GGRNA Home | Help | Advanced search

2024-04-24 08:13:28, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_000956               2494 bp    mRNA    linear   PRI 26-MAY-2013
DEFINITION  Homo sapiens prostaglandin E receptor 2 (subtype EP2), 53kDa
            (PTGER2), mRNA.
ACCESSION   NM_000956
VERSION     NM_000956.3  GI:194473721
KEYWORDS    RefSeq.
SOURCE      Homo sapiens (human)
  ORGANISM  Homo sapiens
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
            Catarrhini; Hominidae; Homo.
REFERENCE   1  (bases 1 to 2494)
  AUTHORS   Hu,S., Sun,W., Wei,W., Wang,D., Jin,J., Wu,J., Chen,J., Wu,H. and
            Wang,Q.
  TITLE     Involvement of the prostaglandin E receptor EP2 in
            paeoniflorin-induced human hepatoma cell apoptosis
  JOURNAL   Anticancer Drugs 24 (2), 140-149 (2013)
   PUBMED   23069790
  REMARK    GeneRIF: The expression of the EP2 receptor and Bcl-2 was
            significantly increased.
REFERENCE   2  (bases 1 to 2494)
  AUTHORS   Wildenhain,S., Ingenhag,D., Ruckert,C., Degistirici,O., Dugas,M.,
            Meisel,R., Hauer,J. and Borkhardt,A.
  TITLE     Homeobox protein HB9 binds to the prostaglandin E receptor 2
            promoter and inhibits intracellular cAMP mobilization in leukemic
            cells
  JOURNAL   J. Biol. Chem. 287 (48), 40703-40712 (2012)
   PUBMED   23048027
  REMARK    GeneRIF: HB9 binds to the prostaglandin E receptor 2 promoter and
            inhibits intracellular cAMP mobilization in leukemic cells.
REFERENCE   3  (bases 1 to 2494)
  AUTHORS   To,S.Q., Takagi,K., Miki,Y., Suzuki,K., Abe,E., Yang,Y., Sasano,H.,
            Simpson,E.R., Knower,K.C. and Clyne,C.D.
  TITLE     Epigenetic mechanisms regulate the prostaglandin E receptor 2 in
            breast cancer
  JOURNAL   J. Steroid Biochem. Mol. Biol. 132 (3-5), 331-338 (2012)
   PUBMED   22929011
  REMARK    GeneRIF: Although EP2 methylation status is inversely correlated to
            expression levels in established breast cancer cell lines, we could
            not identify that such a correlation existed in tumour-associated
            stroma cells.
REFERENCE   4  (bases 1 to 2494)
  AUTHORS   Desai,S., April,H., Nwaneshiudu,C. and Ashby,B.
  TITLE     Comparison of agonist-induced internalization of the human EP2 and
            EP4 prostaglandin receptors: role of the carboxyl terminus in EP4
            receptor sequestration
  JOURNAL   Mol. Pharmacol. 58 (6), 1279-1286 (2000)
   PUBMED   11093764
REFERENCE   5  (bases 1 to 2494)
  AUTHORS   Smock,S.L., Pan,L.C., Castleberry,T.A., Lu,B., Mather,R.J. and
            Owen,T.A.
  TITLE     Cloning, structural characterization, and chromosomal localization
            of the gene encoding the human prostaglandin E(2) receptor EP2
            subtype
  JOURNAL   Gene 237 (2), 393-402 (1999)
   PUBMED   10521663
REFERENCE   6  (bases 1 to 2494)
  AUTHORS   Stillman,B.A., Breyer,M.D. and Breyer,R.M.
  TITLE     Importance of the extracellular domain for prostaglandin EP(2)
            receptor function
  JOURNAL   Mol. Pharmacol. 56 (3), 545-551 (1999)
   PUBMED   10462542
REFERENCE   7  (bases 1 to 2494)
  AUTHORS   Duncan,A.M., Anderson,L.L., Funk,C.D., Abramovitz,M. and Adam,M.
  TITLE     Chromosomal localization of the human prostanoid receptor gene
            family
  JOURNAL   Genomics 25 (3), 740-742 (1995)
   PUBMED   7759114
REFERENCE   8  (bases 1 to 2494)
  AUTHORS   Regan,J.W., Bailey,T.J., Pepperl,D.J., Pierce,K.L., Bogardus,A.M.,
            Donello,J.E., Fairbairn,C.E., Kedzie,K.M., Woodward,D.F. and
            Gil,D.W.
  TITLE     Cloning of a novel human prostaglandin receptor with
            characteristics of the pharmacologically defined EP2 subtype
  JOURNAL   Mol. Pharmacol. 46 (2), 213-220 (1994)
   PUBMED   8078484
REFERENCE   9  (bases 1 to 2494)
  AUTHORS   Bastien,L., Sawyer,N., Grygorczyk,R., Metters,K.M. and Adam,M.
  TITLE     Cloning, functional expression, and characterization of the human
            prostaglandin E2 receptor EP2 subtype
  JOURNAL   J. Biol. Chem. 269 (16), 11873-11877 (1994)
   PUBMED   8163486
REFERENCE   10 (bases 1 to 2494)
  AUTHORS   An,S., Yang,J., Xia,M. and Goetzl,E.J.
  TITLE     Cloning and expression of the EP2 subtype of human receptors for
            prostaglandin E2
  JOURNAL   Biochem. Biophys. Res. Commun. 197 (1), 263-270 (1993)
   PUBMED   8250933
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from CR977661.1, CN484094.1,
            BC093927.1, CF132756.1, BE739744.1, U19487.1 and BM986745.1.
            This sequence is a reference standard in the RefSeqGene project.
            On Jul 26, 2008 this sequence version replaced gi:31881629.
            
            Summary: This gene encodes a receptor for prostaglandin E2, a
            metabolite of arachidonic acid which has different biologic
            activities in a wide range of tissues. Mutations in this gene are
            associated with aspirin-induced susceptibility to asthma. [provided
            by RefSeq, Oct 2009].
            
            Publication Note:  This RefSeq record includes a subset of the
            publications that are available for this gene. Please see the Gene
            record to access additional publications.
            
            ##Evidence-Data-START##
            Transcript exon combination :: U19487.1, BC093927.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025081, ERS025084 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-179               CR977661.1         1-179
            180-325             CN484094.1         157-302
            326-1411            BC093927.1         128-1213
            1412-1536           CF132756.1         184-308
            1537-1770           BE739744.1         19-252              c
            1771-2090           U19487.1           1676-1995
            2091-2494           BM986745.1         1-404               c
FEATURES             Location/Qualifiers
     source          1..2494
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="14"
                     /map="14q22"
     gene            1..2494
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /note="prostaglandin E receptor 2 (subtype EP2), 53kDa"
                     /db_xref="GeneID:5732"
                     /db_xref="HGNC:9594"
                     /db_xref="HPRD:08905"
                     /db_xref="MIM:176804"
     exon            1..1094
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /inference="alignment:Splign:1.39.8"
     variation       86
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1353411"
     misc_feature    162..164
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /note="upstream in-frame stop codon"
     variation       180
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1254598"
     STS             199..1411
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /db_xref="UniSTS:484297"
     variation       218
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367906865"
     variation       251
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377586161"
     CDS             252..1328
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /note="prostanoid EP2 receptor; PGE receptor EP2 subtype;
                     PGE2 receptor EP2 subtype"
                     /codon_start=1
                     /product="prostaglandin E2 receptor EP2 subtype"
                     /protein_id="NP_000947.2"
                     /db_xref="GI:31881630"
                     /db_xref="CCDS:CCDS9708.1"
                     /db_xref="GeneID:5732"
                     /db_xref="HGNC:9594"
                     /db_xref="HPRD:08905"
                     /db_xref="MIM:176804"
                     /translation="
MGNASNDSQSEDCETRQWLPPGESPAISSVMFSAGVLGNLIALALLARRWRGDVGCSAGRRSSLSLFHVLVTELVFTDLLGTCLISPVVLASYARNQTLVALAPESRACTYFAFAMTFFSLATMLMLFAMALERYLSIGHPYFYQRRVSRSGGLAVLPVIYAVSLLFCSLPLLDYGQYVQYCPGTWCFIRHGRTAYLQLYATLLLLLIVSVLACNFSVILNLIRMHRRSRRSRCGPSLGSGRGGPGARRRGERVSMAEETDHLILLAIMTITFAVCSLPFTIFAYMNETSSRKEKWDLQALRFLSINSIIDPWVFAILRPPVLRLMRSVLCCRISLRTQDATQTSCSTQSDASKQADL
"
     misc_feature    321..392
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P43116.2);
                     transmembrane region"
     misc_feature    432..1193
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /note="7 transmembrane receptor (rhodopsin family);
                     Region: 7tm_1; pfam00001"
                     /db_xref="CDD:200918"
     misc_feature    447..524
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P43116.2);
                     transmembrane region"
     misc_feature    585..647
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P43116.2);
                     transmembrane region"
     misc_feature    705..779
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P43116.2);
                     transmembrane region"
     misc_feature    846..920
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P43116.2);
                     transmembrane region"
     misc_feature    1038..1109
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P43116.2);
                     transmembrane region"
     misc_feature    1149..1220
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (P43116.2);
                     transmembrane region"
     variation       252
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369088393"
     variation       278
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373293918"
     variation       283
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143842615"
     variation       284
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200159674"
     variation       326
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:1353410"
     variation       371
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140005651"
     variation       385
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371237403"
     variation       403
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:149858582"
     variation       430
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139726427"
     variation       434
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:373886710"
     variation       447
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199970087"
     variation       458
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376819687"
     variation       467
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143268571"
     variation       468
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371082222"
     variation       491
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146696779"
     variation       498
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:111965614"
     variation       563
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142520476"
     variation       587
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151002714"
     variation       657
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:140871944"
     variation       744
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:150176330"
     variation       788
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:138820478"
     variation       797
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141336040"
     variation       799
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147051461"
     variation       864
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200859761"
     variation       875
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200194449"
     variation       879
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138405848"
     variation       898
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:199670925"
     variation       917
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:143806281"
     variation       918
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:368578200"
     variation       921
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201355660"
     variation       928..929
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:377257557"
     variation       928
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:77558975"
     variation       966
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112051607"
     variation       975
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144220413"
     variation       997
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199687826"
     variation       1022
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:61757786"
     variation       1028
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200330886"
     variation       1037
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:148307308"
     variation       1061
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:34414213"
     exon            1095..2480
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /inference="alignment:Splign:1.39.8"
     variation       1105
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139552094"
     variation       1118
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:45478594"
     variation       1142
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144210519"
     variation       1163
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2229187"
     variation       1167
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200776840"
     variation       1169
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:60167547"
     variation       1193
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:181468557"
     variation       1202
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372997180"
     variation       1205
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377525620"
     variation       1276
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149912921"
     variation       1278
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:111527326"
     variation       1288
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367922312"
     variation       1340
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:199599262"
     variation       1390
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:708502"
     variation       1415
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148744234"
     variation       1442
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371901911"
     STS             1449..1639
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /standard_name="G59837"
                     /db_xref="UniSTS:136986"
     variation       1537
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:17197"
     variation       1573
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:45472599"
     STS             1631..1965
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /standard_name="SHGC-12634"
                     /db_xref="UniSTS:58544"
     variation       1859
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:142305426"
     variation       1996
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:186059271"
     variation       2015
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:45501991"
     variation       2056
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:45461592"
     variation       2089..2092
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace=""
                     /replace="ttta"
                     /db_xref="dbSNP:35932603"
     variation       2090..2093
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace=""
                     /replace="ttat"
                     /db_xref="dbSNP:45460603"
     variation       2190
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189260273"
     variation       2256
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1042618"
     variation       2355..2358
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace=""
                     /replace="tgtt"
                     /db_xref="dbSNP:368242759"
     variation       2432
                     /gene="PTGER2"
                     /gene_synonym="EP2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:181203428"
     polyA_signal    2453..2458
                     /gene="PTGER2"
                     /gene_synonym="EP2"
     polyA_site      2480
                     /gene="PTGER2"
                     /gene_synonym="EP2"
ORIGIN      
cggccttggccggcgcgggtaggcgcgggagcctcgagcgccgctcggatgcagcagccgagccgccactcggcgcgcggcgggagacccagggcaagccgccgtcggcgcgctgggtgcgggaagggggctctggatttcggtccctcccctttttcctctgagtctcggaacgctccggctctcagaccctcttcctcccaggtaaaggccgggagaggagggcgcatctcttttccaggcaccccaccatgggcaatgcctccaatgactcccagtctgaggactgcgagacgcgacagtggcttcccccaggcgaaagcccagccatcagctccgtcatgttctcggccggggtgctggggaacctcatagcactggcgctgctggcgcgccgctggcggggggacgtggggtgcagcgccggccgcaggagctccctctccttgttccacgtgctggtgaccgagctggtgttcaccgacctgctcgggacctgcctcatcagcccagtggtactggcttcgtacgcgcggaaccagaccctggtggcactggcgcccgagagccgcgcgtgcacctacttcgctttcgccatgaccttcttcagcctggccacgatgctcatgctcttcgccatggccctggagcgctacctctcgatcgggcacccctacttctaccagcgccgcgtctcgcgctccgggggcctggccgtgctgcctgtcatctatgcagtctccctgctcttctgctcgctgccgctgctggactatgggcagtacgtccagtactgccccgggacctggtgcttcatccggcacgggcggaccgcttacctgcagctgtacgccaccctgctgctgcttctcattgtctcggtgctcgcctgcaacttcagtgtcattctcaacctcatccgcatgcaccgccgaagccggagaagccgctgcggaccttccctgggcagtggccggggcggccccggggcccgcaggagaggggaaagggtgtccatggcggaggagacggaccacctcattctcctggctatcatgaccatcaccttcgccgtctgctccttgcctttcacgatttttgcatatatgaatgaaacctcttcccgaaaggaaaaatgggacctccaagctcttaggtttttatcaattaattcaataattgacccttgggtctttgccatccttaggcctcctgttctgagactaatgcgttcagtcctctgttgtcggatttcattaagaacacaagatgcaacacaaacttcctgttctacacagtcagatgccagtaaacaggctgacctttgaggtcagtagtttaaaagttcttagttatatagcatctggaagatcattttgaaattgttccttggagaaatgaaaacagtgtgtaaacaaaatgaagctgccctaataaaaaggagtatacaaacatttaagctgtggtcaaggctacagatgtgctgacaaggcacttcatgtaaagtgtcagaaggagctacaaaacctaccctcagtgagcatggtacttggcctttggaggaacaatcggctgcattgaagatccagctgcctattgatttaagctttcctgttgaatgacaaagtatgtggttttgtaatttgtttgaaaccccaaacagtgactgtactttctattttaatcttgctactaccgttatacacatatagtgtacagccagaccagattaaacttcatatgtaatctctaggaagtcaatatgtggaagcaaccaagcctgctgtcttgtgatcacttagcgaaccctttatttgaacaatgaagttgaaaatcataggcaccttttactgtgatgtttgtgtatgtgggagtactctcatcactacagtattactcttacaagagtggactcagtgggttaacatcagttttgtttactcatcctccaggaactgcaggtcaagttgtcaggttatttattttataatgtccatatgctaatagtgatcaagaagactttaggaatggttctctcaacaagaaataatagaaatgtctcaaggcagttaattctcattaatactctttatttatcctatttctgggggaggatgtacgtggccatgtatgaagccaaatattaggcttaaaaactgaaaaatctggttcattcttcagatatactggaacccttttaaagttgatattggggccatgagtaaaatagattttataagatgactgtgttgtaccaaaattcatctgtctatattttatttagggaacatggtttgactcatcttatatgggaaaccatgtagcagtgagtcatatcttaatatatttctaaatgtttggcatgtaaatgtaaactcagcatcaaaatatttcagtgaatttgcactgtttaatcatagttactgtgtaaactcatctgaaatgttacaaaaataaactataaaacaaaaatttgaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:5732 -> Molecular function: GO:0004957 [prostaglandin E receptor activity] evidence: IEA
            GeneID:5732 -> Biological process: GO:0007186 [G-protein coupled receptor signaling pathway] evidence: TAS
            GeneID:5732 -> Biological process: GO:0007189 [adenylate cyclase-activating G-protein coupled receptor signaling pathway] evidence: ISS
            GeneID:5732 -> Biological process: GO:0032496 [response to lipopolysaccharide] evidence: IEA
            GeneID:5732 -> Biological process: GO:0042127 [regulation of cell proliferation] evidence: IEA
            GeneID:5732 -> Biological process: GO:0071380 [cellular response to prostaglandin E stimulus] evidence: ISS
            GeneID:5732 -> Cellular component: GO:0005886 [plasma membrane] evidence: TAS
            GeneID:5732 -> Cellular component: GO:0005887 [integral to plasma membrane] evidence: TAS

by @meso_cacase at DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.