BANP
Protein BANP
Also known as: BANP_HUMAN, BEND1, DKFZp761H172, FLJ10177, FLJ20538, SMAR1, SMARBP1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N9N5
- Gene
- BANP
- Ensembl
- ENSG00000172530
- Chromosome
- 16
- Canonical length
- 519 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear bodies
OverviewNCBI Gene
This gene encodes a protein that binds to matrix attachment regions. The protein forms a complex with p53 and negatively regulates p53 transcription, and functions as a tumor suppressor and cell cycle regulator. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]
Canonical amino-acid sequenceUniProt
519 residues, UniProt reviewed canonical sequence.
>Q8N9N5|BANP
1 MMSEHDLADV VQIAVEDLSP DHPVVLENHV VTDEDEPALK RQRLEINCQD PSIKTICLRL
61 DSIEAKLQAL EATCKSLEEK LDLVTNKQHS PIQVPMVAGS PLGATQTCNK VRCVVPQTTV
121 ILNNDRQNAI VAKMEDPLSN RAPDSLENVI SNAVPGRRQN TIVVKVPGQE DSHHEDGESG
181 SEASDSVSSC GQAGSQSIGS NVTLITLNSE EDYPNGTWLG DENNPEMRVR CAIIPSDMLH
241 ISTNCRTAEK MALTLLDYLF HREVQAVSNL SGQGKHGKKQ LDPLTIYGIR CHLFYKFGIT
301 ESDWYRIKQS IDSKCRTAWR RKQRGQSLAV KSFSRRTPNS SSYCPSEPMM STPPPASELP
361 QPQPQPQALH YALANAQQVQ IHQIGEDGQV QVGHLHIAQV PQGEQVQITQ DSEGNLQIHH
421 VGQDGQLLEA TRIPCLLAPS VFKASSGQVL QGAQLIAVAS SDPAAAGVDG SPLQGSDIQV
481 QYVQLAPVSD HTAGAQTAEA LQPTLQPEMQ LEHGAIQIQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BANP 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)
- 0.52
- Highest tissue expression
- 12 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 12 nTPM
- liver: 9.9 nTPM
- thymus: 9.9 nTPM
- cerebellum: 9.4 nTPM
- ovary: 8.9 nTPM
- lymph node: 8.8 nTPM
Single-cell type
- somatotrophs: 260 nCPM
- neutrophils: 164 nCPM
- pdcs: 162 nCPM
- oocytes: 157 nCPM
- lactotrophs: 142 nCPM
- syncytiotrophoblasts: 139 nCPM
Immune cell
- neutrophil: 63 nTPM
- eosinophil: 40 nTPM
- plasmacytoid DC: 30 nTPM
- memory B-cell: 25 nTPM
- naive CD4 T-cell: 24 nTPM
- myeloid DC: 24 nTPM
Brain region
- cerebellum: 39 nTPM
- white matter: 31 nTPM
- choroid plexus: 31 nTPM
- medulla oblongata: 29 nTPM
- thalamus: 29 nTPM
- pons: 27 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)
- 0.27
- gnomAD pLI
- 0.99
- gnomAD missense Z
- 2.43
- DepMap mean gene effect
- -0.95
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% 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
- BEN domain
- BEN domain
- Protein BANP
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of BANP 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 BANP as an antibody target. Whether an autoantibody or antibody against BANP could matter depends on whether native BANP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BANP 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 BANP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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