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2024-03-28 20:08:01, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_145655               4219 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens glucosaminyl (N-acetyl) transferase 2, I-branching
            enzyme (I blood group) (GCNT2), transcript variant 3, mRNA.
ACCESSION   NM_145655
VERSION     NM_145655.3  GI:85790494
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 4219)
  AUTHORS   Borck,G., Kakar,N., Hoch,J., Friedrich,K., Freudenberg,J.,
            Nurnberg,G., Yilmaz,R., Daud,S., Baloch,D.M., Nurnberg,P.,
            Oldenburg,J., Ahmad,J. and Kubisch,C.
  TITLE     An Alu repeat-mediated genomic GCNT2 deletion underlies congenital
            cataracts and adult i blood group
  JOURNAL   Hum. Genet. 131 (2), 209-216 (2012)
   PUBMED   21761136
  REMARK    GeneRIF: An Alu repeat-mediated genomic GCNT2 deletion underlies
            congenital cataracts and adult i blood group
REFERENCE   2  (bases 1 to 4219)
  AUTHORS   Zhang,H., Meng,F., Wu,S., Kreike,B., Sethi,S., Chen,W., Miller,F.R.
            and Wu,G.
  TITLE     Engagement of I-branching {beta}-1,
            6-N-acetylglucosaminyltransferase 2 in breast cancer metastasis and
            TGF-{beta} signaling
  JOURNAL   Cancer Res. 71 (14), 4846-4856 (2011)
   PUBMED   21750175
  REMARK    GeneRIF: Results show involvement of GCNT2 in EMT and TGF-beta
            signaling, and further glycosylation modification of E-cadherin by
            GCNT2, are the underlying integrative mechanisms for breast cancer
            metastasis.
REFERENCE   3  (bases 1 to 4219)
  AUTHORS   Wussuki-Lior,O., Abu-Horowitz,A., Netzer,I., Almer,Z., Morad,Y.,
            Goldich,Y., Yahalom,V., Pras,E. and Pras,E.
  TITLE     Hematologic biomarkers in childhood cataracts
  JOURNAL   Mol. Vis. 17, 1011-1015 (2011)
   PUBMED   21541272
  REMARK    GeneRIF: In the family with the 'ii' blood group a novel GCNT2
            mutation was found in the cataract patients.
            Publication Status: Online-Only
REFERENCE   4  (bases 1 to 4219)
  AUTHORS   Inaba,N., Hiruma,T., Togayachi,A., Iwasaki,H., Wang,X.H.,
            Furukawa,Y., Sumi,R., Kudo,T., Fujimura,K., Iwai,T., Gotoh,M.,
            Nakamura,M. and Narimatsu,H.
  TITLE     A novel I-branching beta-1,6-N-acetylglucosaminyltransferase
            involved in human blood group I antigen expression
  JOURNAL   Blood 101 (7), 2870-2876 (2003)
   PUBMED   12468428
REFERENCE   5  (bases 1 to 4219)
  AUTHORS   Yu,L.C., Twu,Y.C., Chou,M.L., Reid,M.E., Gray,A.R., Moulds,J.M.,
            Chang,C.Y. and Lin,M.
  TITLE     The molecular genetics of the human I locus and molecular
            background explain the partial association of the adult i phenotype
            with congenital cataracts
  JOURNAL   Blood 101 (6), 2081-2088 (2003)
   PUBMED   12424189
REFERENCE   6  (bases 1 to 4219)
  AUTHORS   Yu,L.C., Twu,Y.C., Chang,C.Y. and Lin,M.
  TITLE     Molecular basis of the adult i phenotype and the gene responsible
            for the expression of the human blood group I antigen
  JOURNAL   Blood 98 (13), 3840-3845 (2001)
   PUBMED   11739194
REFERENCE   7  (bases 1 to 4219)
  AUTHORS   Yeh,J.C., Ong,E. and Fukuda,M.
  TITLE     Molecular cloning and expression of a novel beta-1,
            6-N-acetylglucosaminyltransferase that forms core 2, core 4, and I
            branches
  JOURNAL   J. Biol. Chem. 274 (5), 3215-3221 (1999)
   PUBMED   9915862
REFERENCE   8  (bases 1 to 4219)
  AUTHORS   Bierhuizen,M.F., Mattei,M.G. and Fukuda,M.
  TITLE     Expression of the developmental I antigen by a cloned human cDNA
            encoding a member of a beta-1,6-N-acetylglucosaminyltransferase
            gene family
  JOURNAL   Genes Dev. 7 (3), 468-478 (1993)
   PUBMED   8449405
REFERENCE   9  (bases 1 to 4219)
  AUTHORS   Keats,B., Ott,J. and Conneally,M.
  TITLE     Report of the committee on linkage and gene order
  JOURNAL   Cytogenet. Cell Genet. 51 (1-4), 459-502 (1989)
   PUBMED   2791656
REFERENCE   10 (bases 1 to 4219)
  AUTHORS   Fukuda,M., Fukuda,M.N. and Hakomori,S.
  TITLE     Developmental change and genetic defect in the carbohydrate
            structure of band 3 glycoprotein of human erythrocyte membrane
  JOURNAL   J. Biol. Chem. 254 (10), 3700-3703 (1979)
   PUBMED   438154
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from BX503586.1, AY435147.1 and
            AL832719.1.
            This sequence is a reference standard in the RefSeqGene project.
            On Jan 27, 2006 this sequence version replaced gi:30061505.
            
            Summary: This gene encodes the enzyme responsible for formation of
            the blood group I antigen. The i and I antigens are distinguished
            by linear and branched poly-N-acetyllactosaminoglycans,
            respectively. The encoded protein is the I-branching enzyme, a
            beta-1,6-N-acetylglucosaminyltransferase responsible for the
            conversion of fetal i antigen to adult I antigen in erythrocytes
            during embryonic development. Mutations in this gene have been
            associated with adult i blood group phenotype. Alternatively
            spliced transcript variants encoding different isoforms have been
            described. [provided by RefSeq, Jul 2008].
            
            Transcript Variant: This variant (3) contains a different 5' end
            exon compared to variant 2. The encoded isoform (C) is longer and
            has a distinct N-terminus, compared to isoform B.
            
            Sequence Note: This RefSeq record represents the GCNT2*001.1.1
            allele.
            
            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 :: BX647668.1, BX647576.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025083, ERS025084 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-230               BX503586.1         2-231
            231-4199            AY435147.1         1-3969
            4200-4219           AL832719.1         4201-4220
FEATURES             Location/Qualifiers
     source          1..4219
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="6"
                     /map="6p24.2"
     gene            1..4219
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /note="glucosaminyl (N-acetyl) transferase 2, I-branching
                     enzyme (I blood group)"
                     /db_xref="GeneID:2651"
                     /db_xref="HGNC:4204"
                     /db_xref="MIM:600429"
     exon            1..1155
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /inference="alignment:Splign:1.39.8"
     variation       1
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:55725242"
     variation       2
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:56265438"
     variation       3
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:55706551"
     variation       4
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:55664565"
     variation       5
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:55912586"
     variation       6
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:55964919"
     variation       8
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:56269596"
     variation       11
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:56275392"
     variation       12
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:55824158"
     variation       13
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:55706315"
     variation       14
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:370268348"
     variation       14
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:569693"
     variation       15
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:56093956"
     variation       16
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:56147450"
     variation       17
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:56133708"
     variation       18
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:56201238"
     variation       19
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:55750437"
     variation       22
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:55657895"
     variation       23
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:56387570"
     variation       23
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149927029"
     variation       24
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:56256255"
     variation       25
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:56298720"
     misc_feature    90..92
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /note="upstream in-frame stop codon"
     variation       91
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185292074"
     variation       119
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190193662"
     variation       120
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115219599"
     variation       121
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:73434927"
     variation       131
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:181342389"
     variation       164
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114691812"
     variation       212
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:371364114"
     CDS             231..1439
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /EC_number="2.4.1.150"
                     /note="isoform C is encoded by transcript variant 3; Ii
                     blood group; I beta-1,6-N-acetylglucosaminyltransferase;
                     N-acetyllactosaminide
                     beta-1,6-N-acetylglucosaminyl-transferase;
                     beta-1,6-N-acetylglucosaminyltransferase 2"
                     /codon_start=1
                     /product="N-acetyllactosaminide
                     beta-1,6-N-acetylglucosaminyl-transferase isoform C"
                     /protein_id="NP_663630.2"
                     /db_xref="GI:85790495"
                     /db_xref="CCDS:CCDS4513.1"
                     /db_xref="GeneID:2651"
                     /db_xref="HGNC:4204"
                     /db_xref="MIM:600429"
                     /translation="
MNFWRYCFFAFTLLSVVIFVRFYSSQLSPPKSYEKLNSSSERYFRKTACNHALEKMPVFLWENILPSPLRSVPCKDYLTQNHYITSPLSEEEAAFPLAYVMVIHKDFDTFERLFRAIYMPQNVYCVHVDEKAPAEYKESVRQLLSCFQNAFIASKTESVVYAGISRLQADLNCLKDLVASEVPWKYVINTCGQDFPLKTNREIVQHLKGFKGKNITPGVLPPDHAIKRTKYVHQEHTDKGGFFVKNTNILKTSPPHQLTIYFGTAYVALTRDFVDFVLRDQRAIDLLQWSKDTYSPDEHFWVTLNRVSGVPGSMPNASWTGNLRAIKWSDMEDRHGGCHGHYVHGICIYGNGDLKWLVNSPSLFANKFELNTYPLTVECLELRHRERTLNQSETAIQPSWYF
"
     misc_feature    249..290
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q8NFS9.2);
                     transmembrane region"
     misc_feature    519..1304
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /note="Core-2/I-Branching enzyme; Region: Branch;
                     pfam02485"
                     /db_xref="CDD:202252"
     variation       257
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:183989959"
     variation       261
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146192473"
     variation       278
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:112495317"
     variation       284
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200043261"
     variation       302
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:5874284"
     variation       308
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139386317"
     variation       317
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201305914"
     variation       332
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:188379073"
     variation       346
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:368878274"
     variation       351
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144003460"
     variation       364
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:371732832"
     variation       438
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202027643"
     variation       473
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:201291494"
     variation       489
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:11966400"
     variation       497
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369674837"
     variation       566
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:78368345"
     variation       569
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:148665139"
     variation       583
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139546463"
     variation       594
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:149719341"
     variation       597
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:185966856"
     variation       601
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:147482025"
     variation       609
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200376277"
     variation       611
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144473761"
     variation       619
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147860726"
     variation       627
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142340241"
     variation       679
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145342719"
     variation       735
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:56106312"
     variation       765
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149144819"
     variation       778
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369938064"
     variation       788
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201986799"
     variation       791
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142440506"
     variation       792
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:151328531"
     variation       831
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147898876"
     variation       843
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:370235645"
     variation       845
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201399458"
     variation       847
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:377565758"
     variation       913
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:55795227"
     variation       915
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150468994"
     variation       922
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370612113"
     variation       925
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200314522"
     variation       928
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:182321762"
     variation       937
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:594495"
     variation       954
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367919657"
     variation       989
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202188269"
     variation       993
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199671735"
     variation       1008
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368253480"
     variation       1009
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140303058"
     variation       1033
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372387897"
     variation       1046
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:539351"
     variation       1052
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:137864542"
     variation       1064
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:71548508"
     variation       1065
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150434353"
     variation       1066
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374501897"
     variation       1094
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367830933"
     variation       1155
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:55739763"
     exon            1156..1248
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /inference="alignment:Splign:1.39.8"
     variation       1215
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200302046"
     variation       1221
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377726790"
     variation       1224
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201667728"
     exon            1249..4200
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /inference="alignment:Splign:1.39.8"
     variation       1276
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148284531"
     variation       1279
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:56141211"
     variation       1283
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141252458"
     variation       1284
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369770528"
     variation       1303
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200336999"
     variation       1305
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:74715857"
     variation       1341
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373290948"
     variation       1371
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:9467010"
     variation       1384
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:55940927"
     variation       1385
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370574556"
     variation       1393
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147413525"
     variation       1407
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374648973"
     variation       1414
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371217806"
     variation       1415
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139955928"
     variation       1438
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:55719848"
     variation       1439
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:55969149"
     variation       1458
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200119543"
     STS             1460..1627
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /standard_name="D6S2094"
                     /db_xref="UniSTS:43631"
     variation       1482
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371150329"
     variation       1492
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:145159006"
     variation       1498
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:374570069"
     STS             1502..1628
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /standard_name="STS-Z19550"
                     /db_xref="UniSTS:70275"
     variation       1520
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2230907"
     variation       1543
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:151338305"
     variation       1544
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113642669"
     variation       1635
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:77170997"
     variation       1664
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:6936681"
     variation       1675
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:183281090"
     variation       1837
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:75940068"
     variation       1844
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:189112306"
     variation       2110
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:6938748"
     variation       2121
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:80071169"
     variation       2207
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:73437198"
     variation       2378
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:9467011"
     variation       2445
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377020829"
     variation       2446..2449
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="ttca"
                     /db_xref="dbSNP:369368500"
     variation       2454
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:192166399"
     variation       2460..2461
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="ttca"
                     /db_xref="dbSNP:139647870"
     variation       2468
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:150306520"
     variation       2480
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374453226"
     variation       2551
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:6899538"
     variation       2613
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:13210512"
     variation       2623
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:75229997"
     variation       2756
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:137926677"
     variation       2872
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:182857743"
     variation       2979
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:4621625"
     variation       3168
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187764030"
     variation       3172
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:76447432"
     variation       3198
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370846327"
     variation       3332..3333
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace=""
                     /replace="at"
                     /db_xref="dbSNP:144237076"
     variation       3376
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149471442"
     variation       3455
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:191632896"
     variation       3465
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184105266"
     variation       3548
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:188841276"
     variation       3659
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:375311644"
     variation       3743
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192169515"
     variation       3769
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:145879560"
     variation       3891
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:114854786"
     variation       3899
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184558753"
     variation       3959
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:9460952"
     variation       3960
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190656787"
     variation       3961
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:182331720"
     variation       4035
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:186051583"
     polyA_signal    4177..4182
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
     polyA_site      4200
                     /gene="GCNT2"
                     /gene_synonym="bA360O19.2; bA421M1.1; CCAT; GCNT2C; GCNT5;
                     IGNT; II; NACGT1; NAGCT1; ULG3"
ORIGIN      
gcagaccaaagtgagagagggacgcaccgcatctccaggcacatccaaaaaggatggacgagacaccgaagcagaggatacaggaggattaaaggattcaggaaagcaagcagccctccggagaagctgtcgaaattcaagactggcaagagaagcaaattcaacctctcacaccgatcatttctcattccctgaaaagaagagattgtttccccagggaagtgaaaataatgaacttttggaggtactgcttttttgctttcactctgctcagcgtggtcatttttgtgagattttacagtagccaattgagcccgccaaaaagttatgagaagctgaacagttccagtgaaaggtattttaggaaaactgcctgtaatcacgccttagagaaaatgccagtctttttgtgggaaaatatattaccatcacctttgcgaagtgtcccttgcaaggattacctgacccagaatcactacatcacaagtcccctgtcggaagaagaggctgcattccctttggcctatgtcatggtcatccataaggactttgacacctttgaaaggctctttagggctatctatatgccccaaaatgtctactgtgttcacgtggatgagaaagccccagctgagtataaggaatctgtgaggcagttactgagttgcttccaaaatgctttcattgcttcaaagacagagtctgtggtttatgcaggcatttccagactccaggctgacctgaactgtctgaaagaccttgtcgcctctgaggttccctggaagtacgtcatcaacacctgtggacaagacttccccctgaaaaccaaccgggagatagttcagcatctgaaaggatttaaagggaaaaatatcaccccaggggtgctgcctcctgaccatgcaattaagcgaactaaatatgtccaccaagagcatacagataaaggtggcttttttgtgaaaaatactaatattttgaaaacttcacctccacatcagctgaccatctactttggcactgcctatgtggcgcttaccagagactttgtcgactttgttctacgtgaccaaagggccattgatctactacaatggtcaaaagatacctatagtcctgatgagcatttctgggtgacacttaatagggtttcaggtgttcctggctctatgccaaatgcatcctggactggaaacctcagagctataaagtggagtgacatggaagacagacacggaggctgccacggccactatgtacatggtatttgtatctatggaaacggagacttaaagtggctggttaattcaccaagcctgtttgctaacaagtttgagcttaatacctacccccttactgtggaatgcctagaactgaggcatcgcgaaagaaccctcaatcagagtgaaactgcgatacaacccagctggtatttttgagctattcatgagctactcatgactgaagggaaactgcagctgggaagaggagcctgtttttgtgagagacttttgccttcgtaatgttaaccgtttcaggaccacgtttatagcttcaggacctggctacgtaattatacttaaaatatccactggacactgtgaaatacactaacaggatggctgggtagagcaatctgggcactttggccaattttagtcttgctgtttcttgatgctcacctctatattagtttattgttaggatcaatgataaatttaaatgacctcagatctttgcaccagatactcatcatatacaaatgttttagtaaaaaagagaattgtagataatactgtctaggaaaataagaattaggtttctttgaagaaggaatcttttataacaccttaacagtcaccactgtgctcaaccagacagatagtgaaacagctttctgggtaattcaccaatttcctttaaaacataagctacctgaatggagaatacatcttgtttctgagtttcaacactagcatttttggcttactcatggacaaagttctgtatatagtataaagtcattaacaagaaacaggatatgctttaagacagaattcactgtctgttgcttcagtaaaaggacctcggggaataaaacatttctctcttatatgccagaatgtaggctggtccctatgtcatgtcttccattaagaacactaaaaagtccttgcaagaatggagatatgcattcaagagaggtgctatcacatagatctagtctgaagtctggaacactttcctcttctatgacccctctctccccagtattatcttacttgcaaaatggagaccaaattctatcctgtgaggcttttaattgcaccatagtatgctctgagtagctttacactgcctggtactgatagtagtggctcgatttttaagagccttcaattgtagatgaacatctctgttatttatccctcattcatccatccgttcattcattcagccttcaatcaacatctcttgagtgtctattatgtacaggacatgtactgagacaaaaaggaaacataagagctttttcactctaaaaatcttggcaataatgtcaacaccagaaagcctcctctggagaatcttacagagtgattgtagtttaatacaggaacacacagggctgtgtagcatgataccaggcccaggagatcagtaattacaaattaagggttaaatcagagattattcaacagagagggagaaaggaggagacagagggaggacctgttgtgttccagccattctggtattcctttatgtatctaatttcattcaaacctcacaacagtcttgtgaggcccttatataattactcccattttgcagatgaagtaactgaggcttagaaaggttaatagcaccggggaacaatttctctgggtgagaattgggactctgttgctggtcttctcagttcatttcctgaggtggatttactgagagaaggtgaaataaagccatatttagtataccagagaaggtagattttaagaatggtctcagtgttaatactgagaaaaagtcctgtcagttcagaaaaaatgtgaagtctactttagtattcctgtaatactaaaccgttgagtttctaaatatttatttattctaacaaaaagcaattactacaaatggatgacacatttaatgaacacaattttattttttttctgtaactgtgcttgttgaatgtcaatcatatttaaagggaatgactttgaagtaaaaccttttttcttgctactgaaaaaaatggagttgttttgggtggtaaagtgttaaggaatagggacagctggtcacacaaggaactcttgaaggccacatgtgaaaacctgtcacttgcacagaggccagtcccactaaggtgaccagagtgggctccaagcacaaactgccattggctatagatgggactgtgtccccccaaaattcatgtgttggagccttaaccctcaatgtgatggtatttgagatggggcctttggtaagggaagtttagatgaggtcacgagggtaggaccctcatgatgggatgagtccccttacaagacctctggcttgggccgggcgtggtggctcacacctgtaatcccaacactttgggaggccaaggcaggtagatcacttgatgccaggagttccagaccaggctggccgacatggtgaaaccccatctctactaaaaaatataaaaattagccgggctttgtggcatgtgcctgtaatcccagctatttggcaggctgaggcatgagaatcgcttgaacccaggaggtggaggttacagtgagctgagagtgccccactgcactccagcctgggtgacagagcgagactttgtcccaaaacaaaataggtgaggggatagcgaatgcactcagggtcagcagtggagtttaaaaattgtctcttttcaacttatttaaatgacagcacctgagaagaggaaccgttttacactggatgtttctcatgtagaacaagaaatctttctggaattgatgtttacatgtctgttgttggtcatctctcctgtgtcttaaatactttaatgttggaagagcatagtgtttgggctagtgggtttctgacagcccatgggaatgccctgaaactactgtatctgatgtttgttttcgatgaggttccatgttttgttttcttgggaataaattaatatattgttttccaaaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:2651 -> Molecular function: GO:0008109 [N-acetyllactosaminide beta-1,6-N-acetylglucosaminyltransferase activity] evidence: IEA
            GeneID:2651 -> Biological process: GO:0006024 [glycosaminoglycan biosynthetic process] evidence: TAS
            GeneID:2651 -> Biological process: GO:0006486 [protein glycosylation] evidence: IEA
            GeneID:2651 -> Biological process: GO:0007275 [multicellular organismal development] evidence: TAS
            GeneID:2651 -> Cellular component: GO:0000139 [Golgi membrane] evidence: IEA
            GeneID:2651 -> Cellular component: GO:0016020 [membrane] evidence: TAS
            GeneID:2651 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
ANNOTATIONS from NCBI Entrez Gene (20130726):
            NP_663630 -> EC 2.4.1.150

by @meso_cacase at DBCLS
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