| 1347471 | GPR17 | G protein-coupled receptor 17 | Predicted to enable G protein-coupled receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway. Predicted to act upstream of or within negative regulation of inflammatory response to antigenic stimulus. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025] | 2 | 127646153 | 127652639 | Human | 90 | symbol , COSMIC , Human Proteome Map | gene, protein-coding, VALIDATED [RefSeq] |
| 1353149 | GPR171 | G protein-coupled receptor 171 | Predicted to enable G protein-coupled purinergic nucleotide receptor activity; neuropeptide binding activity; and neuropeptide receptor activity. Predicted to be involved in adenylate cyclase-modulating G protein-coupled receptor signaling pathway; regulation of feeding behavior; and regulation of s ensory perception of pain. Predicted to act upstream of or within negative regulation of myeloid cell differentiation. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025] | 3 | 151197754 | 151203216 | Human | 78 | symbol , COSMIC , Human Proteome Map | gene, protein-coding, VALIDATED [RefSeq] |
| 1347737 | GPR173 | G protein-coupled receptor 173 | This gene encodes a member of the G-protein coupled receptor 1 family. This protein contains 7 transmembrane domains and conserved cysteine residues. [provided by RefSeq, Nov 2009] | X | 53048789 | 53080615 | Human | 60 | symbol , COSMIC , Human Proteome Map | gene, protein-coding, REVIEWED [RefSeq] |
| 1345699 | GPR174 | G protein-coupled receptor 174 | This gene encodes a protein belonging to the G protein-coupled receptor superfamily. These proteins are characterized by the presence of seven alpha-helical transmembrane domains, and they activate or interact with various endogenous or exogenous ligands, including neurotransmitters, hormones, and o dorant and taste substances. This family member is classified as an orphan receptor because the cognate ligand has not been identified. [provided by RefSeq, Sep 2011] | X | 79144688 | 79175318 | Human | 45 | symbol , COSMIC , Human Proteome Map | gene, protein-coding, VALIDATED [RefSeq] |
| 737562 | GPR176 | G protein-coupled receptor 176 | Members of the G protein-coupled receptor family, such as GPR176, are cell surface receptors involved in responses to hormones, growth factors, and neurotransmitters (Hata et al., 1995 [PubMed 7893747]).[supplied by OMIM, Jul 2008] | 15 | 39799008 | 39920266 | Human | 116 | symbol , COSMIC , description , Human Proteome Map | gene, protein-coding, VALIDATED [RefSeq] |
| 1601901 | GPR179 | G protein-coupled receptor 179 | This gene encodes a member of the glutamate receptor subfamily of G protein-coupled receptors. The encoded protein has an EGF-like calcium binding domain and a seven transmembrane domain in the N-terminal region of the protein. Mutations in this gene are associated with congenital stationary night b lindness type 1E. [provided by RefSeq, Apr 2012] | 17 | 38324571 | 38343956 | Human | 153 | symbol , COSMIC , Human Proteome Map | gene, protein-coding, REVIEWED [RefSeq] |
| 14402306 | GPR176-DT | GPR176 divergent transcript | INTERACTS WITH lipopolysaccharide; S-(1,2-dichlorovinyl)-L-cysteine | 15 | 39921024 | 39924899 | Human | 2 | symbol , COSMIC , name , Human Proteome Map | gene, ncrna, VALIDATED [RefSeq] |
| 1346676 | OXER1 | oxoeicosanoid receptor 1 | Enables G protein-coupled receptor activity and icosanoid binding activity. Involved in adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025] | 2 | 42762499 | 42764135 | Human | 33 | old_gene_symbol | gene, protein-coding, VALIDATED [RefSeq] |
| 1350892 | TMEM181 | transmembrane protein 181 | The TMEM181 gene encodes a putative G protein-coupled receptor expressed on the cell surface (Carette et al., 2009 [PubMed 19965467]; Wollscheid et al., 2009 [PubMed 19349973]).[supplied by OMIM, Jan 2010] | 6 | 158536640 | 158635429 | Human | 54 | old_gene_symbol | gene, protein-coding, VALIDATED [RefSeq] |
| 1354338 | TPRA1 | transmembrane protein adipocyte associated 1 | Predicted to enable G protein-coupled receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway. Predicted to act upstream of or within embryonic cleavage and negative regulation of mitotic cell cycle phase transition. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025] | 3 | 127571232 | 127598231 | Human | 84 | old_gene_name , old_gene_symbol | gene, protein-coding, VALIDATED [RefSeq] |
| 1605334 | WLS | Wnt ligand secretion mediator | Enables Wnt-protein binding activity and identical protein binding activity. Involved in positive regulation of cell communication and protein transport. Located in several cellular components, including Golgi apparatus; early endosome; and endoplasmic reticulum membrane. Implicated in Zaki syndrome . [provided by Alliance of Genome Resources, Jul 2025] | 1 | 68098459 | 68232546 | Human | 226 | old_gene_name , old_gene_symbol | gene, protein-coding, VALIDATED [RefSeq] |
| 1346677 | SLC52A1 | solute carrier family 52 member 1 | Biological redox reactions require electron donors and acceptor. Vitamin B2 is the source for the flavin in flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) which are common redox reagents. This gene encodes a member of the riboflavin (vitamin B2) transporter family. Haploinsufficie ncy of this protein can cause maternal riboflavin deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jan 2013] | 17 | 5032602 | 5042414 | Human | 91 | old_gene_symbol | gene, protein-coding, REVIEWED [RefSeq] |
| 1349767 | SLC52A2 | solute carrier family 52 member 2 | This gene encodes a membrane protein which belongs to the riboflavin transporter family. In humans, riboflavin must be obtained by intestinal absorption because it cannot be synthesized by the body. The water-soluble vitamin riboflavin is processed to the coenzymes flavin mononucleotide (FMN) and fl avin adenine dinucleotide (FAD) which then act as intermediaries in many cellular metabolic reactions. Paralogous members of the riboflavin transporter gene family are located on chromosomes 17 and 20. Unlike other members of this family, this gene has higher expression in brain tissue than small intestine. Alternative splicing of this gene results in multiple transcript variants encoding the same protein. Mutations in this gene have been associated with Brown-Vialetto-Van Laere syndrome 2 - an autosomal recessive progressive neurologic disorder characterized by deafness, bulbar dysfunction, and axial and limb hypotonia. [provided by RefSeq, Jul 2012] | 8 | 144358552 | 144361272 | Human | 181 | old_gene_symbol | gene, protein-coding, REVIEWED [RefSeq] |
| 16562210 | AC023908.1 | novel transcript, sense overlapping GPR176 | | | | | Human | | name | gene, lncrna |
