BMF
Bcl-2-modifying factor
Also known as: BMF_HUMAN, FLJ00065
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96LC9
- Gene
- BMF
- Ensembl
- ENSG00000104081
- Chromosome
- 15
- Canonical length
- 184 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
The protein encoded by this gene belongs to the BCL2 protein family. BCL2 family members form hetero- or homodimers and act as anti- or pro-apoptotic regulators that are involved in a wide variety of cellular activities. This protein contains a single BCL2 homology domain 3 (BH3), and has been shown to bind BCL2 proteins and function as an apoptotic activator. This protein is found to be sequestered to myosin V motors by its association with dynein light chain 2, which may be important for sensing intracellular damage and triggering apoptosis. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
184 residues, UniProt reviewed canonical sequence.
>Q96LC9|BMF
1 MEPSQCVEEL EDDVFQPEDG EPVTQPGSLL SADLFAQSLL DCPLSRLQLF PLTHCCGPGL
61 RPTSQEDKAT QTLSPASPSQ GVMLPCGVTE EPQRLFYGNA GYRLPLPASF PAVLPIGEQP
121 PEGQWQHQAE VQIARKLQCI ADQFHRLHVQ QHQQNQNRVW WQILLFLHNL ALNGEENRNG
181 AGPRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BMF 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.66
- Highest tissue expression
- 71 nTPM
Expression across tissuesHPA
Tissue
- thymus: 71 nTPM
- bone marrow: 31 nTPM
- small intestine: 22 nTPM
- tonsil: 22 nTPM
- duodenum: 20 nTPM
- spleen: 18 nTPM
Single-cell type
- kupffer cells: 46 nCPM
- tuft cells: 35 nCPM
- plasma cells: 34 nCPM
- thymocytes: 20 nCPM
- b-cells: 18 nCPM
- monocytes: 17 nCPM
Immune cell
- non-classical monocyte: 4 nTPM
- neutrophil: 3.2 nTPM
- intermediate monocyte: 2.9 nTPM
- memory B-cell: 2.9 nTPM
- classical monocyte: 2.6 nTPM
- eosinophil: 2.5 nTPM
Brain region
- white matter: 14 nTPM
- thalamus: 11 nTPM
- medulla oblongata: 9.8 nTPM
- pons: 9.4 nTPM
- choroid plexus: 8.9 nTPM
- hypothalamus: 8.4 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)
- 1.01
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 0.54
- DepMap mean gene effect
- -0.32
- 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
- anoikis
- negative regulation of autophagy
- positive regulation of apoptotic process
- positive regulation of protein-containing complex assembly
- positive regulation of release of cytochrome c from mitochondria
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Bcl-2-modifying factor
- Bcl-2-modifying factor, apoptosis
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of BMF 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 BMF as an antibody target. Whether an autoantibody or antibody against BMF could matter depends on whether native BMF is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BMF is annotated at the cell surface, where native BMF is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label BMF as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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