LOCUS ABE66436.1 350 aa PRT HUM 26-JUL-2016 DEFINITION Homo sapiens GLIS family zinc finger 3 transcript variant TE1 protein. ACCESSION DQ438879-1 PROTEIN_ID ABE66436.1 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 1585) 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 1585) 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 Qualifiers source /db_xref="H-InvDB:HIT000343339" /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="9" /map="9p24.2" /note="generated by 3' RACE PCR" protein /gene="GLIS3" /note="neonatal diabetes mellitus and congenital hypothyroidism syndrome; alternatively spliced" BEGIN 1 DDDGEMDGIG GKHCCRWIDC SALYDQQEEL VRHIEKVHID QRKGEDFTCF WAGCPRRYKP 61 FNARYKLLIH MRVHSGEKPN KCTFEGCEKA FSRLENLKIH LRSHTGEKPY LCQHPGCQKA 121 FSNSSDRAKH QRTHLDTKPY ACQIPGCTKR YTDPSSLRKH VKAHSSKEQQ ARKKLRSSTE 181 LHPDLLTDCL TVQSLQPATS PRDAAAEGTV GRSPGPGPDL YSAPIFSSNY SSRSGTAAGA 241 VPPPHPVSHP SPGHNVQGSP HNPSSQLPPL TAVDAGAERF APSAPSPHHI SPRRVPAPSS 301 ILQRTQPPYT QQPSGSHLKS YQPETNSSFQ PNGIHVHGKQ EAGSPLSFEK //