LOCUS       DQ438904                 492 bp    mRNA    linear   HUM 26-JUL-2016
DEFINITION  Homo sapiens GLIS family zinc finger 3 transcript variant TS20
            (GLIS3) mRNA, exons 15, 18 and partial cds, alternatively spliced.
ACCESSION   DQ438904
VERSION     DQ438904.1
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 492)
  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 492)
  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..492
                     /db_xref="H-InvDB:HIT000343364"
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="9"
                     /map="9p24.2"
                     /note="generated by 5' RACE PCR"
     gene            1..>492
                     /gene="GLIS3"
     exon            1..355
                     /gene="GLIS3"
                     /number=15
     exon            356..>492
                     /gene="GLIS3"
                     /number=18
     CDS             426..>492
                     /gene="GLIS3"
                     /note="neonatal diabetes mellitus and congenital
                     hypothyroidism syndrome; alternatively spliced"
                     /codon_start=1
                     /product="GLIS family zinc finger 3 transcript variant
                     TS20"
                     /protein_id="ABE66456.1"
                     /translation="MKQEWSQGYRALPSLSNHGSQN"
BASE COUNT          131 a          109 c          116 g          136 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 tacaggtccc
      361 ttatttcgcg tgagtctttg gcgtccacga ccttgagtct gacggaaagt cagtcggcct
      421 caagcatgaa gcaggagtgg tcccagggct acagggccct cccttcgctc tccaaccacg
      481 gctctcagaa tg
//