GPR137B
Integral membrane protein GPR137B
Also known as: G137B_HUMAN, TM7SF1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O60478
- Gene
- GPR137B
- Ensembl
- ENSG00000077585
- Chromosome
- 1
- Canonical length
- 399 aa
- Protein class
- Predicted membrane proteins, Transporters
OverviewNCBI Gene
Involved in positive regulation of TORC1 signaling; positive regulation of protein localization to lysosome; and regulation of autophagy. Located in lysosomal membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
399 residues, UniProt reviewed canonical sequence.
>O60478|GPR137B
1 MRPERPRPRG SAPGPMETPP WDPARNDSLP PTLTPAVPPY VKLGLTVVYT VFYALLFVFI
61 YVQLWLVLRY RHKRLSYQSV FLFLCLFWAS LRTVLFSFYF KDFVAANSLS PFVFWLLYCF
121 PVCLQFFTLT LMNLYFTQVI FKAKSKYSPE LLKYRLPLYL ASLFISLVFL LVNLTCAVLV
181 KTGNWERKVI VSVRVAINDT LFVLCAVSLS ICLYKISKMS LANIYLESKG SSVCQVTAIG
241 VTVILLYTSR ACYNLFILSF SQNKSVHSFD YDWYNVSDQA DLKNQLGDAG YVLFGVVLFV
301 WELLPTTLVV YFFRVRNPTK DLTNPGMVPS HGFSPRSYFF DNPRRYDSDD DLAWNIAPQG
361 LQGGFAPDYY DWGQQTNSFL AQAGTLQDST LDPDKPSLGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GPR137B 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)
- 0.4
- Highest tissue expression
- 126 nTPM
Expression across tissuesHPA
Tissue
- retina: 126 nTPM
- kidney: 64 nTPM
- basal ganglia: 43 nTPM
- epididymis: 38 nTPM
- amygdala: 35 nTPM
- spinal cord: 34 nTPM
Single-cell type
- rod photoreceptor cells: 394 nCPM
- melanocytes: 318 nCPM
- müller glia: 315 nCPM
- kupffer cells: 266 nCPM
- cdc: 264 nCPM
- hofbauer cells: 237 nCPM
Immune cell
- basophil: 18 nTPM
- eosinophil: 9.6 nTPM
- non-classical monocyte: 7.3 nTPM
- intermediate monocyte: 4.1 nTPM
- memory CD8 T-cell: 2.7 nTPM
- T-reg: 1.7 nTPM
Brain region
- basal ganglia: 54 nTPM
- midbrain: 52 nTPM
- thalamus: 51 nTPM
- medulla oblongata: 51 nTPM
- white matter: 51 nTPM
- hypothalamus: 47 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)
- 1.32
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.24
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- autophagy
- negative regulation of bone resorption
- negative regulation of osteoclast differentiation
- positive regulation of protein localization to lysosome
- positive regulation of TORC1 signaling
- regulation of autophagy
- regulation of GTPase activity
- regulation of macrophage activation
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of GPR137B 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 GPR137B as an antibody target. Whether an autoantibody or antibody against GPR137B could matter depends on whether native GPR137B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GPR137B 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 GPR137B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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