LOCUS DQ438897 250 bp mRNA linear HUM 26-JUL-2016 DEFINITION Homo sapiens GLIS family zinc finger 3 transcript variant TS13 (GLIS3) mRNA, exons 9, 18 and partial cds, alternatively spliced. ACCESSION DQ438897 VERSION DQ438897.1 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 250) 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 250) 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..250 /db_xref="H-InvDB:HIT000343357" /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="9" /map="9p24.2" /note="generated by 5' RACE PCR" gene 1..>250 /gene="GLIS3" exon 1..113 /gene="GLIS3" /number=9 CDS 97..>250 /gene="GLIS3" /note="neonatal diabetes mellitus and congenital hypothyroidism syndrome; alternatively spliced" /codon_start=1 /product="GLIS family zinc finger 3 transcript variant TS13" /protein_id="ABE66449.1" /translation="MDDSIRSLISRESLASTTLSLTESQSASSMKQEWSQGYRALPSL SNHGSQN" exon 114..>250 /gene="GLIS3" /number=18 BASE COUNT 53 a 69 c 66 g 62 t ORIGIN 1 agttccaagt tactcactgg agctgacaag tcacctcggg gaccgggaag tcactcaagt 61 gtctggaaat cttggccctg gctgatttgt catcctatgg atgattcaat taggtccctt 121 atttcgcgtg agtctttggc gtccacgacc ttgagtctga cggaaagtca gtcggcctca 181 agcatgaagc aggagtggtc ccagggctac agggccctcc cttcgctctc caaccacggc 241 tctcagaatg //