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EBI Dbfetch

ID   BC050288; SV 1; linear; mRNA; STD; HUM; 2479 BP.
XX
AC   BC050288;
XX
DT   23-APR-2003 (Rel. 75, Created)
DT   15-OCT-2008 (Rel. 97, Last updated, Version 10)
XX
DE   Homo sapiens DnaJ (Hsp40) homolog, subfamily B, member 8, mRNA (cDNA clone
DE   MGC:43650 IMAGE:5270636), complete cds.
XX
KW   MGC.
XX
OS   Homo sapiens (human)
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae;
OC   Homo.
XX
RN   [1]
RP   1-2479
RX   DOI; 10.1073/pnas.242603899
RX   PUBMED; 12477932.
RG   Mammalian Gene Collection Program Team
RA   Strausberg R.L., Feingold E.A., Grouse L.H., Derge J.G., Klausner R.D.,
RA   Collins F.S., Wagner L., Shenmen C.M., Schuler G.D., Altschul S.F.,
RA   Zeeberg B., Buetow K.H., Schaefer C.F., Bhat N.K., Hopkins R.F., Jordan H.,
RA   Moore T., Max S.I., Wang J., Hsieh F., Diatchenko L., Marusina K.,
RA   Farmer A.A., Rubin G.M., Hong L., Stapleton M., Soares M.B., Bonaldo M.F.,
RA   Casavant T.L., Scheetz T.E., Brownstein M.J., Usdin T.B., Toshiyuki S.,
RA   Carninci P., Prange C., Raha S.S., Loquellano N.A., Peters G.J.,
RA   Abramson R.D., Mullahy S.J., Bosak S.A., McEwan P.J., McKernan K.J.,
RA   Malek J.A., Gunaratne P.H., Richards S., Worley K.C., Hale S., Garcia A.M.,
RA   Gay L.J., Hulyk S.W., Villalon D.K., Muzny D.M., Sodergren E.J., Lu X.,
RA   Gibbs R.A., Fahey J., Helton E., Ketteman M., Madan A., Rodrigues S.,
RA   Sanchez A., Whiting M., Madan A., Young A.C., Shevchenko Y., Bouffard G.G.,
RA   Blakesley R.W., Touchman J.W., Green E.D., Dickson M.C., Rodriguez A.C.,
RA   Grimwood J., Schmutz J., Myers R.M., Butterfield Y.S., Krzywinski M.I.,
RA   Skalska U., Smailus D.E., Schnerch A., Schein J.E., Jones S.J., Marra M.A.;
RT   "Generation and initial analysis of more than 15,000 full-length human and
RT   mouse cDNA sequences";
RL   Proc. Natl. Acad. Sci. U.S.A. 99(26):16899-16903(2002).
XX
RN   [2]
RC   NIH-MGC Project URL: http://mgc.nci.nih.gov
RP   1-2479
RG   NIH MGC Project
RA   ;
RT   ;
RL   Submitted (08-APR-2003) to the EMBL/GenBank/DDBJ databases.
RL   National Institutes of Health, Mammalian Gene Collection (MGC), Bethesda,
RL   MD 20892-2590, USA
XX
DR   ASTD; TRAN00000046744.
DR   Ensembl-Gn; ENSG00000179407; Homo_sapiens.
DR   Ensembl-Tr; ENST00000319153; Homo_sapiens.
DR   H-InvDB; HIT000259098.
DR   ImaGenes; IMAGp998O2111682Q.
DR   ImaGenes; IRAKp961L1874Q.
DR   ImaGenes; IRATp970C11104D.
XX
CC   Contact: MGC help desk
CC   Email: cgapbs-r@mail.nih.gov
CC   Tissue Procurement: Miklos Palkovits, M.D., Ph.D.
CC   cDNA Library Preparation: Michael J. Brownstein (NHGRI) &  Shiraki
CC   Toshiyuki and Piero Carninci (RIKEN)
CC   cDNA Library Arrayed by: The I.M.A.G.E. Consortium (LLNL)
CC   DNA Sequencing by: Sequencing Group at the Stanford Human Genome
CC   Center, Stanford University School of Medicine, Stanford, CA  94305
CC   Web site:       http://www-shgc.stanford.edu
CC   Contact:  (Dickson, Mark) mcd@paxil.stanford.edu
CC   Dickson, M., Schmutz, J., Grimwood, J., Rodriquez, A., and Myers,
CC   R. M.
CC   Clone distribution: MGC clone distribution information can be found
CC   through the I.M.A.G.E. Consortium/LLNL at: http://image.llnl.gov
CC   Series: IRAK Plate: 74 Row: l Column: 18
CC   This clone was selected for full length sequencing because it
CC   passed the following selection criteria: matched mRNA gi: 46094077.
CC   Differences found between this sequence and the human reference
CC   genome (build 36) are described in misc_difference features below
CC   and these differences were also compared to chimpanzee genomic
CC   sequences available as of 09/15/2004.
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..2479
FT                   /organism="Homo sapiens"
FT                   /lab_host="DH10B"
FT                   /mol_type="mRNA"
FT                   /clone_lib="NIH_MGC_97"
FT                   /clone="MGC:43650 IMAGE:5270636"
FT                   /tissue_type="Testis"
FT                   /note="Vector: pBluescriptR"
FT                   /db_xref="taxon:9606"
FT   gene            1..2479
FT                   /gene="DNAJB8"
FT                   /note="synonym: MGC33884"
FT   misc_difference 200
FT                   /gene="DNAJB8"
FT                   /note="'C' in cDNA is 'A' in the human genome. The
FT                   chimpanzee genome agrees with the cDNA sequence, suggesting
FT                   that this difference is unlikely to be due to an artifact."
FT   CDS             1662..2360
FT                   /codon_start=1
FT                   /gene="DNAJB8"
FT                   /product="DnaJ (Hsp40) homolog, subfamily B, member 8"
FT                   /db_xref="GDB:11513595"
FT                   /db_xref="GOA:Q8NHS0"
FT                   /db_xref="HGNC:23699"
FT                   /db_xref="InterPro:IPR015609"
FT                   /db_xref="PDB:2DMX"
FT                   /db_xref="UniProtKB/Swiss-Prot:Q8NHS0"
FT                   /protein_id="AAH50288.1"
FT                   /translation="MANYYEVLGVQASASPEDIKKAYRKLALRWHPDKNPDNKEEAEKK
FT                   FKLVSEAYEVLSDSKKRSLYDRAGCDSWRAGGGASTPYHSPFDTGYTFRNPEDIFREFF
FT                   GGLDPFSFEFWDSPFNSDRGGRGHGLRGAFSAGFGEFPAFMEAFSSFNMLGCSGGSHTT
FT                   FSSTSFGGSSSGSSGFKSVMSSTEMINGHKVTTKRIVENGQERVEVEEDGQLKSVTVNG
FT                   KEQLKWMDSK"
FT   misc_difference 1973
FT                   /gene="DNAJB8"
FT                   /note="'C' in cDNA is 'T' in the human genome; no amino
FT                   acid change. The chimpanzee genome agrees with the cDNA
FT                   sequence, suggesting that this difference is unlikely to be
FT                   due to an artifact."
FT   misc_difference 2009
FT                   /gene="DNAJB8"
FT                   /note="'T' in cDNA is 'C' in the human genome; no amino
FT                   acid change. The chimpanzee genome agrees with the human
FT                   genomic sequence and not the cDNA."
FT   misc_difference 2466..2479
FT                   /gene="DNAJB8"
FT                   /note="polyA tail: 14 bases do not align to the human
FT                   genome."
XX
SQ   Sequence 2479 BP; 527 A; 829 C; 629 G; 494 T; 0 other;
     acaccgcctt tgccatcacc accgtcattg ccccctctac taccaccacc atcaccacca        60
     ccgggtctgc ctcagccaga cccaccactg cctctaatta gactgccacc atcatcactg       120
     ccaccaccac tgcccctcca atgccttcct gatgtcacca tctgctttct ctctgctatc       180
     ctcacaccca actccatcac aaccaccacc ttcatctgag ccgccatcac cctcacagta       240
     cacagccctc aaatgtgtac caaggaggag gacatttact acacgctgca ccctgaacag       300
     tctgggacca gcggtcaggg aacaaggaat cgagatgctc acctgcagct cccaggtgag       360
     cggctctcta gagcttgcct gggagctgct gaggagctca cggtattcca ggaagctccc       420
     catccatgcc tcagcctgtg gctcagaagc agggtcttcg cagaagattg ccccgagctg       480
     ttgcaaagct caccattgtc acctgcctgc aacggcctct cttttccact ctccaaatcc       540
     cttgtattgg caggctctag tctggaatta taccggtgat gggattctgg aaaatccctc       600
     agatttctcc aggatgcaag gagaccatgg aagaggaaca agcctgcaag ggacagcagg       660
     tgctaactgc taaccgagac atagtgacaa aaatccagcc acagagataa agaatcaggt       720
     tcatctgtag ctacatccag tggagaagtt ctgctcttca actcctctgc taagccacat       780
     gtgtcagcag gtgtagaatt gagtggaaca cttctttgga tttgctgtcc gctgcagcct       840
     tggccctggt ttcacatccc ctccctcact gactcgctgt gtgaccttga gcactgtgtg       900
     tctctgagcc tggttcatcc aagagtttac cgacggccct cgtgtgccag ccactgtcct       960
     agacagggac agactttccc gcctttgtgg agcttacccc ggaagacctg gccagataat      1020
     gggcacaaaa aaagcaggct cttgtcccca ccccagcctg cctgaacccc accttggcct      1080
     cctcttgcct cagctgctgc ccagccatcg gccgagtgga catacccagg acgcccttgc      1140
     ccgcctcccc caccacggcc acagaccttt gtcactcacc aaggctggaa tcccgtggct      1200
     gatcctgcct ctgccctttg gctcccggga ctcagcccac accacctggg tcacagagca      1260
     tcccattccc acacaccgtt gtggccacct caccagcagg ggcaggccca tatgcccagg      1320
     tttgcctggt gaggagctgg gggcgggggt atgccccgcc ccgggagctg acgtcataaa      1380
     aggagctctg gagggcagcc cactctggcc tggccccaca gcggcagtgt ccctcccctc      1440
     cccccactcc tctcagtggg ggcccctcca gtccctgaga attggtacta cgaaaaggtg      1500
     aactcctggg cagaatcttg cctagagctt gcggagtcca gccaggcccc tgctgaaggg      1560
     ccccagacca ccggccactt ctcccccgtc catctgacca gctgggcccc tgcgcccacc      1620
     tggcctccac gttccctctc ctctcaccca cacccctggc catggctaac tactacgaag      1680
     tgctgggcgt gcaggccagc gcttccccgg aggacatcaa gaaagcctac cgcaagctgg      1740
     cccttcgttg gcaccccgac aagaaccctg acaataagga ggaggcggag aagaagttca      1800
     agctggtgtc tgaggcctat gaggttctgt ctgactccaa gaaacgctcc ctgtatgacc      1860
     gtgctggctg tgacagctgg cgggctggtg gcggggccag cacgccctac cacagcccct      1920
     tcgacaccgg ctacaccttc cgtaaccctg aggacatctt ccgggagttt ttcggtggcc      1980
     tggacccttt ctcctttgag ttctgggata gcccattcaa tagtgaccgt ggtggccggg      2040
     gccatggcct gaggggggcc ttctcggcag gctttggaga atttccggcc ttcatggagg      2100
     ccttctcatc cttcaacatg ctgggctgca gcgggggcag ccacaccacc ttctcatcca      2160
     cctccttcgg gggctccagt tctggcagct cggggttcaa gtcggtgatg tcgtccaccg      2220
     agatgatcaa tggccacaag gtcaccacca agcgcatcgt ggagaacggg caggagcgcg      2280
     tggaggtgga ggaagacggg cagctcaagt cggtgactgt gaacggcaag gagcagctca      2340
     aatggatgga cagcaagtag gcgctggcca cccggccctg ccttcccacc accaccaccg      2400
     tgcatggggc agcaaacacg tggggccgca gacatagcct gatggttaat aaatgtgcca      2460
     agtgaaaaaa aaaaaaaaa                                                   2479
//


  
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