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2024-03-28 22:40:07, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_004185               2063 bp    mRNA    linear   PRI 07-JUL-2013
DEFINITION  Homo sapiens wingless-type MMTV integration site family, member 2B
            (WNT2B), transcript variant WNT-2B1, mRNA.
ACCESSION   NM_004185
VERSION     NM_004185.3  GI:197333757
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 2063)
  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 2063)
  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 2063)
  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 2063)
  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 2063)
  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 2063)
  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 2063)
  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 2063)
  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 2063)
  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 2063)
  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 AB045116.1 and BC141825.1.
            On Aug 29, 2008 this sequence version replaced gi:13518016.
            
            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-2B1) contains different
            segments for its 5' UTR and 5' coding region, compared to
            transcript variant WNT-2B2. The encoded protein (isoform WNT-2B1)
            has a shorter and distinct N-terminus when it is compared to
            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.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-1232              AB045116.1         1-1232
            1233-2063           BC141825.1         1685-2515
FEATURES             Location/Qualifiers
     source          1..2063
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="1"
                     /map="1p13"
     gene            1..2063
                     /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..174
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    58..60
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /note="upstream in-frame stop codon"
     STS             73..1281
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /db_xref="UniSTS:482015"
     variation       84
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:371825913"
     variation       116
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374777255"
     CDS             121..1239
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /note="isoform WNT-2B1 is encoded by transcript variant
                     WNT-2B1; XWNT2, Xenopus, homolog of; wingless-type MMTV
                     integration site family, member 13; protein Wnt-2b"
                     /codon_start=1
                     /product="protein Wnt-2b isoform WNT-2B1"
                     /protein_id="NP_004176.2"
                     /db_xref="GI:13518017"
                     /db_xref="CCDS:CCDS846.1"
                     /db_xref="GeneID:7482"
                     /db_xref="HGNC:12781"
                     /db_xref="HPRD:03574"
                     /db_xref="MIM:601968"
                     /translation="
MLDGLGVVAISIFGIQLKTEGSLRTAVPGIPTQSAFNKCLQRYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWNCTTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRGRHHDQRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLECKCHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVMATQDGANFTAARQGYRRATRTDLVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCECKFHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT
"
     misc_feature    274..1203
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /note="wnt family; Region: wnt; pfam00110"
                     /db_xref="CDD:201009"
     misc_feature    283..1203
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /note="found in Wnt-1; Region: WNT1; smart00097"
                     /db_xref="CDD:128408"
     misc_feature    382..1200
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /note="Region: WNT-core domain"
     misc_feature    910..912
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /note="glycosylation site"
     misc_feature    910..912
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="glycosylation site"
     variation       139
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142980721"
     variation       156
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:189656664"
     exon            175..245
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /inference="alignment:Splign:1.39.8"
     exon            246..466
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /inference="alignment:Splign:1.39.8"
     variation       264
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377342580"
     variation       268
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370244148"
     variation       304
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374175549"
     variation       323
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:79888517"
     variation       325
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199744667"
     variation       326
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368523301"
     variation       352
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201662450"
     variation       365
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140445206"
     variation       431
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145011115"
     variation       432
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372534893"
     variation       441
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142129756"
     variation       442
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140255509"
     variation       457
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:184557937"
     variation       458
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141257308"
     exon            467..744
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /inference="alignment:Splign:1.39.8"
     variation       519
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:137855546"
     variation       520
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150473635"
     variation       522
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202077038"
     variation       531
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116923670"
     variation       554
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149608763"
     variation       576
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189277982"
     variation       587
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373636614"
     variation       602
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35058556"
     variation       607
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147459875"
     variation       614
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:142716277"
     variation       645
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149716293"
     variation       666
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200972987"
     variation       670
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:351371"
     variation       682
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146253356"
     variation       709
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372960279"
     variation       731
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:180824040"
     variation       739
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377518381"
     exon            745..1009
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /inference="alignment:Splign:1.39.8"
     variation       769
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:140289496"
     variation       795
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112638528"
     STS             799..1135
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /standard_name="Wnt2b"
                     /db_xref="UniSTS:465418"
     variation       821
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375265204"
     variation       838
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201153849"
     variation       879
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:141070301"
     variation       894
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201268308"
     variation       918
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368272752"
     variation       919
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150246330"
     variation       926
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143127439"
     STS             945..1086
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /standard_name="Wnt2b"
                     /db_xref="UniSTS:466087"
     variation       949
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199991957"
     variation       963
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372397139"
     variation       1003
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:138326201"
     exon            1010..2018
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /inference="alignment:Splign:1.39.8"
     variation       1023
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146027356"
     variation       1046
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201658677"
     variation       1064
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368029359"
     variation       1070
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192061205"
     variation       1080
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371343411"
     variation       1100
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201872478"
     variation       1112
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:374641766"
     variation       1115
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144189370"
     variation       1122
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:141296639"
     variation       1159
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368700550"
     variation       1188
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139266843"
     variation       1189
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:111919963"
     variation       1196
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:372190907"
     variation       1203
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2227860"
     variation       1206
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145437043"
     variation       1233
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:910697"
     variation       1268
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200355523"
     variation       1534
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17030446"
     variation       1537
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:373531874"
     variation       1614
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1569932"
     STS             1630..1791
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /standard_name="RH102745"
                     /db_xref="UniSTS:97079"
     variation       1673
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113309659"
     variation       1688
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190688758"
     variation       1692
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376487188"
     variation       1797..1798
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace=""
                     /replace="at"
                     /db_xref="dbSNP:139624875"
     variation       1858
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143485662"
     variation       1879
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2273368"
     variation       1920
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:181978420"
     variation       1925
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184488483"
     polyA_signal    1975..1980
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
     polyA_site      1993
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
     polyA_site      1994
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
     variation       2008
                     /gene="WNT2B"
                     /gene_synonym="WNT13; XWNT2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:146289905"
ORIGIN      
aaaccctgaagagcccaagcaatgtggttgtaaaatttgcaaaataagattaaatcttaactgcaatctgttaacactgctgtctcctttcactctttctcctatatcacactttcccacatgttggatggccttggagtggtagccataagcatttttggaattcaactaaaaactgaaggatccttgaggacggcagtacctggcatacctacacagtcagcgttcaacaagtgtttgcaaaggtacattggggcactgggggcacgagtgatctgtgacaatatccctggtttggtgagccggcagcggcagctgtgccagcgttacccagacatcatgcgttcagtgggcgagggtgcccgagaatggatccgagagtgtcagcaccaattccgccaccaccgctggaactgtaccaccctggaccgggaccacaccgtctttggccgtgtcatgctcagaagtagccgagaggcagcttttgtatatgccatctcatcagcaggggtagtccacgctattactcgcgcctgtagccagggtgaactgagtgtgtgcagctgtgacccctacacccgtggccgacaccatgaccagcgtggggactttgactggggtggctgcagtgacaacatccactacggtgtccgttttgccaaggccttcgtggatgccaaggagaagaggcttaaggatgcccgggccctcatgaacttacataataaccgctgtggtcgcacggctgtgcggcggtttctgaagctggagtgtaagtgccatggcgtgagtggttcctgtactctgcgcacctgctggcgtgcactctcagatttccgccgcacaggtgattacctgcggcgacgctatgatggggctgtgcaggtgatggccacccaagatggtgccaacttcaccgcagcccgccaaggctatcgccgtgccacccggactgatcttgtctactttgacaactctccagattactgtgtcttggacaaggctgcaggttccctaggcactgcaggccgtgtctgcagcaagacatcaaaaggaacagacggttgtgaaatcatgtgctgtggccgagggtacgacacaactcgagtcacccgtgttacccagtgtgagtgcaaattccactggtgctgtgctgtacggtgcaaggaatgcagaaatactgtggacgtccatacttgcaaagcccccaagaaggcagagtggctggaccaaacctgaacacacagatacctcactcatccctccaattcaagcctctcaactcaaaagcacaagatccttgcatgcacaccttcctccaccctccaccctgggctgctaccgcttctatttaaggatgtagagagtaatccatagggaccatggtgtcctggctggttccttagccctgggaaggagttgtcaggggatataagaaactgagcaagctccctgatttcccgctctggagatttgaagggagagtagaagagatagggggtctttagagtgaaatgagttgcactaaagtacgtagttgaggctccttttttctttcctttgcaccagcttcccgatacttcttggtgtgcaagaggaagggtacctgtagagagcttctttttgtttctacctggccaaagttagatgggacaaagatgaatggcatgtcccttctctgaagtccgtttgagcagaactacctggtaccccgaaagaaaatcttaggctaccacattctattattgagagcctgagatgttagccatagtggacaaggttccattcacatgctcatatgtttataaactgtgttttgtagaagaaaaagaatcataacaatacaaacacacattcattctctctttttctctctaccattctcaacctgtattggacagcactgcctcttttgcttacttgctgcctgttcaaactgaggtggaatgcagtggttcccatgcttaacaaatcattaaaacaccctagaacactcctaggatagattaatgtagtaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
//

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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