BATF2
Basic leucine zipper transcriptional factor ATF-like 2
Also known as: BATF2_HUMAN, MGC20410
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N1L9
- Gene
- BATF2
- Ensembl
- ENSG00000168062
- Chromosome
- 11
- Canonical length
- 274 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoli
OverviewNCBI Gene
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in defense response to protozoan; myeloid dendritic cell differentiation; and regulation of transcription by RNA polymerase II. Part of RNA polymerase II transcription regulator complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
274 residues, UniProt reviewed canonical sequence.
>Q8N1L9|BATF2
1 MHLCGGNGLL TQTDPKEQQR QLKKQKNRAA AQRSRQKHTD KADALHQQHE SLEKDNLALR
61 KEIQSLQAEL AWWSRTLHVH ERLCPMDCAS CSAPGLLGCW DQAEGLLGPG PQGQHGCREQ
121 LELFQTPGSC YPAQPLSPGP QPHDSPSLLQ CPLPSLSLGP AVVAEPPVQL SPSPLLFASH
181 TGSSLQGSSS KLSALQPSLT AQTAPPQPLE LEHPTRGKLG SSPDNPSSAL GLARLQSREH
241 KPALSAATWQ GLVVDPSPHP LLAFPLLSSA QVHFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BATF2 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)
- 0.68
- Highest tissue expression
- 13 nTPM
Expression across tissuesHPA
Tissue
- spleen: 13 nTPM
- salivary gland: 13 nTPM
- pancreas: 9.2 nTPM
- duodenum: 8.8 nTPM
- appendix: 8.2 nTPM
- colon: 8.1 nTPM
Single-cell type
- colonocytes: 21 nCPM
- enterocytes: 18 nCPM
- goblet cells: 17 nCPM
- pancreatic acinar cells: 13 nCPM
- breast lactating cells: 13 nCPM
- enteric stem cells: 12 nCPM
Immune cell
- neutrophil: 7.4 nTPM
- intermediate monocyte: 5.3 nTPM
- non-classical monocyte: 2.8 nTPM
- classical monocyte: 2.1 nTPM
- eosinophil: 1 nTPM
- memory B-cell: 1 nTPM
Brain region
- medulla oblongata: 5.3 nTPM
- pons: 4.9 nTPM
- spinal cord: 4.8 nTPM
- thalamus: 3 nTPM
- basal ganglia: 2.5 nTPM
- choroid plexus: 2.5 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)
- 1.07
- gnomAD pLI
- 0.59
- gnomAD missense Z
- 0.37
- DepMap mean gene effect
- -0.07
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- defense response to protozoan
- integrated stress response signaling
- myeloid dendritic cell differentiation
- regulation of transcription by RNA polymerase II
Molecular functions
- DNA-binding transcription factor activity, RNA polymerase II-specific
- RNA polymerase II cis-regulatory region sequence-specific DNA binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of BATF2 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 BATF2 as an antibody target. Whether an autoantibody or antibody against BATF2 could matter depends on whether native BATF2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BATF2 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 BATF2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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