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2024-03-28 17:33:04, 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:

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

by @meso_cacase at DBCLS
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