ZNF48
Zinc finger protein 48
Also known as: DKFZp762K013, FLJ31751, MGC43952, ZNF48_HUMAN, ZNF553
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96MX3
- Gene
- ZNF48
- Ensembl
- ENSG00000180035
- Chromosome
- 16
- Canonical length
- 618 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Mitochondria
OverviewNCBI Gene
Enables identical protein 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
618 residues, UniProt reviewed canonical sequence.
>Q96MX3|ZNF48
1 MERAVEPWGP DLHRPEEREP QRGARTGLGS ENVISQPNEF EHTPQEDDLG FKEEDLAPDH
61 EVGNASLKPE GIQNWDDLWV QREGLGKPQP RDRGPRLLGE PRWGQASSDR AAVCGECGKS
121 FRQMSDLVKH QRTHTGEKPY KCGVCGKGFG DSSARIKHQR THSGEKPYRA RPPAQGPPKI
181 PRSRIPAGER PTICGECGKS FRQSSDLVKH QRTHTGEKPY KCGICGKGFG DSSARIKHQR
241 THRGEQPPRP VVPRRQPSRA ATAATQGPKA QDKPYICTDC GKRFVLSCSL LSHQRSHLGP
301 KPFGCDVCGK EFARGSDLVK HLRVHTGEKP YLCPECGKGF ADSSARVKHL RTHSGERPHA
361 CPECDRTFSL SSTLLRHRLT HMEPQDFSFP GYPLPALIPS PPPPPLGTSP PLTPRSPSHS
421 GEPFGLPGLE PEPGGPQAGE PPPPLAGDKP HKCPECGKGF RRSSDLVKHH RVHTGEKPYL
481 CPECGKGFAD SSARVKHLRT HRGERARPPP PSTLLRPHNP PGPVPMAPRP RVRAQPSGPS
541 QPHVCGFCGK EFPRSSDLVK HRRTHTGEKP YKCAECGKGF GDSSARIKHQ RGHLVLTPFG
601 IGDGRARPLK QEAATGLELocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF48 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)
- 0.54
- Highest tissue expression
- 8.7 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 8.7 nTPM
- cerebral cortex: 8.6 nTPM
- colon: 7.6 nTPM
- thymus: 7.6 nTPM
- endometrium: 6.9 nTPM
- parathyroid gland: 6.1 nTPM
Single-cell type
- retinal pigment epithelial cells: 21 nCPM
- cardiomyocytes: 18 nCPM
- thymocytes: 17 nCPM
- mast cells: 17 nCPM
- oocytes: 14 nCPM
- smooth muscle cells: 14 nCPM
Immune cell
- gdT-cell: 0.9 nTPM
- NK-cell: 0.9 nTPM
- MAIT T-cell: 0.6 nTPM
- naive CD8 T-cell: 0.6 nTPM
- memory CD8 T-cell: 0.5 nTPM
- naive CD4 T-cell: 0.5 nTPM
Brain region
- cerebral cortex: 15 nTPM
- cerebellum: 14 nTPM
- hippocampal formation: 13 nTPM
- basal ganglia: 13 nTPM
- amygdala: 13 nTPM
- white matter: 13 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)
- 0.69
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 1.27
- DepMap mean gene effect
- 0
- 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
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ZNF48 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 ZNF48 as an antibody target. Whether an autoantibody or antibody against ZNF48 could matter depends on whether native ZNF48 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF48 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 ZNF48 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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