BRINP2
BMP/retinoic acid-inducible neural-specific protein 2
Also known as: BRNP2_HUMAN, DBCCR1L2, FAM5B
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9C0B6
- Gene
- BRINP2
- Ensembl
- ENSG00000198797
- Chromosome
- 1
- Canonical length
- 783 aa
- Protein class
- Predicted secreted proteins, Transporters
- Secretome location
- Secreted in other tissues
OverviewNCBI Gene
Predicted to be involved in cellular response to retinoic acid; central nervous system neuron differentiation; and negative regulation of mitotic cell cycle. Predicted to act upstream of or within locomotion and nervous system development. Predicted to be located in extracellular region. Predicted to be active in cytoplasm; dendrite; and neuronal cell body. Implicated in oral squamous cell carcinoma. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
783 residues, UniProt reviewed canonical sequence.
>Q9C0B6|BRINP2
1 MRWQCGTRFR GLRPAVAPWT ALLALGLPGW VLAVSATAAA VVPEQHASVA GQHPLDWLLT
61 DRGPFHRAQE YADFMERYRQ GFTTRYRIYR EFARWKVNNL ALERKDFFSL PLPLAPEFIR
121 NIRLLGRRPN LQQVTENLIK KYGTHFLLSA TLGGEESLTI FVDKQKLGRK TETTGGASII
181 GGSGNSTAVS LETLHQLAAS YFIDRESTLR RLHHIQIATG AIKVTETRTG PLGCSNYDNL
241 DSVSSVLVQS PENKVQLLGL QVLLPEYLRE RFVAAALSYI TCSSEGELVC KENDCWCKCS
301 PTFPECNCPD ADIQAMEDSL LQIQDSWATH NRQFEESEEF QALLKRLPDD RFLNSTAISQ
361 FWAMDTSLQH RYQQLGAGLK VLFKKTHRIL RRLFNLCKRC HRQPRFRLPK ERSLSYWWNR
421 IQSLLYCGES TFPGTFLEQS HSCTCPYDQS SCQGPIPCAL GEGPACAHCA PDNSTRCGSC
481 NPGYVLAQGL CRPEVAESLE NFLGLETDLQ DLELKYLLQK QDSRIEVHSI FISNDMRLGS
541 WFDPSWRKRM LLTLKSNKYK PGLVHVMLAL SLQICLTKNS TLEPVMAIYV NPFGGSHSES
601 WFMPVNEGSF PDWERTNVDA AAQCQNWTIT LGNRWKTFFE TVHVYLRSRI KSLDDSSNET
661 IYYEPLEMTD PSKNLGYMKI NTLQVFGYSL PFDPDAIRDL ILQLDYPYTQ GSQDSALLQL
721 IELRDRVNQL SPPGKVRLDL FSCLLRHRLK LANNEVGRIQ SSLRAFNSKL PNPVEYETGK
781 LCSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BRINP2 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.36
- Highest tissue expression
- 27 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 27 nTPM
- amygdala: 19 nTPM
- basal ganglia: 13 nTPM
- hippocampal formation: 11 nTPM
- hypothalamus: 9.6 nTPM
- adrenal gland: 8.5 nTPM
Single-cell type
- astrocytes: 176 nCPM
- oligodendrocyte progenitor cells: 140 nCPM
- pituitary stem cells: 117 nCPM
- brain excitatory neurons: 113 nCPM
- brain inhibitory neurons: 76 nCPM
- adrenal medulla cells: 75 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebral cortex: 47 nTPM
- amygdala: 41 nTPM
- thalamus: 39 nTPM
- basal ganglia: 33 nTPM
- white matter: 32 nTPM
- hypothalamus: 28 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)
- 0.21
- gnomAD pLI
- 1
- gnomAD missense Z
- 0.86
- DepMap mean gene effect
- 0.01
- 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
Biological processes
- cellular response to retinoic acid
- central nervous system neuron differentiation
- locomotion
- multicellular organism growth
- negative regulation of mitotic cell cycle
- positive regulation of neuron differentiation
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads BRINP2 as an antibody target. Whether an autoantibody or antibody against BRINP2 could matter depends on whether native BRINP2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BRINP2 is annotated as secreted, so native BRINP2 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label BRINP2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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