LOCUS       AB050193                1760 bp    mRNA    linear   HUM 01-JUL-2008
DEFINITION  Homo sapiens h-scot-t mRNA for succinyl CoA: 3-oxo acid CoA
            transferase, complete cds.
ACCESSION   AB050193
VERSION     AB050193.2
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 1760)
  AUTHORS   Kohroki,J. and Tanaka,H.
  TITLE     Direct Submission
  JOURNAL   Submitted (18-OCT-2000) to the DDBJ/EMBL/GenBank databases.
            Contact:Hiromitsu Tanaka
            Faculty of Pharmaceutical Sciences, Nagasaki International
            University; Sasebo, Nagasaki 859-3298, Japan
REFERENCE   2
  AUTHORS   Tanaka,H., Kohroki,J., Iguchi,N., Onishi,M. and Nishimune,Y.
  TITLE     Cloning and characterization of a human orthologue of
            testis-specific succinyl CoA: 3-oxo acid CoA transferase (Scot-t)
            cDNA.
  JOURNAL   Mol. Hum. Reprod. 8, 16-23 (2002)
COMMENT     
FEATURES             Location/Qualifiers
     source          1..1760
                     /cell_type="haploid germ cell"
                     /country="Japan"
                     /db_xref="H-InvDB:HIT000059551"
                     /db_xref="taxon:9606"
                     /mol_type="mRNA"
                     /note="SNP information was identified using a genomic DNA
                     of a blood"
                     /organism="Homo sapiens"
                     /sex="male"
                     /tissue_type="testis"
     CDS             20..1573
                     /codon_start=1
                     /gene="h-scot-t"
                     /note="SCOT-t"
                     /note="haploid germ cell specific succinyl CoA
                     transferase"
                     /product="succinyl CoA: 3-oxo acid CoA transferase"
                     /protein_id="BAB40810.2"
                     /transl_table=1
                     /translation="MAALRLLASVLGRGVPAGGSGLALSQGCARCFATSPRLRAKFYA
                     DPVEMVKDISDGATVMIGGFGLCGIPENLIAALLRTRVKDLQVVSSNVGVEDFGLGLL
                     LAARQVRRIVCSYVGENTLCESQYLAGELELELTPQGTLAERIRAGGAGVPAFYTPTG
                     YGTLVQEGGAPIRYTPDGHLALMSQPREVREFNGDHFLLERAIRADFALVKGWKADRA
                     GNVVFRRSARNFNVPMCKAADVTAVEVEEIVEVGAFPPEDIHVPNIYVDRVIKGQKYE
                     KRIERLTILKEEDGDAGKEEDARTRIIRRAALEFEDGMYANLGIGIPLLASNFISPSM
                     TVHLHSENGILGLGPFPTEDEVDADLINAGKQTVTVLPGGCFFASDDSFAMIRGGHIQ
                     LTMLGAMQVSKYGDLANWMIPGKKVKGMGGAMDLVSSQKTRVVVTMQHCTKDNTPKIM
                     EKCTMPLTGKRCVDRIITEKAVFDVHRKKELTLRELWEGLTVDDIKKSTGCAFAVSPN
                     LRPMQQVAP"
     variation       132
                     /note="SNP information"
                     /note="This substitution causes an amino acid
                     substitution from Leu to Pro"
                     /replace="c"
     variation       280
                     /note="SNP information in Australian"
                     /note="This substitution dose not cause an amino acid"
                     /replace="a"
     variation       873
                     /note="SNP information"
                     /note="This substitution causes an amino acid
                     substitution from Leu to Arg"
                     /replace="g"
     variation       1002
                     /note="SNP information in Australian"
                     /note="This substitution causes an amino acid
                     substitution from Asn to Ser"
                     /replace="g"
     variation       1074
                     /note="SNP information"
                     /note="This substitution causes an amino acid
                     substitution from Thr to Met"
                     /replace="t"
     variation       1395
                     /note="SNP information"
                     /note="This substitution causes an amino acid
                     substitution from Gly to Val"
                     /replace="t"
     variation       1458
                     /note="SNP information"
                     /note="This substitution causes an amino acid
                     substitution from Glu to Gly"
                     /replace="g"
     variation       1499
                     /note="SNP information"
                     /note="This substitution causes an amino acid
                     substitution from Asp to Asn"
                     /replace="a"
     variation       1616
                     /note="3'UTR"
                     /note="SNP information"
                     /replace="a"
     variation       1670
                     /note="3'UTR"
                     /note="SNP information"
                     /replace="c"
BASE COUNT          368 a          519 c          581 g          292 t
ORIGIN      
        1 gggccgaccc gggccgacta tggcggcgct gcggctcctg gcgtcagtgc tcgggcgcgg
       61 ggtccccgcc ggcggctcag ggctcgcgct gtcccagggc tgcgcccgct gctttgccac
      121 cagtccccgg ctccgtgcca agttctacgc ggacccggtg gagatggtga aggacatctc
      181 tgacggggcg accgtcatga tcgggggctt cgggctctgc gggatccccg agaacctgat
      241 cgccgcgctg ctcaggaccc gcgtgaaaga cctgcaggtg gtcagcagca acgtgggcgt
      301 ggaggacttc ggcctgggcc tcctgctggc cgccaggcag gtccgtcgca tcgtctgttc
      361 ctacgtgggc gagaacaccc tgtgcgagag ccagtacctg gcaggagagc tggagctgga
      421 gctcacgccc cagggcaccc tggccgagcg catccgcgcg gggggcgccg gggtgcccgc
      481 cttctacacc cccacgggct acgggaccct ggtccaggaa gggggcgccc ccatccgcta
      541 caccccggac ggccacctgg cgctcatgag ccagccccga gaggtgaggg agttcaacgg
      601 cgaccacttc cttttggagc gcgccatccg ggcagacttc gccctggtga aagggtggaa
      661 ggccgaccgg gcaggaaacg tggtcttcag gagaagcgcc cgcaatttca acgtgcccat
      721 gtgcaaagct gcagacgtca cggcggtgga ggtggaagag atcgtggagg tgggggcttt
      781 ccccccagaa gacatccacg ttcctaacat ttatgtagat cgcgtgataa aggggcagaa
      841 atacgagaaa cgaattgagc gcttaacgat cctgaaagag gaagatggag acgctggaaa
      901 ggaagaggac gccaggacgc gcatcatcag acgcgcagct ctggaatttg aggacggcat
      961 gtacgccaat ctgggcatag gcatccccct gctggccagc aacttcatca gtcccagcat
     1021 gactgtccat cttcacagtg agaacgggat cctgggcctg ggcccgtttc ccacggaaga
     1081 tgaggtggat gccgacctca tcaatgcagg caagcagacg gtcacggtgc ttcccggggg
     1141 ctgcttcttc gccagcgacg actccttcgc catgatccga gggggacaca tccaactaac
     1201 catgcttgga gccatgcagg tttccaaata cggcgacctg gcgaactgga tgatccctgg
     1261 caagaaggtg aaaggcatgg gcggtgccat ggacttggtg tccagtcaga agaccagagt
     1321 ggtggtcacc atgcagcact gcacaaagga caacaccccc aagatcatgg agaaatgcac
     1381 catgccgctg accgggaagc ggtgcgtgga ccgcatcatc accgagaagg ccgtgtttga
     1441 cgtgcacagg aagaaagagc tgacgctgag ggagctctgg gagggcctga cggtggacga
     1501 catcaaaaag agcacggggt gtgcctttgc tgtgtccccg aacctcaggc ccatgcagca
     1561 ggtggcaccc tgacgggacc tggatctggg cggggtggtg cgctcctcag ggcgggtgcc
     1621 accgggttcc ccaggggaat acatgtcccc agctctggga ggggtttgct actggcctcc
     1681 tactttcctc cctaggtgga cagtgctcct ctagagagct gcgactttaa ttaaaaacaa
     1741 caggaaaaca gaaaaaaaaa
//