LOCUS AK301020 1926 bp mRNA linear HUM 24-JUL-2008 DEFINITION Homo sapiens cDNA FLJ53497 complete cds, highly similar to Meckel syndrome type 1 protein. ACCESSION AK301020 VERSION AK301020.1 KEYWORDS FLI_CDNA; oligo capping. 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 1926) AUTHORS Isogai,T. and Yamamoto,J. TITLE Direct Submission JOURNAL Submitted (09-OCT-2007) to the DDBJ/EMBL/GenBank databases. Contact:Takao Isogai Reverse Proteomics Research Institute; 1-9-11 Kaji-cho, Chiyoda-ku, Tokyo 101-0044, Japan E-mail :flj-cdna@nifty.com REFERENCE 2 AUTHORS Wakamatsu,A., Yamamoto,J., Kimura,K., Ishii,S., Watanabe,K., Sugiyama,A., Murakawa,K., Kaida,T., Tsuchiya,K., Fukuzumi,Y., Kumagai,A., Oishi,Y., Yamamoto,S., Ono,Y., Komori,Y., Yamazaki,M., Kisu,Y., Nishikawa,T., Sugano,S., Nomura,N. and Isogai,T. TITLE NEDO human cDNA sequencing project focused on splicing variants JOURNAL Unpublished (2007) COMMENT Human cDNA sequencing project focused on splicing variants of mRNA in NEDO functional analysis of protein and research application project supported by Ministry of Economy, Trade and Industry, Japan; cDNA selection for complete cds sequencing: Reverse Proteomics Research Institute (REPRORI), Hitachi, Ltd., Japan (Hitachi) and Japan Biological Informatics Consortium, Japan (JBIC); cDNA complete cds sequencing: JBIC; cDNA library construction: Helix Research Institute supported by Japan Key Technology Center, Japan (HRI); cDNA 5'- & 3'-end sequencing: Research Association for Biotechnology, Japan, Biotechnology Center, National Institute of Technology and Evaluation, Japan and HRI; cDNA mapping to human genome: Central Research Laboratory, Hitachi; evaluation and annotation: REPRORI. FEATURES Location/Qualifiers source 1..1926 /clone="SMINT2019108" /clone_lib="SMINT2" /db_xref="H-InvDB:HIT000495644" /db_xref="taxon:9606" /mol_type="mRNA" /note="cloning vector: pME18SFL3" /organism="Homo sapiens" /tissue_type="small intestine" CDS 518..1588 /codon_start=1 /note="highly similar to Meckel syndrome type 1 protein" /protein_id="BAG62637.1" /transl_table=1 /translation="MHIMADLGPYKKLGYKKYEHVLCTLKVDSNGVITVKPDFTGLKG PYRIETEGEKQELWKYTIDNVSPHAQPEEEERERRVFKDLYGRHKEYLSSLVGTDFEM TVPGALRLFVNGEVVSAQGYEYDNLYVHFFVELPTAHWSSPAFQQLSGVTQTYTTKSL AMDKVAHFSYPFTFEAFFLHEDESSDALPEWPVLYCEVLSLDFWQRYRVEGYGAVVLP ATPGSHTLTVSTWRPVELGTVAELRRFFIGGSLELEDLSYVRIPGSFKGERLSRFGLR TETTGTVTFRLHCLQQSRAFMESSSLQKRMRSVLDRLEGFSQQSSIHNVLEAFRRARR RMQEARESLPQDLVSPSGTLVS" BASE COUNT 443 a 529 c 528 g 426 t ORIGIN 1 gctgtcatgg cggagaccgt ctggagcact gacaccgggg aggcagtgta tcgctcccgg 61 gaccccgtgc gcaacttgcg cctccgagtc cacctgcaaa gaatcacatc aagcaacttt 121 cttcattatc agcctgctgc cgagctcggg aaggacctca tagacttggc cacttttagg 181 cctcagccaa ctgccagtgg acaccgccca gaggaagacg aagaggagga gattgtgatt 241 gggtggcagg agaagctctt tagccagttt gaagtagatc tgtaccaaaa tgaaacagcc 301 tgtcagagtc ctttggatta tcagtaccgt caggagatcc tgaagctgga gaattcgggt 361 ggcaagaaaa accgacgaat ctttacctac actgactctg atagatacac caatttggag 421 gagggagggc ggcatcctca agtcacgcat cgtcacctgg gagccctcag aagagtttgt 481 caggaacaac cacgtcatta acacccctct tcagacaatg cacatcatgg cagacctggg 541 gccctataaa aagcttggct ataagaagta tgaacatgtc ctgtgtactc tgaaggtgga 601 tagcaatggt gtgatcacag taaagcctga cttcacgggc ctcaaaggac cctacaggat 661 tgagacggag ggggagaagc aggagctgtg gaaatatacg atcgacaatg tttcccccca 721 cgcacagccg gaggaggagg agcgggaacg gcgagtgttc aaggatcttt atggccggca 781 caaggagtat ctcagcagcc tcgtaggcac cgactttgag atgactgtcc caggtgccct 841 ccggctcttt gtaaatggag aggtcgtttc agcccaaggc tatgagtatg acaatctcta 901 cgtccacttc tttgtagaat tgccaactgc tcactggtca agcccagcat tccagcagct 961 ctcaggagta acacagacct acaccaccaa gtccctggca atggacaagg tggctcactt 1021 ctcctaccca ttcacgtttg aagccttctt cctccatgag gatgaatctt ctgatgcact 1081 cccggagtgg cctgtgctct actgtgaggt cctctcgctg gacttctggc agaggtaccg 1141 tgtggaaggc tatggggctg tggtgctgcc tgccactcca ggctcacaca ccctgacagt 1201 ctccacgtgg agacctgtgg agcttggcac ggtggctgag ctgaggaggt ttttcattgg 1261 cggttctctg gaactggagg acctctccta tgtacggata ccaggatcct tcaaggggga 1321 acgcctgagc cgctttggac tccgcacaga gaccacaggc actgtcacct tccgcttgca 1381 ctgtctgcag cagtccaggg ccttcatgga atcgagctcc cttcagaaaa ggatgcggag 1441 tgtgttggac cgtctggaag ggttcagcca gcagagttcc attcacaatg tgctagaggc 1501 cttccgtcga gcccggcgcc gcatgcagga ggcccgggaa agcctcccgc aggacctagt 1561 gagcccctct ggaaccctgg tctcctagct cacagcagcc ctggcccaca gtgcaagagg 1621 acaagatggg ggatatctga ggccagtgct ctcctgcctc ttcgtctttc tgattagaga 1681 ccacgttggt ctgctgagaa ccagaaaagc tgggaaattc ccggctggcc cctctgccta 1741 gccttctgca gggtcttctc cctaccctgt ggaaataaag ccagagaccc tgtggccccc 1801 cctttatatt tgcagccact gtcaatgggc atcacagcaa ggcaggcttt ttgatctgaa 1861 gctgtttggg gtgaccccat agtgagtctg gccttgactc acttttctgg cttgtctcac 1921 agtagc //