TMEM87B
Transmembrane protein 87B
Also known as: FLJ14681, TM87B_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96K49
- Gene
- TMEM87B
- Ensembl
- ENSG00000153214
- Chromosome
- 2
- Canonical length
- 555 aa
- Protein class
- Disease related genes, Potential drug targets, Predicted membrane proteins, Transporters
- Subcellular location
- Golgi apparatus,Vesicles
OverviewNCBI Gene
This gene encodes a protein that may interact with human papillomavirus type 18 E6 oncogene. The protein is also likely to be involved in endosome-to-trans-Golgi network retrograde transport. The gene is expressed in adult and fetal tissues, including brain and heart. This gene is a component of the 2q13 deletion syndrome. Mutations in this gene may be associated with congenital heart defects. [provided by RefSeq, Aug 2016]
Canonical amino-acid sequenceUniProt
555 residues, UniProt reviewed canonical sequence.
>Q96K49|TMEM87B
1 MVAACRSVAG LLPRRRRCFP ARAPLLRVAL CLLCWTPAAV RAVPELGLWL ETVNDKSGPL
61 IFRKTMFNST DIKLSVKSFH CSGPVKFTIV WHLKYHTCHN EHSNLEELFQ KHKLSVDEDF
121 CHYLKNDNCW TTKNENLDCN SDSQVFPSLN NKELINIRNV SNQERSMDVV ARTQKDGFHI
181 FIVSIKTENT DASWNLNVSL SMIGPHGYIS ASDWPLMIFY MVMCIVYILY GILWLTWSAC
241 YWKDILRIQF WIAAVIFLGM LEKAVFYSEY QNISNTGLST QGLLIFAELI SAIKRTLARL
301 LVIIVSLGYG IVKPRLGTVM HRVIGLGLLY LIFAAVEGVM RVIGGSNHLA VVLDDIILAV
361 IDSIFVWFIF ISLAQTMKTL RLRKNTVKFS LYRHFKNTLI FAVLASIVFM GWTTKTFRIA
421 KCQSDWMERW VDDAFWSFLF SLILIVIMFL WRPSANNQRY AFMPLIDDSD DEIEEFMVTS
481 ENLTEGIKLR ASKSVSNGTA KPATSENFDE DLKWVEENIP SSFTDVALPV LVDSDEEIMT
541 RSEMAEKMFS SEKIMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TMEM87B 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
- 7
- Mean surface accessibility (rSASA)
- 0.37
- Highest tissue expression
- 29 nTPM
Expression across tissuesHPA
Tissue
- prostate: 29 nTPM
- small intestine: 28 nTPM
- duodenum: 26 nTPM
- colon: 26 nTPM
- rectum: 26 nTPM
- stomach: 21 nTPM
Single-cell type
- prostatic glandular cells: 188 nCPM
- breast lactating cells: 172 nCPM
- mucous neck cells: 117 nCPM
- goblet cells: 114 nCPM
- adrenal cortex cells: 111 nCPM
- gonadotrophs: 109 nCPM
Immune cell
- non-classical monocyte: 6.3 nTPM
- T-reg: 6.3 nTPM
- memory CD4 T-cell: 5.8 nTPM
- MAIT T-cell: 5.6 nTPM
- memory B-cell: 5.6 nTPM
- basophil: 5.4 nTPM
Brain region
- midbrain: 16 nTPM
- thalamus: 12 nTPM
- pons: 12 nTPM
- medulla oblongata: 10 nTPM
- hypothalamus: 10 nTPM
- spinal cord: 10 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)
- 1.03
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.68
- DepMap mean gene effect
- -0.1
- DepMap dependency class
- none
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
- endosome to Golgi
- retrograde transport
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TMEM87B as an antibody target. Whether an autoantibody or antibody against TMEM87B could matter depends on whether native TMEM87B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TMEM87B 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 TMEM87B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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