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2024-03-30 00:19:22, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_197972               1615 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens NME/NM23 family member 7 (NME7), transcript variant 2,
            mRNA.
ACCESSION   NM_197972
VERSION     NM_197972.1  GI:37574613
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 1615)
  AUTHORS   Heit,J.A., Armasu,S.M., Asmann,Y.W., Cunningham,J.M.,
            Matsumoto,M.E., Petterson,T.M. and De Andrade,M.
  TITLE     A genome-wide association study of venous thromboembolism
            identifies risk variants in chromosomes 1q24.2 and 9q
  JOURNAL   J. Thromb. Haemost. 10 (8), 1521-1531 (2012)
   PUBMED   22672568
REFERENCE   2  (bases 1 to 1615)
  AUTHORS   Smith,N.L., Huffman,J.E., Strachan,D.P., Huang,J., Dehghan,A.,
            Trompet,S., Lopez,L.M., Shin,S.Y., Baumert,J., Vitart,V., Bis,J.C.,
            Wild,S.H., Rumley,A., Yang,Q., Uitterlinden,A.G., Stott,D.J.,
            Davies,G., Carter,A.M., Thorand,B., Polasek,O., McKnight,B.,
            Campbell,H., Rudnicka,A.R., Chen,M.H., Buckley,B.M., Harris,S.E.,
            Peters,A., Pulanic,D., Lumley,T., de Craen,A.J., Liewald,D.C.,
            Gieger,C., Campbell,S., Ford,I., Gow,A.J., Luciano,M.,
            Porteous,D.J., Guo,X., Sattar,N., Tenesa,A., Cushman,M.,
            Slagboom,P.E., Visscher,P.M., Spector,T.D., Illig,T., Rudan,I.,
            Bovill,E.G., Wright,A.F., McArdle,W.L., Tofler,G., Hofman,A.,
            Westendorp,R.G., Starr,J.M., Grant,P.J., Karakas,M., Hastie,N.D.,
            Psaty,B.M., Wilson,J.F., Lowe,G.D., O'Donnell,C.J., Witteman,J.C.,
            Jukema,J.W., Deary,I.J., Soranzo,N., Koenig,W. and Hayward,C.
  TITLE     Genetic predictors of fibrin D-dimer levels in healthy adults
  JOURNAL   Circulation 123 (17), 1864-1872 (2011)
   PUBMED   21502573
REFERENCE   3  (bases 1 to 1615)
  AUTHORS   Germain,M., Saut,N., Greliche,N., Dina,C., Lambert,J.C., Perret,C.,
            Cohen,W., Oudot-Mellakh,T., Antoni,G., Alessi,M.C., Zelenika,D.,
            Cambien,F., Tiret,L., Bertrand,M., Dupuy,A.M., Letenneur,L.,
            Lathrop,M., Emmerich,J., Amouyel,P., Tregouet,D.A. and Morange,P.E.
  TITLE     Genetics of venous thrombosis: insights from a new genome wide
            association study
  JOURNAL   PLoS ONE 6 (9), E25581 (2011)
   PUBMED   21980494
REFERENCE   4  (bases 1 to 1615)
  AUTHORS   Ehret,G.B., O'Connor,A.A., Weder,A., Cooper,R.S. and Chakravarti,A.
  TITLE     Follow-up of a major linkage peak on chromosome 1 reveals
            suggestive QTLs associated with essential hypertension: GenNet
            study
  JOURNAL   Eur. J. Hum. Genet. 17 (12), 1650-1657 (2009)
   PUBMED   19536175
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   5  (bases 1 to 1615)
  AUTHORS   Trynka,G., Zhernakova,A., Romanos,J., Franke,L., Hunt,K.A.,
            Turner,G., Bruinenberg,M., Heap,G.A., Platteel,M., Ryan,A.W., de
            Kovel,C., Holmes,G.K., Howdle,P.D., Walters,J.R., Sanders,D.S.,
            Mulder,C.J., Mearin,M.L., Verbeek,W.H., Trimble,V., Stevens,F.M.,
            Kelleher,D., Barisani,D., Bardella,M.T., McManus,R., van Heel,D.A.
            and Wijmenga,C.
  TITLE     Coeliac disease-associated risk variants in TNFAIP3 and REL
            implicate altered NF-kappaB signalling
  JOURNAL   Gut 58 (8), 1078-1083 (2009)
   PUBMED   19240061
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   6  (bases 1 to 1615)
  AUTHORS   Cheung,C.L., Chan,B.Y., Chan,V., Ikegawa,S., Kou,I., Ngai,H.,
            Smith,D., Luk,K.D., Huang,Q.Y., Mori,S., Sham,P.C. and Kung,A.W.
  TITLE     Pre-B-cell leukemia homeobox 1 (PBX1) shows functional and possible
            genetic association with bone mineral density variation
  JOURNAL   Hum. Mol. Genet. 18 (4), 679-687 (2009)
   PUBMED   19064610
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   7  (bases 1 to 1615)
  AUTHORS   Desvignes,T., Pontarotti,P., Fauvel,C. and Bobe,J.
  TITLE     Nme protein family evolutionary history, a vertebrate perspective
  JOURNAL   BMC Evol. Biol. 9, 256 (2009)
   PUBMED   19852809
  REMARK    Publication Status: Online-Only
REFERENCE   8  (bases 1 to 1615)
  AUTHORS   Hippe,H.J., Luedde,M., Lutz,S., Koehler,H., Eschenhagen,T.,
            Frey,N., Katus,H.A., Wieland,T. and Niroomand,F.
  TITLE     Regulation of cardiac cAMP synthesis and contractility by
            nucleoside diphosphate kinase B/G protein beta gamma dimer
            complexes
  JOURNAL   Circ. Res. 100 (8), 1191-1199 (2007)
   PUBMED   17363702
  REMARK    GeneRIF: Compared with wild-type betagamma nucleoside diphosphate
            kinase overexpression of Gbeta nucleoside diphosphate kinase
            suppressed basal cAMP formation up to 55%.
REFERENCE   9  (bases 1 to 1615)
  AUTHORS   Lacombe,M.L., Milon,L., Munier,A., Mehus,J.G. and Lambeth,D.O.
  TITLE     The human Nm23/nucleoside diphosphate kinases
  JOURNAL   J. Bioenerg. Biomembr. 32 (3), 247-258 (2000)
   PUBMED   11768308
  REMARK    Review article
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            CD107958.1, AK094513.1 and BC006983.1.
            
            ##Evidence-Data-START##
            Transcript exon combination :: AK094513.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025082, ERS025084 [ECO:0000348]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-146               CD107958.1         44-189
            147-1586            AK094513.1         145-1584
            1587-1615           BC006983.1         1464-1492
FEATURES             Location/Qualifiers
     source          1..1615
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="1"
                     /map="1q24"
     gene            1..1615
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /note="NME/NM23 family member 7"
                     /db_xref="GeneID:29922"
                     /db_xref="HGNC:20461"
                     /db_xref="HPRD:11394"
                     /db_xref="MIM:613465"
     exon            1..241
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /inference="alignment:Splign:1.39.8"
     variation       complement(67)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:17345517"
     variation       complement(124)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:182440832"
     variation       complement(191)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:371770204"
     variation       complement(204)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201280194"
     misc_feature    232..234
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /note="upstream in-frame stop codon"
     variation       complement(235)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:375459194"
     variation       complement(238)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371164733"
     exon            242..318
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /inference="alignment:Splign:1.39.8"
     variation       complement(246)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372956824"
     variation       complement(275)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144677908"
     CDS             316..1338
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /EC_number="2.7.4.6"
                     /note="isoform b is encoded by transcript variant 2;
                     nucleoside diphosphate kinase 7; nucleoside-diphosphate
                     kinase 7; NDK 7; NDP kinase 7; non-metastatic cells 7,
                     protein expressed in (nucleoside-diphosphate kinase)"
                     /codon_start=1
                     /product="nucleoside diphosphate kinase 7 isoform b"
                     /protein_id="NP_932076.1"
                     /db_xref="GI:37574614"
                     /db_xref="CCDS:CCDS44274.1"
                     /db_xref="GeneID:29922"
                     /db_xref="HGNC:20461"
                     /db_xref="HPRD:11394"
                     /db_xref="MIM:613465"
                     /translation="
MHDVKNHRTFLKRTKYDNLHLEDLFIGNKVNVFSRQLVLIDYGDQYTARQLGSRKEKTLALIKPDAISKAGEIIEIINKAGFTITKLKMMMLSRKEALDFHVDHQSRPFFNELIQFITTGPIIAMEILRDDAICEWKRLLGPANSGVARTDASESIRALFGTDGIRNAAHGPDSFASAAREMELFFPSSGGCGPANTAKFTNCTCCIVKPHAVSEGLLGKILMAIRDAGFEISAMQMFNMDRVNVEEFYEVYKGVVTEYHDMVTEMYSGPCVAMEIQQNNATKTFREFCGPADPEIARHLRPGTLRAIFGKTKIQNAVHCTDLPEDGLLEVQYFFKILDN
"
     misc_feature    <322..480
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /note="Repeat of unknown function (DUF1126); Region:
                     DUF1126; cl02728"
                     /db_xref="CDD:207712"
     misc_feature    481..873
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /note="Nucleoside diphosphate kinase 7 domain A (NDPk7A):
                     The nm23-H7 class of nucleoside diphosphate kinase (NDPk7)
                     consists of an N-terminal DM10 domain and two functional
                     catalytic NDPk modules, NDPk7A and NDPk7B. The function of
                     the DM10 domain, which also...; Region: NDPk7A; cd04415"
                     /db_xref="CDD:58530"
     misc_feature    order(502..504,616..618,640..642,724..726,742..744,
                     784..786,814..816,823..825,829..834,856..858)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /note="active site"
                     /db_xref="CDD:58530"
     misc_feature    order(514..516,523..531,538..540,547..549,574..582)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /note="multimer interface [polypeptide binding]; other
                     site"
                     /db_xref="CDD:58530"
     misc_feature    919..1320
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /note="Nucleoside diphosphate kinase 7 domain B (NDPk7B):
                     The nm23-H7 class of nucleoside diphosphate kinase (NDPk7)
                     consists of an N-terminal DM10 domain and two functional
                     catalytic NDPk modules, NDPk7A and NDPk7B. The function of
                     the DM10 domain, which also...; Region: NDPk7B; cd04412"
                     /db_xref="CDD:58527"
     misc_feature    order(940..942,1060..1062,1087..1089,1171..1173,
                     1189..1191,1231..1233,1261..1263,1270..1272,1276..1281,
                     1303..1305)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /note="active site"
                     /db_xref="CDD:58527"
     misc_feature    order(952..954,967..975,982..984,991..993,1018..1026)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /note="multimer interface [polypeptide binding]; other
                     site"
                     /db_xref="CDD:58527"
     exon            319..485
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /inference="alignment:Splign:1.39.8"
     variation       complement(321)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:150210914"
     variation       complement(338)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141747474"
     variation       complement(339)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201299047"
     variation       complement(352)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369065175"
     variation       complement(377)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376236268"
     variation       complement(429)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200282699"
     variation       complement(477)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201878585"
     variation       complement(485)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:147020111"
     exon            486..596
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /inference="alignment:Splign:1.39.8"
     variation       complement(516)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143018147"
     variation       complement(522)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:149023832"
     variation       complement(565)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185014515"
     exon            597..647
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /inference="alignment:Splign:1.39.8"
     variation       complement(617)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201587017"
     variation       complement(633)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200126131"
     exon            648..855
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /inference="alignment:Splign:1.39.8"
     variation       complement(655)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140135005"
     variation       complement(656)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377403791"
     variation       complement(661)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:144536973"
     variation       complement(695)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376824095"
     variation       complement(761)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139755731"
     variation       complement(821)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148704057"
     variation       complement(822)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143907031"
     variation       complement(833)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199705261"
     exon            856..961
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /inference="alignment:Splign:1.39.8"
     variation       complement(868)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:138141740"
     variation       complement(890)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377724965"
     variation       complement(897)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:373271409"
     variation       complement(908)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138939685"
     variation       complement(921)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:150154816"
     variation       complement(926)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369297997"
     variation       complement(928)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200644365"
     variation       complement(932)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:137920841"
     variation       complement(947)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143515962"
     exon            962..1026
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /inference="alignment:Splign:1.39.8"
     variation       complement(977)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375383227"
     variation       complement(995)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:187396504"
     exon            1027..1095
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /inference="alignment:Splign:1.39.8"
     variation       complement(1028)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374917505"
     variation       complement(1035)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202081199"
     variation       complement(1053..1054)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:36013941"
     variation       complement(1054..1055)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:34165486"
     variation       complement(1086)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144390206"
     exon            1096..1197
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /inference="alignment:Splign:1.39.8"
     variation       complement(1101)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149843431"
     variation       complement(1123)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377259893"
     variation       complement(1139)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:142020252"
     variation       complement(1171)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138530600"
     exon            1198..1305
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /inference="alignment:Splign:1.39.8"
     variation       complement(1207)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372946555"
     variation       complement(1208)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150610040"
     variation       complement(1243)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201432827"
     variation       complement(1251)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:200097150"
     variation       complement(1270)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:368848783"
     variation       complement(1282)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:59827137"
     variation       complement(1299)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148239352"
     exon            1306..1589
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /inference="alignment:Splign:1.39.8"
     variation       complement(1314)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201176827"
     variation       complement(1327)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:77280637"
     variation       complement(1339)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375605707"
     variation       complement(1364)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:188194894"
     variation       complement(1365)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:369306366"
     variation       complement(1374)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:375795890"
     variation       complement(1397)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116473357"
     variation       complement(1406)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:3180378"
     variation       complement(1426)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1138486"
     variation       complement(1461)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:113442279"
     variation       complement(1473)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:12091"
     variation       complement(1514)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138857215"
     variation       complement(1530)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150136713"
     variation       complement(1557)
                     /gene="NME7"
                     /gene_synonym="MN23H7; nm23-H7"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112941951"
ORIGIN      
acagaataatggcgtctcgtagccccaggcgacagcgtggaggggcgggtctgtcgattggatgaacgcagctgagattactcccagccactaaggacgaagaggtggggcggtggcgtcccacgcctcgtgcgacagtgggcggggctttgttgcctgagtaaccgtatgatggtggtggtggtggtgtcttcctgtctcaacgatacctattttctagtgctgagatcctgagacaatgagtggtatgatccaaatgcttcacttcttcgacgttatgagcttttattttacccaggggatggatctgttgaaatgcatgatgtaaagaatcatcgcacctttttaaagcggaccaaatatgataacctgcacttggaagatttatttataggcaacaaagtgaatgtcttttctcgacaactggtattaattgactatggggatcaatatacagctcgccagctgggcagtaggaaagaaaaaacgctagccctaattaaaccagatgcaatatcaaaggctggagaaataattgaaataataaacaaagctggatttactataaccaaactcaaaatgatgatgctttcaaggaaagaagcattggattttcatgtagatcaccagtcaagaccctttttcaatgagctgatccagtttattacaactggtcctattattgccatggagattttaagagatgatgctatatgtgaatggaaaagactgctgggacctgcaaactctggagtggcacgcacagatgcttctgaaagcattagagccctctttggaacagatggcataagaaatgcagcgcatggccctgattcttttgcttctgcggccagagaaatggagttgttttttccttcaagtggaggttgtgggccggcaaacactgctaaatttactaattgtacctgttgcattgttaaaccccatgctgtcagtgaaggactgttgggaaagatcctgatggctatccgagatgcaggttttgaaatctcagctatgcagatgttcaatatggatcgggttaatgttgaggaattctatgaagtttataaaggagtagtgaccgaatatcatgacatggtgacagaaatgtattctggcccttgtgtagcaatggagattcaacagaataatgctacaaagacatttcgagaattttgtggacctgctgatcctgaaattgcccggcatttacgccctggaactctcagagcaatctttggtaaaactaagatccagaatgctgttcactgtactgatctgccagaggatggcctattagaggttcaatacttcttcaagatcttggataattagtggtgtggaaagtaaagaagtcacaggttgggacatttagacaagagtgaatcacacacgaggaatgtgttcattcttttattgtccgttgttttaacctgactgaatacaagatcaacaagagcactgtactcctggcaattattacatatgttagaacatggattttgcactgtagacaacatttaacaccagtctatggggtactgcattgctttttataaagttcaaaataaagatttattttcaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:29922 -> Molecular function: GO:0004550 [nucleoside diphosphate kinase activity] evidence: IEA
            GeneID:29922 -> Molecular function: GO:0005524 [ATP binding] evidence: IEA
            GeneID:29922 -> Molecular function: GO:0046872 [metal ion binding] evidence: IEA
            GeneID:29922 -> Biological process: GO:0003351 [epithelial cilium movement] evidence: IEA
            GeneID:29922 -> Biological process: GO:0006183 [GTP biosynthetic process] evidence: IEA
            GeneID:29922 -> Biological process: GO:0006228 [UTP biosynthetic process] evidence: IEA
            GeneID:29922 -> Biological process: GO:0006241 [CTP biosynthetic process] evidence: IEA
            GeneID:29922 -> Biological process: GO:0007368 [determination of left/right symmetry] evidence: IEA
            GeneID:29922 -> Biological process: GO:0007420 [brain development] evidence: IEA
            GeneID:29922 -> Biological process: GO:0042073 [intraflagellar transport] evidence: IEA
            GeneID:29922 -> Biological process: GO:0060830 [ciliary receptor clustering involved in smoothened signaling pathway] evidence: IEA
            GeneID:29922 -> Biological process: GO:0060972 [left/right pattern formation] evidence: IEA
            GeneID:29922 -> Cellular component: GO:0005813 [centrosome] evidence: IDA
ANNOTATIONS from NCBI Entrez Gene (20130726):
            NP_932076 -> EC 2.7.4.6

by @meso_cacase at DBCLS
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