ZNF544
Zinc finger protein 544
Also known as: AF020591, ZN544_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6NX49
- Gene
- ZNF544
- Ensembl
- ENSG00000198131
- Chromosome
- 19
- Canonical length
- 715 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Predicted to enable DNA binding activity and zinc ion binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
715 residues, UniProt reviewed canonical sequence.
>Q6NX49|ZNF544
1 MEARSMLVPP QASVCFEDVA MAFTQEEWEQ LDLAQRTLYR EVTLETWEHI VSLGLFLSKS
61 DVISQLEQEE DLCRAEQEAP RDWKATLEEN RLNSEKDRAR EELSHHVEVY RSGPEEPPSL
121 VLGKVQDQSN QLREHQENSL RFMVLTSERL FAQREHCELE LGGGYSLPST LSLLPTTLPT
181 STGFPKPNSQ VKELKQNSAF INHEKNGADG KHCESHQCAR AFCQSIYLSK LGNVETGKKN
241 PYEYIVSGDS LNYGSSLCFH GRTFSVKKSD DCKDYGNLFS HSVSLNEQKP VHFGKSQYEC
301 DECRETCSES LCLVQTERSG PGETPFRCEE RCAAFPMASS FSDCNIIQTT EKPSVCNQCG
361 KSFSCCKLIH QRTHTGEKPF ECTQCGKSFS QSYDLVIHQR THTGEKPYEC DLCGKSFTQR
421 SKLITHQRIH TGEKPYQCIE CRKSFRWNSN LIVHQRIHTG EKPYECTHCG KSFSQSYELV
481 THKRTHTGEK PFKCTQCGKS FSQKYDLVVH QRTHTGEKPY ECNLCGKSFS QSSKLITHQR
541 IHTGEKPYQC IECGKSFRWN SNLVIHQRIH TGEKPYDCTH CGKSFSQSYQ LVAHKRTHTG
601 EKPYECNECG KAFNRSTQLI RHLQIHTGEK PYKCNQCNKA FARSSYLVMH QRTHTGEKPF
661 ECSQCGKAFS GSSNLLSHHR IHSGEKPYEC SDCGKSFRQQ SQLVVHRRTH TGEKPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF544 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)
- 0.44
- Highest tissue expression
- 36 nTPM
Expression across tissuesHPA
Tissue
- epididymis: 36 nTPM
- parathyroid gland: 24 nTPM
- fallopian tube: 23 nTPM
- testis: 22 nTPM
- retina: 21 nTPM
- thyroid gland: 19 nTPM
Single-cell type
- late spermatids: 52 nCPM
- late primary spermatocytes: 38 nCPM
- early primary spermatocytes: 26 nCPM
- early spermatids: 26 nCPM
- megakaryocytes: 19 nCPM
- differentiating spermatogonia: 12 nCPM
Immune cell
- NK-cell: 17 nTPM
- eosinophil: 15 nTPM
- naive B-cell: 14 nTPM
- naive CD8 T-cell: 12 nTPM
- memory B-cell: 11 nTPM
- memory CD8 T-cell: 9.5 nTPM
Brain region
- cerebellum: 62 nTPM
- choroid plexus: 62 nTPM
- hippocampal formation: 42 nTPM
- midbrain: 41 nTPM
- medulla oblongata: 40 nTPM
- cerebral cortex: 40 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)
- 1.58
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.72
- DepMap mean gene effect
- 0.02
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% 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 ZNF544 as an antibody target. Whether an autoantibody or antibody against ZNF544 could matter depends on whether native ZNF544 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF544 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 ZNF544 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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