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2025-05-09 17:10:23, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_153448 1591 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens ESX homeobox 1 (ESX1), mRNA.
ACCESSION NM_153448
VERSION NM_153448.3 GI:283806665
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 1591)
AUTHORS Bonaparte,E., Moretti,M., Colpi,G.M., Nerva,F., Contalbi,G.,
Vaccalluzzo,L., Tabano,S., Grati,F.R., Gazzano,G., Sirchia,S.M.,
Simoni,G., Gallina,A. and Miozzo,M.
TITLE ESX1 gene expression as a robust marker of residual spermatogenesis
in azoospermic men
JOURNAL Hum. Reprod. 25 (6), 1398-1403 (2010)
PUBMED 20356899
REMARK GeneRIF: ESX1 emerges as a potentially reliable molecular marker of
residual spermatogenesis in azoospermic men
REFERENCE 2 (bases 1 to 1591)
AUTHORS Wang,X. and Zhang,J.
TITLE Rapid evolution of primate ESX1, an X-linked placenta- and
testis-expressed homeobox gene
JOURNAL Hum. Mol. Genet. 16 (17), 2053-2060 (2007)
PUBMED 17588961
REFERENCE 3 (bases 1 to 1591)
AUTHORS Loschiavo,M., Nguyen,Q.K., Duselis,A.R. and Vrana,P.B.
TITLE Mapping and identification of candidate loci responsible for
Peromyscus hybrid overgrowth
JOURNAL Mamm. Genome 18 (1), 75-85 (2007)
PUBMED 17242862
REFERENCE 4 (bases 1 to 1591)
AUTHORS Murthi,P., Doherty,V.L., Said,J.M., Donath,S., Brennecke,S.P. and
Kalionis,B.
TITLE Homeobox gene ESX1L expression is decreased in human pre-term
idiopathic fetal growth restriction
JOURNAL Mol. Hum. Reprod. 12 (5), 335-340 (2006)
PUBMED 16613891
REMARK GeneRIF: In FGR-affected placentae, ESX1L levels were lower than in
gestation-matched controls, indicating a potential role for the
ESX1L gene within the growth control mechanism of the fetus,
through its effect on placental function.
REFERENCE 5 (bases 1 to 1591)
AUTHORS Yanagihara,M., Ishikawa,S., Naito,M., Nakajima,J., Aburatani,H. and
Hatakeyama,M.
TITLE Paired-like homeoprotein ESXR1 acts as a sequence-specific
transcriptional repressor of the human K-ras gene
JOURNAL Oncogene 24 (38), 5878-5887 (2005)
PUBMED 15897875
REFERENCE 6 (bases 1 to 1591)
AUTHORS Figueiredo,A.L., Salles,M.G., Albano,R.M. and Porto,L.C.
TITLE Molecular and morphologic analyses of expression of ESX1L in
different stages of human placental development
JOURNAL J. Cell. Mol. Med. 8 (4), 545-550 (2004)
PUBMED 15601583
REMARK GeneRIF: ESX1L is expressed during all stages of placental
development and is localized to sparse areas of trophoblast in
terminal villi in association with cytotrophoblastic cells
REFERENCE 7 (bases 1 to 1591)
AUTHORS Ozawa,H., Ashizawa,S., Naito,M., Yanagihara,M., Ohnishi,N.,
Maeda,T., Matsuda,Y., Jo,Y., Higashi,H., Kakita,A. and
Hatakeyama,M.
TITLE Paired-like homeodomain protein ESXR1 possesses a cleavable
C-terminal region that inhibits cyclin degradation
JOURNAL Oncogene 23 (39), 6590-6602 (2004)
PUBMED 15235584
REMARK GeneRIF: proteolytic processing of ESXR1 plays a role in concerted
regulation of the cell cycle and transcription in human cells
REFERENCE 8 (bases 1 to 1591)
AUTHORS Fohn,L.E. and Behringer,R.R.
TITLE ESX1L, a novel X chromosome-linked human homeobox gene expressed in
the placenta and testis
JOURNAL Genomics 74 (1), 105-108 (2001)
PUBMED 11374906
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AK097704.1 and BC053599.1.
This sequence is a reference standard in the RefSeqGene project.
On Jan 13, 2010 this sequence version replaced gi:38455418.
Summary: This gene encodes a dual-function 65 kDa protein that
undergoes proteolytic cleavage to produce a 45 kDa N-terminal
fragment with a paired-like homeodomain and a 20 kDa C-terminal
fragment with a proline-rich domain. The C-terminal fragment
localizes to the cytoplasm while the N-terminal fragment localizes
exclusively to the nucleus. In contrast to human, the mouse homolog
has a novel PN/PF motif in the C-terminus and is paternally
imprinted in placental tissue. This gene likely plays a role in
placental development and spermatogenesis. [provided by RefSeq, Jan
2010].
##Evidence-Data-START##
Transcript exon combination :: BC053599.1, BC042633.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025084, ERS025085 [ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-11 AK097704.1 16-26
12-1027 BC053599.1 1-1016
1028-1108 AK097704.1 1043-1123
1109-1591 BC053599.1 1098-1580
FEATURES Location/Qualifiers
source 1..1591
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="X"
/map="Xq22.1"
gene 1..1591
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/note="ESX homeobox 1"
/db_xref="GeneID:80712"
/db_xref="HGNC:14865"
/db_xref="HPRD:06503"
/db_xref="HPRD:08945"
/db_xref="MIM:300154"
exon 1..151
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/inference="alignment:Splign:1.39.8"
variation complement(12)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376260931"
variation complement(22)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:377423337"
variation complement(59)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:373167155"
variation complement(60)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369664343"
misc_feature 64..66
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/note="upstream in-frame stop codon"
CDS 70..1290
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/note="ESX1-related protein; extraembryonic,
spermatogenesis, homeobox 1 homolog"
/codon_start=1
/product="homeobox protein ESX1"
/protein_id="NP_703149.1"
/db_xref="GI:23592228"
/db_xref="CCDS:CCDS14516.1"
/db_xref="GeneID:80712"
/db_xref="HGNC:14865"
/db_xref="HPRD:06503"
/db_xref="HPRD:08945"
/db_xref="MIM:300154"
/translation="
MESLRGYTHSDIGYRSLAVGEDIEEVNDEKLTVTSLMARGGEDEENTRSKPEYGTEAENNVGTEGSVPSDDQDREGGGGHEPEQQQEEPPLTKPEQQQEEPPLLELKQEQEEPPQTTVEGPQPAEGPQTAEGPQPPERKRRRRTAFTQFQLQELENFFDESQYPDVVARERLAARLNLTEDRVQVWFQNRRAKWKRNQRVLMLRNTATADLAHPLDMFLGGAYYAAPALDPALCVHLVPQLPRPPVLPVPPMPPRPPMVPMPPRPPIAPMPPMAPVPPGSRMAPVPPGPRMAPVPPWPPMAPVPPWPPMAPVPTGPPMAPVPPGPPMARVPPGPPMARVPPGPPMAPLPPGPPMAPLPPGPPMAPLPPGPPMAPLPPRSHVPHTGLAPVHITWAPVINSYYACPFF
"
misc_feature 481..498
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q8N693.3);
Region: Nuclear localization signal (Potential)"
misc_feature 487..663
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/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(487..501,505..507,556..558,574..576,613..615,
619..624,631..636,640..648,652..657)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/note="DNA binding site [nucleotide binding]"
/db_xref="CDD:28970"
misc_feature order(493..495,502..504,622..624,631..636,643..645)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/note="specific DNA base contacts [nucleotide binding];
other site"
/db_xref="CDD:28970"
misc_feature 799..1203
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q8N693.3);
Region: 15 X 9 AA tandem repeats of P-P-x-x-P-x-P-P-x"
variation complement(78)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201322852"
variation complement(87)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:147351224"
variation complement(97)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:186958219"
variation complement(124)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="g"
/replace="t"
/db_xref="dbSNP:202022977"
variation complement(139)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:200141038"
exon 152..575
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/inference="alignment:Splign:1.39.8"
variation complement(160)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140169186"
variation complement(170)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147516186"
variation complement(201)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="g"
/replace="t"
/db_xref="dbSNP:149394798"
variation complement(230)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="g"
/replace="t"
/db_xref="dbSNP:76590545"
variation complement(239)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200824381"
variation complement(271)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:138817762"
variation complement(279)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:376654393"
variation complement(294)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150207642"
variation complement(297)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:372065561"
variation complement(333)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200053829"
variation complement(379)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:56255243"
variation complement(381)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:141891783"
variation complement(386..387)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace=""
/replace="tg"
/db_xref="dbSNP:72224483"
variation complement(417)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:138260698"
variation complement(437)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="c"
/db_xref="dbSNP:368352917"
variation complement(460)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375606449"
variation complement(475)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:370791049"
variation complement(477)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="c"
/db_xref="dbSNP:145629484"
variation complement(495)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140432334"
variation complement(544)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:201574313"
variation complement(567)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="g"
/replace="t"
/db_xref="dbSNP:146746547"
exon 576..621
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/inference="alignment:Splign:1.39.8"
variation complement(577)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:370262145"
variation complement(605)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:143139589"
variation complement(611)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201519494"
exon 622..1480
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/inference="alignment:Splign:1.39.8"
variation complement(647)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:41305431"
variation complement(656)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144948361"
variation complement(662)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200652460"
variation complement(709)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:149916765"
variation complement(722)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="t"
/db_xref="dbSNP:371028979"
variation complement(772)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199653056"
variation complement(790)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376291238"
variation complement(794)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:139543229"
variation complement(823)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373095481"
variation complement(870)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:369362892"
variation complement(877)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:375826244"
variation complement(903)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369054321"
variation complement(907)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144173947"
variation complement(910)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:111666814"
variation complement(934)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:141524947"
variation complement(937)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:148783552"
variation complement(940)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374876713"
variation complement(943)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200455087"
variation complement(971)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200908797"
variation complement(972)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373133940"
variation complement(976)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200592570"
variation complement(985)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="t"
/db_xref="dbSNP:201963432"
variation complement(990)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:184828935"
variation complement(1009)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="c"
/db_xref="dbSNP:9697856"
variation complement(1028)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:191202058"
variation complement(1098)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368249985"
variation complement(1109)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:200088361"
variation complement(1111)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:76090537"
variation complement(1136)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:201142803"
variation complement(1138)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:199856640"
variation complement(1190)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:369886617"
variation complement(1192)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:78191648"
variation complement(1200)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace=""
/replace="gggccgcccatggcgcctctgccaccc"
/db_xref="dbSNP:11267975"
variation complement(1201)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:377155869"
variation complement(1246)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:12383583"
variation complement(1252)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="g"
/db_xref="dbSNP:372235695"
variation complement(1278)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375756428"
variation complement(1281)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:138294460"
variation complement(1285)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:184749315"
variation complement(1286)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145648737"
variation complement(1288)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:9803338"
variation complement(1302)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="c"
/db_xref="dbSNP:368022150"
variation complement(1305)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:192729779"
variation complement(1317)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371465085"
variation complement(1336)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:201413646"
variation complement(1369)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="c"
/replace="t"
/db_xref="dbSNP:113852635"
variation complement(1420)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="c"
/db_xref="dbSNP:188475442"
variation complement(1479)
/gene="ESX1"
/gene_synonym="ESX1L; ESXR1"
/replace="a"
/replace="t"
/db_xref="dbSNP:183421159"
ORIGIN
cccgggatcgccgcggaaccacgcacagagtctgcagaagtgcacagctttatcgacagcgcttgaagcatggagtctcttcgcgggtacacccacagtgatattggctaccgcagcctggcagtcggcgaggacatcgaggaagtgaatgatgagaaacttaccgtgacctcgctgatggcaaggggaggagaggacgaggagaatacacggtccaaacctgagtacggaacagaagcggaaaacaacgttggcacggaagggtccgtcccctcggacgaccaagaccgtgagggtggcggcggccacgagccggagcaacagcaggaggagccgcccctgaccaagccggagcaacagcaggaggagccgcccctgctcgagctgaagcaagagcaggaggagccgccccagacgaccgtggaggggccacagccggcggaggggccacaaaccgctgagggaccacagcccccagagaggaaacgccgccgccgcaccgcgttcacgcagtttcagctgcaggagctagagaactttttcgatgaatctcaatatcccgacgttgtggcgcgagagagacttgcagcacgcctgaatttgactgaagacagagtgcaggtttggtttcagaacagaagagccaagtggaaacgaaatcagagggtgctaatgttgagaaacactgctactgctgacctggcccaccctttggacatgttcttgggtggggcctattatgctgctcctgctctggatcctgctttgtgtgttcatctggtgccacaactacctagaccacctgtgctgcctgtgccacctatgccacccaggccacccatggtccctatgccacccaggccacccatagcacctatgccacccatggcgcctgtgccacccggctcacgcatggcgcctgtgccacccgggccacgcatggcgcctgtgccaccctggccgcccatggcgcctgtgccaccctggccgcccatggcgcctgtgccaaccgggccgcccatggcgcctgtgccacccgggccgcccatggcgcgtgtgccacccgggccgcccatggcgcgtgtgccacccgggccgcccatggcgcctctgccacccgggccgcccatggcgcctctgccacccgggccgcccatggcgcctctgccacccgggccgcccatggcgcctctgccacccaggtcacatgtgcctcacactggcctggctcctgtacacatcacatgggcccctgtcatcaacagttattatgcatgtccctttttctaaagtaaggtattcataacagtttttccaaagttctttcctgccagatagaaattgtgcacagcacagcatcaagtaattcgttagatgcttgttaaatgaagtgggtaggtgaacaaagttaacgaatgccctgttatttttgtaggccacataattgtagtattttcaataaagatgtgacttaatagtaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:80712 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA
GeneID:80712 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IDA
GeneID:80712 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA
GeneID:80712 -> Biological process: GO:0006357 [regulation of transcription from RNA polymerase II promoter] evidence: IEA
GeneID:80712 -> Biological process: GO:0045892 [negative regulation of transcription, DNA-dependent] evidence: IDA
GeneID:80712 -> Biological process: GO:0051726 [regulation of cell cycle] evidence: IDA
GeneID:80712 -> Biological process: GO:0060713 [labyrinthine layer morphogenesis] evidence: IEA
GeneID:80712 -> Biological process: GO:0060716 [labyrinthine layer blood vessel development] evidence: IEA
GeneID:80712 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
GeneID:80712 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
by
@meso_cacase at
DBCLS
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