LOCUS AAA36329.1 349 aa PRT HUM 27-APR-1993 DEFINITION Homo sapiens protein ( Human GT mitochondrial solute carrier protein homologue mRNA, complete cds. ). ACCESSION M31659-1 PROTEIN_ID AAA36329.1 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 1719) AUTHORS Zarrilli,R., Oates,E.L., McBride,O.W., Lerman,M.I., Chan,J.Y., Santisteban,P., Ursini,M.V., Notkins,A.L. and Kohn,L.D. TITLE Sequence and chromosomal assignment of a novel cDNA identified by immunoscreening of a thyroid expression library: similarity to a family of mitochondrial solute carrier proteins JOURNAL Mol. Endocrinol. 3 (9), 1498-1505 (1989) PUBMED 2575220 COMMENT Original source text: Human (Graves' disease patient) thyroid, cDNA to mRNA, clone hGT-7. The region between base pairs 195-297 appears to be an aberrantly spliced intron. An acceptor splice consensus sequence is present at the 3' end of this region, but no donor site is found at its 5' end. Upon readthrough of this intron boundary, a stop codon is found at positions 245-247. FEATURES Qualifiers source /db_xref="H-InvDB:HIT000195437" /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" protein /note="GT mitochondrial solute carrier protein homologue; putative" intron_pos 44:1 (1/1) BEGIN 1 MAAATAAAAL AAADPPPAMP GAAGAGGPTT RRDFYWLRSF LAGSIAGCCA KTTVAPLDRV 61 KVLLQAHNHH YKHLGVFSAL RAVPQKEGFL GLYKGNGAMM IRIFPYGAIQ FMAFEHYKTL 121 ITTKLGISGH VHRLMAGSMA GMTAVICTDP VDMVRVRLAF QVKGEHRYTG IIHAFKTIYA 181 KEGGFFGFYR GLMPTILGMA PYAGVSFFTF GTLKSVGLSH APTLLGSPSS DNPNVLVLKT 241 HVNLLCGGVA RAIAQTISYP FDVTRRRMQL GTVLPEFEKC LTMRDTMKYD YGHHGIRKGL 301 YRGLSLNYIR CIPSQAVAFY NIRTYEAVFS PQLKKNYGWF FLIHSQREK //