LOCUS       DQ438900                 736 bp    mRNA    linear   HUM 26-JUL-2016
DEFINITION  Homo sapiens GLIS family zinc finger 3 transcript variant TS16
            (GLIS3) mRNA, exons 9, 10.3, 18 and partial cds, alternatively
            spliced.
ACCESSION   DQ438900
VERSION     DQ438900.1
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 736)
  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 736)
  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..736
                     /db_xref="H-InvDB:HIT000343360"
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="9"
                     /map="9p24.2"
                     /note="generated by 5' RACE PCR"
     gene            1..>736
                     /gene="GLIS3"
     exon            1..113
                     /gene="GLIS3"
                     /number=9
     exon            114..599
                     /gene="GLIS3"
                     /number=10.3
     exon            600..>736
                     /gene="GLIS3"
                     /number=18
     CDS             670..>736
                     /gene="GLIS3"
                     /note="neonatal diabetes mellitus and congenital
                     hypothyroidism syndrome; alternatively spliced"
                     /codon_start=1
                     /product="GLIS family zinc finger 3 transcript variant
                     TS16"
                     /protein_id="ABE66452.1"
                     /translation="MKQEWSQGYRALPSLSNHGSQN"
BASE COUNT          175 a          210 c          187 g          164 t
ORIGIN      
        1 agttccaagt tactcactgg agctgacaag tcacctcggg gaccgggaag tcactcaagt
       61 gtctggaaat cttggccctg gctgatttgt catcctatgg atgattcaat taggcttata
      121 acccacacca tggataactt attggacttt gcctgaaagg agtcattagt gacattggat
      181 atttgaccgt cttggccaca ggtttttcag aatgaatgga agatcatgca gcatgagtct
      241 ccaccggaca tcgggaaccc cacaggggcc taggatggtc agtggtcatc acattcctgc
      301 catccgagcc cactccggga ctcctggccc ctcgccctgt ggcagcacat cgagtcccac
      361 tatggcaagc cttgctaaca acctccatct caagatgccc tcaggaggag ggatggctcc
      421 tcagaacaac gtggctgaga gccgcatcca tctgcctgcc ttaagcccca ggagacaaat
      481 gctcaccaat gggaagccgc gattccaggt cacccaggct ggaggcatgt cagggtcaca
      541 tactttaaag ccaaagcagc aggagtttgg aagccctttt cctccaaatc ctgggaaagg
      601 tcccttattt cgcgtgagtc tttggcgtcc acgaccttga gtctgacgga aagtcagtcg
      661 gcctcaagca tgaagcagga gtggtcccag ggctacaggg ccctcccttc gctctccaac
      721 cacggctctc agaatg
//