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GP142_HUMAN
ID   GP142_HUMAN             Reviewed;         462 AA.
AC   Q7Z601; A4CYJ8; Q86SL3;
DT   10-MAY-2005, integrated into UniProtKB/Swiss-Prot.
DT   01-OCT-2003, sequence version 1.
DT   03-AUG-2022, entry version 138.
DE   RecName: Full=Probable G-protein coupled receptor 142;
DE   AltName: Full=G-protein coupled receptor PGR2;
GN   Name=GPR142; Synonyms=PGR2;
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].
RX   PubMed=14623098; DOI=10.1016/s0014-5793(03)01196-7;
RA   Fredriksson R., Hoeglund P.J., Gloriam D.E.I., Lagerstroem M.C.,
RA   Schioeth H.B.;
RT   "Seven evolutionarily conserved human rhodopsin G protein-coupled receptors
RT   lacking close relatives.";
RL   FEBS Lett. 554:381-388(2003).
RN   [2]
RP   NUCLEOTIDE SEQUENCE [MRNA], AND TISSUE SPECIFICITY.
RX   PubMed=15845401; DOI=10.1016/j.bbrc.2005.03.174;
RA   Matsuo A., Matsumoto S., Nagano M., Masumoto K.H., Takasaki J.,
RA   Matsumoto M., Kobori M., Katoh M., Shigeyoshi Y.;
RT   "Molecular cloning and characterization of a novel Gq-coupled orphan
RT   receptor GPRg1 exclusively expressed in the central nervous system.";
RL   Biochem. Biophys. Res. Commun. 331:363-369(2005).
RN   [3]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 122-436, AND VARIANT ASN-132.
RX   PubMed=12679517; DOI=10.1073/pnas.0230374100;
RA   Vassilatis D.K., Hohmann J.G., Zeng H., Li F., Ranchalis J.E.,
RA   Mortrud M.T., Brown A., Rodriguez S.S., Weller J.R., Wright A.C.,
RA   Bergmann J.E., Gaitanaris G.A.;
RT   "The G protein-coupled receptor repertoires of human and mouse.";
RL   Proc. Natl. Acad. Sci. U.S.A. 100:4903-4908(2003).
CC   -!- FUNCTION: Orphan receptor.
CC   -!- SUBCELLULAR LOCATION: Cell membrane; Multi-pass membrane protein.
CC   -!- TISSUE SPECIFICITY: Exclusively expressed in the central nervous
CC       system, most abundantly in the ventrolateral region of caudate putamen,
CC       the habenular nucleus, the zona incerta, and the medial mammillary
CC       nucleus. {ECO:0000269|PubMed:15845401}.
CC   -!- SIMILARITY: Belongs to the G-protein coupled receptor 1 family.
CC       {ECO:0000255|PROSITE-ProRule:PRU00521}.
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DR   EMBL; AY288421; AAP72130.1; -; mRNA.
DR   EMBL; AB196530; BAD97441.1; -; mRNA.
DR   EMBL; AY255622; AAO85134.1; -; mRNA.
DR   CCDS; CCDS11698.1; -.
DR   RefSeq; NP_001318005.1; NM_001331076.1.
DR   RefSeq; NP_001318006.1; NM_001331077.1.
DR   RefSeq; NP_861455.1; NM_181790.1.
DR   AlphaFoldDB; Q7Z601; -.
DR   SMR; Q7Z601; -.
DR   BioGRID; 131570; 2.
DR   STRING; 9606.ENSP00000335158; -.
DR   BindingDB; Q7Z601; -.
DR   ChEMBL; CHEMBL2069161; -.
DR   GuidetoPHARMACOLOGY; 132; -.
DR   iPTMnet; Q7Z601; -.
DR   PhosphoSitePlus; Q7Z601; -.
DR   BioMuta; GPR142; -.
DR   DMDM; 83288229; -.
DR   PaxDb; Q7Z601; -.
DR   PeptideAtlas; Q7Z601; -.
DR   PRIDE; Q7Z601; -.
DR   Antibodypedia; 51646; 181 antibodies from 29 providers.
DR   DNASU; 350383; -.
DR   Ensembl; ENST00000335666.4; ENSP00000335158.4; ENSG00000257008.7.
DR   GeneID; 350383; -.
DR   KEGG; hsa:350383; -.
DR   UCSC; uc032fqt.2; human.
DR   CTD; 350383; -.
DR   DisGeNET; 350383; -.
DR   GeneCards; GPR142; -.
DR   HGNC; HGNC:20088; GPR142.
DR   HPA; ENSG00000257008; Not detected.
DR   MIM; 609046; gene.
DR   neXtProt; NX_Q7Z601; -.
DR   OpenTargets; ENSG00000257008; -.
DR   PharmGKB; PA134891802; -.
DR   VEuPathDB; HostDB:ENSG00000257008; -.
DR   eggNOG; KOG3656; Eukaryota.
DR   GeneTree; ENSGT00940000160948; -.
DR   HOGENOM; CLU_009579_24_1_1; -.
DR   InParanoid; Q7Z601; -.
DR   OMA; LKWVHCF; -.
DR   OrthoDB; 994073at2759; -.
DR   PhylomeDB; Q7Z601; -.
DR   TreeFam; TF334275; -.
DR   PathwayCommons; Q7Z601; -.
DR   BioGRID-ORCS; 350383; 11 hits in 1058 CRISPR screens.
DR   GeneWiki; GPR142; -.
DR   GenomeRNAi; 350383; -.
DR   Pharos; Q7Z601; Tchem.
DR   PRO; PR:Q7Z601; -.
DR   Proteomes; UP000005640; Chromosome 17.
DR   RNAct; Q7Z601; protein.
DR   Bgee; ENSG00000257008; Expressed in islet of Langerhans and 57 other tissues.
DR   ExpressionAtlas; Q7Z601; baseline and differential.
DR   GO; GO:0030054; C:cell junction; IDA:HPA.
DR   GO; GO:0005829; C:cytosol; IDA:HPA.
DR   GO; GO:0016021; C:integral component of membrane; IEA:UniProtKB-KW.
DR   GO; GO:0005886; C:plasma membrane; IDA:HPA.
DR   GO; GO:0004930; F:G protein-coupled receptor activity; IEA:UniProtKB-KW.
DR   GO; GO:0007186; P:G protein-coupled receptor signaling pathway; IBA:GO_Central.
DR   InterPro; IPR000276; GPCR_Rhodpsn.
DR   InterPro; IPR017452; GPCR_Rhodpsn_7TM.
DR   Pfam; PF00001; 7tm_1; 1.
DR   PRINTS; PR00237; GPCRRHODOPSN.
DR   PROSITE; PS00237; G_PROTEIN_RECEP_F1_1; 1.
DR   PROSITE; PS50262; G_PROTEIN_RECEP_F1_2; 1.
PE   2: Evidence at transcript level;
KW   Cell membrane; G-protein coupled receptor; Membrane; Receptor;
KW   Reference proteome; Transducer; Transmembrane; Transmembrane helix.
FT   CHAIN           1..462
FT                   /note="Probable G-protein coupled receptor 142"
FT                   /id="PRO_0000069620"
FT   TOPO_DOM        1..152
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        153..173
FT                   /note="Helical; Name=1"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        174..195
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        196..216
FT                   /note="Helical; Name=2"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        217..233
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        234..254
FT                   /note="Helical; Name=3"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        255..278
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        279..299
FT                   /note="Helical; Name=4"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        300..316
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        317..337
FT                   /note="Helical; Name=5"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        338..357
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        358..378
FT                   /note="Helical; Name=6"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        379..397
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        398..418
FT                   /note="Helical; Name=7"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        419..462
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   REGION          87..123
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   VARIANT         132
FT                   /note="H -> N (in dbSNP:rs2382647)"
FT                   /evidence="ECO:0000269|PubMed:12679517"
FT                   /id="VAR_061219"
SQ   SEQUENCE   462 AA;  51106 MW;  E9120B52372C75CA CRC64;
     MSIMMLPMEQ KIQWVPTSLQ DITAVLGTEA YTEEDKSMVS HAQKSQHSCL SHSRWLRSPQ
     VTGGSWDLRI RPSKDSSSFR QAQCLRKDPG ANNHLESQGV RGTAGDADRE LRGPSEKATA
     GQPRVTLLPT PHVSGLSQEF ESHWPEIAER SPCVAGVIPV IYYSVLLGLG LPVSLLTAVA
     LARLATRTRR PSYYYLLALT ASDIIIQVVI VFAGFLLQGA VLARQVPQAV VRTANILEFA
     ANHASVWIAI LLTVDRYTAL CHPLHHRAAS SPGRTRRAIA AVLSAALLTG IPFYWWLDMW
     RDTDSPRTLD EVLKWAHCLT VYFIPCGVFL VTNSAIIHRL RRRGRSGLQP RVGKSTAILL
     GITTLFTLLW APRVFVMLYH MYVAPVHRDW RVHLALDVAN MVAMLHTAAN FGLYCFVSKT
     FRATVRQVIH DAYLPCTLAS QPEGMAAKPV MEPPGLPTGA EV
 
 
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