LOCUS       DQ438901                 633 bp    mRNA    linear   HUM 26-JUL-2016
DEFINITION  Homo sapiens GLIS family zinc finger 3 transcript variant TS17
            (GLIS3) mRNA, exons 8.1, 18 and partial cds, alternatively spliced.
ACCESSION   DQ438901
VERSION     DQ438901.1
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 633)
  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 633)
  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..633
                     /db_xref="H-InvDB:HIT000343361"
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="9"
                     /map="9p24.2"
                     /note="generated by 5' RACE PCR"
     gene            1..>633
                     /gene="GLIS3"
     exon            1..496
                     /gene="GLIS3"
                     /number=8.1
     exon            497..>633
                     /gene="GLIS3"
                     /number=18
     CDS             567..>633
                     /gene="GLIS3"
                     /note="neonatal diabetes mellitus and congenital
                     hypothyroidism syndrome; alternatively spliced"
                     /codon_start=1
                     /product="GLIS family zinc finger 3 transcript variant
                     TS17"
                     /protein_id="ABE66453.1"
                     /translation="MKQEWSQGYRALPSLSNHGSQN"
BASE COUNT          109 a          217 c          193 g          114 t
ORIGIN      
        1 cgggaccccc tgtacgccgt ccgcgccgtc cagggtcaca ccggcgacgg aacccgccgg
       61 cagcaattag ccagcatccc ggggtcggcc cccagaagca ttccccggcc caggacgagg
      121 atgaacagga caggcgaggc acaaagtcgc aactgaactt tttagaaaca ttatttgtgt
      181 gtgtatgtgt gtagcagggg agaatgagct gatgccgagg gtccagccac cccgcctctg
      241 cctcctcctc cccctgccgc cgctgccctc gcagacgcgc gcgcacacac ggcacttggg
      301 ccgggtttcc gcgctccgtc cccccgtttg gatgggggtt ttcatttccg aaggaggcac
      361 agcccgcgga gcgctctgaa gggctggagc cccaagttac tcctcgccag cgccggccgc
      421 ccgctgtcac tcgcgctggc cggccggggg aagggacccg cacgccgggc tttgttgtgg
      481 aaatcccggt tacctggtcc cttatttcgc gtgagtcttt ggcgtccacg accttgagtc
      541 tgacggaaag tcagtcggcc tcaagcatga agcaggagtg gtcccagggc tacagggccc
      601 tcccttcgct ctccaaccac ggctctcaga atg
//