PEX11B
Peroxisomal membrane protein 11B
Also known as: PEX11beta, PX11B_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O96011
- Gene
- PEX11B
- Ensembl
- ENSG00000131779
- Chromosome
- 1
- Canonical length
- 259 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Vesicles
- Quaternary structure
- Homodimer
OverviewNCBI Gene
The protein encoded by this gene facilitates peroxisomal proliferation and interacts with PEX19. The encoded protein is found in the peroxisomal membrane. Several transcript variants, some protein-coding and some not protein-coding, have been found for this gene. [provided by RefSeq, Dec 2012]
Canonical amino-acid sequenceUniProt
259 residues, UniProt reviewed canonical sequence.
>O96011|PEX11B
1 MDAWVRFSAQ SQARERLCRA AQYACSLLGH ALQRHGASPE LQKQIRQLES HLSLGRKLLR
61 LGNSADALES AKRAVHLSDV VLRFCITVSH LNRALYFACD NVLWAGKSGL APRVDQEKWA
121 QRSFRYYLFS LIMNLSRDAY EIRLLMEQES SACSRRLKGS GGGVPGGSET GGLGGPGTPG
181 GGLPQLALKL RLQVLLLARV LRGHPPLLLD VVRNACDLFI PLDKLGLWRC GPGIVGLCGL
241 VSSILSILTL IYPWLRLKPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PEX11B 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)
- 0.35
- Highest tissue expression
- 49 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 49 nTPM
- basal ganglia: 40 nTPM
- hypothalamus: 40 nTPM
- skeletal muscle: 40 nTPM
- hippocampal formation: 36 nTPM
- cerebellum: 36 nTPM
Single-cell type
- oocytes: 65 nCPM
- early primary spermatocytes: 60 nCPM
- parietal cells: 51 nCPM
- esophageal suprabasal cells: 50 nCPM
- megakaryocytes: 50 nCPM
- cytotrophoblasts: 49 nCPM
Immune cell
- plasmacytoid DC: 95 nTPM
- memory B-cell: 94 nTPM
- basophil: 90 nTPM
- naive B-cell: 85 nTPM
- total PBMC: 83 nTPM
- T-reg: 80 nTPM
Brain region
- hypothalamus: 41 nTPM
- cerebral cortex: 37 nTPM
- basal ganglia: 35 nTPM
- pons: 35 nTPM
- white matter: 32 nTPM
- hippocampal formation: 32 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about PEX11B.
Disease | AllUniProt
Conditions PEX11B is implicated in, by any mechanism.
- Peroxisome biogenesis disorder 14B (PBD14B) MIM:614920
Disease | GeneticClinVar
14 pathogenic / likely-pathogenic of 261 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Peroxisome biogenesis disorder 14B
- Peroxisome biogenesis disorder
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)
- 1.08
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.31
- DepMap mean gene effect
- -0.29
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 10% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PEX11B 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 PEX11B as an antibody target. Whether an autoantibody or antibody against PEX11B could matter depends on whether native PEX11B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PEX11B 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 PEX11B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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