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2024-04-24 14:25:38, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_013364 3771 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens paraneoplastic Ma antigen 3 (PNMA3), mRNA.
ACCESSION NM_013364
VERSION NM_013364.4 GI:142976815
KEYWORDS RefSeq.
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 3771)
AUTHORS Wills,N.M., Moore,B., Hammer,A., Gesteland,R.F. and Atkins,J.F.
TITLE A functional -1 ribosomal frameshift signal in the human
paraneoplastic Ma3 gene
JOURNAL J. Biol. Chem. 281 (11), 7082-7088 (2006)
PUBMED 16407312
REMARK GeneRIF: analysis of a ribosomal frameshift signal in the human
paraneoplastic Ma3 gene
REFERENCE 2 (bases 1 to 3771)
AUTHORS Schuller,M., Jenne,D. and Voltz,R.
TITLE The human PNMA family: novel neuronal proteins implicated in
paraneoplastic neurological disease
JOURNAL J. Neuroimmunol. 169 (1-2), 172-176 (2005)
PUBMED 16214224
REFERENCE 3 (bases 1 to 3771)
AUTHORS Rosenfeld,M.R., Eichen,J.G., Wade,D.F., Posner,J.B. and Dalmau,J.
TITLE Molecular and clinical diversity in paraneoplastic immunity to Ma
proteins
JOURNAL Ann. Neurol. 50 (3), 339-348 (2001)
PUBMED 11558790
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from DR001205.1, AF083116.1,
AC152006.1 and AI689415.1.
This sequence is a reference standard in the RefSeqGene project.
On Apr 6, 2007 this sequence version replaced gi:108936947.
Summary: This gene is a member of the paraneoplastic antigen MA
(PNMA) gene family, whose protein products share homology with
retroviral Gag proteins. They are highly expressed in the brain and
also in a range of tumors associated with serious neurological
phenotypes. PMID:16407312 reports the presence of a functional -1
ribosomal frameshift signal (consisting of a heptanucleotide shift
motif followed 3' by a pseudoknot structure) in this gene, however,
the frame-shifted product has not been characterized. [provided by
RefSeq, Jul 2008].
##Evidence-Data-START##
Transcript exon combination :: DR001205.1, AK312299.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025082, ERS025084 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-310 DR001205.1 1-310
311-1465 AF083116.1 2-1156
1466-3588 AC152006.1 15510-17632
3589-3771 AI689415.1 1-183 c
FEATURES Location/Qualifiers
source 1..3771
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="X"
/map="Xq28"
gene 1..3771
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/note="paraneoplastic Ma antigen 3"
/db_xref="GeneID:29944"
/db_xref="HGNC:18742"
/db_xref="MIM:300675"
exon 1..230
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/inference="alignment:Splign:1.39.8"
variation 190
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="g"
/replace="t"
/db_xref="dbSNP:185487943"
exon 231..3751
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/inference="alignment:Splign:1.39.8"
variation 247
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="c"
/db_xref="dbSNP:112872629"
variation 290
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:371971890"
variation 303
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="c"
/db_xref="dbSNP:73244173"
misc_feature 313..315
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/note="upstream in-frame stop codon"
STS 317..1748
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/db_xref="UniSTS:484360"
variation 317
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:368216116"
variation 320
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200901878"
CDS 337..1728
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/note="paraneoplastic cancer-testis-brain antigen"
/codon_start=1
/product="paraneoplastic antigen Ma3"
/protein_id="NP_037496.3"
/db_xref="GI:142976816"
/db_xref="CCDS:CCDS35435.2"
/db_xref="GeneID:29944"
/db_xref="HGNC:18742"
/db_xref="MIM:300675"
/translation="
MPLTLLQDWCRGEHLNTRRCMLILGIPEDCGEDEFEETLQEACRHLGRYRVIGRMFRREENAQAILLELAQDIDYALLPREIPGKGGPWEVIVKPRNSDGEFLNRLNRFLEEERRTVSDMNRVLGSDTNCSAPRVTISPEFWTWAQTLGAAVQPLLEQMLYRELRVFSGNTISIPGALAFDAWLEHTTEMLQMWQVPEGEKRRRLMECLRGPALQVVSGLRASNASITVEECLAALQQVFGPVESHKIAQVKLCKAYQEAGEKVSSFVLRLEPLLQRAVENNVVSRRNVNQTRLKRVLSGATLPDKLRDKLKLMKQRRKPPGFLALVKLLREEEEWEATLGPDRESLEGLEVAPRPPARITGVGAVPLPASGNSFDVRPSQGYRRRRGRGQHRRGGVARAGSRGSRKRKRHTFCYSCGEDGHIRVQCINPSNLLLVKQKKQAAVESGNGNWAWDKSHPKSKAK
"
variation 364
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="t"
/db_xref="dbSNP:138344782"
variation 388
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="g"
/db_xref="dbSNP:190348179"
variation 393
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:202140456"
variation 402
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:372698524"
variation 425
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:149639020"
variation 429
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200483739"
variation 430
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:183036677"
variation 444
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:377280936"
variation 553
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:369898586"
variation 591
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="g"
/replace="t"
/db_xref="dbSNP:201029233"
variation 597
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:187756882"
variation 679
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="c"
/db_xref="dbSNP:146193731"
variation 684
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:137859993"
variation 686
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:373422837"
variation 703
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:376393730"
variation 709
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="g"
/db_xref="dbSNP:369206827"
variation 813
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:142457335"
variation 823
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:145960568"
variation 854
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="g"
/db_xref="dbSNP:148668161"
variation 923
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="g"
/replace="t"
/db_xref="dbSNP:202200283"
variation 942
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="g"
/replace="t"
/db_xref="dbSNP:200243171"
variation 1056
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376776291"
variation 1113
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:141778950"
variation 1192
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:371312702"
variation 1200
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:373086110"
variation 1201
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:150765757"
variation 1213
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:139222403"
variation 1251
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:73244174"
variation 1259
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:371005134"
variation 1294
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="c"
/db_xref="dbSNP:373760526"
variation 1300
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:145275859"
variation 1423
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200461938"
variation 1466
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:6526155"
variation 1480
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:36042591"
variation 1486
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:144738062"
variation 1490
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:201293043"
variation 1493
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:35603712"
variation 1514
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370578186"
variation 1558
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:148950007"
variation 1596
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:374897376"
variation 1608
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="g"
/db_xref="dbSNP:143788367"
variation 1619
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:148136883"
variation 1643
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="t"
/db_xref="dbSNP:201419986"
variation 1660
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="g"
/db_xref="dbSNP:367981870"
variation 1666
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:202098633"
misc_feature 1674..1680
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/note="Region: frameshift motif"
misc_feature 1687..1732
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/note="the presumptive pseudoknot structure is necessary
for -1 frameshifting; Region: pseudoknot structure"
variation 1754
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="g"
/db_xref="dbSNP:16996820"
STS 1771..2566
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/standard_name="PNMA3__5734"
/db_xref="UniSTS:463809"
variation 2056
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:5970424"
variation 2224
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:5969945"
variation 2262
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:149395183"
variation 2312
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="g"
/db_xref="dbSNP:144779148"
variation 2377
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="c"
/db_xref="dbSNP:113728199"
variation 2506..2508
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace=""
/replace="agg"
/db_xref="dbSNP:72127091"
variation 2508
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200655921"
variation 2516..2518
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace=""
/replace="gga"
/db_xref="dbSNP:57597943"
variation 2853
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:3830028"
variation 2859
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:192053077"
variation 2915
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:145951598"
variation 2926
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:5970425"
variation 2936
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="t"
/db_xref="dbSNP:370821486"
variation 2955
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:182772471"
variation 2987
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="g"
/db_xref="dbSNP:187487835"
variation 3001
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:192762020"
variation 3050
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="g"
/db_xref="dbSNP:11539741"
variation 3066
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:184001061"
variation 3067
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:143273000"
variation 3068
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376509367"
variation 3071
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="g"
/db_xref="dbSNP:2301186"
variation 3160
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:1045059"
variation 3242
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:41302162"
variation 3256
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2301182"
variation 3285
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:1045069"
variation 3371
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2301183"
variation 3447
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:9035"
variation 3454
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:187317140"
variation 3463
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:55968837"
variation 3472
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:2301184"
variation 3479
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:55810952"
STS 3494..3708
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/standard_name="STS-N70548"
/db_xref="UniSTS:37744"
variation 3504
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:56298832"
variation 3508
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="t"
/db_xref="dbSNP:55971669"
variation 3512
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:184640906"
variation 3523
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:139179449"
variation 3529
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:55989575"
variation 3552
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="g"
/replace="t"
/db_xref="dbSNP:372609981"
variation 3608
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:45520141"
variation 3658
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="c"
/db_xref="dbSNP:368234443"
variation 3659
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:372508952"
variation 3700
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="c"
/replace="t"
/db_xref="dbSNP:2301185"
variation 3702
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="c"
/db_xref="dbSNP:7122"
variation 3712
/gene="PNMA3"
/gene_synonym="MA3; MA5"
/replace="a"
/replace="g"
/db_xref="dbSNP:146139188"
polyA_signal 3724..3729
/gene="PNMA3"
/gene_synonym="MA3; MA5"
polyA_site 3751
/gene="PNMA3"
/gene_synonym="MA3; MA5"
ORIGIN
ccgccgccgcgcccccgccccgtgtccgcactgcagagagccgcggcgagcaggcgccggcgcactggcccacgtgctgcgcgagcgagggagagccacagtctgagcgaacgtccgcgctgggagccaggggtgcccgacccccgtccgccgccgccgccgccgccgcgcatagcccccggagagccctctggggaccccgaccagaagggaccttgccctgggagaaggctgtggagacctgggccttctgcgatcaccctaggagttgatccagatatgtgcctcacgccctgatcactccccccaaattagtatccgcagagattcgaggacatgccgttgaccttgttacaggactggtgtcggggggaacacctgaacacccggaggtgcatgctcatcctggggatccccgaggactgtggcgaggatgagtttgaggagacactccaggaggcttgcaggcacctgggcagatacagggtgattggcaggatgtttaggagggaggagaacgcccaggcgattctactggagctggcacaagatatcgactatgctttgctcccaagggaaataccaggaaagggggggccctgggaagtgattgtaaaaccccgtaactcagatggggaatttctcaacagactgaaccgcttcttagaggaggagaggcggaccgtgtcagatatgaaccgagtcctcgggtcggacaccaattgttcggctccaagagtgactatatcaccagagttctggacctgggcccagactctgggggcagcagtgcagcctctgctagaacaaatgttgtaccgagaactaagagtgttttctgggaacaccatatccatcccaggtgcactggcctttgatgcctggcttgagcacaccactgagatgctacagatgtggcaggtgcccgagggggaaaagaggcggaggctgatggaatgcttacggggccctgctctccaggtggtcagtgggctccgggccagcaatgcttccataactgtggaggagtgcctggctgccttgcagcaggtgttcggacctgtggagagccataaaattgcccaggtgaagttgtgtaaagcctatcaggaggcaggagagaaagtatctagctttgtgttacgtttggaacccctgctccaaagagctgtagaaaacaatgtggtatcacgtagaaacgtgaatcagactcgcctgaaacgagtcttaagtggggccacccttcctgacaaactccgagataagcttaagctgatgaaacagcgaaggaagcctcctggtttcctggccctggtgaagctcctgcgtgaggaggaggaatgggaggccactttaggtccagatagggagagtctggaggggctggaagtagccccaaggccacctgccaggatcactggggttggggcagtacctctccctgcctctggcaacagttttgatgtgaggccttcccagggctaccggcgccggaggggcagaggccaacaccgaaggggtggtgtggcaagggctggctctcgaggctcaagaaaacggaaacgccacacattctgctatagctgtggggaagacggccacatcagggtacagtgcatcaacccctccaacctgctcttggtaaagcagaagaaacaggctgcagttgagtcgggaaacgggaactgggcttgggacaagagccatcccaagtccaaggccaagtaggctcgggagaacagggcaacatttcctaccacaggccaaggagacaaaagagatattggaaggaggggaaagagaagcccagacaaacagcagatgagttgagtggggcagagggacagggcagccagaccaaggccaagccttctcacccttggccagctggaagggacttcagcaaccaagaccacctggcaacaggctcagtgggggtcaggtccaggtccccgaagaggtgctggagaggaaagcagggagccactgcatccagcacatggggtgcctgggcctcagatggggaccccaaagaagcagaagctgaagaaggtacggctgggggttctgtcctgctcatccaaccacccctaaatacccaccctgtggactttgagctgaacatgcccactggcccccaggccacatgggacctggaggagcctacctggggcctgcccctgccagcaggtgccagggctggtgaggaagagctggggggcagaggtaaagccctgcaggggaggccacagggtccatcccgtcttcaggatcatctacactgcactaggggagccccaggaaggcagcaccctggaggccctgtgccagtgaggacaggagaccctaaggccccgggagcccagtgccagccagaggttgtgcaggcaaggagaccaaagattgatgagaagacccccagcaggggtactgggtacccggcaggccagtgccctcacagttgacttggaccagggtggctgtgaagggaagtctttgttgcaaaggaggaggaggaaaagggaggacttggtagggttttgtttcttctgcttgtttctgtacagggccaccagactcctggagagatcaagcaaggagaacctggggctgccatggccaaagcaactcaacagatgccaatgccaattccaaggccagccacaaccctgccaccttggggaatccagcctggaggcatcccctaagcagccagccatggcctgggtggaggcacctgaagacgtctgtcccaaactcccccagccctgagctgggagatgacagggggaaagaggccctctcaagggtgccagatgcctgggtctcccaagaggggtcccccaactcaccgttcccgggacaggctgccccctgttccaggaagctcatcctcacctgtgtaggcccctgtagtgacccacgcgtccagcagacgcccacccaccgctagccgttgttcctgtgcaaagtagtgtgctatgcacccacccaggtggccgcctctgggcccaaggcacatgctgtgagcttcctgtgagcccaggctctgctcactgctgtcccgcgtcatgagcaccacctctgctttccctgtgtagatctaggccagtggctgcttgttcttgtggagctgtgtgtgttcttctctgagcagctcctccccggagtcccccagcacagtcccaggagatgacaggaaggaagcaccagggcaaggcggacgctcaccctgtgaccacgatggtgaccgtgactgtgggaggaagaactggacccaggacggagcggggctgccctgcctgaggctcccgaggagctttgtgctttggtgttccacccctgttgttactcatgactcagtttccttgacctggtagggtgttccctgctgtgttttccagtgtcctgtgactgtcctgtgcgggccatagggcagggccctgtcccagcagatgggcttgggagggggctccctaaagccagtggacactgccagagtctaccttcctggcaagaggcagaccccggggccctcaggaaggagggagttggcagcgggggctgcagcaggagtaggagcagatgaggcgtcttgccaggaacctcaggaggagggggcccgggacctgtgtgggacctgtgtcctgtggtggccgtttgcagtttctctctgtgttgtgattcccttctcttcaacgttttcagtacgtgtttctcttcaataaacttcattcagtgttccagccggaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:29944 -> Molecular function: GO:0003676 [nucleic acid binding] evidence: IEA
GeneID:29944 -> Molecular function: GO:0008270 [zinc ion binding] evidence: IEA
GeneID:29944 -> Biological process: GO:0006915 [apoptotic process] evidence: NAS
GeneID:29944 -> Cellular component: GO:0005730 [nucleolus] evidence: IEA
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