BNIP1
Vesicle transport protein SEC20
Also known as: Nip1, SEC20, SEC20_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q12981
- Gene
- BNIP1
- Ensembl
- ENSG00000113734
- Chromosome
- 5
- Canonical length
- 228 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Endoplasmic reticulum
OverviewNCBI Gene
This gene is a member of the BCL2/adenovirus E1B 19 kd-interacting protein (BNIP) family. It interacts with the E1B 19 kDa protein, which protects cells from virally-induced cell death. The encoded protein also interacts with E1B 19 kDa-like sequences of BCL2, another apoptotic protector. In addition, this protein is involved in vesicle transport into the endoplasmic reticulum. Alternative splicing of this gene results in four protein products with identical N- and C-termini. [provided by RefSeq, Mar 2011]
Canonical amino-acid sequenceUniProt
228 residues, UniProt reviewed canonical sequence.
>Q12981|BNIP1
1 MAAPQDVHVR ICNQEIVKFD LEVKALIQDI RDCSGPLSAL TELNTKVKEK FQQLRHRIQD
61 LEQLAKEQDK ESEKQLLLQE VENHKKQMLS NQASWRKANL TCKIAIDNLE KAELLQGGDL
121 LRQRKTTKES LAQTSSTITE SLMGISRMMA QQVQQSEEAM QSLVTSSRTI LDANEEFKSM
181 SGTIQLGRKL ITKYNRRELT DKLLIFLALA LFLATVLYIV KKRLFPFLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BNIP1 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.37
- Highest tissue expression
- 32 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 32 nTPM
- pancreas: 18 nTPM
- tongue: 15 nTPM
- testis: 14 nTPM
- skeletal muscle: 13 nTPM
- choroid plexus: 13 nTPM
Single-cell type
- oocytes: 78 nCPM
- late primary spermatocytes: 51 nCPM
- syncytiotrophoblasts: 44 nCPM
- cytotrophoblasts: 33 nCPM
- migrating cytotrophoblasts: 31 nCPM
- esophageal basal cells: 29 nCPM
Immune cell
- gdT-cell: 17 nTPM
- plasmacytoid DC: 16 nTPM
- memory CD4 T-cell: 15 nTPM
- MAIT T-cell: 14 nTPM
- T-reg: 14 nTPM
- myeloid DC: 13 nTPM
Brain region
- hypothalamus: 14 nTPM
- thalamus: 13 nTPM
- pons: 13 nTPM
- midbrain: 13 nTPM
- white matter: 13 nTPM
- medulla oblongata: 12 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about BNIP1.
Disease | AllUniProt
Conditions BNIP1 is implicated in, by any mechanism.
- Spondyloepiphyseal dysplasia, Holling type (SEDH) MIM:621345
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)
- 1.25
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.47
- DepMap mean gene effect
- -0.67
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- apoptotic process
- endoplasmic reticulum membrane fusion
- endoplasmic reticulum organization
- execution phase of apoptosis
- negative regulation of apoptotic process
- response to activity
- response to oxygen-glucose deprivation
- response to starvation
- retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum
- apoptotic process in response to mitochondrial fragmentation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Sec20
- Sec20, C-terminal
- Sec20
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of BNIP1 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 BNIP1 as an antibody target. Whether an autoantibody or antibody against BNIP1 could matter depends on whether native BNIP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BNIP1 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 BNIP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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