BCL2L13
Bcl-2-like protein 13
Also known as: B2L13_HUMAN, BCL-RAMBO, MIL1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BXK5
- Gene
- BCL2L13
- Ensembl
- ENSG00000099968
- Chromosome
- 22
- Canonical length
- 485 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Mitochondria
OverviewNCBI Gene
This gene encodes a mitochondrially-localized protein with conserved B-cell lymphoma 2 homology motifs. Overexpression of the encoded protein results in apoptosis. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]
Canonical amino-acid sequenceUniProt
485 residues, UniProt reviewed canonical sequence.
>Q9BXK5|BCL2L13
1 MASSSTVPLG FHYETKYVVL SYLGLLSQEK LQEQHLSSPQ GVQLDIASQS LDQEILLKVK
61 TEIEEELKSL DKEISEAFTS TGFDRHTSPV FSPANPESSM EDCLAHLGEK VSQELKEPLH
121 KALQMLLSQP VTYQAFRECT LETTVHASGW NKILVPLVLL RQMLLELTRR GQEPLSALLQ
181 FGVTYLEDYS AEYIIQQGGW GTVFSLESEE EEYPGITAED SNDIYILPSD NSGQVSPPES
241 PTVTTSWQSE SLPVSLSASQ SWHTESLPVS LGPESWQQIA MDPEEVKSLD SNGAGEKSEN
301 NSSNSDIVHV EKEEVPEGME EAAVASVVLP ARELQEALPE APAPLLPHIT ATSLLGTREP
361 DTEVITVEKS SPATSLFVEL DEEEVKAATT EPTEVEEVVP ALEPTETLLS EKEINAREES
421 LVEELSPASE KKPVPPSEGK SRLSPAGEMK PMPLSEGKSI LLFGGAAAVA ILAVAIGVAL
481 ALRKKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BCL2L13 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)
- 0.53
- Highest tissue expression
- 41 nTPM
Expression across tissuesHPA
Tissue
- retina: 41 nTPM
- tongue: 38 nTPM
- skeletal muscle: 37 nTPM
- liver: 15 nTPM
- heart muscle: 14 nTPM
- parathyroid gland: 14 nTPM
Single-cell type
- ocular epithelial cells: 471 nCPM
- retinal bipolar cells: 330 nCPM
- myonuclei: 305 nCPM
- retinal ganglion cells: 232 nCPM
- syncytiotrophoblasts: 179 nCPM
- renal collecting duct intercalated cells: 177 nCPM
Immune cell
- classical monocyte: 9.5 nTPM
- intermediate monocyte: 8 nTPM
- NK-cell: 6.5 nTPM
- non-classical monocyte: 6.4 nTPM
- myeloid DC: 5.4 nTPM
- basophil: 5.1 nTPM
Brain region
- midbrain: 45 nTPM
- cerebral cortex: 41 nTPM
- pons: 40 nTPM
- medulla oblongata: 37 nTPM
- thalamus: 36 nTPM
- hypothalamus: 36 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)
- 0.8
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.3
- DepMap mean gene effect
- -0.14
- DepMap dependency class
- selective
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
- canonical glycolysis
- fat cell differentiation
- mitochondrion organization
- mitophagy
- oxidative phosphorylation
- regulation of apoptotic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of BCL2L13 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 BCL2L13 as an antibody target. Whether an autoantibody or antibody against BCL2L13 could matter depends on whether native BCL2L13 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BCL2L13 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 BCL2L13 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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