ID GPR85_HUMAN Reviewed; 370 AA. AC P60893; Q9JHI6; Q9NPD1; DT 13-APR-2004, integrated into UniProtKB/Swiss-Prot. DT 13-APR-2004, sequence version 1. DT 24-JAN-2024, entry version 154. DE RecName: Full=Probable G-protein coupled receptor 85; DE AltName: Full=Super conserved receptor expressed in brain 2; GN Name=GPR85; Synonyms=SREB2; OS Homo sapiens (Human). OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; OC Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; OC Homo. OX NCBI_TaxID=9606; RN [1] RP NUCLEOTIDE SEQUENCE [MRNA], AND TISSUE SPECIFICITY. RC TISSUE=Brain; RX PubMed=10978537; DOI=10.1016/s0167-4781(00)00182-2; RA Hellebrand S., Schaller H.C., Wittenberger T.; RT "The brain-specific G-protein coupled receptor GPR85 with identical protein RT sequence in man and mouse maps to human chromosome 7q31."; RL Biochim. Biophys. Acta 1493:269-272(2000). RN [2] RP NUCLEOTIDE SEQUENCE [MRNA], AND TISSUE SPECIFICITY. RC TISSUE=Brain; RX PubMed=10833454; DOI=10.1006/bbrc.2000.2829; RA Matsumoto M., Saito T., Takasaki J., Kamohara M., Sugimoto T., RA Kobayashi M., Tadokoro M., Matsumoto S., Ohishi T., Furuichi K.; RT "An evolutionarily conserved G-protein coupled receptor family, SREB, RT expressed in the central nervous system."; RL Biochem. Biophys. Res. Commun. 272:576-582(2000). RN [3] RP NUCLEOTIDE SEQUENCE [GENOMIC DNA]. RA Suwa M., Sato T., Okouchi I., Arita M., Futami K., Matsumoto S., RA Tsutsumi S., Aburatani H., Asai K., Akiyama Y.; RT "Genome-wide discovery and analysis of human seven transmembrane helix RT receptor genes."; RL Submitted (JUL-2001) to the EMBL/GenBank/DDBJ databases. RN [4] RP NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]. RC TISSUE=Amygdala; RX PubMed=17974005; DOI=10.1186/1471-2164-8-399; RA Bechtel S., Rosenfelder H., Duda A., Schmidt C.P., Ernst U., RA Wellenreuther R., Mehrle A., Schuster C., Bahr A., Bloecker H., Heubner D., RA Hoerlein A., Michel G., Wedler H., Koehrer K., Ottenwaelder B., Poustka A., RA Wiemann S., Schupp I.; RT "The full-ORF clone resource of the German cDNA consortium."; RL BMC Genomics 8:399-399(2007). RN [5] RP NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. RX PubMed=12853948; DOI=10.1038/nature01782; RA Hillier L.W., Fulton R.S., Fulton L.A., Graves T.A., Pepin K.H., RA Wagner-McPherson C., Layman D., Maas J., Jaeger S., Walker R., Wylie K., RA Sekhon M., Becker M.C., O'Laughlin M.D., Schaller M.E., Fewell G.A., RA Delehaunty K.D., Miner T.L., Nash W.E., Cordes M., Du H., Sun H., RA Edwards J., Bradshaw-Cordum H., Ali J., Andrews S., Isak A., Vanbrunt A., RA Nguyen C., Du F., Lamar B., Courtney L., Kalicki J., Ozersky P., RA Bielicki L., Scott K., Holmes A., Harkins R., Harris A., Strong C.M., RA Hou S., Tomlinson C., Dauphin-Kohlberg S., Kozlowicz-Reilly A., Leonard S., RA Rohlfing T., Rock S.M., Tin-Wollam A.-M., Abbott A., Minx P., Maupin R., RA Strowmatt C., Latreille P., Miller N., Johnson D., Murray J., RA Woessner J.P., Wendl M.C., Yang S.-P., Schultz B.R., Wallis J.W., RA Spieth J., Bieri T.A., Nelson J.O., Berkowicz N., Wohldmann P.E., RA Cook L.L., Hickenbotham M.T., Eldred J., Williams D., Bedell J.A., RA Mardis E.R., Clifton S.W., Chissoe S.L., Marra M.A., Raymond C., Haugen E., RA Gillett W., Zhou Y., James R., Phelps K., Iadanoto S., Bubb K., Simms E., RA Levy R., Clendenning J., Kaul R., Kent W.J., Furey T.S., Baertsch R.A., RA Brent M.R., Keibler E., Flicek P., Bork P., Suyama M., Bailey J.A., RA Portnoy M.E., Torrents D., Chinwalla A.T., Gish W.R., Eddy S.R., RA McPherson J.D., Olson M.V., Eichler E.E., Green E.D., Waterston R.H., RA Wilson R.K.; RT "The DNA sequence of human chromosome 7."; RL Nature 424:157-164(2003). RN [6] RP VARIANTS THR-152 AND LEU-221, CHARACTERIZATION OF VARIANTS THR-152 AND RP LEU-221, SUBCELLULAR LOCATION, AND INTERACTION WITH DLG4 AND DLG3. RX PubMed=25780553; DOI=10.1186/s13229-015-0012-5; RA Fujita-Jimbo E., Tanabe Y., Yu Z., Kojima K., Mori M., Li H., Iwamoto S., RA Yamagata T., Momoi M.Y., Momoi T.; RT "The association of GPR85 with PSD-95-neuroligin complex and autism RT spectrum disorder: a molecular analysis."; RL Mol. Autism 6:17-17(2015). CC -!- FUNCTION: Orphan receptor. CC -!- SUBUNIT: Interacts with DLG4 and DLG3. {ECO:0000269|PubMed:25780553}. CC -!- SUBCELLULAR LOCATION: Cell membrane {ECO:0000250}; Multi-pass membrane CC protein {ECO:0000250}. Endoplasmic reticulum CC {ECO:0000269|PubMed:25780553}. CC -!- TISSUE SPECIFICITY: Highly expressed in brain and testis. Lower levels CC in small intestine, placenta and spleen. In brain regions, detected in CC all regions tested, but somewhat lower levels in the corpus callosum, CC medulla and spinal cord. {ECO:0000269|PubMed:10833454, CC ECO:0000269|PubMed:10978537}. CC -!- SIMILARITY: Belongs to the G-protein coupled receptor 1 family. CC {ECO:0000255|PROSITE-ProRule:PRU00521}. CC --------------------------------------------------------------------------- CC Copyrighted by the UniProt Consortium, see https://www.uniprot.org/terms CC Distributed under the Creative Commons Attribution (CC BY 4.0) License CC --------------------------------------------------------------------------- DR EMBL; AF250237; AAF79956.1; -; mRNA. DR EMBL; AB040800; BAA96646.1; -; mRNA. DR EMBL; AB065688; BAC05911.1; -; Genomic_DNA. DR EMBL; AL161959; CAB82307.1; -; mRNA. DR EMBL; AC073346; AAQ93365.1; -; Genomic_DNA. DR CCDS; CCDS5758.1; -. DR PIR; T47131; T47131. DR RefSeq; NP_001139737.1; NM_001146265.1. DR RefSeq; NP_001139738.1; NM_001146266.1. DR RefSeq; NP_001139739.1; NM_001146267.1. DR RefSeq; NP_061843.3; NM_018970.6. DR RefSeq; XP_005250508.1; XM_005250451.2. DR RefSeq; XP_016867841.1; XM_017012352.1. DR AlphaFoldDB; P60893; -. DR SMR; P60893; -. DR BioGRID; 119932; 11. DR IntAct; P60893; 1. DR STRING; 9606.ENSP00000297146; -. DR ChEMBL; CHEMBL4523868; -. DR GlyCosmos; P60893; 3 sites, No reported glycans. DR GlyGen; P60893; 3 sites. DR iPTMnet; P60893; -. DR PhosphoSitePlus; P60893; -. DR BioMuta; GPR85; -. DR DMDM; 46397442; -. DR MassIVE; P60893; -. DR PaxDb; 9606-ENSP00000297146; -. DR PeptideAtlas; P60893; -. DR ProteomicsDB; 57234; -. DR Antibodypedia; 17381; 182 antibodies from 26 providers. DR DNASU; 54329; -. DR Ensembl; ENST00000297146.7; ENSP00000297146.2; ENSG00000164604.14. DR Ensembl; ENST00000424100.2; ENSP00000396763.1; ENSG00000164604.14. DR Ensembl; ENST00000449591.2; ENSP00000401178.1; ENSG00000164604.14. DR Ensembl; ENST00000610164.1; ENSP00000476863.1; ENSG00000164604.14. DR GeneID; 54329; -. DR KEGG; hsa:54329; -. DR MANE-Select; ENST00000424100.2; ENSP00000396763.1; NM_001146267.2; NP_001139739.1. DR UCSC; uc003vgp.2; human. DR AGR; HGNC:4536; -. DR CTD; 54329; -. DR DisGeNET; 54329; -. DR GeneCards; GPR85; -. DR HGNC; HGNC:4536; GPR85. DR HPA; ENSG00000164604; Group enriched (brain, retina, skeletal muscle). DR MIM; 605188; gene. DR neXtProt; NX_P60893; -. DR OpenTargets; ENSG00000164604; -. DR PharmGKB; PA28929; -. DR VEuPathDB; HostDB:ENSG00000164604; -. DR eggNOG; KOG3656; Eukaryota. DR GeneTree; ENSGT00890000139436; -. DR HOGENOM; CLU_055518_0_0_1; -. DR InParanoid; P60893; -. DR OMA; WCPYLVA; -. DR OrthoDB; 2962814at2759; -. DR PhylomeDB; P60893; -. DR TreeFam; TF331163; -. DR PathwayCommons; P60893; -. DR SignaLink; P60893; -. DR BioGRID-ORCS; 54329; 14 hits in 1149 CRISPR screens. DR GenomeRNAi; 54329; -. DR Pharos; P60893; Tbio. DR PRO; PR:P60893; -. DR Proteomes; UP000005640; Chromosome 7. DR RNAct; P60893; Protein. DR Bgee; ENSG00000164604; Expressed in cortical plate and 128 other cell types or tissues. DR ExpressionAtlas; P60893; baseline and differential. DR GO; GO:0005783; C:endoplasmic reticulum; IDA:UniProtKB. DR GO; GO:0005886; C:plasma membrane; IDA:LIFEdb. DR GO; GO:0004930; F:G protein-coupled receptor activity; IBA:GO_Central. DR GO; GO:0007165; P:signal transduction; TAS:UniProtKB. DR CDD; cd15218; 7tmA_SREB2_GPR85; 1. DR Gene3D; 1.20.1070.10; Rhodopsin 7-helix transmembrane proteins; 1. DR InterPro; IPR000276; GPCR_Rhodpsn. DR InterPro; IPR017452; GPCR_Rhodpsn_7TM. DR PANTHER; PTHR19268; G PROTEIN-COUPLED RECEPTOR; 1. DR PANTHER; PTHR19268:SF7; G-PROTEIN COUPLED RECEPTOR 85-RELATED; 1. DR Pfam; PF00001; 7tm_1; 1. DR PRINTS; PR00237; GPCRRHODOPSN. DR SUPFAM; SSF81321; Family A G protein-coupled receptor-like; 1. DR PROSITE; PS50262; G_PROTEIN_RECEP_F1_2; 1. DR Genevisible; P60893; HS. PE 1: Evidence at protein level; KW Cell membrane; Disulfide bond; Endoplasmic reticulum; KW G-protein coupled receptor; Glycoprotein; Membrane; Receptor; KW Reference proteome; Transducer; Transmembrane; Transmembrane helix. FT CHAIN 1..370 FT /note="Probable G-protein coupled receptor 85" FT /id="PRO_0000069591" FT TOPO_DOM 1..25 FT /note="Extracellular" FT /evidence="ECO:0000255" FT TRANSMEM 26..46 FT /note="Helical; Name=1" FT /evidence="ECO:0000255" FT TOPO_DOM 47..57 FT /note="Cytoplasmic" FT /evidence="ECO:0000255" FT TRANSMEM 58..78 FT /note="Helical; Name=2" FT /evidence="ECO:0000255" FT TOPO_DOM 79..96 FT /note="Extracellular" FT /evidence="ECO:0000255" FT TRANSMEM 97..117 FT /note="Helical; Name=3" FT /evidence="ECO:0000255" FT TOPO_DOM 118..137 FT /note="Cytoplasmic" FT /evidence="ECO:0000255" FT TRANSMEM 138..158 FT /note="Helical; Name=4" FT /evidence="ECO:0000255" FT TOPO_DOM 159..188 FT /note="Extracellular" FT /evidence="ECO:0000255" FT TRANSMEM 189..209 FT /note="Helical; Name=5" FT /evidence="ECO:0000255" FT TOPO_DOM 210..286 FT /note="Cytoplasmic" FT /evidence="ECO:0000255" FT TRANSMEM 287..307 FT /note="Helical; Name=6" FT /evidence="ECO:0000255" FT TOPO_DOM 308..313 FT /note="Extracellular" FT /evidence="ECO:0000255" FT TRANSMEM 314..334 FT /note="Helical; Name=7" FT /evidence="ECO:0000255" FT TOPO_DOM 335..370 FT /note="Cytoplasmic" FT /evidence="ECO:0000255" FT CARBOHYD 3 FT /note="N-linked (GlcNAc...) asparagine" FT /evidence="ECO:0000255" FT CARBOHYD 83 FT /note="N-linked (GlcNAc...) asparagine" FT /evidence="ECO:0000255" FT CARBOHYD 182 FT /note="N-linked (GlcNAc...) asparagine" FT /evidence="ECO:0000255" FT DISULFID 94..172 FT /evidence="ECO:0000255|PROSITE-ProRule:PRU00521" FT VARIANT 152 FT /note="M -> T (found in a patient with autism spectrum FT disorder; uncertain significance; induces response to FT endoplasmic reticulum stress; negative regulation of FT dendrite morphogenesis)" FT /evidence="ECO:0000269|PubMed:25780553" FT /id="VAR_074204" FT VARIANT 221 FT /note="V -> L (found in a patient with autism spectrum FT disorder; uncertain significance; induces response to FT endoplasmic reticulum stress; negative regulation of FT dendrite morphogenesis)" FT /evidence="ECO:0000269|PubMed:25780553" FT /id="VAR_074205" SQ SEQUENCE 370 AA; 41995 MW; 7B67A39F6166AAEB CRC64; MANYSHAADN ILQNLSPLTA FLKLTSLGFI IGVSVVGNLL ISILLVKDKT LHRAPYYFLL DLCCSDILRS AICFPFVFNS VKNGSTWTYG TLTCKVIAFL GVLSCFHTAF MLFCISVTRY LAIAHHRFYT KRLTFWTCLA VICMVWTLSV AMAFPPVLDV GTYSFIREED QCTFQHRSFR ANDSLGFMLL LALILLATQL VYLKLIFFVH DRRKMKPVQF VAAVSQNWTF HGPGASGQAA ANWLAGFGRG PTPPTLLGIR QNANTTGRRR LLVLDEFKME KRISRMFYIM TFLFLTLWGP YLVACYWRVF ARGPVVPGGF LTAAVWMSFA QAGINPFVCI FSNRELRRCF STTLLYCRKS RLPREPYCVI //