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 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
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