TGFBR3L
Transforming growth factor-beta receptor type 3-like protein
Also known as: GEMP, TGR3L_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- H3BV60
- Gene
- TGFBR3L
- Ensembl
- ENSG00000260001
- Chromosome
- 19
- Canonical length
- 292 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Vesicles
OverviewNCBI Gene
Predicted to enable glycosaminoglycan binding activity; transforming growth factor beta receptor activity; and type II transforming growth factor beta receptor binding activity. Predicted to contribute to transforming growth factor beta binding activity. Predicted to be involved in several processes, including epithelial to mesenchymal transition; regulation of transforming growth factor beta receptor signaling pathway; and transforming growth factor beta receptor signaling pathway. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
292 residues, UniProt reviewed canonical sequence.
>H3BV60|TGFBR3L
1 MLGTVLLLAL LPGITTLPSG PPAPPFPAAP GPWLRRPLFS LKLSDTEDVF PRRAGPLEVP
61 ADSRVFVQAA LARPSPRWGL ALHRCSVTPS SRPAPGPALA LLREGCPADT SVAFPPPPPP
121 SPGAARPARF SFRLRPVFNA SVQFLHCQLS RCRRLRGVRR APAPLTPPPP PPPSRCLPQD
181 EACADTGSGS AEGLAADGPH LHTLTQPIVV TVPRPPPRPP KSVPGRAVRP EPPAPAPAAL
241 EPAPVVALVL AAFVLGAALA AGLGLVCAHS APHAPGPPAR ASPSGPQPRR SQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TGFBR3L 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
- 1
- Mean surface accessibility (rSASA)
- 0.5
- Highest tissue expression
- 33 nTPM
Expression across tissuesHPA
Tissue
- pituitary gland: 33 nTPM
- liver: 3.4 nTPM
- duodenum: 1.9 nTPM
- small intestine: 1.5 nTPM
- cerebellum: 1.4 nTPM
- endometrium: 1.4 nTPM
Single-cell type
- gonadotrophs: 949 nCPM
- pancreatic islet cells: 24 nCPM
- somatotrophs: 19 nCPM
- late spermatids: 18 nCPM
- pituitary stem cells: 17 nCPM
- smooth muscle cells: 16 nCPM
Immune cell
- basophil: 0.5 nTPM
- neutrophil: 0.5 nTPM
- gdT-cell: 0.3 nTPM
- memory CD8 T-cell: 0.3 nTPM
- naive CD8 T-cell: 0.3 nTPM
- eosinophil: 0.2 nTPM
Brain region
- cerebellum: 7.5 nTPM
- cerebral cortex: 6.9 nTPM
- white matter: 5.4 nTPM
- basal ganglia: 5.1 nTPM
- hypothalamus: 5 nTPM
- pons: 5 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)
- 1.38
- gnomAD pLI
- 0.08
- gnomAD missense Z
- 0.67
- DepMap mean gene effect
- -0.07
- DepMap dependency class
- selective
OntologyGO
Biological processes
- cell migration
- epithelial to mesenchymal transition
- regulation of transforming growth factor beta receptor signaling pathway
- transforming growth factor beta receptor signaling pathway
Molecular functions
- glycosaminoglycan binding
- transforming growth factor beta receptor activity
- type II transforming growth factor beta receptor binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TGFBR3L 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 TGFBR3L as an antibody target. Whether an autoantibody or antibody against TGFBR3L could matter depends on whether native TGFBR3L is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TGFBR3L is annotated at the cell surface, where native TGFBR3L 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 TGFBR3L as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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