nCPM
- smooth muscle cells: 2.8 nCPM
- cardiomyocytes: 1.3 nCPM
- oligodendrocyte progenitor cells: 1 nCPM
Immune cell
- neutrophil: 0.2 nTPM
- basophil: 0.1 nTPM
- eosinophil: 0.1 nTPM
- naive CD4 T-cell: 0.1 nTPM
- T-reg: 0.1 nTPM
- classical monocyte: 0 nTPM
Brain region
- cerebellum: 0.9 nTPM
- thalamus: 0.8 nTPM
- amygdala: 0.7 nTPM
- cerebral cortex: 0.7 nTPM
- white matter: 0.7 nTPM
- basal ganglia: 0.6 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)
- 1.36
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.12
- DepMap mean gene effect
- -0.2
- 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
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
- transcription cis-regulatory region binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads KLF17 as an antibody target. Whether an autoantibody or antibody against KLF17 could matter depends on whether native KLF17 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KLF17 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 KLF17 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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