ZNF649
Zinc finger protein 649
Also known as: FLJ12644, ZN649_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BS31
- Gene
- ZNF649
- Ensembl
- ENSG00000198093
- Chromosome
- 19
- Canonical length
- 505 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
OverviewNCBI Gene
Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of osteoblast differentiation and regulation of transcription by RNA polymerase II. Predicted to act upstream of or within negative regulation of DNA-templated transcription. Located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
505 residues, UniProt reviewed canonical sequence.
>Q9BS31|ZNF649
1 MTKAQESLTL EDVAVDFTWE EWQFLSPAQK DLYRDVMLEN YSNLVSVGYQ AGKPDALTKL
61 EQGEPLWTLE DEIHSPAHPE IEKADDHLQQ PLQNQKILKR TGQRYEHGRT LKSYLGLTNQ
121 SRRYNRKEPA EFNGDGAFLH DNHEQMPTEI EFPESRKPIS TKSQFLKHQQ THNIEKAHEC
181 TDCGKAFLKK SQLTEHKRIH TGKKPHVCSL CGKAFYKKYR LTEHERAHRG EKPHGCSLCG
241 KAFYKRYRLT EHERAHKGEK PYGCSECGKA FPRKSELTEH QRIHTGIKPH QCSECGRAFS
301 RKSLLVVHQR THTGEKPHTC SECGKGFIQK GNLNIHQRTH TGEKPYGCID CGKAFSQKSC
361 LVAHQRYHTG KTPFVCPECG QPCSQKSGLI RHQKIHSGEK PYKCSDCGKA FLTKTMLIVH
421 HRTHTGERPY GCDECEKAYF YMSCLVKHKR IHSREKRGDS VKVENPSTAS HSLSPSEHVQ
481 GKSPVNMVTV AMVAGQCEFA HILHSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF649 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)
- 0.48
- Highest tissue expression
- 20 nTPM
Expression across tissuesHPA
Tissue
- prostate: 20 nTPM
- retina: 12 nTPM
- breast: 9.4 nTPM
- ovary: 9 nTPM
- parathyroid gland: 8.9 nTPM
- placenta: 8.3 nTPM
Single-cell type
- prostatic glandular cells: 20 nCPM
- lactotrophs: 16 nCPM
- oligodendrocytes: 14 nCPM
- corticotrophs: 13 nCPM
- oligodendrocyte progenitor cells: 12 nCPM
- tuft cells: 12 nCPM
Immune cell
- MAIT T-cell: 12 nTPM
- T-reg: 10 nTPM
- naive B-cell: 9.1 nTPM
- eosinophil: 7.7 nTPM
- NK-cell: 7.7 nTPM
- naive CD4 T-cell: 7.4 nTPM
Brain region
- white matter: 50 nTPM
- hypothalamus: 42 nTPM
- cerebellum: 42 nTPM
- medulla oblongata: 40 nTPM
- cerebral cortex: 38 nTPM
- thalamus: 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)
- 0.95
- gnomAD pLI
- 0.07
- gnomAD missense Z
- 1.41
- DepMap mean gene effect
- 0.12
- DepMap dependency class
- none
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
- DNA-binding transcription factor activity
- 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 ZNF649 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 ZNF649 as an antibody target. Whether an autoantibody or antibody against ZNF649 could matter depends on whether native ZNF649 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF649 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 ZNF649 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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