ZNF248
Zinc finger protein 248
Also known as: bA162G10.3, ZN248_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8NDW4
- Gene
- ZNF248
- Ensembl
- ENSG00000198105
- Chromosome
- 10
- Canonical length
- 579 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA 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
579 residues, UniProt reviewed canonical sequence.
>Q8NDW4|ZNF248
1 MNKSQEQVSF KDVCVDFTQE EWYLLDPAQK ILYRDVILEN YSNLVSVGYC ITKPEVIFKI
61 EQGEEPWILE KGFPSQCHPE RKWKVDDVLE SSQENEDDHF WELLFHNNKT VSVENGDRGS
121 KTFNLGTDPV SLRNYPYKIC DSCEMNLKNI SGLIISKKNC SRKKPDEFNV CEKLLLDIRH
181 EKIPIGEKSY KYDQKRNAIN YHQDLSQPSF GQSFEYSKNG QGFHDEAAFF TNKRSQIGET
241 VCKYNECGRT FIESLKLNIS QRPHLEMEPY GCSICGKSFC MNLRFGHQRA LTKDNPYEYN
301 EYGEIFCDNS AFIIHQGAYT RKILREYKVS DKTWEKSALL KHQIVHMGGK SYDYNENGSN
361 FSKKSHLTQL RRAHTGEKTF ECGECGKTFW EKSNLTQHQR THTGEKPYEC TECGKAFCQK
421 PHLTNHQRTH TGEKPYECKQ CGKTFCVKSN LTEHQRTHTG EKPYECNACG KSFCHRSALT
481 VHQRTHTGEK PFICNECGKS FCVKSNLIVH QRTHTGEKPY KCNECGKTFC EKSALTKHQR
541 THTGEKPYEC NACGKTFSQR SVLTKHQRIH TRVKALSTSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF248 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)
- 0.53
- Highest tissue expression
- 30 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 30 nTPM
- pituitary gland: 18 nTPM
- colon: 17 nTPM
- retina: 16 nTPM
- cervix: 16 nTPM
- seminal vesicle: 15 nTPM
Single-cell type
- thyrotrophs: 279 nCPM
- lactotrophs: 265 nCPM
- somatotrophs: 245 nCPM
- myonuclei: 212 nCPM
- choroid plexus epithelial cells: 191 nCPM
- retinal amacrine cells: 190 nCPM
Immune cell
- naive CD4 T-cell: 6.1 nTPM
- naive CD8 T-cell: 5.3 nTPM
- naive B-cell: 5.2 nTPM
- MAIT T-cell: 4.5 nTPM
- memory B-cell: 4.2 nTPM
- gdT-cell: 4 nTPM
Brain region
- cerebellum: 54 nTPM
- white matter: 45 nTPM
- cerebral cortex: 44 nTPM
- hypothalamus: 37 nTPM
- basal ganglia: 36 nTPM
- midbrain: 33 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)
- 0.49
- gnomAD pLI
- 0.33
- gnomAD missense Z
- 0.48
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% 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-specific
- RNA polymerase II transcription regulatory region sequence-specific DNA binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ZNF248 as an antibody target. Whether an autoantibody or antibody against ZNF248 could matter depends on whether native ZNF248 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF248 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 ZNF248 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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