LOCUS       DQ438894                 700 bp    mRNA    linear   HUM 26-JUL-2016
DEFINITION  Homo sapiens GLIS family zinc finger 3 transcript variant TS10
            (GLIS3) mRNA, exons 15, 17, 18 and partial cds, alternatively
            spliced.
ACCESSION   DQ438894
VERSION     DQ438894.1
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 700)
  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 700)
  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..700
                     /db_xref="H-InvDB:HIT000343354"
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="9"
                     /map="9p24.2"
                     /note="generated by 5' RACE PCR"
     gene            1..>700
                     /gene="GLIS3"
     exon            1..355
                     /gene="GLIS3"
                     /number=15
     exon            356..563
                     /gene="GLIS3"
                     /number=17
     CDS             433..>700
                     /gene="GLIS3"
                     /note="neonatal diabetes mellitus and congenital
                     hypothyroidism syndrome; alternatively spliced"
                     /codon_start=1
                     /product="GLIS family zinc finger 3 transcript variant
                     TS10"
                     /protein_id="ABE66446.1"
                     /translation="MMVQRLGLISPPASQVSTACNQISPSLQRAMNAANLNIPPSDTR
                     SLISRESLASTTLSLTESQSASSMKQEWSQGYRALPSLSNHGSQN"
     exon            564..>700
                     /gene="GLIS3"
                     /number=18
BASE COUNT          186 a          168 c          165 g          181 t
ORIGIN      
        1 actgacctca tccatagtgt ggtgtttggt ctatgagcag ttgattcacc agttttcaga
       61 gcccaagtct aaaatcacag atcctgtggg ggatctggga gcatctgcct tacctttatg
      121 aaggttatgg tcagttaagc cttgctttca atgggctcac ttcgctatgg gaagaaaatt
      181 ctgcagttgt taaaaacaaa aggacactgc cttttccaag ggagctgaca gctattggtt
      241 tttccggaga ggattactgg tgaagacagt tatgaagaac aagtaactct tgtaaataaa
      301 cagcatgttc ttgcttaaat atttcccaga acagttctaa agaaatataa tacaggggct
      361 cttggctttg ggcctcagtg caagtccatt ggaaaaggca gctgcaacaa tctagtggtc
      421 accagcagtc ccatgatggt tcagcgactg ggactcattt cacctccagc aagccaggtc
      481 tctacagcat gcaaccagat cagtcctagc ttacagaggg caatgaatgc agccaacctg
      541 aatatacctc cttcagatac caggtccctt atttcgcgtg agtctttggc gtccacgacc
      601 ttgagtctga cggaaagtca gtcggcctca agcatgaagc aggagtggtc ccagggctac
      661 agggccctcc cttcgctctc caaccacggc tctcagaatg
//