ZFAND2A
AN1-type zinc finger protein 2A
Also known as: AIRAP, ZFN2A_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N6M9
- Gene
- ZFAND2A
- Ensembl
- ENSG00000178381
- Chromosome
- 7
- Canonical length
- 145 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Predicted to enable zinc ion binding activity. Predicted to be involved in proteasome-mediated ubiquitin-dependent protein catabolic process and protein targeting to ER. Predicted to act upstream of or within cellular response to arsenic-containing substance and positive regulation of proteasomal ubiquitin-dependent protein catabolic process. Predicted to be located in nucleus. Predicted to be part of proteasome complex. Predicted to be active in endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
145 residues, UniProt reviewed canonical sequence.
>Q8N6M9|ZFAND2A
1 MEFPDLGKHC SEKTCKQLDF LPVKCDACKQ DFCKDHFPYA AHKCPFAFQK DVHVPVCPLC
61 NTPIPVKKGQ IPDVVVGDHI DRDCDSHPGK KKEKIFTYRC SKEGCKKKEM LQMVCAQCHG
121 NFCIQHRHPL DHSCRHGSRP TIKAGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZFAND2A 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
- 78 nTPM
Expression across tissuesHPA
Tissue
- liver: 78 nTPM
- bone marrow: 76 nTPM
- cerebral cortex: 58 nTPM
- amygdala: 55 nTPM
- hippocampal formation: 53 nTPM
- spinal cord: 52 nTPM
Single-cell type
- oocytes: 3,864 nCPM
- pancreatic duct cells: 615 nCPM
- epididymal principal cells: 419 nCPM
- esophageal apical cells: 223 nCPM
- colonocytes: 182 nCPM
- pancreatic acinar cells: 173 nCPM
Immune cell
- basophil: 72 nTPM
- T-reg: 40 nTPM
- naive B-cell: 35 nTPM
- plasmacytoid DC: 35 nTPM
- eosinophil: 34 nTPM
- NK-cell: 33 nTPM
Brain region
- cerebral cortex: 67 nTPM
- white matter: 46 nTPM
- hippocampal formation: 39 nTPM
- cerebellum: 39 nTPM
- hypothalamus: 36 nTPM
- pons: 36 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)
- 1.69
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.95
- DepMap mean gene effect
- 0.09
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular response to arsenic-containing substance
- positive regulation of proteasomal ubiquitin-dependent protein catabolic process
- proteasome-mediated ubiquitin-dependent protein catabolic process
- protein targeting to ER
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ZFAND2A as an antibody target. Whether an autoantibody or antibody against ZFAND2A could matter depends on whether native ZFAND2A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZFAND2A 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 ZFAND2A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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