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2024-04-19 20:07:20, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_002139 2097 bp mRNA linear PRI 31-MAY-2013
DEFINITION Homo sapiens RNA binding motif protein, X-linked (RBMX), transcript
variant 1, mRNA.
ACCESSION NM_002139
VERSION NM_002139.3 GI:258645145
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 2097)
AUTHORS Matsunaga,S., Takata,H., Morimoto,A., Hayashihara,K., Higashi,T.,
Akatsuchi,K., Mizusawa,E., Yamakawa,M., Ashida,M., Matsunaga,T.M.,
Azuma,T., Uchiyama,S. and Fukui,K.
TITLE RBMX: a regulator for maintenance and centromeric protection of
sister chromatid cohesion
JOURNAL Cell Rep 1 (4), 299-308 (2012)
PUBMED 22832223
REMARK GeneRIF: RBMX is a cohesion regulator that maintains the proper
cohesion of sister chromatids.
REFERENCE 2 (bases 1 to 2097)
AUTHORS Adamson,B., Smogorzewska,A., Sigoillot,F.D., King,R.W. and
Elledge,S.J.
TITLE A genome-wide homologous recombination screen identifies the
RNA-binding protein RBMX as a component of the DNA-damage response
JOURNAL Nat. Cell Biol. 14 (3), 318-328 (2012)
PUBMED 22344029
REMARK GeneRIF: Data show that RBMX accumulated at DNA lesions through
multiple domains in a poly(ADP-ribose) polymerase 1-dependent
manner and promoted HR by facilitating proper BRCA2 expression.
Publication Status: Online-Only
REFERENCE 3 (bases 1 to 2097)
AUTHORS Shin,K.H., Kim,R.H., Yu,B., Kang,M.K., Elashoff,D., Christensen,R.,
Pucar,A. and Park,N.H.
TITLE Expression and mutation analysis of heterogeneous nuclear
ribonucleoprotein G in human oral cancer
JOURNAL Oral Oncol. 47 (11), 1011-1016 (2011)
PUBMED 21840245
REMARK GeneRIF: studied the genetic and expression states of hnRNP G in
normal, premalignant and malignant human oral tissues to further
understand the relationship between the hnRNP G alterations and the
development of human oral cancer
REFERENCE 4 (bases 1 to 2097)
AUTHORS Heinrich,B., Zhang,Z., Raitskin,O., Hiller,M., Benderska,N.,
Hartmann,A.M., Bracco,L., Elliott,D., Ben-Ari,S., Soreq,H.,
Sperling,J., Sperling,R. and Stamm,S.
TITLE Heterogeneous nuclear ribonucleoprotein G regulates splice site
selection by binding to CC(A/C)-rich regions in pre-mRNA
JOURNAL J. Biol. Chem. 284 (21), 14303-14315 (2009)
PUBMED 19282290
REFERENCE 5 (bases 1 to 2097)
AUTHORS Shin,K.H., Kim,R.H., Kim,R.H., Kang,M.K. and Park,N.H.
TITLE hnRNP G elicits tumor-suppressive activity in part by upregulating
the expression of Txnip
JOURNAL Biochem. Biophys. Res. Commun. 372 (4), 880-885 (2008)
PUBMED 18541147
REMARK GeneRIF: These studies indicate that hnRNP G promotes the
expression of Txnip and mediates its tumor-suppressive effect.
REFERENCE 6 (bases 1 to 2097)
AUTHORS Mazeyrat,S., Saut,N., Mattei,M.G. and Mitchell,M.J.
TITLE RBMY evolved on the Y chromosome from a ubiquitously transcribed
X-Y identical gene
JOURNAL Nat. Genet. 22 (3), 224-226 (1999)
PUBMED 10391207
REFERENCE 7 (bases 1 to 2097)
AUTHORS Delbridge,M.L., Lingenfelter,P.A., Disteche,C.M. and Graves,J.A.
TITLE The candidate spermatogenesis gene RBMY has a homologue on the
human X chromosome
JOURNAL Nat. Genet. 22 (3), 223-224 (1999)
PUBMED 10391206
REFERENCE 8 (bases 1 to 2097)
AUTHORS Venables,J.P., Vernet,C., Chew,S.L., Elliott,D.J., Cowmeadow,R.B.,
Wu,J., Cooke,H.J., Artzt,K. and Eperon,I.C.
TITLE T-STAR/ETOILE: a novel relative of SAM68 that interacts with an
RNA-binding protein implicated in spermatogenesis
JOURNAL Hum. Mol. Genet. 8 (6), 959-969 (1999)
PUBMED 10332027
REFERENCE 9 (bases 1 to 2097)
AUTHORS Soulard,M., Della Valle,V., Siomi,M.C., Pinol-Roma,S., Codogno,P.,
Bauvy,C., Bellini,M., Lacroix,J.C., Monod,G., Dreyfuss,G. et al.
TITLE hnRNP G: sequence and characterization of a glycosylated
RNA-binding protein
JOURNAL Nucleic Acids Res. 21 (18), 4210-4217 (1993)
PUBMED 7692398
REFERENCE 10 (bases 1 to 2097)
AUTHORS Le Coniat,M., Soulard,M., Della Valle,V., Larsen,C.J. and Berger,R.
TITLE Localization of the human gene encoding heterogeneous nuclear RNA
ribonucleoprotein G (hnRNP-G) to chromosome 6p12
JOURNAL Hum. Genet. 88 (5), 593-595 (1992)
PUBMED 1551662
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from BM147410.1, DC337568.1,
BC007435.2 and BM993214.1.
On Sep 18, 2009 this sequence version replaced gi:56699408.
Summary: This gene belongs to the RBMY gene family which includes
candidate Y chromosome spermatogenesis genes. This gene, an active
X chromosome homolog of the Y chromosome RBMY gene, is widely
expressed whereas the RBMY gene evolved a male-specific function in
spermatogenesis. Pseudogenes of this gene, found on chromosomes 1,
4, 9, 11, and 6, were likely derived by retrotransposition from the
original gene. Alternatively spliced transcript variants encoding
different isoforms have been identified. A snoRNA gene (SNORD61) is
found in one of its introns. [provided by RefSeq, Sep 2009].
Transcript Variant: This variant (1) represents the more frequently
occurring transcript and it encodes the longer protein (isoform 1).
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: BC006550.2, BM480306.1 [ECO:0000332]
RNAseq introns :: mixed/partial sample support
ERS025081, ERS025082 [ECO:0000350]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-209 BM147410.1 1-209
210-239 DC337568.1 155-184
240-2067 BC007435.2 176-2003
2068-2097 BM993214.1 1-30 c
FEATURES Location/Qualifiers
source 1..2097
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="X"
/map="Xq26.3"
gene 1..2097
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/note="RNA binding motif protein, X-linked"
/db_xref="GeneID:27316"
/db_xref="HGNC:9910"
/db_xref="MIM:300199"
exon 1..184
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/inference="alignment:Splign:1.39.8"
misc_feature 163..165
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/note="upstream in-frame stop codon"
exon 185..319
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/inference="alignment:Splign:1.39.8"
variation 210
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/replace="a"
/replace="c"
/db_xref="dbSNP:2011584"
CDS 211..1386
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/note="isoform 1 is encoded by transcript variant 1; RNA
binding motif protein, X chromosome; heterogeneous nuclear
ribonucleoprotein G; hnRNP G; glycoprotein p43;
RNA-binding motif protein, X chromosome"
/codon_start=1
/product="RNA-binding motif protein, X chromosome isoform
1"
/protein_id="NP_002130.2"
/db_xref="GI:56699409"
/db_xref="CCDS:CCDS14661.1"
/db_xref="GeneID:27316"
/db_xref="HGNC:9910"
/db_xref="MIM:300199"
/translation="
MVEADRPGKLFIGGLNTETNEKALEAVFGKYGRIVEVLLMKDRETNKSRGFAFVTFESPADAKDAARDMNGKSLDGKAIKVEQATKPSFESGRRGPPPPPRSRGPPRGLRGGRGGSGGTRGPPSRGGHMDDGGYSMNFNMSSSRGPLPVKRGPPPRSGGPPPKRSAPSGPVRSSSGMGGRAPVSRGRDSYGGPPRREPLPSRRDVYLSPRDDGYSTKDSYSSRDYPSSRDTRDYAPPPRDYTYRDYGHSSSRDDYPSRGYSDRDGYGRDRDYSDHPSGGSYRDSYESYGNSRSAPPTRGPPPSYGGSSRYDDYSSSRDGYGGSRDSYSSSRSDLYSSGRDRVGRQERGLPPSMERGYPPPRDSYSSSSRGAPRGGGRGGSRSDRGGGRSRY
"
misc_feature 211..213
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/experiment="experimental evidence, no additional details
recorded"
/note="N-acetylmethionine, in Heterogeneous nuclear
ribonucleoprotein G, alternate; propagated from
UniProtKB/Swiss-Prot (P38159.3); acetylation site"
misc_feature 214..216
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/experiment="experimental evidence, no additional details
recorded"
/note="N-acetylvaline, in Heterogeneous nuclear
ribonucleoprotein G, N-terminally processed; propagated
from UniProtKB/Swiss-Prot (P38159.3); acetylation site"
misc_feature 229..468
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/note="RNA recognition motif in heterogeneous nuclear
ribonucleoprotein G (hnRNP G), Y chromosome RNA
recognition motif 1 (hRBMY), testis-specific heterogeneous
nuclear ribonucleoprotein G-T (hnRNP G-T) and similar
proteins; Region: RRM_RBMX_like; cd12382"
/db_xref="CDD:240828"
misc_feature order(235..237,241..243,247..261,322..324,328..339,
343..363,367..369,442..444,448..450,454..468)
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/note="RNA binding site [nucleotide binding]; other site"
/db_xref="CDD:240828"
misc_feature <235..>465
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/note="RNA-binding proteins (RRM domain) [General function
prediction only]; Region: COG0724"
/db_xref="CDD:223796"
misc_feature 298..300
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/experiment="experimental evidence, no additional details
recorded"
/note="N6-acetyllysine; propagated from
UniProtKB/Swiss-Prot (P38159.3); acetylation site"
misc_feature 382..384
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 382..384
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 472..474
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P38159.3); phosphorylation site"
misc_feature 472..474
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 481..483
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 727..861
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/note="RBM1CTR (NUC064) family; Region: RBM1CTR;
pfam08081"
/db_xref="CDD:149260"
misc_feature 733..735
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 763..765
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/experiment="experimental evidence, no additional details
recorded"
/note="methylation site"
misc_feature 766..918
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (P38159.3);
Region: Necessary for the association to nascent RNAPII
transcripts and nuclear localization"
misc_feature 832..834
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 832..834
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1195..1197
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P38159.3); phosphorylation site"
misc_feature 1204..1206
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P38159.3); phosphorylation site"
misc_feature 1207..1383
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (P38159.3);
Region: Necessary for RNA-binding"
misc_feature 1264..1266
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P38159.3); phosphorylation site"
misc_feature 1264..1266
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
exon 320..426
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/inference="alignment:Splign:1.39.8"
exon 427..598
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/inference="alignment:Splign:1.39.8"
exon 599..751
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/inference="alignment:Splign:1.39.8"
variation 673
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/replace="c"
/replace="t"
/db_xref="dbSNP:11558422"
exon 752..866
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/inference="alignment:Splign:1.39.8"
variation 834
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056264"
exon 867..992
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/inference="alignment:Splign:1.39.8"
variation 962
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/replace="c"
/replace="t"
/db_xref="dbSNP:11556431"
exon 993..1075
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/inference="alignment:Splign:1.39.8"
variation 1018
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/replace="c"
/replace="t"
/db_xref="dbSNP:374604645"
exon 1076..2082
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/inference="alignment:Splign:1.39.8"
variation 1215
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/replace="a"
/replace="c"
/db_xref="dbSNP:16978599"
variation 1220
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/replace="a"
/replace="g"
/db_xref="dbSNP:35899675"
variation 1276
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/replace="g"
/replace="t"
/db_xref="dbSNP:35085326"
variation 1296
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/replace="c"
/replace="t"
/db_xref="dbSNP:34606958"
variation 1479
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/replace="a"
/replace="g"
/db_xref="dbSNP:15259"
variation 1536
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/replace="c"
/replace="t"
/db_xref="dbSNP:2230685"
STS 1666..2011
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/standard_name="DXS7491"
/db_xref="UniSTS:29985"
variation 1691
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/replace="c"
/replace="t"
/db_xref="dbSNP:850"
variation 1859
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/replace="c"
/replace="t"
/db_xref="dbSNP:849"
variation 2017
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
/replace="a"
/replace="t"
/db_xref="dbSNP:10147"
polyA_signal 2044..2049
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
polyA_site 2067
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
polyA_site 2082
/gene="RBMX"
/gene_synonym="hnRNP-G; HNRNPG; HNRPG; RBMXP1; RBMXRT;
RNMX"
ORIGIN
ggtccttcagcctcgttcccgggcagtataaagtttgctgtctcctttgttcgccctcgttgcgcagtagtgctagcggcttcgcggttcggtcctcgcacccggcagccgccactggtgctgagctgctaggaagcccctatcgccgagctcgttggagcttgaacccattgtcacccctccgactcaccggcccaaaaaaaaaaaaacatggttgaagcagatcgcccaggaaagctcttcattggtgggcttaatacggaaacaaatgagaaagctcttgaagcagtatttggcaaatatggacgaatagtggaagtactcttgatgaaagaccgtgaaaccaacaaatcaagaggatttgcttttgtcacctttgaaagcccagcagacgctaaggatgcagccagagacatgaatggaaagtcattagatggaaaagccatcaaggtggaacaagccaccaaaccatcatttgaaagtggtagacgtggaccgcctccacctccaagaagtagaggccctccaagaggtcttagaggtggaagaggaggaagtggaggaaccaggggacctccctcacggggaggacacatggatgacggtggatattccatgaattttaacatgagttcttccaggggaccactcccagtaaaaagaggaccaccaccaagaagtgggggtcctcctcctaagagatctgcaccttcaggaccagttcgcagtagcagtggaatgggaggaagagctcctgtatcacgtggaagagatagttatggaggtccacctcgaagggaaccgctgccctctcgtagagatgtttatttgtccccaagagatgatgggtattctactaaagacagctattcaagcagagattacccaagttctcgtgatactagagattatgcaccaccaccacgagattatacttaccgtgattatggtcattccagttcacgtgatgactatccatcaagaggatatagcgatagagatggatatggtcgtgatcgtgactattcagatcatccaagtggaggttcctacagagattcatatgagagttatggtaactcacgtagtgctccacctacacgagggcccccgccatcttatggtggaagcagtcgctatgatgattacagcagctcacgtgacggatatggtggaagtcgagacagttactcaagcagccgaagtgatctctactcaagtggtcgtgatcgggttggcagacaagaaagagggcttcccccttctatggaaagggggtaccctcctccacgtgattcctacagcagttcaagccgcggagcaccaagaggtggtggccgtggaggaagccgatctgatagagggggaggcagaagcagatactagaaacaaacaaaactttggaccaaaatcccagttcaaagaaacaaaaagtggaaactattctatcataactacccaaggactactaaaaggaaaaattgtgttactttttttaaattccctgttaagttcccctccataatttttatgttcttgtgaggaaaaaagtaaaacatgtttaattttatttgactttcgcattgcttttcaacaagcaaatgttaaatgtgttaagacttgtactagtgttgtaactttccaagtaaaagtatcccctaaaggccacttcctatctgatttttcccagcaaatgaggcaggcaattctaagatcttccacaaaacatctagccatctaaaatggagagatgaatcattctacctatacaaacaagctagctattagagggtggttggggtatgctactcataagatttcagggtgtcttccaactgaaatctcaatgttctcagtacgaaaaacctgaaatcacatgcctatgtaaggaaagtgctattcacccagtaaacccaaaaaagcaaatggataatgctggccattttgcctttctgacatttccttgggaatctgcaagaacctcccctttcccttcccccaataagaccatttaagtgtgtgttaaacaactacagaatactaaataaaaagtttggccaaaaccaaccatgaagctgcaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:27316 -> Molecular function: GO:0000166 [nucleotide binding] evidence: IEA
GeneID:27316 -> Molecular function: GO:0001047 [core promoter binding] evidence: IDA
GeneID:27316 -> Molecular function: GO:0003682 [chromatin binding] evidence: IDA
GeneID:27316 -> Molecular function: GO:0003723 [RNA binding] evidence: IDA
GeneID:27316 -> Molecular function: GO:0003723 [RNA binding] evidence: NAS
GeneID:27316 -> Molecular function: GO:0003729 [mRNA binding] evidence: IDA
GeneID:27316 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:27316 -> Biological process: GO:0000381 [regulation of alternative mRNA splicing, via spliceosome] evidence: IDA
GeneID:27316 -> Biological process: GO:0000398 [mRNA splicing, via spliceosome] evidence: IC
GeneID:27316 -> Biological process: GO:0000398 [mRNA splicing, via spliceosome] evidence: TAS
GeneID:27316 -> Biological process: GO:0006366 [transcription from RNA polymerase II promoter] evidence: IDA
GeneID:27316 -> Biological process: GO:0006509 [membrane protein ectodomain proteolysis] evidence: IDA
GeneID:27316 -> Biological process: GO:0008380 [RNA splicing] evidence: TAS
GeneID:27316 -> Biological process: GO:0010467 [gene expression] evidence: TAS
GeneID:27316 -> Biological process: GO:0045944 [positive regulation of transcription from RNA polymerase II promoter] evidence: IDA
GeneID:27316 -> Biological process: GO:0048025 [negative regulation of mRNA splicing, via spliceosome] evidence: ISS
GeneID:27316 -> Biological process: GO:0048026 [positive regulation of mRNA splicing, via spliceosome] evidence: ISS
GeneID:27316 -> Biological process: GO:0051260 [protein homooligomerization] evidence: ISS
GeneID:27316 -> Biological process: GO:0071347 [cellular response to interleukin-1] evidence: IDA
GeneID:27316 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
GeneID:27316 -> Cellular component: GO:0005654 [nucleoplasm] evidence: TAS
GeneID:27316 -> Cellular component: GO:0005719 [nuclear euchromatin] evidence: IDA
GeneID:27316 -> Cellular component: GO:0044530 [supraspliceosomal complex] evidence: IDA
GeneID:27316 -> Cellular component: GO:0070062 [extracellular vesicular exosome] evidence: IDA
GeneID:27316 -> Cellular component: GO:0071013 [catalytic step 2 spliceosome] evidence: IDA
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