GGRNA Home | Help | Advanced search

2024-04-18 19:14:01, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001165975            3107 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens phosphodiesterase 1B, calmodulin-dependent (PDE1B),
            transcript variant 2, mRNA.
ACCESSION   NM_001165975
VERSION     NM_001165975.2  GI:342187232
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 3107)
  AUTHORS   Bailey,S.D., Xie,C., Do,R., Montpetit,A., Diaz,R., Mohan,V.,
            Keavney,B., Yusuf,S., Gerstein,H.C., Engert,J.C. and Anand,S.
  CONSRTM   DREAM investigators
  TITLE     Variation at the NFATC2 locus increases the risk of
            thiazolidinedione-induced edema in the Diabetes REduction
            Assessment with ramipril and rosiglitazone Medication (DREAM) study
  JOURNAL   Diabetes Care 33 (10), 2250-2253 (2010)
   PUBMED   20628086
  REMARK    GeneRIF: Observational study of gene-disease association,
            gene-environment interaction, and pharmacogenomic / toxicogenomic.
            (HuGE Navigator)
REFERENCE   2  (bases 1 to 3107)
  AUTHORS   Talmud,P.J., Drenos,F., Shah,S., Shah,T., Palmen,J., Verzilli,C.,
            Gaunt,T.R., Pallas,J., Lovering,R., Li,K., Casas,J.P., Sofat,R.,
            Kumari,M., Rodriguez,S., Johnson,T., Newhouse,S.J., Dominiczak,A.,
            Samani,N.J., Caulfield,M., Sever,P., Stanton,A., Shields,D.C.,
            Padmanabhan,S., Melander,O., Hastie,C., Delles,C., Ebrahim,S.,
            Marmot,M.G., Smith,G.D., Lawlor,D.A., Munroe,P.B., Day,I.N.,
            Kivimaki,M., Whittaker,J., Humphries,S.E. and Hingorani,A.D.
  CONSRTM   ASCOT investigators; NORDIL investigators; BRIGHT Consortium
  TITLE     Gene-centric association signals for lipids and apolipoproteins
            identified via the HumanCVD BeadChip
  JOURNAL   Am. J. Hum. Genet. 85 (5), 628-642 (2009)
   PUBMED   19913121
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   3  (bases 1 to 3107)
  AUTHORS   Vandeput,F., Wolda,S.L., Krall,J., Hambleton,R., Uher,L.,
            McCaw,K.N., Radwanski,P.B., Florio,V. and Movsesian,M.A.
  TITLE     Cyclic nucleotide phosphodiesterase PDE1C1 in human cardiac
            myocytes
  JOURNAL   J. Biol. Chem. 282 (45), 32749-32757 (2007)
   PUBMED   17726023
REFERENCE   4  (bases 1 to 3107)
  AUTHORS   Bender,A.T. and Beavo,J.A.
  TITLE     PDE1B2 regulates cGMP and a subset of the phenotypic
            characteristics acquired upon macrophage differentiation from a
            monocyte
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 103 (2), 460-465 (2006)
   PUBMED   16407168
  REMARK    GeneRIF: PDE1B2 regulates a subset of phenotypic changes that occur
            upon phorbol-12-myristate-13-acetate-induced differentiation and
            likely also plays a role in differentiated macrophages by
            regulating agonist-stimulated cGMP levels
REFERENCE   5  (bases 1 to 3107)
  AUTHORS   Bender,A.T., Ostenson,C.L., Wang,E.H. and Beavo,J.A.
  TITLE     Selective up-regulation of PDE1B2 upon monocyte-to-macrophage
            differentiation
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 102 (2), 497-502 (2005)
   PUBMED   15625104
  REMARK    GeneRIF: Selective up-regulation of PDE1B2 upon
            monocyte-to-macrophage differentiation.
REFERENCE   6  (bases 1 to 3107)
  AUTHORS   Yu,J., Wolda,S.L., Frazier,A.L., Florio,V.A., Martins,T.J.,
            Snyder,P.B., Harris,E.A., McCaw,K.N., Farrell,C.A., Steiner,B.,
            Bentley,J.K., Beavo,J.A., Ferguson,K. and Gelinas,R.
  TITLE     Identification and characterisation of a human
            calmodulin-stimulated phosphodiesterase PDE1B1
  JOURNAL   Cell. Signal. 9 (7), 519-529 (1997)
   PUBMED   9419816
REFERENCE   7  (bases 1 to 3107)
  AUTHORS   Spence,S., Rena,G., Sullivan,M., Erdogan,S. and Houslay,M.D.
  TITLE     Receptor-mediated stimulation of lipid signalling pathways in CHO
            cells elicits the rapid transient induction of the PDE1B isoform of
            Ca2+/calmodulin-stimulated cAMP phosphodiesterase
  JOURNAL   Biochem. J. 321 (PT 1), 157-163 (1997)
   PUBMED   9003415
REFERENCE   8  (bases 1 to 3107)
  AUTHORS   Jiang,X., Li,J., Paskind,M. and Epstein,P.M.
  TITLE     Inhibition of calmodulin-dependent phosphodiesterase induces
            apoptosis in human leukemic cells
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 93 (20), 11236-11241 (1996)
   PUBMED   8855339
REFERENCE   9  (bases 1 to 3107)
  AUTHORS   Loughney,K., Martins,T.J., Harris,E.A., Sadhu,K., Hicks,J.B.,
            Sonnenburg,W.K., Beavo,J.A. and Ferguson,K.
  TITLE     Isolation and characterization of cDNAs corresponding to two human
            calcium, calmodulin-regulated, 3',5'-cyclic nucleotide
            phosphodiesterases
  JOURNAL   J. Biol. Chem. 271 (2), 796-806 (1996)
   PUBMED   8557689
REFERENCE   10 (bases 1 to 3107)
  AUTHORS   Repaske,D.R., Swinnen,J.V., Jin,S.L., Van Wyk,J.J. and Conti,M.
  TITLE     A polymerase chain reaction strategy to identify and clone cyclic
            nucleotide phosphodiesterase cDNAs. Molecular cloning of the cDNA
            encoding the 63-kDa calmodulin-dependent phosphodiesterase
  JOURNAL   J. Biol. Chem. 267 (26), 18683-18688 (1992)
   PUBMED   1326532
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from BX538092.1, BP342896.1 and
            BC032226.1.
            On Jul 30, 2011 this sequence version replaced gi:260166686.
            
            Summary: The protein encoded by this gene belongs to the cyclic
            nucleotide phosphodiesterase (PDE) family, and PDE1 subfamily.
            Members of the PDE1 family are calmodulin-dependent PDEs that are
            stimulated by a calcium-calmodulin complex. This PDE has
            dual-specificity for the second messengers, cAMP and cGMP, with a
            preference for cGMP as a substrate. cAMP and cGMP function as key
            regulators of many important physiological processes. Alternatively
            spliced transcript variants encoding different isoforms have been
            described for this gene.[provided by RefSeq, Jul 2011].
            
            Transcript Variant: This variant (2) contains an alternate 5'
            terminal exon (with an AUG codon) compared to variant 1. This
            results in a shorter isoform (2) with a distinct N-terminus
            compared to isoform 1.
            
            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 :: AJ401609.1, AK302931.1 [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
            1-96                BX538092.1         1-96
            97-605              BP342896.1         76-584
            606-2364            BX538092.1         509-2267
            2365-3107           BC032226.1         2450-3192
FEATURES             Location/Qualifiers
     source          1..3107
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="12"
                     /map="12q13"
     gene            1..3107
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /note="phosphodiesterase 1B, calmodulin-dependent"
                     /db_xref="GeneID:5153"
                     /db_xref="HGNC:8775"
                     /db_xref="MIM:171891"
     exon            1..194
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /inference="alignment:Splign:1.39.8"
     variation       97
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:10747699"
     variation       101
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376202872"
     variation       129
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111971905"
     CDS             142..1692
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /EC_number="3.1.4.17"
                     /note="isoform 2 is encoded by transcript variant 2;
                     calcium/calmodulin-dependent 3',5'-cyclic nucleotide
                     phosphodiesterase 1B; calcium/calmodulin-stimulated cyclic
                     nucleotide phosphodiesterase; presumed 63kDa form of the
                     type 1 cyclic nucleotide phosphodiesterase family known as
                     PDE1B; calmodulin-stimulated phosphodiesterase PDE1B1;
                     cam-PDE 1B; 63 kDa Cam-PDE"
                     /codon_start=1
                     /product="calcium/calmodulin-dependent 3',5'-cyclic
                     nucleotide phosphodiesterase 1B isoform 2"
                     /protein_id="NP_001159447.1"
                     /db_xref="GI:260166687"
                     /db_xref="CCDS:CCDS53800.1"
                     /db_xref="GeneID:5153"
                     /db_xref="HGNC:8775"
                     /db_xref="MIM:171891"
                     /translation="
MANPVPVQRSHLQGPILRLRYMVKQLENGEINIEELKKNLEYTASLLEAVYIDETRQILDTEDELQELRSDAVPSEVRDWLASTFTQQARAKGRRAEEKPKFRSIVHAVQAGIFVERMFRRTYTSVGPTYSTAVLNCLKNLDLWCFDVFSLNQAADDHALRTIVFELLTRHNLISRFKIPTVFLMSFLDALETGYGKYKNPYHNQIHAADVTQTVHCFLLRTGMVHCLSEIELLAIIFAAAIHDYEHTGTTNSFHIQTKSECAIVYNDRSVLENHHISSVFRLMQDDEMNIFINLTKDEFVELRALVIEMVLATDMSCHFQQVKTMKTALQQLERIDKPKALSLLLHAADISHPTKQWLVHSRWTKALMEEFFRQGDKEAELGLPFSPLCDRTSTLVAQSQIGFIDFIVEPTFSVLTDVAEKSVQPLADEDSKSKNQPSFQWRQPSLDVEVGDPNPDVVSFRSTWVKRIQENKQKWKERAASGITNQMSIDELSPCEEEAPPSPAEDEHNQNGNLD
"
     misc_feature    310..492
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /note="3'5'-cyclic nucleotide phosphodiesterase
                     N-terminal; Region: PDEase_I_N; pfam08499"
                     /db_xref="CDD:203961"
     misc_feature    745..1440
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /note="3'5'-cyclic nucleotide phosphodiesterase; Region:
                     PDEase_I; pfam00233"
                     /db_xref="CDD:109297"
     variation       163
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199827682"
     exon            195..308
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /inference="alignment:Splign:1.39.8"
     variation       199
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147900601"
     variation       200
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374027304"
     variation       202
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:61733023"
     variation       205
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139920915"
     variation       232
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376974140"
     variation       273
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:2887906"
     variation       289
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200096201"
     variation       307
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373781937"
     exon            309..491
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /inference="alignment:Splign:1.39.8"
     variation       323
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371717266"
     variation       374
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142799171"
     variation       375
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372746803"
     variation       421
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374242340"
     variation       434
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:377170220"
     variation       483
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151025806"
     exon            492..558
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /inference="alignment:Splign:1.39.8"
     variation       500
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376631753"
     variation       540
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369117826"
     variation       551
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373914778"
     variation       558
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140892078"
     exon            559..675
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /inference="alignment:Splign:1.39.8"
     variation       565
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112699956"
     variation       596
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:11615709"
     variation       666
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377445884"
     exon            676..816
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /inference="alignment:Splign:1.39.8"
     STS             706..896
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /standard_name="MARC_21181-21182:1027091922:1"
                     /db_xref="UniSTS:268504"
     variation       742
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:150159795"
     variation       747
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146735076"
     variation       762
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:115951482"
     variation       776
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200815928"
     variation       802
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145391059"
     exon            817..917
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /inference="alignment:Splign:1.39.8"
     variation       827
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:137936270"
     variation       828
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:113265707"
     variation       833
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373565313"
     variation       850
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:143034173"
     variation       855
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376805586"
     variation       873
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148185581"
     variation       885
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115481291"
     exon            918..1043
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /inference="alignment:Splign:1.39.8"
     variation       932
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:375085069"
     variation       960
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:12812036"
     variation       962
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:12811532"
     variation       1018
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201756814"
     variation       1020
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150688398"
     variation       1027
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:12811737"
     exon            1044..1145
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /inference="alignment:Splign:1.39.8"
     variation       1104
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:139284651"
     variation       1129
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200839405"
     variation       1131
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199536319"
     exon            1146..1266
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /inference="alignment:Splign:1.39.8"
     variation       1262
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:143206355"
     exon            1267..1348
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /inference="alignment:Splign:1.39.8"
     exon            1349..1457
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /inference="alignment:Splign:1.39.8"
     variation       1350
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:147497085"
     variation       1357
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372439210"
     variation       1408
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:376262595"
     variation       1424
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147477377"
     variation       1440
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:150000693"
     variation       1443
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:148673155"
     exon            1458..1588
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /inference="alignment:Splign:1.39.8"
     variation       1469
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148711763"
     variation       1487
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:142239113"
     variation       1526
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202001120"
     variation       1557
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1249950"
     variation       1573
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140368041"
     variation       1584
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200779298"
     exon            1589..1709
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /inference="alignment:Splign:1.39.8"
     variation       1592
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:183676395"
     variation       1595
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:144100250"
     variation       1599
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146475493"
     variation       1625
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:371822951"
     variation       1636
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140787002"
     variation       1656
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150107941"
     exon            1710..3089
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /inference="alignment:Splign:1.39.8"
     STS             1710..2548
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /standard_name="PDE1B_3295"
                     /db_xref="UniSTS:462390"
     variation       1886..1887
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:35108378"
     variation       1890
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372424493"
     variation       1921..1922
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:34320482"
     variation       1940
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376600771"
     variation       2051
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143775746"
     STS             2061..2347
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /standard_name="SHGC-148605"
                     /db_xref="UniSTS:176493"
     variation       2260
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11170978"
     variation       2275
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:5798310"
     variation       2343
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371896018"
     variation       2365
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:884510"
     variation       2592
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:191560225"
     variation       2631
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:76676851"
     variation       2665
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1249499"
     variation       2673
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148127859"
     variation       2688
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:183626030"
     variation       2702
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1144996"
     STS             2740..2927
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /standard_name="RH78688"
                     /db_xref="UniSTS:48654"
     variation       2746
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111571643"
     STS             2882..3071
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /standard_name="A007D03"
                     /db_xref="UniSTS:80815"
     variation       2908
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144107699"
     variation       2909
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:10783631"
     variation       2984..2985
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:71444859"
     variation       3014
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189001857"
     variation       3058
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3825195"
     polyA_signal    3070..3075
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
     polyA_site      3089
                     /gene="PDE1B"
                     /gene_synonym="PDE1B1; PDES1B"
ORIGIN      
gttctctctggtcagttgctcagttctactgggacctggaggaggaaggcaggggccaaagaggaagttgtcccctcttgggggccctggggctcctggggtcaggattttgatactctgaagcaggaaactttgattcccatggcaaaccctgttcctgttcagaggagccacctccagggccccattctcaggctgcgctacatggtgaagcagttggagaatggggagataaacattgaggagctgaagaaaaatctggagtacacagcttctctgctggaagccgtctacatagatgagacacggcaaatcttggacacggaggacgagctgcaggagctgcggtcagatgccgtgccttcggaggtgcgggactggctggcctccaccttcacccagcaggcccgggccaaaggccgccgagcagaggagaagcccaagttccgaagcattgtgcacgctgtgcaggctgggatcttcgtggaacggatgttccggagaacatacacctctgtgggccccacttactctactgcggttctcaactgtctcaagaacctggatctctggtgctttgatgtcttttccttgaaccaggcagcagatgaccatgccctgaggaccattgtttttgagttgctgactcggcataacctcatcagccgcttcaagattcccactgtgtttttgatgagtttcctggatgccttggagacaggctatgggaagtacaagaatccttaccacaaccagatccacgcagccgatgttacccagacagtccattgcttcttgctccgcacagggatggtgcactgcctgtcggagattgagctcctggccatcatctttgctgcagctatccatgattatgagcacacgggcactaccaacagcttccacatccagaccaagtcagaatgtgccatcgtgtacaatgatcgttcagtgctggagaatcaccacatcagctctgttttccgattgatgcaggatgatgagatgaacattttcatcaacctcaccaaggatgagtttgtagaactccgagccctggtcattgagatggtgttggccacagacatgtcctgccatttccagcaagtgaagaccatgaagacagccttgcaacagctggagaggattgacaagcccaaggccctgtctctactgctccatgctgctgacatcagccacccaaccaagcagtggttggtccacagccgttggaccaaggccctcatggaggaattcttccgtcagggtgacaaggaggcagagttgggcctgcccttttctccactctgtgaccgcacttccactctagtggcacagtctcagatagggttcatcgacttcattgtggagcccacattctctgtgctgactgacgtggcagagaagagtgttcagcccctggcggatgaggactccaagtctaaaaaccagcccagctttcagtggcgccagccctctctggatgtggaagtgggagaccccaaccctgatgtggtcagctttcgttccacctgggtcaagcgcattcaggagaataagcagaaatggaaggaacgggcagcaagtggcatcaccaaccagatgtccattgacgagctgtccccctgtgaagaagaggcccccccatcccctgccgaagatgaacacaaccagaatgggaatctggattagccctggggctggcccaggtcttcattgagtccaaagtgtttgatgtcatcagcaccatccatcaggactggctcccccatctgctccaagggagcgtggtcgtggaagaaacaacccacctgaaggccaaatgccagagatttggggttggggaaagggcccctccccacctgacacccactggggtgcactttaatgttccggcagcaagactggggaacttcaggctcccagtggtcactgtgcccatccctcagcctctggattctcttcatggccaggtggctgccagggagcggggagcttcctggaggcttcccagggccttggggaagggtcagagatgccagccccctgggacctcccccatcctttttgcctccaagtttctaagcaatacattttgggggttccctcagccccccaccccagatcttagctggcaggtctgggtgccccttttcctcccctgggaagggctggaataggatagaaagctgggggttttcagagccctatgtgtggggaggggagtggattccttcagggcatggtacctttctaggacctgggaatggggtggagaggacatcctcttcaccccagaattgcgctgcttcagccccatctccagcctgatcctctgaatcttccttccctccctttctgatacagtgactggggcaaaaggagccattgtgaccaggggctgcgggaggcctttcctgggaccttccttgggactggtctgggcccctggggcttgtcgcctgccctgagtccggagccctttgcctccttcctctcccctggggctgggaggctccatccgaccaatgtctgtaaagtgctttgaggatctccccagcaaagcaccttcagaatgtatcgacaccagctgggttagggtcaagggtgcctggggagggtgagtaatcctgcattgctaaaagagagggtctgtcccctcctctccacgtcccagaactggcccagctgcaggcactaagaagctcctcccctgagacaagtgaggggtagtcggtgaaaggcagatggacaaggggctcagggctgctgccttcctgtcctctggagagaacccagccaggcgcggtgccccttcctctcctcaggctcctccttgcccccaccttgccccaggaaaggccaaagtccaggtgactgccctccttctttcttgtaaataccaaccatgcatttgtacagtgggccctgttcatgcgaaatccacatccatggtctcctagacctgctaccctggtacttccaccctaccccaccccgagaagggcagagacgcatgtgactcacccctgcccttggtttcccagacccctgctatagccagagaacaataaagaagggagaccaggaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:5153 -> Molecular function: GO:0004115 [3',5'-cyclic-AMP phosphodiesterase activity] evidence: IEA
            GeneID:5153 -> Molecular function: GO:0004117 [calmodulin-dependent cyclic-nucleotide phosphodiesterase activity] evidence: TAS
            GeneID:5153 -> Molecular function: GO:0005516 [calmodulin binding] evidence: IEA
            GeneID:5153 -> Molecular function: GO:0046872 [metal ion binding] evidence: IEA
            GeneID:5153 -> Molecular function: GO:0048101 [calcium- and calmodulin-regulated 3',5'-cyclic-GMP phosphodiesterase activity] evidence: IEA
            GeneID:5153 -> Biological process: GO:0001505 [regulation of neurotransmitter levels] evidence: IEA
            GeneID:5153 -> Biological process: GO:0001975 [response to amphetamine] evidence: IEA
            GeneID:5153 -> Biological process: GO:0006198 [cAMP catabolic process] evidence: IDA
            GeneID:5153 -> Biological process: GO:0006915 [apoptotic process] evidence: TAS
            GeneID:5153 -> Biological process: GO:0007165 [signal transduction] evidence: TAS
            GeneID:5153 -> Biological process: GO:0007173 [epidermal growth factor receptor signaling pathway] evidence: TAS
            GeneID:5153 -> Biological process: GO:0007202 [activation of phospholipase C activity] evidence: TAS
            GeneID:5153 -> Biological process: GO:0007596 [blood coagulation] evidence: TAS
            GeneID:5153 -> Biological process: GO:0007626 [locomotory behavior] evidence: IEA
            GeneID:5153 -> Biological process: GO:0008542 [visual learning] evidence: IEA
            GeneID:5153 -> Biological process: GO:0008543 [fibroblast growth factor receptor signaling pathway] evidence: TAS
            GeneID:5153 -> Biological process: GO:0030224 [monocyte differentiation] evidence: IEP
            GeneID:5153 -> Biological process: GO:0036006 [cellular response to macrophage colony-stimulating factor stimulus] evidence: IDA
            GeneID:5153 -> Biological process: GO:0042053 [regulation of dopamine metabolic process] evidence: IEA
            GeneID:5153 -> Biological process: GO:0042428 [serotonin metabolic process] evidence: IEA
            GeneID:5153 -> Biological process: GO:0045087 [innate immune response] evidence: TAS
            GeneID:5153 -> Biological process: GO:0046069 [cGMP catabolic process] evidence: IDA
            GeneID:5153 -> Biological process: GO:0048011 [neurotrophin TRK receptor signaling pathway] evidence: TAS
            GeneID:5153 -> Biological process: GO:0097011 [cellular response to granulocyte macrophage colony-stimulating factor stimulus] evidence: IDA
            GeneID:5153 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
            GeneID:5153 -> Cellular component: GO:0005730 [nucleolus] evidence: IDA
            GeneID:5153 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
            GeneID:5153 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
            GeneID:5153 -> Cellular component: GO:0043025 [neuronal cell body] evidence: IEA
ANNOTATIONS from NCBI Entrez Gene (20130726):
            NP_001159447 -> EC 3.1.4.17

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