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2025-05-09 20:11:16, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001012659 5065 bp mRNA linear PRI 17-MAR-2013 DEFINITION Homo sapiens arginine-fifty homeobox (ARGFX), mRNA. ACCESSION NM_001012659 VERSION NM_001012659.1 GI:61969665 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 5065) AUTHORS Li,G. and Holland,P.W. TITLE The origin and evolution of ARGFX homeobox loci in mammalian radiation JOURNAL BMC Evol. Biol. 10, 182 (2010) PUBMED 20565723 REMARK Publication Status: Online-Only REFERENCE 2 (bases 1 to 5065) AUTHORS Booth,H.A. and Holland,P.W. TITLE Annotation, nomenclature and evolution of four novel homeobox genes expressed in the human germ line JOURNAL Gene 387 (1-2), 7-14 (2007) PUBMED 17005330 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. This record has been curated by NCBI staff in collaboration with Anne Booth and Peter Holland. The reference sequence was derived from AC069239.16. Summary: Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 amino acids referred to as the homeodomain. This gene is a member of the ARGFX homeobox gene family. [provided by RefSeq, Jul 2008]. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-83 AC069239.16 30152-30234 c 84-198 AC069239.16 27349-27463 c 199-315 AC069239.16 21265-21381 c 316-464 AC069239.16 13100-13248 c 465-5065 AC069239.16 7543-12143 c FEATURES Location/Qualifiers source 1..5065 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="3" /map="3q13.33" gene 1..5065 /gene="ARGFX" /note="arginine-fifty homeobox" /db_xref="GeneID:503582" /db_xref="HGNC:30146" /db_xref="HPRD:18525" /db_xref="MIM:611164" exon 1..83 /gene="ARGFX" /inference="alignment:Splign:1.39.8" variation 44 /gene="ARGFX" /replace="a" /replace="g" /db_xref="dbSNP:375210747" misc_feature 78..80 /gene="ARGFX" /note="upstream in-frame stop codon" exon 84..198 /gene="ARGFX" /inference="alignment:Splign:1.39.8" CDS 96..1043 /gene="ARGFX" /codon_start=1 /product="arginine-fifty homeobox" /protein_id="NP_001012677.1" /db_xref="GI:61969666" /db_xref="CCDS:CCDS33834.1" /db_xref="GeneID:503582" /db_xref="HGNC:30146" /db_xref="HPRD:18525" /db_xref="MIM:611164" /translation="
MRNRMAPENPQPDPFINRNYSNMKVIPPQDPASPSFTLLSKLECSGTVSAYCSLNLPGSTDPPTSASRVAATTAIRRRHKERTSFTHQQYEELEALFSQTMFPDRNLQEKLALRLDLPESTVKVWFRNRRFKLKKQQQQQSAKQRNQILPSKKNVPTSPRTSPSPYAFSPVISDFYSSLPSQPLDPSNWAWNSTFTESSTSDFQMQDTQWERLVASVPALYSDAYDIFQIIELYNLPDENEISSSSFHCLYQYLSPTKYQVGGQGSSLSIFAGPAVGLSPAQTWPNMTSQAFEAYSLTDSLEFQKTSNMVDLGFL
"
misc_feature 333..>473
/gene="ARGFX"
/note="Homeodomain; DNA binding domains involved in the
transcriptional regulation of key eukaryotic developmental
processes; may bind to DNA as monomers or as homo- and/or
heterodimers, in a sequence-specific manner; Region:
homeodomain; cd00086"
/db_xref="CDD:28970"
misc_feature order(333..344,348..350,399..401,417..419,456..458,
462..467)
/gene="ARGFX"
/note="DNA binding site [nucleotide binding]"
/db_xref="CDD:28970"
misc_feature order(336..338,345..347,465..467)
/gene="ARGFX"
/note="specific DNA base contacts [nucleotide binding];
other site"
/db_xref="CDD:28970"
variation 104
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:200448128"
variation 129
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:147644178"
variation 139
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:202191342"
variation 149
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:201721488"
variation 162
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:147017228"
variation 163
/gene="ARGFX"
/replace="g"
/replace="t"
/db_xref="dbSNP:188489586"
variation 190
/gene="ARGFX"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201565904"
variation 196
/gene="ARGFX"
/replace="c"
/replace="g"
/db_xref="dbSNP:145075970"
exon 199..315
/gene="ARGFX"
/inference="alignment:Splign:1.39.8"
variation 297
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:140537962"
exon 316..464
/gene="ARGFX"
/inference="alignment:Splign:1.39.8"
variation 321
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:149102809"
variation 332
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:201467868"
variation 339
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:138183438"
variation 371
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:199794514"
variation 372
/gene="ARGFX"
/replace="a"
/replace="c"
/db_xref="dbSNP:199578428"
variation 396
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:201664081"
variation 430
/gene="ARGFX"
/replace="a"
/replace="c"
/db_xref="dbSNP:201114172"
variation 440
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:148181426"
variation 449
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:185718718"
exon 465..5065
/gene="ARGFX"
/inference="alignment:Splign:1.39.8"
variation 480
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:201405550"
variation 498
/gene="ARGFX"
/replace="a"
/replace="c"
/db_xref="dbSNP:199525328"
variation 507
/gene="ARGFX"
/replace="a"
/replace="c"
/db_xref="dbSNP:183447701"
variation 528
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:141209862"
variation 529
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:9813391"
variation 570
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:202064163"
variation 572
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:142123906"
variation 577
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:146404354"
variation 584
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:139420670"
variation 622
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:149627701"
variation 638
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:376913494"
variation 651
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:144775023"
variation 657
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:144237895"
variation 658
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:148714358"
variation 659
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:201079029"
variation 661
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:144768421"
variation 676
/gene="ARGFX"
/replace="a"
/replace="c"
/db_xref="dbSNP:200387142"
variation 682
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:61750878"
variation 740
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:139699736"
variation 742
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:112431334"
variation 743
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:145252171"
variation 821
/gene="ARGFX"
/replace="a"
/replace="t"
/db_xref="dbSNP:138917850"
variation 931
/gene="ARGFX"
/replace="a"
/replace="c"
/db_xref="dbSNP:192920748"
variation 958
/gene="ARGFX"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:79657977"
variation 967
/gene="ARGFX"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:199782325"
variation 972
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:373740963"
variation 1020
/gene="ARGFX"
/replace="a"
/replace="t"
/db_xref="dbSNP:148566270"
variation 1022
/gene="ARGFX"
/replace="c"
/replace="g"
/db_xref="dbSNP:199657126"
variation 1223
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:115045570"
variation 1241
/gene="ARGFX"
/replace="g"
/replace="t"
/db_xref="dbSNP:116595666"
variation 1271..1272
/gene="ARGFX"
/replace=""
/replace="c"
/db_xref="dbSNP:35191130"
variation 1397
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:185446877"
variation 1439
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:145628833"
variation 1539
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:187960668"
STS 1611..1860
/gene="ARGFX"
/standard_name="D10S16"
/db_xref="UniSTS:155756"
STS 1611..1725
/gene="ARGFX"
/standard_name="D10S16"
/db_xref="UniSTS:155756"
STS 1624..2151
/gene="ARGFX"
/standard_name="GDB:312794"
/db_xref="UniSTS:30247"
STS 1668..1772
/gene="ARGFX"
/standard_name="D11S3114"
/db_xref="UniSTS:152207"
STS 1679..2151
/gene="ARGFX"
/standard_name="L17971"
/db_xref="UniSTS:43966"
STS 1748..2152
/gene="ARGFX"
/standard_name="L17705"
/db_xref="UniSTS:66091"
STS 1752..2671
/gene="ARGFX"
/standard_name="GDB:631813"
/db_xref="UniSTS:158430"
STS 1765..2152
/gene="ARGFX"
/standard_name="L17877"
/db_xref="UniSTS:61334"
variation 1819
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:371788576"
variation 1921
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:192964034"
variation 1982
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:147748191"
variation 2036
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:373874014"
variation 2076
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:11711973"
variation 2092
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:114502094"
variation 2189
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:141916184"
variation 2325
/gene="ARGFX"
/replace="g"
/replace="t"
/db_xref="dbSNP:11712050"
variation 2407
/gene="ARGFX"
/replace=""
/replace="at"
/db_xref="dbSNP:3044706"
variation 2408
/gene="ARGFX"
/replace="a"
/replace="t"
/db_xref="dbSNP:201864700"
variation 2408
/gene="ARGFX"
/replace=""
/replace="ta"
/db_xref="dbSNP:35713310"
variation 2409
/gene="ARGFX"
/replace="a"
/replace="t"
/db_xref="dbSNP:200632755"
variation 2527..2528
/gene="ARGFX"
/replace=""
/replace="ag"
/db_xref="dbSNP:200036693"
variation 2635
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:374449236"
STS 2651..2754
/gene="ARGFX"
/standard_name="D11S3114"
/db_xref="UniSTS:152207"
variation 2668..2669
/gene="ARGFX"
/replace=""
/replace="t"
/db_xref="dbSNP:36106917"
STS 2687..2898
/gene="ARGFX"
/standard_name="sY3084"
/db_xref="UniSTS:515126"
STS 2735..3284
/gene="ARGFX"
/standard_name="D8S2279"
/db_xref="UniSTS:473907"
STS 2735..2835
/gene="ARGFX"
/standard_name="D8S2279"
/db_xref="UniSTS:473907"
variation 2738
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:144196638"
variation 2753
/gene="ARGFX"
/replace="a"
/replace="c"
/db_xref="dbSNP:12171301"
variation 2762
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:111644352"
STS 2824..2925
/gene="ARGFX"
/standard_name="D11S3663"
/db_xref="UniSTS:152897"
STS 2853..3901
/gene="ARGFX"
/standard_name="GDB:315881"
/db_xref="UniSTS:156545"
variation 2926..2931
/gene="ARGFX"
/replace=""
/replace="aaaaat"
/db_xref="dbSNP:201179558"
variation 2929..2930
/gene="ARGFX"
/replace=""
/replace="aa"
/db_xref="dbSNP:57481564"
variation 2996
/gene="ARGFX"
/replace="c"
/replace="g"
/db_xref="dbSNP:184248326"
variation 3092
/gene="ARGFX"
/replace="g"
/replace="t"
/db_xref="dbSNP:1718353"
variation 3145
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:188205049"
variation 3206
/gene="ARGFX"
/replace=""
/replace="a"
/db_xref="dbSNP:34783142"
variation 3220
/gene="ARGFX"
/replace="a"
/replace="t"
/db_xref="dbSNP:61798088"
variation 3222
/gene="ARGFX"
/replace="a"
/replace="t"
/db_xref="dbSNP:61798089"
variation 3251
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:201503811"
variation 3262
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:6790254"
variation 3339
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:147781703"
variation 3483
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:140176733"
variation 3484
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:374864009"
variation 3511
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:192396038"
variation 3631
/gene="ARGFX"
/replace="a"
/replace="t"
/db_xref="dbSNP:570735"
variation 3634
/gene="ARGFX"
/replace="a"
/replace="t"
/db_xref="dbSNP:570732"
variation 3643
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:184729641"
variation 3709
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:188788703"
variation 3717
/gene="ARGFX"
/replace="a"
/replace="c"
/db_xref="dbSNP:150330332"
STS 3845..4108
/gene="ARGFX"
/standard_name="D11S3316"
/db_xref="UniSTS:152558"
STS 3893..3961
/gene="ARGFX"
/standard_name="D1S1423"
/db_xref="UniSTS:149619"
variation 3916..3917
/gene="ARGFX"
/replace=""
/replace="t"
/db_xref="dbSNP:11386339"
variation 3968
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:199633068"
variation 4056
/gene="ARGFX"
/replace="c"
/replace="t"
/db_xref="dbSNP:7638024"
variation 4075..4076
/gene="ARGFX"
/replace=""
/replace="t"
/db_xref="dbSNP:35654921"
variation 4084
/gene="ARGFX"
/replace=""
/replace="g"
/db_xref="dbSNP:5852272"
variation 4213
/gene="ARGFX"
/replace="a"
/replace="c"
/db_xref="dbSNP:80017115"
variation 4336
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:181700331"
variation 4478
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:149925874"
variation 4720
/gene="ARGFX"
/replace="a"
/replace="g"
/db_xref="dbSNP:6783657"
variation 4756
/gene="ARGFX"
/replace="c"
/replace="g"
/db_xref="dbSNP:112991755"
variation 4946
/gene="ARGFX"
/replace="a"
/replace="c"
/db_xref="dbSNP:149089777"
ORIGIN
ggacacactaaggaaactgcatttccagagagagacacaccacgtaggactgaaaatggttactctaaggggattcgtgacagatttcagaaaccatgaggaacagaatggccccagagaatccccagccagaccctttcatcaataggaattattccaacatgaaggtgataccaccacaggatccagctagtcccagtttcactctgttatccaagctggagtgcagtggcacggtctcggcttactgcagcctcaacctcccaggttcaactgatcctcccacctcagcctcccgagtagctgcgactacagcaatacggagaaggcataaagaacgtacttctttcacccaccaacagtatgaggagctagaagctctgtttagccagaccatgttcccagatagaaatcttcaggagaaactagctttgagactcgacctaccggagtcaacagtaaaggtttggttcaggaaccggcgattcaaattgaagaagcagcagcagcagcaatcagcaaagcaacgaaaccagatccttccatccaagaagaatgtgcccacctcccccagaacatcccccagtccttatgctttttctcctgtgatttcagatttctacagctcccttccatctcagcccttagacccttccaattgggcatggaactctaccttcactgagagttctaccagtgacttccaaatgcaagatactcagtgggagaggctggtggcctcggttcctgctttgtactctgatgcctatgacatattccaaatcatagaactgtacaatcttcctgatgagaatgagatatccagctcttctttccactgtctgtatcagtatctctcacccacaaagtaccaggtaggaggacagggttcctctctcagcatctttgctggtccagctgtaggcctatctcctgcacaaacctggcccaatatgacaagccaagcctttgaagcctacagtctaacagatagcctggaattccagaaaacctccaatatggtagacttgggatttctctgaccagagtactaataaatatagatcatttagaaaagtggtcttcttgcctcttgtacatgactgtttttttcctttgtctcattttaacccaacatctgggtctgtgtctctgatttccatgtaaatgttgcaaaaagagttttccaagtagagctgggcactacgtaatcagccccacaagtctccctgagaagcctgcctagtccctttcatggccaatgagactccaaaattcccttcccaaaactatcttggattttctaaaagtaggacagtggttttgggggttatccacttttatttttttgaaactagctctcattctgtcacccaggctggaatacagtggtacagtcacggctcacaaaagccttgacctcctgggctcaggtgatcctcccacctcagcctcctgagtagctaggactacagatgctcgccaccacacctggctaattttttttttttgagactgagtctcgcactgtcacccagggtggagtgcagtggcgggatctcagctcagtgcaacctccacctcctggggttcaagtgattctcctgtgtcagcctcctgagtagctgggattacaggcgtgtgccaccatgcctggctaacttttgtatttttagtagagacggggtttcaccacgttgcccaggctggtcttgaactcctgacctccagtgatccgcctgccttgacctcccaaagtgctgggattacagacatgagccaccgagcctggccaatttttgtgttttttgtagagacgaggttttgccatgttgcccaggctggtctccaactcctggacttaacgccatccacctgccacagcctcccaaagtgctaggaatacaggagtgcaccatcgcacccggctgggttatctagtttaaaaacactttttttcaaggaaaccgaagaaaccatcatccacttttctctctgtatcattctgattttagtatatgtgttgtggaagtgagtacactatcatccacttttaatgacagaaagttataaacttacattttgtttccaatttttcattttttgtttgttatttgttttttgtagacagcactctgtcacccaggctggagtgcagtggcaccatcttggctcactgcagcctctgcctcctgggctcaaacagtcctcccacctcagccttctgagtagctgagactacagacatgcgccaccatgtctggctaatttttgtatttttagtggagatggggtttcgccttgttgcccaggctgaatttgggtttttttaaaatgagactttcagtcctaatttgaggggaaattactgtcaccactagttttaatatagtacaatgaaaaaataatatatatatatatagtacaatggtccagacataataagaggtgtaaaaactatcacaggaagaaataaaaacagatttttgaaggtgagatgataaacttgcaaaactcacaaaataaagagtcaaacttttagaatgacaagttagcatattttccagccacatgatcaacctacaaaattaataccatttctgaacaccagtaataaagaaacataagggctgggggtggtggctcatgcctgtaatcccagcactttgggaggccgaggcgggcggatcacgaggtcaggagattgagaccagcctgactaacatggtgaaatcccgtctctactaaaaatacaaaaaaaaaaaaaaaaaaaagccaggcatggtggcacacacctgtaatcccagctactcgggaggctgaggaaggagaattgcttgaacctgggaggtggaggttgcagtgagctgaggtcgcaccactgcactccagcctggacaacagagcaagactctgtctcaaaaaaaaaataaaaaataaaaaataaaaaataaaagaaacataagataagtacctctcaatgaaaaatgtaaaagtacctagaaattcacaaaaaaattaatacctctgtggagaaaacttcaaaacttaaaaaaggacatagaaaatgttttgaataggccaggcgcagtggctcacacctgtaatcccagcacgttgggaggccaaggcgggcagatcacgaggtcaagagatcaagaccatcctggccaacatggtgaaatcctgcctctactaaaaatacaaaaaaaaaaaaaaattagctgggcatggtggcacacacctgtagtcccagctacttgggaggctgaggcaggagaatcacaaggattgaaactatgcagtgtgttctccaaacatgatggaacgaaattagaaatcaataaaatttgggaaattcacaaatatgtggatattaaacaacacattcctaaataaccagtggttaaagaggtaatcacagtctgagcaacatggcaaaaccctgtgtctacaaaaaataaaaaattagctgggcatgacggccagagcccatggtcccagctactcgagaggctgaggtaagagcatcccttgagccacagaggtcgaggctgcagtgagctgtgactgtgccactgcactccagcttgagcaacacagtgatactgtctcaataaataaataaatagaagaaatcatgagtaaaattggaaaacacttttaactgaaaaaaacaaaagcacaacaaaccaaaacatgggatgaagctaaatcaatgcttagaaggaaatttatagcttcaaatacttatatacatattttttaaaagtagctttacataggaaggaagtggcatagttttatcaatatctgtcaaattaaacttcaaggcaaaacttttttattgagatggagtcttgctctgtcacccaggccgtgcaatctcggctcactgcaacctccgcctcctgggtcaaatgattctcctgctttagcctcccaagtagctgggactacaggtgtacgccaccacacccagctaatttttgtatttttagtagggacaggttttgccatgttgcccaggctggcctcaaactcctgagctcaagtgatcctcccgtctcagcctcccaaagggctgagattacaggtgtgagctacctcacctggccaaaacagtttttttagaaatgaagtatattagacaacaacaaaaggaacaactaacctgaaatatataataactttgaacttaaatatacttaacaacatataccaaaaatatatgaggcaaattttagcaaaaattaaaattcttaagaaaacttcactaatatatagtcataatgtggtatattcatagaacattctcaataattgataataacagtccaaagaaagcagaaagaaggaaagcctagaacagaaataaatgaaatagagaatagaaaagcaatacagaaaaaaaattatgaaatcaaaagctggttctttgaaaagatctacaaaatggcaaacatttagctagattgaccaccccctcaaaagactcaaattactagaatcagaaacaaaagtcaagattttattaccaaacttatagaaataaaaattattagaaagaaatactatgaacaattgaatgccaacaaattagataaatgaaatggacaaattcctaggaagacacagaataccaaatctgactccacaagaaatagatgttgtgaatagagcttgctatggtatgaatgtgtcccccacagctcatgcgttggaaacttaatccccaaagcaacagctttgagaggtgagacctttaagggttactaggcagagcccccatgaatggattaatgccattattgtgggagtgggttagttatctcagaagtgggttcctgataaaaggatgagttcggccttcttcttccccaaaatctttatccccacccccacctctatctttctctctctctcttacctcctcctctcccttccttctgccatgggaggatgaaacatgaaggccctggccaggtgtggcccctccatcttccgtctgagactggaagacttcccagccttcagaactgtaagaaataaatctctcttcata
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:503582 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA
GeneID:503582 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA
GeneID:503582 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA
GeneID:503582 -> Cellular component: GO:0005634 [nucleus] evidence: IEA
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