LOCUS       BC051907                2813 bp    mRNA    linear   HUM 15-JUL-2006
DEFINITION  Homo sapiens fragile X mental retardation, autosomal homolog 2,
            mRNA (cDNA clone MGC:60375 IMAGE:6149976), complete cds.
ACCESSION   BC051907
VERSION     BC051907.1
KEYWORDS    MGC.
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 2813)
  AUTHORS   Strausberg,R.L., Feingold,E.A., Grouse,L.H., Derge,J.G.,
            Klausner,R.D., Collins,F.S., Wagner,L., Shenmen,C.M., Schuler,G.D.,
            Altschul,S.F., Zeeberg,B., Buetow,K.H., Schaefer,C.F., Bhat,N.K.,
            Hopkins,R.F., Jordan,H., Moore,T., Max,S.I., Wang,J., Hsieh,F.,
            Diatchenko,L., Marusina,K., Farmer,A.A., Rubin,G.M., Hong,L.,
            Stapleton,M., Soares,M.B., Bonaldo,M.F., Casavant,T.L.,
            Scheetz,T.E., Brownstein,M.J., Usdin,T.B., Toshiyuki,S.,
            Carninci,P., Prange,C., Raha,S.S., Loquellano,N.A., Peters,G.J.,
            Abramson,R.D., Mullahy,S.J., Bosak,S.A., McEwan,P.J.,
            McKernan,K.J., Malek,J.A., Gunaratne,P.H., Richards,S.,
            Worley,K.C., Hale,S., Garcia,A.M., Gay,L.J., Hulyk,S.W.,
            Villalon,D.K., Muzny,D.M., Sodergren,E.J., Lu,X., Gibbs,R.A.,
            Fahey,J., Helton,E., Ketteman,M., Madan,A., Rodrigues,S.,
            Sanchez,A., Whiting,M., Madan,A., Young,A.C., Shevchenko,Y.,
            Bouffard,G.G., Blakesley,R.W., Touchman,J.W., Green,E.D.,
            Dickson,M.C., Rodriguez,A.C., Grimwood,J., Schmutz,J., Myers,R.M.,
            Butterfield,Y.S., Krzywinski,M.I., Skalska,U., Smailus,D.E.,
            Schnerch,A., Schein,J.E., Jones,S.J. and Marra,M.A.
  CONSRTM   Mammalian Gene Collection Program Team
  TITLE     Generation and initial analysis of more than 15,000 full-length
            human and mouse cDNA sequences
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 99 (26), 16899-16903 (2002)
   PUBMED   12477932
REFERENCE   2  (bases 1 to 2813)
  CONSRTM   NIH MGC Project
  TITLE     Direct Submission
  JOURNAL   Submitted (01-MAY-2003) National Institutes of Health, Mammalian
            Gene Collection (MGC), Bethesda, MD 20892-2590, USA
  REMARK    NIH-MGC Project URL: http://mgc.nci.nih.gov
COMMENT     Contact: MGC help desk
            Email: cgapbs-r@mail.nih.gov
            Tissue Procurement: ATCC/DCTD/DTP
            cDNA Library Preparation: Life Technologies, Inc.
            cDNA Library Arrayed by: The I.M.A.G.E. Consortium (LLNL)
            DNA Sequencing by: Sequencing Group at the Stanford Human Genome
            Center, Stanford University School of Medicine, Stanford, CA  94305
            Web site:       http://www-shgc.stanford.edu
            Contact:  (Dickson, Mark) mcd@paxil.stanford.edu
            Dickson, M., Schmutz, J., Grimwood, J., Rodriquez, A., and Myers,
            R. M.
            
            Clone distribution: MGC clone distribution information can be found
            through the I.M.A.G.E. Consortium/LLNL at: http://image.llnl.gov
            Series: IRAK Plate: 110 Row: k Column: 15
            This clone was selected for full length sequencing because it
            passed the following selection criteria: matched mRNA gi: 6598321.
FEATURES             Location/Qualifiers
     source          1..2813
                     /db_xref="H-InvDB:HIT000053741"
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /clone="MGC:60375 IMAGE:6149976"
                     /tissue_type="Skin, melanotic melanoma."
                     /clone_lib="NIH_MGC_72"
                     /lab_host="DH10B"
                     /note="Vector: pCMV-SPORT6"
     gene            1..2813
                     /gene="FXR2"
                     /db_xref="GeneID:9513"
                     /db_xref="HGNC:HGNC:4024"
                     /db_xref="MIM:605339"
     CDS             197..2218
                     /gene="FXR2"
                     /codon_start=1
                     /product="fragile X mental retardation, autosomal homolog
                     2"
                     /protein_id="AAH51907.1"
                     /db_xref="GeneID:9513"
                     /db_xref="HGNC:HGNC:4024"
                     /db_xref="MIM:605339"
                     /translation="MGGLASGGDVEPGLPVEVRGSNGAFYKGFVKDVHEDSVTIFFEN
                     NWQSERQIPFGDVRLPPPADYNKEITEGDEVEVYSRANEQEPCGWWLARVRMMKGDFY
                     VIEYAACDATYNEIVTLERLRPVNPNPLATKGSFFKVTMAVPEDLREACSNENVHKEF
                     KKALGANCIFLNITNSELFILSTTEAPVKRASLLGDMHFRSLRTKLLLMSRNEEATKH
                     LETSKQLAAAFQEEFTVREDLMGLAIGTHGANIHQARKVPGVTAIELGEETCTFRIYG
                     ETPEACRQARSYLEFSEDSVQVPRNLVGKVIGKNGKVIQEIVDKSGVVRVRVEGDNDK
                     KNPREEGMVPFIFVGTRENISNAQALLEYHLSYLQEVEQLRLERLQIDEQLRQIGLGF
                     RPPGSGRGSGGSDKAGYSTDESSSSSLHATRTYGGSYGGRGRGRRTGGPAYGPSSDVS
                     TASETESEKREEPNRAGPGDRDPPTRGEESRRRPTGGRGRGPPPAPRPTSRYNSSSIS
                     SVLKDPDSNPYSLLDTSEPEPPVDSEPGEPPPASARRRRSRRRRTDEDRTVMDGGLES
                     DGPNMTENGLEDESRPQRRNRSRRRRNRGNRTDGSISGDRQPVTVADYISRAESQSRQ
                     RPPLERTKPSEDSLSGQKGDSVSKLPKGPSENGELSAPLELGSMVNGVS"
BASE COUNT          626 a          796 c          841 g          550 t
ORIGIN      
        1 ggcggacggg gagcggcccg gccccggccc cctgctcgtt ggctgtggca gggccgccgt
       61 ggggccggcc cggctcccgc cccccgcggc tccccctccg gctcctcctc cggggagacg
      121 ccgggggcct ggcccggccc gcactcagac tgctgctgca gccgccgccg ggggagtcgg
      181 aggcggtggc ggcgccatgg gcggcctggc ctctgggggg gatgtggagc cgggactgcc
      241 cgtcgaggtg cgcggctcca acggggcctt ctacaagggc tttgtgaagg atgtccatga
      301 agactctgtc accatcttct ttgaaaacaa ctggcagagt gagagacaaa ttccttttgg
      361 ggatgtccgg ctaccacctc cagctgacta taataaggag atcacagaag gggatgaagt
      421 ggaggtttat tctcgagcca atgaacagga accttgtggc tggtggctgg cccgggtgcg
      481 gatgatgaag ggagatttct atgtcattga atatgctgcc tgtgatgcca cctacaatga
      541 aattgttacc ctggagcgac ttcggccagt taatcccaat ccccttgcaa ccaaaggcag
      601 cttcttcaag gttaccatgg ctgtgcccga ggatctgaga gaagcctgct ccaatgaaaa
      661 cgtccataaa gagttcaaga aagccctggg agccaactgc atctttctca acatcacaaa
      721 cagtgagctc ttcattctgt caaccacaga agcccctgtg aagcgagcat ctctgctggg
      781 tgatatgcat ttccgaagcc tgcgcaccaa actgctactt atgtcccgca atgaagaagc
      841 taccaagcac ctagagacaa gcaagcagtt ggcagcagcc ttccaagagg agttcacagt
      901 gcgagaggac ctgatgggac tggcaattgg gactcacggt gccaacatcc atcaggcccg
      961 aaaagtacct ggggtgaccg ccattgagtt gggtgaagag acctgcactt tccgcatcta
     1021 tggggagact cccgaggctt gccgacaggc ccgaagctac cttgagtttt ctgaggactc
     1081 agtgcaagtg cccaggaacc tggttggcaa agtgattgga aagaacggga aagtgatcca
     1141 ggagattgtg gataaatctg gtgtggtgag ggttcgagtg gaaggtgata atgacaagaa
     1201 gaaccccagg gaggagggaa tggttccctt catttttgtt ggcacccgag agaacatcag
     1261 caatgcccag gctttgctgg agtatcacct ctcctacctg caggaggtag agcagcttcg
     1321 cttggagagg ctacaaattg atgagcagct tcggcagatt gggctgggct ttcgccctcc
     1381 tgggagtggg cggggcagcg gtggcagcga caaggctgga tatagcactg atgagagctc
     1441 ctcctcctcc ctccatgcga ctcgaaccta tgggggcagc tatgggggcc gtggccgtgg
     1501 ccggaggaca ggcggtcctg cctatggccc cagctcagat gtgtctacag cttcagagac
     1561 tgagtcagag aagagagagg agcccaaccg agctgggcct ggcgacaggg atcccccaac
     1621 ccgaggggaa gaaagccgga ggcggccgac tgggggccgg ggtaggggac ccccacctgc
     1681 cccccggccc acttcgagat acaattcttc atctattagc tcagtgctga aggatccaga
     1741 cagtaatccc tacagcctat tggacacgtc tgaaccagag cccccggttg attcagaacc
     1801 tggggaaccc cccccagcaa gtgccaggcg ccgccgctcc cgccgccgcc gcactgatga
     1861 agacaggacc gtcatggatg gaggcctgga atcagatggg cccaacatga cagagaatgg
     1921 cctggaagat gaatcaagac ctcaacgtcg taatcgcagc cgccgccgcc gtaaccgtgg
     1981 taatcggact gatggctcta tcagtggaga ccgccagcca gtgactgtgg ctgactatat
     2041 ctcacgagca gagtctcaga gccgccagag gccacccctg gaacgcacta aaccctcaga
     2101 agactctctt tcaggacaga agggtgactc tgtcagcaag cttcctaagg gcccctcgga
     2161 gaatggggag ctctccgccc ccttggagtt gggtagtatg gtgaatgggg tttcataaaa
     2221 cctccaacct gcacccctcc cttctccatc tcgcttgctg cccaacacca tggccctcac
     2281 aggcccaact gacctgcgct ggagctgctc ttatctaggg gggagggggg tggcacagca
     2341 gcttgggtac cccccaacct ccaggagcta gtggaggggt gtgtaacagg gtcatacccc
     2401 ctccctcttg tccaccctac ccccagggta aggggagcct ctctccttcc ccatcagact
     2461 ggatgtgcct ttatcctcta atgccccaat ctctctctga acacccccat tctccacctg
     2521 ttggtggggg gtgctcctcg acccacccag atttgaccgt tcagggggcc tcccctgcta
     2581 tccctcctcc catcctgtac cccccatttc tggggcctca tcactgtgga agacggggat
     2641 agtaagagat aagtgggtgg gaggcacggg gaaggttttg gagtagaacc aggggtgtgt
     2701 atgaaggggg gtgacaaggt ccccctgggg aggggaccaa ccttgtctgg tggatgagaa
     2761 ggcgtattta tttttcactg tacagtattt aaaaagagaa aaaaaaaaaa aaa
//