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2024-03-29 08:35:28, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_024494               2515 bp    mRNA    linear   PRI 07-JUL-2013
DEFINITION  Homo sapiens wingless-type MMTV integration site family, member 2B
            (WNT2B), transcript variant WNT-2B2, mRNA.
ACCESSION   NM_024494
VERSION     NM_024494.2  GI:197333756
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 2515)
  AUTHORS   Wang,H., Fan,L., Xia,X., Rao,Y., Ma,Q., Yang,J., Lu,Y., Wang,C.,
            Ma,D. and Huang,X.
  TITLE     Silencing Wnt2B by siRNA interference inhibits metastasis and
            enhances chemotherapy sensitivity in ovarian cancer
  JOURNAL   Int. J. Gynecol. Cancer 22 (5), 755-761 (2012)
   PUBMED   22635028
  REMARK    GeneRIF: High Wnt2B overexpression is associated with ovarian
            cancer metastasis and drug resistance.
REFERENCE   2  (bases 1 to 2515)
  AUTHORS   Zhang,X., Yang,H., Lee,J.J., Kim,E., Lippman,S.M., Khuri,F.R.,
            Spitz,M.R., Lotan,R., Hong,W.K. and Wu,X.
  TITLE     MicroRNA-related genetic variations as predictors for risk of
            second primary tumor and/or recurrence in patients with early-stage
            head and neck cancer
  JOURNAL   Carcinogenesis 31 (12), 2118-2123 (2010)
   PUBMED   20819778
  REMARK    GeneRIF: Observational study of gene-disease association and
            gene-gene interaction. (HuGE Navigator)
REFERENCE   3  (bases 1 to 2515)
  AUTHORS   Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B,
            Yusuf S, Gerstein HC, Engert JC 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   4  (bases 1 to 2515)
  AUTHORS   Fernandez-Rozadilla C, de Castro L, Clofent J, Brea-Fernandez A,
            Bessa X, Abuli A, Andreu M, Jover R, Xicola R, Llor X, Castells A,
            Castellvi-Bel S, Carracedo A and Ruiz-Ponte C.
  CONSRTM   Gastrointestinal Oncology Group of the Spanish Gastroenterological
            Association
  TITLE     Single nucleotide polymorphisms in the Wnt and BMP pathways and
            colorectal cancer risk in a Spanish cohort
  JOURNAL   PLoS ONE 5 (9) (2010)
   PUBMED   20844743
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
            Publication Status: Online-Only
REFERENCE   5  (bases 1 to 2515)
  AUTHORS   Talmud PJ, Drenos F, Shah S, Shah T, Palmen J, Verzilli C, Gaunt
            TR, Pallas J, Lovering R, Li K, Casas JP, Sofat R, Kumari M,
            Rodriguez S, Johnson T, Newhouse SJ, Dominiczak A, Samani NJ,
            Caulfield M, Sever P, Stanton A, Shields DC, Padmanabhan S,
            Melander O, Hastie C, Delles C, Ebrahim S, Marmot MG, Smith GD,
            Lawlor DA, Munroe PB, Day IN, Kivimaki M, Whittaker J, Humphries SE
            and Hingorani AD.
  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   6  (bases 1 to 2515)
  AUTHORS   Katoh,M., Kirikoshi,H., Saitoh,T., Sagara,N. and Koike,J.
  TITLE     Alternative splicing of the WNT-2B/WNT-13 gene
  JOURNAL   Biochem. Biophys. Res. Commun. 275 (1), 209-216 (2000)
   PUBMED   10944466
REFERENCE   7  (bases 1 to 2515)
  AUTHORS   Van Den Berg,D.J., Sharma,A.K., Bruno,E. and Hoffman,R.
  TITLE     Role of members of the Wnt gene family in human hematopoiesis
  JOURNAL   Blood 92 (9), 3189-3202 (1998)
   PUBMED   9787155
REFERENCE   8  (bases 1 to 2515)
  AUTHORS   Bergstein,I., Eisenberg,L.M., Bhalerao,J., Jenkins,N.A.,
            Copeland,N.G., Osborne,M.P., Bowcock,A.M. and Brown,A.M.
  TITLE     Isolation of two novel WNT genes, WNT14 and WNT15, one of which
            (WNT15) is closely linked to WNT3 on human chromosome 17q21
  JOURNAL   Genomics 46 (3), 450-458 (1997)
   PUBMED   9441749
REFERENCE   9  (bases 1 to 2515)
  AUTHORS   Katoh,M., Hirai,M., Sugimura,T. and Terada,M.
  TITLE     Cloning, expression and chromosomal localization of Wnt-13, a novel
            member of the Wnt gene family
  JOURNAL   Oncogene 13 (4), 873-876 (1996)
   PUBMED   8761309
REFERENCE   10 (bases 1 to 2515)
  AUTHORS   Smolich,B.D., McMahon,J.A., McMahon,A.P. and Papkoff,J.
  TITLE     Wnt family proteins are secreted and associated with the cell
            surface
  JOURNAL   Mol. Biol. Cell 4 (12), 1267-1275 (1993)
   PUBMED   8167409
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from BC141825.1.
            On Aug 29, 2008 this sequence version replaced gi:13518020.
            
            Summary: This gene encodes a member of the wingless-type MMTV
            integration site (WNT) family of highly conserved, secreted
            signaling factors. WNT family members function in a variety of
            developmental processes including regulation of cell growth and
            differentiation and are characterized by a WNT-core domain. This
            gene may play a role in human development as well as human
            carcinogenesis. This gene produces two alternatively spliced
            transcript variants. [provided by RefSeq, Aug 2008].
            
            Transcript Variant: This variant (WNT-2B2) represents the shorter
            transcript yet it encodes the longer protein (isoform WNT-2B2).
            
            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 :: BC141825.1, AK312696.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025084, ERS025085 [ECO:0000348]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-2515              BC141825.1         1-2515
FEATURES             Location/Qualifiers
     source          1..2515
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="1"
                     /map="1p13"
     gene            1..2515
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /note="wingless-type MMTV integration site family, member
                     2B"
                     /db_xref="GeneID:7482"
                     /db_xref="HGNC:12781"
                     /db_xref="HPRD:03574"
                     /db_xref="MIM:601968"
     exon            1..697
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /inference="alignment:Splign:1.39.8"
     variation       51
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:373617635"
     variation       116
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:13373888"
     variation       361
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:11102484"
     variation       405
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145615759"
     variation       406
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:370981921"
     variation       412
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148494162"
     misc_feature    438..440
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /note="upstream in-frame stop codon"
     STS             497..2034
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /db_xref="UniSTS:486849"
     CDS             516..1691
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /note="isoform WNT-2B2 is encoded by transcript variant
                     WNT-2B2; XWNT2, Xenopus, homolog of; wingless-type MMTV
                     integration site family, member 13; protein Wnt-2b"
                     /codon_start=1
                     /product="protein Wnt-2b isoform WNT-2B2"
                     /protein_id="NP_078613.1"
                     /db_xref="GI:13518021"
                     /db_xref="CCDS:CCDS847.1"
                     /db_xref="GeneID:7482"
                     /db_xref="HGNC:12781"
                     /db_xref="HPRD:03574"
                     /db_xref="MIM:601968"
                     /translation="
MLRPGGAEEAAQLPLRRASAPVPVPSPAAPDGSRASARLGLACLLLLLLLTLPARVDTSWWYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWNCTTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRGRHHDQRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLECKCHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVMATQDGANFTAARQGYRRATRTDLVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCECKFHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT
"
     misc_feature    726..1655
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /note="wnt family; Region: wnt; pfam00110"
                     /db_xref="CDD:201009"
     misc_feature    735..1655
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /note="found in Wnt-1; Region: WNT1; smart00097"
                     /db_xref="CDD:128408"
     misc_feature    834..1652
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /note="Region: WNT-core domain"
     misc_feature    1362..1364
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="glycosylation site"
     variation       540
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:36006679"
     variation       557
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200421272"
     variation       564
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201895225"
     variation       567
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:3828075"
     variation       588
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:374417605"
     variation       593
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377064373"
     variation       597
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199522950"
     exon            698..918
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /inference="alignment:Splign:1.39.8"
     variation       716
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377342580"
     variation       720
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370244148"
     variation       756
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374175549"
     variation       775
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:79888517"
     variation       777
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199744667"
     variation       778
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368523301"
     variation       804
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201662450"
     variation       817
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140445206"
     variation       883
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145011115"
     variation       884
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372534893"
     variation       893
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142129756"
     variation       894
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140255509"
     variation       909
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:184557937"
     variation       910
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141257308"
     exon            919..1196
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /inference="alignment:Splign:1.39.8"
     variation       971
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:137855546"
     variation       972
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150473635"
     variation       974
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202077038"
     variation       983
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116923670"
     variation       1006
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149608763"
     variation       1028
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189277982"
     variation       1039
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373636614"
     variation       1054
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35058556"
     variation       1059
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147459875"
     variation       1066
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:142716277"
     variation       1097
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149716293"
     variation       1118
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200972987"
     variation       1122
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:351371"
     variation       1134
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146253356"
     variation       1161
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372960279"
     variation       1183
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:180824040"
     variation       1191
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377518381"
     exon            1197..1461
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /inference="alignment:Splign:1.39.8"
     variation       1221
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:140289496"
     variation       1247
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112638528"
     STS             1251..1587
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /standard_name="Wnt2b"
                     /db_xref="UniSTS:465418"
     variation       1273
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375265204"
     variation       1290
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201153849"
     variation       1331
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:141070301"
     variation       1346
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201268308"
     variation       1370
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368272752"
     variation       1371
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150246330"
     variation       1378
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143127439"
     STS             1397..1538
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /standard_name="Wnt2b"
                     /db_xref="UniSTS:466087"
     variation       1401
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199991957"
     variation       1415
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372397139"
     variation       1455
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:138326201"
     exon            1462..2470
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /inference="alignment:Splign:1.39.8"
     variation       1475
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146027356"
     variation       1498
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201658677"
     variation       1516
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368029359"
     variation       1522
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192061205"
     variation       1532
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371343411"
     variation       1552
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201872478"
     variation       1564
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:374641766"
     variation       1567
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144189370"
     variation       1574
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:141296639"
     variation       1611
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368700550"
     variation       1640
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139266843"
     variation       1641
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111919963"
     variation       1648
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:372190907"
     variation       1655
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2227860"
     variation       1658
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145437043"
     variation       1685
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:910697"
     variation       1720
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200355523"
     variation       1986
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17030446"
     variation       1989
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:373531874"
     variation       2066
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1569932"
     STS             2082..2243
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /standard_name="RH102745"
                     /db_xref="UniSTS:97079"
     variation       2125
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113309659"
     variation       2140
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190688758"
     variation       2144
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376487188"
     variation       2249..2250
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace=""
                     /replace="at"
                     /db_xref="dbSNP:139624875"
     variation       2310
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143485662"
     variation       2331
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2273368"
     variation       2372
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:181978420"
     variation       2377
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184488483"
     polyA_signal    2427..2432
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
     polyA_site      2445
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
     polyA_site      2446
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
     variation       2460
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:146289905"
ORIGIN      
ggagccgcggcgtcccgtcgcagcgtgcgggagcaggtgggggtgcagcgcggtggcgcgcgggagccccgaggggcggaggcggctgctacacctagggcgtcgcggagcgccccgggcttggcgcgggcggagccgccctaagggccgcgcgtgtccccggcctcggccccgccccgtcccgtccaatgagagcccgcggccgaaggggctgtccgcacactaggcccgcagctcccttcagcgccgcagaccccctgacaccgcacccggtcctcaggcagcgcgccccagaccccgggttcggcacgccgtcgtcggcttccggacatcgcaacttgcgcccctctcggggatcctcctcccgggctctggaccccaggtgatcctaggtccccagccgccggcgaacaccatggccccccaggggggtgaggtaggagcagcctgagtacccccagaaggtgccccgtccacgcccctccgggctgcgcggcgggagtcttcggggagctatgctgagaccgggtggtgcggaggaagctgcgcagctcccgcttcggcgcgccagcgccccggtccctgtgccgtcgcccgcggcccccgacggctcccgggcttcggcccgcctaggtcttgcctgccttctgctcctgctgctgctgacgctgccggcccgcgtagacacgtcctggtggtacattggggcactgggggcacgagtgatctgtgacaatatccctggtttggtgagccggcagcggcagctgtgccagcgttacccagacatcatgcgttcagtgggcgagggtgcccgagaatggatccgagagtgtcagcaccaattccgccaccaccgctggaactgtaccaccctggaccgggaccacaccgtctttggccgtgtcatgctcagaagtagccgagaggcagcttttgtatatgccatctcatcagcaggggtagtccacgctattactcgcgcctgtagccagggtgaactgagtgtgtgcagctgtgacccctacacccgtggccgacaccatgaccagcgtggggactttgactggggtggctgcagtgacaacatccactacggtgtccgttttgccaaggccttcgtggatgccaaggagaagaggcttaaggatgcccgggccctcatgaacttacataataaccgctgtggtcgcacggctgtgcggcggtttctgaagctggagtgtaagtgccatggcgtgagtggttcctgtactctgcgcacctgctggcgtgcactctcagatttccgccgcacaggtgattacctgcggcgacgctatgatggggctgtgcaggtgatggccacccaagatggtgccaacttcaccgcagcccgccaaggctatcgccgtgccacccggactgatcttgtctactttgacaactctccagattactgtgtcttggacaaggctgcaggttccctaggcactgcaggccgtgtctgcagcaagacatcaaaaggaacagacggttgtgaaatcatgtgctgtggccgagggtacgacacaactcgagtcacccgtgttacccagtgtgagtgcaaattccactggtgctgtgctgtacggtgcaaggaatgcagaaatactgtggacgtccatacttgcaaagcccccaagaaggcagagtggctggaccaaacctgaacacacagatacctcactcatccctccaattcaagcctctcaactcaaaagcacaagatccttgcatgcacaccttcctccaccctccaccctgggctgctaccgcttctatttaaggatgtagagagtaatccatagggaccatggtgtcctggctggttccttagccctgggaaggagttgtcaggggatataagaaactgagcaagctccctgatttcccgctctggagatttgaagggagagtagaagagatagggggtctttagagtgaaatgagttgcactaaagtacgtagttgaggctccttttttctttcctttgcaccagcttcccgatacttcttggtgtgcaagaggaagggtacctgtagagagcttctttttgtttctacctggccaaagttagatgggacaaagatgaatggcatgtcccttctctgaagtccgtttgagcagaactacctggtaccccgaaagaaaatcttaggctaccacattctattattgagagcctgagatgttagccatagtggacaaggttccattcacatgctcatatgtttataaactgtgttttgtagaagaaaaagaatcataacaatacaaacacacattcattctctctttttctctctaccattctcaacctgtattggacagcactgcctcttttgcttacttgctgcctgttcaaactgaggtggaatgcagtggttcccatgcttaacaaatcattaaaacaccctagaacactcctaggatagattaatgtagtaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:7482 -> Molecular function: GO:0005109 [frizzled binding] evidence: IBA
            GeneID:7482 -> Biological process: GO:0002062 [chondrocyte differentiation] evidence: IEP
            GeneID:7482 -> Biological process: GO:0002088 [lens development in camera-type eye] evidence: ISS
            GeneID:7482 -> Biological process: GO:0008584 [male gonad development] evidence: IEP
            GeneID:7482 -> Biological process: GO:0016055 [Wnt receptor signaling pathway] evidence: IMP
            GeneID:7482 -> Biological process: GO:0021871 [forebrain regionalization] evidence: IEP
            GeneID:7482 -> Biological process: GO:0030182 [neuron differentiation] evidence: IBA
            GeneID:7482 -> Biological process: GO:0030182 [neuron differentiation] evidence: ISS
            GeneID:7482 -> Biological process: GO:0045165 [cell fate commitment] evidence: IBA
            GeneID:7482 -> Biological process: GO:0060070 [canonical Wnt receptor signaling pathway] evidence: IEA
            GeneID:7482 -> Biological process: GO:0060492 [lung induction] evidence: IEA
            GeneID:7482 -> Biological process: GO:0060638 [mesenchymal-epithelial cell signaling] evidence: IEA
            GeneID:7482 -> Biological process: GO:0061072 [iris morphogenesis] evidence: ISS
            GeneID:7482 -> Biological process: GO:0061303 [cornea development in camera-type eye] evidence: ISS
            GeneID:7482 -> Biological process: GO:0071425 [hematopoietic stem cell proliferation] evidence: IDA
            GeneID:7482 -> Biological process: GO:0090190 [positive regulation of branching involved in ureteric bud morphogenesis] evidence: IEA
            GeneID:7482 -> Biological process: GO:0090263 [positive regulation of canonical Wnt receptor signaling pathway] evidence: IDA
            GeneID:7482 -> Cellular component: GO:0005576 [extracellular region] evidence: TAS
            GeneID:7482 -> Cellular component: GO:0005578 [proteinaceous extracellular matrix] evidence: IEA
            GeneID:7482 -> Cellular component: GO:0005615 [extracellular space] evidence: NAS

by @meso_cacase at DBCLS
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