2025-05-09 20:35:55, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_024567 3233 bp mRNA linear PRI 15-JUN-2013 DEFINITION Homo sapiens homeobox containing 1 (HMBOX1), transcript variant 1, mRNA. ACCESSION NM_024567 VERSION NM_024567.3 GI:209180432 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 3233) AUTHORS Gong,J., Liu,R., Zhuang,R., Zhang,Y., Fang,L., Xu,Z., Jin,L., Wang,T., Song,C., Yang,K., Wei,Y., Yang,A., Jin,B. and Chen,L. TITLE miR-30c-1* promotes natural killer cell cytotoxicity against human hepatoma cells by targeting the transcription factor HMBOX1 JOURNAL Cancer Sci. 103 (4), 645-652 (2012) PUBMED 22320217 REMARK GeneRIF: our results revealed a novel regulatory mechanism: miR-30c-1(*) promoted NK cell cytotoxicity against hepatoma cells by targeting HMBOX1. REFERENCE 2 (bases 1 to 3233) AUTHORS Comuzzie,A.G., Cole,S.A., Laston,S.L., Voruganti,V.S., Haack,K., Gibbs,R.A. and Butte,N.F. TITLE Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population JOURNAL PLoS ONE 7 (12), E51954 (2012) PUBMED 23251661 REFERENCE 3 (bases 1 to 3233) AUTHORS Wu,L., Zhang,C., Zheng,X., Tian,Z. and Zhang,J. TITLE HMBOX1, homeobox transcription factor, negatively regulates interferon-gamma production in natural killer cells JOURNAL Int. Immunopharmacol. 11 (11), 1895-1900 (2011) PUBMED 21839858 REMARK GeneRIF: HMBOX1 may function as a negative regulator of IFN-gamma in NK cells. REFERENCE 4 (bases 1 to 3233) AUTHORS Wu,L., Zhang,C. and Zhang,J. TITLE HMBOX1 negatively regulates NK cell functions by suppressing the NKG2D/DAP10 signaling pathway JOURNAL Cell. Mol. Immunol. 8 (5), 433-440 (2011) PUBMED 21706044 REMARK GeneRIF: HMBOX1 negatively regulates the expression of NKG2D and the activation of the NKG2D/DAP10 signaling pathway in NK cells. REFERENCE 5 (bases 1 to 3233) AUTHORS Aghai,Z.H., Saslow,J.G., Meniru,C., Porter,C., Eydelman,R., Bhat,V., Stahl,G., Sannoh,S., Pyon,K., Hewitt,C. and Bhandari,V. TITLE High-mobility group box-1 protein in tracheal aspirates from premature infants: relationship with bronchopulmonary dysplasia and steroid therapy JOURNAL J Perinatol 30 (9), 610-615 (2010) PUBMED 20182437 REMARK GeneRIF: higher HMGB1(homeobox containing 1) levels in Tracheal aspirates are associated with the development of bronchopulmonary dysplasia or death in ventilated premature infants. REFERENCE 6 (bases 1 to 3233) AUTHORS Zhang,M., Chen,S., Li,Q., Ling,Y., Zhang,J. and Yu,L. TITLE Characterization of a novel human HMBOX1 splicing variant lacking the homeodomain and with attenuated transcription repressor activity JOURNAL Mol. Biol. Rep. 37 (6), 2767-2772 (2010) PUBMED 19757162 REMARK GeneRIF: These findings suggest a distinct role of HMBOX1b, and the control of mRNA splicing might be involved in homeobox genes regulation. REFERENCE 7 (bases 1 to 3233) AUTHORS Dai,J., Wu,L., Zhang,C., Zheng,X., Tian,Z. and Zhang,J. TITLE Recombinant expression of a novel human transcriptional repressor HMBOX1 and preparation of anti-HMBOX1 monoclonal antibody JOURNAL Cell. Mol. Immunol. 6 (4), 261-268 (2009) PUBMED 19728927 REMARK GeneRIF: decreased expression in hepatic carcinoma REFERENCE 8 (bases 1 to 3233) AUTHORS De Marco,A., Biancotto,C., Knezevich,A., Maiuri,P., Vardabasso,C. and Marcello,A. TITLE Intragenic transcriptional cis-activation of the human immunodeficiency virus 1 does not result in allele-specific inhibition of the endogenous gene JOURNAL Retrovirology 5, 98 (2008) PUBMED 18983639 REMARK Publication Status: Online-Only REFERENCE 9 (bases 1 to 3233) AUTHORS Chen,S., Saiyin,H., Zeng,X., Xi,J., Liu,X., Li,X. and Yu,L. TITLE Isolation and functional analysis of human HMBOX1, a homeobox containing protein with transcriptional repressor activity JOURNAL Cytogenet. Genome Res. 114 (2), 131-136 (2006) PUBMED 16825764 REMARK GeneRIF: Hmbox1 is widely expressed in pancreas and the expression of this gene can also be detected in pallium, hippocampus and hypothalamus COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from BC069242.1 and AC108449.5. On Oct 9, 2008 this sequence version replaced gi:47059039. Transcript Variant: This variant (1) represents the longer transcript. Both variants encode the same protein. Sequence Note: This RefSeq record was created from transcript and genomic sequence data because no single transcript was available for the full length of the gene. The extent of this transcript is supported by transcript alignments. ##Evidence-Data-START## Transcript exon combination :: BC069242.1 [ECO:0000332] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-1883 BC069242.1 1-1883 1884-3233 AC108449.5 53313-54662 FEATURES Location/Qualifiers source 1..3233 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="8" /map="8p21.1" gene 1..3233 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /note="homeobox containing 1" /db_xref="GeneID:79618" /db_xref="HGNC:26137" /db_xref="HPRD:07964" exon 1..312 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /inference="alignment:Splign:1.39.8" variation 96 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="t" /db_xref="dbSNP:117901466" variation 174 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:371954919" variation 288 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="g" /db_xref="dbSNP:144108418" exon 313..343 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /inference="alignment:Splign:1.39.8" exon 344..423 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /inference="alignment:Splign:1.39.8" variation 356 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="c" /db_xref="dbSNP:190364776" variation 386 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="t" /db_xref="dbSNP:375170302" misc_feature 395..397 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /note="upstream in-frame stop codon" variation 396 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:143238324" CDS 401..1663 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /note="homeobox telomere-binding protein 1; homeobox-containing protein PBHNF" /codon_start=1 /product="homeobox-containing protein 1" /protein_id="NP_078843.2" /db_xref="GI:47059040" /db_xref="CCDS:CCDS6071.1" /db_xref="GeneID:79618" /db_xref="HGNC:26137" /db_xref="HPRD:07964" /translation="
MLSSFPVVLLETMSHYTDEPRFTIEQIDLLQRLRRTGMTKHEILHALETLDRLDQEHSDKFGRRSSYGGSSYGNSTNNVPASSSTATASTQTQHSGMSPSPSNSYDTSPQPCTTNQNGRENNERLSTSNGKMSPTRYHANSMGQRSYSFEASEEDLDVDDKVEELMRRDSSVIKEEIKAFLANRRISQAVVAQVTGISQSRISHWLLQQGSDLSEQKKRAFYRWYQLEKTNPGATLSMRPAPIPIEDPEWRQTPPPVSATSGTFRLRRGSRFTWRKECLAVMESYFNENQYPDEAKREEIANACNAVIQKPGKKLSDLERVTSLKVYNWFANRRKEIKRRANIEAAILESHGIDVQSPGGHSNSDDVDGNDYSEQDDSTSHSDHQDPISLAVEMAAVNHTILALARQGANEIKTEALDDD
" misc_feature 1202..1420 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /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:238039" misc_feature order(1202..1216,1220..1222,1271..1273,1289..1291, 1373..1375,1379..1384,1391..1396,1400..1408,1412..1417) /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /note="DNA binding site [nucleotide binding]" /db_xref="CDD:238039" misc_feature order(1208..1210,1217..1219,1382..1384,1391..1396, 1403..1405) /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /note="specific DNA base contacts [nucleotide binding]; other site" /db_xref="CDD:238039" variation 415 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="t" /db_xref="dbSNP:369410329" exon 424..900 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /inference="alignment:Splign:1.39.8" variation 513 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="t" /db_xref="dbSNP:372949481" variation 534 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:377394078" variation 535 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="t" /db_xref="dbSNP:368975966" variation 538 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="t" /db_xref="dbSNP:150056601" variation 553 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="t" /db_xref="dbSNP:145379672" variation 596 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:375109128" variation 622 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="t" /db_xref="dbSNP:376798312" variation 670 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="c" /db_xref="dbSNP:370727503" variation 685 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:374107196" variation 697 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:148768782" variation 819 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:113918455" variation 824 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:111980547" variation 856 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:367563195" variation 894 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="g" /replace="t" /db_xref="dbSNP:201679029" exon 901..986 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /inference="alignment:Splign:1.39.8" exon 987..1097 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /inference="alignment:Splign:1.39.8" variation 1002 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:374483267" variation 1055 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="c" /db_xref="dbSNP:144731490" variation 1069 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="t" /db_xref="dbSNP:147891204" exon 1098..1251 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /inference="alignment:Splign:1.39.8" variation 1099 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="t" /db_xref="dbSNP:372681580" variation 1127 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:376040742" variation 1133 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:370049630" variation 1147 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:373691508" variation 1169 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="g" /replace="t" /db_xref="dbSNP:371498035" variation 1195 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="t" /db_xref="dbSNP:201671682" exon 1252..1334 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /inference="alignment:Splign:1.39.8" variation 1307 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:372399969" exon 1335..1430 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /inference="alignment:Splign:1.39.8" variation 1337 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:57483862" exon 1431..1525 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /inference="alignment:Splign:1.39.8" exon 1526..3233 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /inference="alignment:Splign:1.39.8" variation 1600 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="t" /db_xref="dbSNP:377441971" variation 1617 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:371243883" variation 1630 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="t" /db_xref="dbSNP:202238043" variation 1631 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:141568231" variation 1645 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:370641360" variation 1667 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:376300184" variation 1748 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="g" /db_xref="dbSNP:142408867" variation 1752 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:185761956" variation 1756 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="t" /db_xref="dbSNP:11831" variation 1814 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:150865526" variation 1865..1866 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="" /replace="ggtt" /db_xref="dbSNP:3830316" variation 1866..1867 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="" /replace="aacc" /db_xref="dbSNP:35389793" variation 1867..1868 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="" /replace="ccaa" /db_xref="dbSNP:146960848" variation 1875..1876 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="" /replace="acca" /replace="ccaa" /db_xref="dbSNP:5890436" variation 1876..1877 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="" /replace="ccaa" /db_xref="dbSNP:34303559" variation 1877..1878 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="" /replace="caac" /db_xref="dbSNP:72378921" variation 1881..1882 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="" /replace="aacc" /db_xref="dbSNP:34984916" variation 1884 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="c" /db_xref="dbSNP:73669467" variation 1992 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="t" /db_xref="dbSNP:139785494" variation 1995 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:374383298" variation 2021 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="g" /replace="t" /db_xref="dbSNP:144497394" STS 2067..2312 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /standard_name="WI-20805" /db_xref="UniSTS:52353" variation 2085 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="t" /db_xref="dbSNP:14015" variation 2201..2203 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="" /replace="tat" /db_xref="dbSNP:373733278" variation 2238 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="t" /db_xref="dbSNP:14118" STS 2249..2389 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /standard_name="D8S2113" /db_xref="UniSTS:57588" variation 2267 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="t" /db_xref="dbSNP:146433919" variation 2360 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:140779972" variation 2373 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="t" /db_xref="dbSNP:187475748" variation 2401..2406 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="" /replace="gtcatt" /db_xref="dbSNP:375419031" variation 2406..2407 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="" /replace="a" /db_xref="dbSNP:372815934" variation 2406 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="t" /db_xref="dbSNP:1128136" variation 2407..2414 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="" /replace="aaaaaaaa" /db_xref="dbSNP:200587602" variation 2407 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="" /replace="a" /replace="aaaaaaaa" /db_xref="dbSNP:11356150" variation 2407 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="t" /db_xref="dbSNP:78932143" variation 2415 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="" /replace="a" /replace="aaaaaaaa" /db_xref="dbSNP:34577722" variation 2426 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="c" /db_xref="dbSNP:74597687" variation 2429 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="c" /db_xref="dbSNP:62502811" variation 2455 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="t" /db_xref="dbSNP:79251998" variation 2456 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="t" /db_xref="dbSNP:80024799" variation 2514 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="t" /db_xref="dbSNP:10088428" variation 2618 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="a" /replace="g" /db_xref="dbSNP:149659731" STS 3072..3210 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /standard_name="RH103807" /db_xref="UniSTS:98132" variation 3149 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="t" /db_xref="dbSNP:373069277" variation 3152 /gene="HMBOX1" /gene_synonym="HNF1LA; HOT1; PBHNF" /replace="c" /replace="t" /db_xref="dbSNP:192657387" ORIGIN
cctcaagtctctttcctcacttctttctcttcacttaaaacaatttttttggaggggttttggggaggaagtgagcggacgctggggatgggtctcgtaagcggccggattgagaggagggaggaagcagggggcttccgagtgggtgacccagacgcgggctgtggggtggggcagttcgtggggtccggtcctggaaaggcgtcgactgccccccaactcttctggtttcctctacgatgagcggaaggtttgaatcctggaggtggggtctccggtgtggagttctggaaactgtgaggtgatttgcagctggtggaatggaacagtgaagaagcattggaatggtagataacgcagatcatctctggaaaggatattgatccgcctcatgtaaagtatgcttagttcctttccagtggttttgctggaaaccatgtctcattatacagatgaacccagatttaccatagagcagatagatctgcttcagcgacttcggcgtactggaatgactaaacatgaaattctccatgccttggaaactttggaccgtcttgatcaagagcatagtgacaagtttggaagaaggtccagctatggaggaagttcatatgggaatagtactaacaatgtcccagcatcttcctctacagctacagcttccacacagacgcagcattcgggaatgtccccgtcacctagcaacagttatgatacttccccacagccttgcactaccaatcaaaatgggagggagaataatgagcgattatctacatccaatggaaagatgtcaccaactcgctaccatgcaaacagcatgggtcagaggtcatacagttttgaagcctcagaagaggacctagatgtagatgataaagtggaagaattaatgaggagggacagcagtgtgataaaagaggaaatcaaagcctttcttgccaatcggaggatttcccaagcagttgttgcacaggtaacaggtatcagtcagagccggatctctcattggctgttgcagcagggatcagacctgagtgaacagaagaaaagagcattttaccgatggtatcaacttgagaagacaaaccctggcgctacactaagtatgagaccagcccccattccaatagaggaccctgaatggagacaaacgcctcccccagtctctgccacatctggtactttccgactgcgacgagggagtcgatttacctggagaaaggagtgcctggctgttatggaaagttacttcaatgagaatcaatacccagatgaagcaaagagggaagaaattgcaaacgcttgcaatgcagttatacagaagccaggcaaaaagctgtcagatctggaaagagttacctccctgaaagtatataattggtttgctaacagaaggaaggagatcaagaggagagccaatattgaagcagcaatcctggagagtcatgggatagatgtgcagagtccaggaggccactcaaacagtgatgatgtcgacgggaatgactactctgagcaggatgacagtacgagccatagtgaccaccaagaccccatctcattagctgtggaaatggcagcagtcaaccacactatcttggcattggcccgacaaggagccaacgaaatcaagacagaggccctggatgatgactgatcagggaggttaaacatgacaagttaacttagtttagacgtagcaccttagcagactttcctcggtccttaacatgtgttcttacagtataacttgcagtttcttgtatgtcaggtagctgttagggtcttgttctgtgaagatggcatggtgccctcagcctttgcatatactctctcagtattaactcccagtaaataataaccaaccaaccaaccaaacttccctctcccagcccccgaggctagaaaatcttgctgctccgtcttagcattccaagaaagtgcttccaggtatttagatagccctcagttctcaaatattagactacgtgtaaaatcttgggtacctttagattcttgtaacactagtctgtactcccttttccttccccaagactgataggatgcaagctgaggtcgtggcacaggaatgacagacaccatttggggagtatccacagagtcaaaggaacactagaatccccacctcagcgtgaggataattgatttccagctgcaataagccgtgcctcattatagccacactgtggctagattatacttctttgggtgctgtgctaagaatgtcaatggaaaaagccgatctcagattttgtttgaagttaacatgcctgacacagacatcctttcctctcacaagctgtgtgacttagtagataaaatactgccttctgcctttgggaccatgattaaaaacaaagacaaaaaccaaaagtcattaaaaaaaaaaaaaaaaaaaacccagcttgagagcattggaaaaaaaaaatatgagctgaatgtctaatggatgctaagtccagttttcagaaccactgtacattccacggcacagttagcagtgcctgcctggaaaagttttggaggtcatcgtggaagttgctttgcctcctgtcagtgtcccctttccctgctaccaaaaaagtctttcaaggatggagctaaggtcaaaaatgagtgaaaaaacttgcagtgtttgtatccattaaacggaagccccctcactctgagaggtcactagaggacttcatagtggggttgtgctgcttatcacagatgcagacacttgcccagataggagcagagaaaagcaggggacgtttcctactcacattgtggctgtatgagaacacgatgggactgctttgctgttctctttactctgtccttggagaggtgtgaaaagctgtattgctacaggcaatttatttaataattggaagccatattgataatggatgtggtaatatttgtaaagtttaatctactttaagcggcagtaactaatggaatttttttccttgatcacatatgtagcacttttgttactttttaaagatatttatatttgataaatctttttttcattttgagaactcaaaataccaaacagtgaacttgcattctaaagtcaccctgtgatcaccttgtcatctagtagcaaaatgatgaactattcatgcatcaaagaaaattacatctgctggccttgtatgaaaatgatctcttggcatcccgattaaatgacacactgtcactgtgggtaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:79618 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA GeneID:79618 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA GeneID:79618 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA GeneID:79618 -> Biological process: GO:0045892 [negative regulation of transcription, DNA-dependent] evidence: IDA GeneID:79618 -> Biological process: GO:0045893 [positive regulation of transcription, DNA-dependent] evidence: IEA GeneID:79618 -> Cellular component: GO:0005634 [nucleus] evidence: IDA GeneID:79618 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
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