TBC1D10B
TBC1 domain family member 10B
Also known as: DKFZP434P1750, EPI64B, FLJ13130, Rab27A-GAPbeta, TB10B_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q4KMP7
- Gene
- TBC1D10B
- Ensembl
- ENSG00000169221
- Chromosome
- 16
- Canonical length
- 808 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Small G proteins of the RAB family (see MIM 179508) function in intracellular vesicle trafficking by switching from the GTP-bound state to the GDP-bound state with the assistance of guanine nucleotide exchange factors (GEFs; see MIM 609700) and GTPase-activating proteins (GAPs). TBC1D10B functions as a GAP for several proteins of the Rab family (Ishibashi et al., 2009 [PubMed 19077034]).[supplied by OMIM, Nov 2010]
Canonical amino-acid sequenceUniProt
808 residues, UniProt reviewed canonical sequence.
>Q4KMP7|TBC1D10B
1 METGTAPLVA PPRRHGAPAA PSPPPRGSRA GPVVVVAPGP PVTTATSAPV TLVAPGEARP
61 AWVPGSAETS APAPAPAPAP APAVTGSTVV VLTLEASPEA PKPQLPSGPE SPEPAAVAGV
121 ETSRALAAGA DSPKTEEARP SPAPGPGTPT GTPTRTPSRT APGALTAKPP LAPKPGTTVA
181 SGVTARSASG QVTGGHGAAA ATSASAGQAP EDPSGPGTGP SGTCEAPVAV VTVTPAPEPA
241 ENSQDLGSTS SLGPGISGPR GQAPDTLSYL DSVSLMSGTL ESLADDVSSM GSDSEINGLA
301 LRKTDKYGFL GGSQYSGSLE SSIPVDVARQ RELKWLDMFS NWDKWLSRRF QKVKLRCRKG
361 IPSSLRAKAW QYLSNSKELL EQNPGKFEEL ERAPGDPKWL DVIEKDLHRQ FPFHEMFAAR
421 GGHGQQDLYR ILKAYTIYRP DEGYCQAQAP VAAVLLMHMP AEQAFWCLVQ ICDKYLPGYY
481 SAGLEAIQLD GEIFFALLRR ASPLAHRHLR RQRIDPVLYM TEWFMCIFAR TLPWASVLRV
541 WDMFFCEGVK IIFRVALVLL RHTLGSVEKL RSCQGMYETM EQLRNLPQQC MQEDFLVHEV
601 TNLPVTEALI ERENAAQLKK WRETRGELQY RPSRRLHGSR AIHEERRRQQ PPLGPSSSLL
661 SLPGLKSRGS RAAGGAPSPP PPVRRASAGP APGPVVTAEG LHPSLPSPTG NSTPLGSSKE
721 TRKQEKERQK QEKERQKQEK EREKERQKQE KEREKQEKER EKQEKERQKQ EKKAQGRKLS
781 LRRKADGPPG PHDGGDRPSA EARQDAYFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TBC1D10B 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)
- 0.5
- Highest tissue expression
- 34 nTPM
Expression across tissuesHPA
Tissue
- testis: 34 nTPM
- skeletal muscle: 31 nTPM
- spinal cord: 25 nTPM
- cerebellum: 20 nTPM
- cerebral cortex: 18 nTPM
- skin: 18 nTPM
Single-cell type
- late spermatids: 58 nCPM
- neutrophils: 56 nCPM
- megakaryocytes: 50 nCPM
- neutrophil progenitors: 48 nCPM
- monocyte progenitors: 43 nCPM
- monocytes: 27 nCPM
Immune cell
- eosinophil: 1.7 nTPM
- neutrophil: 1.3 nTPM
- gdT-cell: 1.2 nTPM
- memory CD8 T-cell: 1.2 nTPM
- NK-cell: 1 nTPM
- total PBMC: 1 nTPM
Brain region
- white matter: 50 nTPM
- medulla oblongata: 48 nTPM
- cerebral cortex: 44 nTPM
- thalamus: 42 nTPM
- spinal cord: 41 nTPM
- basal ganglia: 41 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)
- 0.21
- gnomAD pLI
- 1
- gnomAD missense Z
- 1.95
- DepMap mean gene effect
- -0.18
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% 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
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TBC1D10B as an antibody target. Whether an autoantibody or antibody against TBC1D10B could matter depends on whether native TBC1D10B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TBC1D10B is annotated at the cell surface, where native TBC1D10B 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 TBC1D10B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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