GPR35
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RefSeq (protein) | |||||||||
Location (UCSC) | Chr 2: 240.61 – 240.63 Mb | Chr 1: 92.88 – 92.91 Mb | |||||||
PubMed search | [3] | [4] |
View/Edit Human | View/Edit Mouse |
G protein-coupled receptor 35 also known as GPR35 is a
crypts of Lieberkühn
.
Ligands
Endogenous ligands
Although GPR35 is still considered an orphan receptor, there have been attempts to deorphanize it by identifying
endogenous molecules that can activate the receptor. All of the currently proposed ligands are either unselective towards GPR35, or they lack high potency, a characteristic feature of natural ligands.[6]
The following list includes the most prominent examples:
- kynurenic acid[7][8]
- LPA species[7]
- cyclic guanosine monophosphate[9]
- DHICA[10]
- T3[10]
- reverse T3[10]
Synthetic agonists
Other synthetic
agonists
of GPR35 include:
Antagonists
Antagonists of GPR35 include:
Both ML145 and ML144 unfurl their antagonistic activity through inverse agonism. They are, however, highly species-selective, and practically inactive at the rodent receptor orthologues.[17]
Clinical significance
Deletion of GPR35 gene may be responsible for brachydactyly mental retardation syndrome and is mutated in 2q37 monosomy and 2q37 deletion syndrome.[18] In one study GPR35 has been recognised as a potential oncogene in stomach cancer.[19]
References
- ^ a b c GRCh38: Ensembl release 89: ENSG00000178623 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000026271 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- PMID 9479505.
- ^ PMID 25805994.
- ^ PMID 20826425.
- PMID 23396314.
- ^ PMID 22523636.
- ^ S2CID 9421354.
- S2CID 43142927.
- ^ PMID 24113750.
- PMID 23608776.
- PMID 22409573.
- ^ )
- PMID 22967846.
- S2CID 42975740.
- S2CID 22753833.