LOCUS       DQ438903                 435 bp    mRNA    linear   HUM 26-JUL-2016
DEFINITION  Homo sapiens GLIS family zinc finger 3 transcript variant TS19
            (GLIS3) mRNA, exons 10.5, 18 and partial cds, alternatively
            spliced.
ACCESSION   DQ438903
VERSION     DQ438903.1
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 435)
  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 435)
  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..435
                     /db_xref="H-InvDB:HIT000343363"
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="9"
                     /map="9p24.2"
                     /note="generated by 5' RACE PCR"
     gene            1..>435
                     /gene="GLIS3"
     exon            1..298
                     /gene="GLIS3"
                     /number=10.5
     exon            299..>435
                     /gene="GLIS3"
                     /number=18
     CDS             369..>435
                     /gene="GLIS3"
                     /note="neonatal diabetes mellitus and congenital
                     hypothyroidism syndrome; alternatively spliced"
                     /codon_start=1
                     /product="GLIS family zinc finger 3 transcript variant
                     TS19"
                     /protein_id="ABE66455.1"
                     /translation="MKQEWSQGYRALPSLSNHGSQN"
BASE COUNT           99 a          139 c          112 g           85 t
ORIGIN      
        1 atccgagccc actccgggac tcctggcccc tcgccctgtg gcagcacatc gagtcccact
       61 atggcaagcc ttgctaacaa cctccatctc aagatgccct caggaggagg gatggctcct
      121 cagaacaacg tggctgagag ccgcatccat ctgcctgcct taagccccag gagacaaatg
      181 ctcaccaatg ggaagccgcg attccaggtc acccaggctg gaggcatgtc agggtcacat
      241 actttaaagc caaagcagca ggagtttgga agcccttttc ctccaaatcc tgggaaaggt
      301 cccttatttc gcgtgagtct ttggcgtcca cgaccttgag tctgacggaa agtcagtcgg
      361 cctcaagcat gaagcaggag tggtcccagg gctacagggc cctcccttcg ctctccaacc
      421 acggctctca gaatg
//