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
//