LOCUS       DQ438899                 797 bp    mRNA    linear   HUM 26-JUL-2016
DEFINITION  Homo sapiens GLIS family zinc finger 3 transcript variant TS15
            (GLIS3) mRNA, exons 8.2, 10.3, 18 and partial cds, alternatively
            spliced.
ACCESSION   DQ438899
VERSION     DQ438899.1
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 797)
  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 797)
  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..797
                     /db_xref="H-InvDB:HIT000343359"
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="9"
                     /map="9p24.2"
                     /note="generated by 5' RACE PCR"
     gene            1..>797
                     /gene="GLIS3"
     exon            1..174
                     /gene="GLIS3"
                     /number=8.2
     exon            175..660
                     /gene="GLIS3"
                     /number=10.3
     exon            661..>797
                     /gene="GLIS3"
                     /number=18
     CDS             731..>797
                     /gene="GLIS3"
                     /note="neonatal diabetes mellitus and congenital
                     hypothyroidism syndrome; alternatively spliced"
                     /codon_start=1
                     /product="GLIS family zinc finger 3 transcript variant
                     TS15"
                     /protein_id="ABE66451.1"
                     /translation="MKQEWSQGYRALPSLSNHGSQN"
BASE COUNT          172 a          241 c          219 g          165 t
ORIGIN      
        1 cccgtttgga tgggggtttt catttccgaa ggaggcacag cccgcggagc gctctgaagg
       61 gctggagccc caagttactc ctcgccagcg ccggccgccc gctgtcactc gcgctggccg
      121 gccgggggaa gggacccgca cgccgggctt tgttgtggaa atcccggtta cctggcttat
      181 aacccacacc atggataact tattggactt tgcctgaaag gagtcattag tgacattgga
      241 tatttgaccg tcttggccac aggtttttca gaatgaatgg aagatcatgc agcatgagtc
      301 tccaccggac atcgggaacc ccacaggggc ctaggatggt cagtggtcat cacattcctg
      361 ccatccgagc ccactccggg actcctggcc cctcgccctg tggcagcaca tcgagtccca
      421 ctatggcaag ccttgctaac aacctccatc tcaagatgcc ctcaggagga gggatggctc
      481 ctcagaacaa cgtggctgag agccgcatcc atctgcctgc cttaagcccc aggagacaaa
      541 tgctcaccaa tgggaagccg cgattccagg tcacccaggc tggaggcatg tcagggtcac
      601 atactttaaa gccaaagcag caggagtttg gaagcccttt tcctccaaat cctgggaaag
      661 gtcccttatt tcgcgtgagt ctttggcgtc cacgaccttg agtctgacgg aaagtcagtc
      721 ggcctcaagc atgaagcagg agtggtccca gggctacagg gccctccctt cgctctccaa
      781 ccacggctct cagaatg
//