BMERB1
bMERB domain-containing protein 1
Also known as: C16orf45, FLJ32618, MERB1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96MC5
- Gene
- BMERB1
- Ensembl
- ENSG00000166780
- Chromosome
- 16
- Canonical length
- 204 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
Predicted to be involved in negative regulation of microtubule depolymerization. Predicted to act upstream of or within negative regulation of cell motility involved in cerebral cortex radial glia guided migration. Predicted to be active in microtubule cytoskeleton. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
204 residues, UniProt reviewed canonical sequence.
>Q96MC5|BMERB1
1 MELKQSLSTH LEAEKPLRRY GAVEETAWKT ERLGRNQLDI ISMAETTMMP EEIELEMAKI
61 QRLREVLVRR ESELRFMMDD IQLCKDIMDL KQELQNLVAI PEKEKTKLQK QREDELIQKI
121 HKLVQKRDFL VDDAEVERLR EQEEDKEMAD FLRIKLKPLD KVTKSPASSR AEKKAEPPPS
181 KPTVAKTGLA LIKDCCGATQ CNIMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BMERB1 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.54
- Highest tissue expression
- 190 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 190 nTPM
- hippocampal formation: 150 nTPM
- amygdala: 144 nTPM
- hypothalamus: 111 nTPM
- cerebellum: 109 nTPM
- basal ganglia: 97 nTPM
Single-cell type
- late spermatids: 313 nCPM
- oligodendrocyte progenitor cells: 156 nCPM
- brain excitatory neurons: 130 nCPM
- other brain neurons: 127 nCPM
- distal convoluted tubule cells: 125 nCPM
- brain inhibitory neurons: 116 nCPM
Immune cell
- gdT-cell: 8.8 nTPM
- memory CD8 T-cell: 5.2 nTPM
- naive CD8 T-cell: 2.8 nTPM
- T-reg: 2.6 nTPM
- memory B-cell: 2.2 nTPM
- memory CD4 T-cell: 2 nTPM
Brain region
- pons: 183 nTPM
- cerebral cortex: 159 nTPM
- hippocampal formation: 150 nTPM
- white matter: 123 nTPM
- amygdala: 114 nTPM
- medulla oblongata: 112 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)
- 0.78
- gnomAD pLI
- 0.14
- DepMap mean gene effect
- 0
- 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
- cell motility involved in cerebral cortex radial glia guided migration
- microtubule depolymerization
- negative regulation of microtubule depolymerization
- negative regulation of cell motility involved in cerebral cortex radial glia guided migration
Cellular components
Protein domainsUniProt · Pfam · InterPro
- bMERB domain
- Bivalent Mical/EHBP Rab binding domain
- BMERB domain-containing protein 1
InteractionsUniProt · HPA
Protein binding partners of BMERB1 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 BMERB1 as an antibody target. Whether an autoantibody or antibody against BMERB1 could matter depends on whether native BMERB1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BMERB1 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 BMERB1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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