LOCUS       AF378119                1416 bp    mRNA    linear   HUM 16-AUG-2002
DEFINITION  Homo sapiens ornithine transporter 2 (ORNT2) mRNA, complete cds;
            nuclear gene for mitochondrial product.
ACCESSION   AF378119
VERSION     AF378119.1
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 1416)
  AUTHORS   Camacho,J.A. III, Obie,C., Biery,B., Almashanu,S., Steel,G.,
            Andrade,D., Porter,J., Kong,J., Mitchell,G. and Valle,D.
  TITLE     Characterization of second mitochondrial ornithine transporter
            ORNT2
  JOURNAL   Unpublished
REFERENCE   2  (bases 1 to 1416)
  AUTHORS   Camacho,J.A. III, Obie,C., Biery,B., Almashanu,S., Steel,G.,
            Andrade,D., Porter,J., Kong,J., Mitchell,G. and Valle,D.
  TITLE     Gene redundancy in patients with
            hyperornithinemia-hyperammonemia-homocitrullinemia (HHH) syndrome
  JOURNAL   Unpublished
REFERENCE   3  (bases 1 to 1416)
  AUTHORS   Camacho,J.A. III, Obie,C., Biery,B., Almashanu,S., Steel,G.,
            Andrade,D., Porter,J., Kong,J., Mitchell,G. and Valle,D.
  TITLE     Direct Submission
  JOURNAL   Submitted (06-MAY-2001) Human Genetics, University of Oklahoma
            Health Sciences Center, 975 NE 10th Street, Biomedical, Oklahoma
            City, OK 73104, USA
FEATURES             Location/Qualifiers
     source          1..1416
                     /db_xref="H-InvDB:HIT000078590"
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="5"
                     /map="5q31"
     gene            1..1416
                     /gene="ORNT2"
     CDS             181..1086
                     /gene="ORNT2"
                     /function="transports ornithine from cytoplasm to
                     mitochondrial matrix"
                     /note="cationic amino acid transporter; similar to Homo
                     sapiens ORNT1 gene which is defective in
                     hyperornithinemia-hyperammonemia-homocitrullinemia HHH
                     syndrome"
                     /codon_start=1
                     /product="ornithine transporter 2"
                     /protein_id="AAM94902.1"
                     /translation="MKSGPGIQAAIDLTAGAAGGTACVLTGQPFDTIKVKMQTFPDLY
                     KGLTDCFLKTYAQVGLRGFYKGTGPALMAYVAENSVLFMCYGFCQQFVRKVAGMDKQA
                     KLSDLQTAAAGSFASAFAALALCPTELVKCRLQTMYEMEMSGKIAKSHNTIWSVVKGI
                     LKKDGPLGFYHGLSSTLLQEGPGYFFFFGGYELSRSFFASGRSKDELGPVHLMLSGGV
                     AGICLWLVVFPVDCIKSRIQVLSMYGKQAGFIGTLLSVVRNEGIVALYSGLKATMIRA
                     IPANGALFVAYEYSRKMMMKQLEAY"
BASE COUNT          334 a          339 c          375 g          368 t
ORIGIN      
        1 cggagcgtag ggttgagcgg cttcccccgc actggggtga gagcccagaa caggcggtag
       61 agccacccca ccacccccaa ctccattccc cgcgctcgct gcggctggac gtgaaaagcc
      121 ggtctcacgc tctggggagt tagtcgcctt ccactgggac cctcagacga gtgagcgaac
      181 atgaagtccg gtcctggcat ccaagccgcc atcgacctca cagcgggggc cgcagggggg
      241 acagcgtgtg tactgactgg gcagcccttc gacacaataa aagtgaagat gcagacgttc
      301 cctgacctgt acaagggcct caccgactgc ttcctgaaga catacgccca agtgggtctc
      361 cggggcttct acaagggcac cggcccggca cttatggcct acgtcgccga aaactcggtc
      421 ctcttcatgt gctacgggtt ctgccagcag tttgtcagga aagtggctgg aatggacaag
      481 caggcaaagc tgagtgatct ccagactgca gccgcggggt ccttcgcctc tgcatttgct
      541 gcactggctc tctgccccac tgagcttgtg aagtgccggc tacagaccat gtatgaaatg
      601 gagatgtcag ggaagatagc aaaaagccat aatacaattt ggtctgtcgt gaagggtatc
      661 cttaaaaagg atggcccctt gggcttctac catggactct cgagtactct acttcaagaa
      721 ggaccgggtt atttcttttt ctttggtggc tatgaactga gccgatcgtt ttttgcgtca
      781 gggagatcaa aagatgaact aggccctgtc catttgatgt taagtggtgg agttgctgga
      841 atttgcctgt ggcttgtcgt gttcccagtg gattgtatta aatccagaat tcaagttctt
      901 tccatgtatg ggaaacaggc aggatttatt ggtaccctct taagtgttgt gagaaatgaa
      961 ggaatagtag ccttatattc tggactgaaa gctactatga ttcgagcaat ccctgccaat
     1021 ggggcactgt ttgtggccta cgaatacagc aggaagatga tgatgaaaca gttggaagca
     1081 tactgaagtg tcttggtgaa cctggatccg agtccatgag tttgaggact acagttcatc
     1141 acagggttca gcagagtaca agaccactgt ctaattttga cttcatggga attttggttt
     1201 tatcttccct tcttctaccc taaatcttaa ctttatggaa gggcctctat tttacatcat
     1261 ataatttctg cccataattg tattgaaata ggaaagttgc tgctcttgca cttgctggaa
     1321 tgtacagggt gggctggttg gccctatgta cctaatctga aaaactaaat atcgttctgt
     1381 cagggccttt gcataaagcc atttgtgtgt acctgc
//