ZNF43
Zinc finger protein 43
Also known as: HTF6, KOX27, ZNF39L1, ZNF43_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P17038
- Gene
- ZNF43
- Ensembl
- ENSG00000198521
- Chromosome
- 19
- Canonical length
- 809 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
OverviewNCBI Gene
This gene belongs to the C2H2-type zinc finger gene family. The zinc finger proteins are involved in gene regulation and development, and are quite conserved throughout evolution. Like this gene product, a third of the zinc finger proteins containing C2H2 fingers also contain the KRAB domain, which has been found to be involved in protein-protein interactions. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
809 residues, UniProt reviewed canonical sequence.
>P17038|ZNF43
1 MGPLTFMDVA IEFCLEEWQC LDIAQQNLYR NVMLENYRNL VFLGIAVSKP DLITCLEQEK
61 EPWEPMRRHE MVAKPPVMCS HFTQDFWPEQ HIKDPFQKAT LRRYKNCEHK NVHLKKDHKS
121 VDECKVHRGG YNGFNQCLPA TQSKIFLFDK CVKAFHKFSN SNRHKISHTE KKLFKCKECG
181 KSFCMLPHLA QHKIIHTRVN FCKCEKCGKA FNCPSIITKH KRINTGEKPY TCEECGKVFN
241 WSSRLTTHKK NYTRYKLYKC EECGKAFNKS SILTTHKIIR TGEKFYKCKE CAKAFNQSSN
301 LTEHKKIHPG EKPYKCEECG KAFNWPSTLT KHKRIHTGEK PYTCEECGKA FNQFSNLTTH
361 KRIHTAEKFY KCTECGEAFS RSSNLTKHKK IHTEKKPYKC EECGKAFKWS SKLTEHKLTH
421 TGEKPYKCEE CGKAFNWPST LTKHNRIHTG EKPYKCEVCG KAFNQFSNLT THKRIHTAEK
481 PYKCEECGKA FSRSSNLTKH KKIHIEKKPY KCEECGKAFK WSSKLTEHKI THTGEKPYKC
541 EECGKAFNHF SILTKHKRIH TGEKPYKCEE CGKAFTQSSN LTTHKKIHTG EKFYKCEECG
601 KAFTQSSNLT THKKIHTGGK PYKCEECGKA FNQFSTLTKH KIIHTEEKPY KCEECGKAFK
661 WSSTLTKHKI IHTGEKPYKC EECGKAFKLS STLSTHKIIH TGEKPYKCEK CGKAFNRSSN
721 LIEHKKIHTG EQPYKCEECG KAFNYSSHLN THKRIHTKEQ PYKCKECGKA FNQYSNLTTH
781 NKIHTGEKLY KPEDVTVILT TPQTFSNIKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF43 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)
- 0.43
- Highest tissue expression
- 10 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 10 nTPM
- ovary: 9.6 nTPM
- thymus: 9.4 nTPM
- testis: 8.2 nTPM
- thyroid gland: 8.2 nTPM
- lymph node: 7.8 nTPM
Single-cell type
- renal connecting tubule cells: 99 nCPM
- neutrophil progenitors: 71 nCPM
- thymocytes: 71 nCPM
- hematopoietic stem cells: 70 nCPM
- megakaryocyte-erythroid progenitors: 66 nCPM
- renal collecting duct principal cells: 63 nCPM
Immune cell
- basophil: 31 nTPM
- naive B-cell: 19 nTPM
- memory B-cell: 19 nTPM
- naive CD4 T-cell: 19 nTPM
- naive CD8 T-cell: 13 nTPM
- memory CD4 T-cell: 12 nTPM
Brain region
- cerebellum: 59 nTPM
- white matter: 51 nTPM
- hypothalamus: 48 nTPM
- cerebral cortex: 46 nTPM
- pons: 45 nTPM
- basal ganglia: 44 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)
- 1.76
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.75
- DepMap mean gene effect
- -0.07
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ZNF43 as an antibody target. Whether an autoantibody or antibody against ZNF43 could matter depends on whether native ZNF43 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF43 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 ZNF43 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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