BEND2
BEN domain-containing protein 2
Also known as: BEND2_HUMAN, CXorf20, MGC33653
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8NDZ0
- Gene
- BEND2
- Ensembl
- ENSG00000177324
- Chromosome
- X
- Canonical length
- 799 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
This gene encodes a protein which has two BEN domains in the C-terminus. These domains are found in proteins which participate in protein and DNA interactions which occur during chromatin restructuring or transcription. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]
Canonical amino-acid sequenceUniProt
799 residues, UniProt reviewed canonical sequence.
>Q8NDZ0|BEND2
1 MSERTQEQDF VIITVDDSDD NNDCSIEMVE VSETADNSTN DIADDSTYVT ADNPTDDTAT
61 QPNFPGGNDG HHRPLQMSYG SGSVTQAGVQ WHDHSSLQPQ PLGLKQFFHL SLPSSWDDRR
121 TPPCPVAHGD QIVSQINHPV HLRRYSYNSE EVDFPKRGRF YTPEVQSSIS PPAERQETHA
181 WASPAVTSLE SAACHELQEA DLSESLSYPR IVSSSSLQQY VAQGGSFPCF GMPWNFISGG
241 AESTNAVISF ANATTAVPMA VLSRRESSLA NNPGVVNYSA LPENENVGPG RALSSFCFHP
301 NLEMPERPAN SSKNSTETAN YPTLMGNYNG QNTASLSVFI PPYFAEKIIL TEMPGTTETN
361 VENNSQTVYY PALSGNTSAP YPASSYLPIT SNFESGPQMS YGTMSYSTEM KNNCDQDDAS
421 ASACLTPDFA LLPLNILVKV DTNTENSVNT MNRSTLLDSD SGQDSSSSSV CIPPKYGYLG
481 DPKRNVRVLK IHLLAVQNMA KPKQAACYLV RILFSKEILI SSSVDIHLKD SQSLDPNKMA
541 ALREYLATTF PTCDLHEHGK DWQDCISGIN SMIYCLCSEG KSTPKTVRKN KKRTNRVASA
601 SADRNDQRGR DGGEGCSWMF QPMNNSKMRE KRNLQPNSNA IPEGMREPST DNPEEPGEAW
661 SYFGRPWRNI RMPCSVLTLA KTKSCASLSA RYLIQKLFTK DVLVQSNVYG NLKHGLCALD
721 PNKISALREF LQENYPICDL SENGRDWKSC VTSINSGIRS LRHDVRRAEA RSQSLPAVTP
781 PELEQESKPG DPDATDPSTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BEND2 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)
- 0.6
- Highest tissue expression
- 5 nTPM
Expression across tissuesHPA
Tissue
- testis: 5 nTPM
- bone marrow: 0.2 nTPM
- spleen: 0.2 nTPM
- adipose tissue: 0 nTPM
- adrenal gland: 0 nTPM
- amygdala: 0 nTPM
Single-cell type
- platelets: 314 nCPM
- early primary spermatocytes: 125 nCPM
- megakaryocytes: 25 nCPM
- peritubular myoid cells: 22 nCPM
- leydig cells: 21 nCPM
- thymic myoid cells: 16 nCPM
Immune cell
- basophil: 2.5 nTPM
- total PBMC: 1.8 nTPM
- neutrophil: 0.6 nTPM
- classical monocyte: 0.1 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- white matter: 1.1 nTPM
- cerebellum: 1 nTPM
- cerebral cortex: 1 nTPM
- pons: 1 nTPM
- thalamus: 1 nTPM
- choroid plexus: 0.9 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)
- 0.54
- gnomAD pLI
- 0.09
- gnomAD missense Z
- 0.71
- DepMap mean gene effect
- 0.13
- DepMap dependency class
- none
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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads BEND2 as an antibody target. Whether an autoantibody or antibody against BEND2 could matter depends on whether native BEND2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BEND2 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 BEND2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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