LOCUS DQ438902 311 bp mRNA linear HUM 26-JUL-2016 DEFINITION Homo sapiens GLIS family zinc finger 3 transcript variant TS18 (GLIS3) mRNA, exons 8.2, 18 and partial cds, alternatively spliced. ACCESSION DQ438902 VERSION DQ438902.1 KEYWORDS . 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 311) AUTHORS Senee,V., Chelala,C., Duchatelet,S., Feng,D., Blanc,H., Cossec,J.C., Charon,C., Nicolino,M., Boileau,P., Cavener,D.R., Bougneres,P., Taha,D. and Julier,C. TITLE Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism JOURNAL Nat. Genet. 38 (6), 682-687 (2006) PUBMED 16715098 REFERENCE 2 (bases 1 to 311) AUTHORS Julier,C. TITLE Direct Submission JOURNAL Submitted (09-MAR-2006) INSERM U730, Genetique des Maladies Infectieuses et Autoimmunes, Institut Pasteur, 28 rue du Docteur Roux, Paris 75015, France FEATURES Location/Qualifiers source 1..311 /db_xref="H-InvDB:HIT000343362" /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="9" /map="9p24.2" /note="generated by 5' RACE PCR" gene 1..>311 /gene="GLIS3" exon 1..174 /gene="GLIS3" /number=8.2 exon 175..>311 /gene="GLIS3" /number=18 CDS 245..>311 /gene="GLIS3" /note="neonatal diabetes mellitus and congenital hypothyroidism syndrome; alternatively spliced" /codon_start=1 /product="GLIS family zinc finger 3 transcript variant TS18" /protein_id="ABE66454.1" /translation="MKQEWSQGYRALPSLSNHGSQN" BASE COUNT 50 a 100 c 98 g 63 t ORIGIN 1 cccgtttgga tgggggtttt catttccgaa ggaggcacag cccgcggagc gctctgaagg 61 gctggagccc caagttactc ctcgccagcg ccggccgccc gctgtcactc gcgctggccg 121 gccgggggaa gggacccgca cgccgggctt tgttgtggaa atcccggtta cctggtccct 181 tatttcgcgt gagtctttgg cgtccacgac cttgagtctg acggaaagtc agtcggcctc 241 aagcatgaag caggagtggt cccagggcta cagggccctc ccttcgctct ccaaccacgg 301 ctctcagaat g //