LOCUS DQ438907 169 bp mRNA linear HUM 26-JUL-2016 DEFINITION Homo sapiens GLIS family zinc finger 3 transcript variant TS22 (GLIS3) mRNA, exons 20.2, 25 and partial cds, alternatively spliced. ACCESSION DQ438907 VERSION DQ438907.1 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 169) 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 169) 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..169 /db_xref="H-InvDB:HIT000343367" /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="9" /map="9p24.2" /note="generated by 5' RACE PCR" gene 1..>169 /gene="GLIS3" exon 1..74 /gene="GLIS3" /number=20.2 CDS 49..>169 /gene="GLIS3" /note="neonatal diabetes mellitus and congenital hypothyroidism syndrome; alternatively spliced" /codon_start=1 /product="GLIS family zinc finger 3 transcript variant TS22" /protein_id="ABE66458.1" /translation="MLNNTLYRSLKVARRPFQGLKISRSTCGATQARSRICASI" exon 75..>169 /gene="GLIS3" /number=25 BASE COUNT 48 a 33 c 49 g 39 t ORIGIN 1 aatgtggtga ggacaaagga ctgcagaggc ctggctagga gggtccagat gcttaataat 61 actttgtata gaagtttgaa ggttgcgaga aggccttttc aaggcttgaa aatctcaaga 121 tccacttgcg gagccacaca ggcgagaagc cgtatttgtg ccagcatcc //