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2024-04-26 01:33:53, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_002431 1397 bp mRNA linear PRI 07-JUL-2013
DEFINITION Homo sapiens menage a trois homolog 1, cyclin H assembly factor
(Xenopus laevis) (MNAT1), transcript variant 1, mRNA.
ACCESSION NM_002431
VERSION NM_002431.3 GI:295789083
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 1397)
AUTHORS Kennedy,R.B., Ovsyannikova,I.G., Pankratz,V.S., Haralambieva,I.H.,
Vierkant,R.A. and Poland,G.A.
TITLE Genome-wide analysis of polymorphisms associated with cytokine
responses in smallpox vaccine recipients
JOURNAL Hum. Genet. 131 (9), 1403-1421 (2012)
PUBMED 22610502
REFERENCE 2 (bases 1 to 1397)
AUTHORS Briggs FB, Goldstein BA, McCauley JL, Zuvich RL, De Jager PL, Rioux
JD, Ivinson AJ, Compston A, Hafler DA, Hauser SL, Oksenberg JR,
Sawcer SJ, Pericak-Vance MA, Haines JL and Barcellos LF.
CONSRTM International Multiple Sclerosis Genetics Consortium
TITLE Variation within DNA repair pathway genes and risk of multiple
sclerosis
JOURNAL Am. J. Epidemiol. 172 (2), 217-224 (2010)
PUBMED 20522537
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 3 (bases 1 to 1397)
AUTHORS Wu,X., Spitz,M.R., Lee,J.J., Lippman,S.M., Ye,Y., Yang,H.,
Khuri,F.R., Kim,E., Gu,J., Lotan,R. and Hong,W.K.
TITLE Novel susceptibility loci for second primary tumors/recurrence in
head and neck cancer patients: large-scale evaluation of genetic
variants
JOURNAL Cancer Prev Res (Phila) 2 (7), 617-624 (2009)
PUBMED 19584075
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 4 (bases 1 to 1397)
AUTHORS Li,Y., Jin,G., Wang,H., Liu,H., Qian,J., Gu,S., Ma,H., Miao,R.,
Hu,Z., Sun,W., Wang,Y., Jin,L., Wei,Q., Shen,H., Huang,W. and Lu,D.
TITLE Polymorphisms of CAK genes and risk for lung cancer: a case-control
study in Chinese population
JOURNAL Lung Cancer 58 (2), 171-183 (2007)
PUBMED 17707548
REMARK GeneRIF: These results suggested that genetic variants in CAK
genes, Cdk7, cyclin H, MAT1, might modulate the risk of lung cancer
in a gene-gene interaction mode, which consist to the biochemical
interaction of corresponding proteins.
GeneRIF: Observational study of gene-disease association, gene-gene
interaction, and gene-environment interaction. (HuGE Navigator)
REFERENCE 5 (bases 1 to 1397)
AUTHORS Luo,P., Wang,A., Payne,K.J., Peng,H., Wang,J.G., Parrish,Y.K.,
Rogerio,J.W., Triche,T.J., He,Q. and Wu,L.
TITLE Intrinsic retinoic acid receptor alpha-cyclin-dependent
kinase-activating kinase signaling involves coordination of the
restricted proliferation and granulocytic differentiation of human
hematopoietic stem cells
JOURNAL Stem Cells 25 (10), 2628-2637 (2007)
PUBMED 17628022
REMARK GeneRIF: Retinoic-acid-induced RAR-CAK signaling events appear to
proceed intrinsically during granulocytic development of normal
primitive hematopoietic cells. ALDH-governed RA availability may
mediate this process by initiating RAR-CAK signaling.
REFERENCE 6 (bases 1 to 1397)
AUTHORS Aprelikova,O., Xiong,Y. and Liu,E.T.
TITLE Both p16 and p21 families of cyclin-dependent kinase (CDK)
inhibitors block the phosphorylation of cyclin-dependent kinases by
the CDK-activating kinase
JOURNAL J. Biol. Chem. 270 (31), 18195-18197 (1995)
PUBMED 7629134
REFERENCE 7 (bases 1 to 1397)
AUTHORS Desai,D., Wessling,H.C., Fisher,R.P. and Morgan,D.O.
TITLE Effects of phosphorylation by CAK on cyclin binding by CDC2 and
CDK2
JOURNAL Mol. Cell. Biol. 15 (1), 345-350 (1995)
PUBMED 7799941
REFERENCE 8 (bases 1 to 1397)
AUTHORS Le Goff,P., Montano,M.M., Schodin,D.J. and Katzenellenbogen,B.S.
TITLE Phosphorylation of the human estrogen receptor. Identification of
hormone-regulated sites and examination of their influence on
transcriptional activity
JOURNAL J. Biol. Chem. 269 (6), 4458-4466 (1994)
PUBMED 8308015
REFERENCE 9 (bases 1 to 1397)
AUTHORS Jacob,G.A., Luse,S.W. and Luse,D.S.
TITLE Abortive initiation is increased only for the weakest members of a
set of down mutants of the adenovirus 2 major late promoter
JOURNAL J. Biol. Chem. 266 (33), 22537-22544 (1991)
PUBMED 1939271
REFERENCE 10 (bases 1 to 1397)
AUTHORS Conaway,R.C. and Conaway,J.W.
TITLE ATP activates transcription initiation from promoters by RNA
polymerase II in a reversible step prior to RNA synthesis
JOURNAL J. Biol. Chem. 263 (6), 2962-2968 (1988)
PUBMED 2449431
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from CD701743.1 and BC000820.1.
On May 5, 2010 this sequence version replaced gi:49574512.
Summary: The protein encoded by this gene, along with cyclin H and
CDK7, forms the CDK-activating kinase (CAK) enzymatic complex. This
complex activates several cyclin-associated kinases and can also
associate with TFIIH to activate transcription by RNA polymerase
II. Two transcript variants encoding different isoforms have been
found for this gene. [provided by RefSeq, Sep 2011].
Transcript Variant: This variant (1) represents the longer
transcript and encodes the longer 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 :: BC000820.1, X92669.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025081, ERS025082 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-36 CD701743.1 18-53
37-1397 BC000820.1 16-1376
FEATURES Location/Qualifiers
source 1..1397
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="14"
/map="14q23"
gene 1..1397
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/note="menage a trois homolog 1, cyclin H assembly factor
(Xenopus laevis)"
/db_xref="GeneID:4331"
/db_xref="HGNC:7181"
/db_xref="HPRD:04042"
/db_xref="MIM:602659"
exon 1..211
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/inference="alignment:Splign:1.39.8"
variation 32
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="g"
/db_xref="dbSNP:149302953"
variation 96
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="g"
/db_xref="dbSNP:144521688"
variation 108
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201631440"
variation 117..118
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace=""
/replace="c"
/db_xref="dbSNP:372971676"
CDS 123..1052
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/note="isoform 1 is encoded by transcript variant 1;
menage a trois 1 (CAK assembly factor); cyclin G1
interacting protein; CDK-activating kinase assembly factor
MAT1; RING finger protein 66; RING finger protein MAT1;
CDK7/cyclin-H assembly factor; cyclin-G1-interacting
protein"
/codon_start=1
/product="CDK-activating kinase assembly factor MAT1
isoform 1"
/protein_id="NP_002422.1"
/db_xref="GI:4505225"
/db_xref="CCDS:CCDS9750.1"
/db_xref="GeneID:4331"
/db_xref="HGNC:7181"
/db_xref="HPRD:04042"
/db_xref="MIM:602659"
/translation="
MDDQGCPRCKTTKYRNPSLKLMVNVCGHTLCESCVDLLFVRGAGNCPECGTPLRKSNFRVQLFEDPTVDKEVEIRKKVLKIYNKREEDFPSLREYNDFLEEVEEIVFNLTNNVDLDNTKKKMEIYQKENKDVIQKNKLKLTREQEELEEALEVERQENEQRRLFIQKEEQLQQILKRKNKQAFLDELESSDLPVALLLAQHKDRSTQLEMQLEKPKPVKPVTFSTGIKMGQHISLAPIHKLEEALYEYQPLQIETYGPHVPELEMLGRLGYLNHVRAASPQDLAGGYTSSLACHRALQDAFSGLFWQPS
"
misc_feature 123..1049
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/note="CDK-activating kinase assembly factor MAT1; Region:
cdk7; TIGR00570"
/db_xref="CDD:129661"
misc_feature 138..281
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/note="RING-finger (Really Interesting New Gene) domain, a
specialized type of Zn-finger of 40 to 60 residues that
binds two atoms of zinc; defined by the 'cross-brace'
motif C-X2-C-X(9-39)-C-X(1-3)-
H-X(2-3)-(N/C/H)-X2-C-X(4-48)C-X2-C; probably involved
in...; Region: RING; cd00162"
/db_xref="CDD:29102"
misc_feature order(138..140,147..149,198..200,204..206,213..215,
222..224,258..260,267..269)
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/note="cross-brace motif; other site"
/db_xref="CDD:29102"
misc_feature 273..275
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphothreonine; propagated from
UniProtKB/Swiss-Prot (P51948.1); phosphorylation site"
misc_feature 546..605
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (P51948.1);
Region: UIM"
misc_feature 957..959
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P51948.1); phosphorylation site"
variation 124
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="t"
/db_xref="dbSNP:142747516"
variation 148
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200037170"
variation 176
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="t"
/db_xref="dbSNP:4151150"
variation 177
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2020891"
variation 183
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="g"
/db_xref="dbSNP:141089655"
variation 194
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="t"
/db_xref="dbSNP:370869313"
exon 212..364
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/inference="alignment:Splign:1.39.8"
variation 225
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="g"
/db_xref="dbSNP:149858892"
variation 240
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="g"
/replace="t"
/db_xref="dbSNP:79519204"
variation 260
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="t"
/db_xref="dbSNP:369837694"
variation 291
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201099092"
variation 344
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="t"
/db_xref="dbSNP:113043441"
exon 365..438
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/inference="alignment:Splign:1.39.8"
variation 372
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="c"
/db_xref="dbSNP:118051600"
variation 392
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="t"
/db_xref="dbSNP:369430026"
exon 439..542
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/inference="alignment:Splign:1.39.8"
variation 449
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="g"
/db_xref="dbSNP:148083759"
variation 453
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="c"
/db_xref="dbSNP:193166798"
variation 501
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201502849"
exon 543..683
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/inference="alignment:Splign:1.39.8"
variation 556
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="g"
/db_xref="dbSNP:150481557"
variation 585
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="t"
/db_xref="dbSNP:145803434"
variation 586
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="g"
/db_xref="dbSNP:373266719"
variation 646
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="g"
/replace="t"
/db_xref="dbSNP:199880102"
variation 648
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="g"
/db_xref="dbSNP:182013117"
variation 665
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="g"
/db_xref="dbSNP:138553416"
exon 684..809
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/inference="alignment:Splign:1.39.8"
variation 756
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="t"
/db_xref="dbSNP:368804790"
variation 776
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="g"
/db_xref="dbSNP:140312266"
variation 788
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="g"
/db_xref="dbSNP:143441995"
exon 810..931
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/inference="alignment:Splign:1.39.8"
variation 814
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="c"
/db_xref="dbSNP:374456541"
variation 815
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="g"
/db_xref="dbSNP:372780456"
variation 827
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="g"
/db_xref="dbSNP:188250258"
variation 838
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201138725"
variation 861
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="g"
/db_xref="dbSNP:76568192"
variation 865
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="c"
/db_xref="dbSNP:201141212"
variation 866
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="c"
/db_xref="dbSNP:200165574"
variation 930
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="g"
/db_xref="dbSNP:371843650"
exon 932..1383
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/inference="alignment:Splign:1.39.8"
variation 954
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="g"
/replace="t"
/db_xref="dbSNP:147991108"
variation 967
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="c"
/db_xref="dbSNP:35188899"
variation 993
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="g"
/db_xref="dbSNP:374997842"
variation 996
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201950562"
variation 1013
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="t"
/db_xref="dbSNP:141776858"
variation 1019
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="t"
/db_xref="dbSNP:113746860"
variation 1028
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="g"
/replace="t"
/db_xref="dbSNP:370014148"
STS 1066..1292
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/standard_name="RH69606"
/db_xref="UniSTS:30690"
variation 1071
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="t"
/db_xref="dbSNP:372625949"
variation 1102
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="t"
/db_xref="dbSNP:4151409"
variation 1115
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="t"
/db_xref="dbSNP:141991211"
STS 1133..1293
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/standard_name="RH47826"
/db_xref="UniSTS:66208"
STS 1135..1291
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/standard_name="RH70941"
/db_xref="UniSTS:50240"
STS 1135..1272
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/standard_name="RH70690"
/db_xref="UniSTS:50241"
variation 1135
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="g"
/db_xref="dbSNP:78104565"
variation 1152
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="t"
/db_xref="dbSNP:112869712"
variation 1241
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="c"
/db_xref="dbSNP:114206370"
variation 1273
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="c"
/replace="t"
/db_xref="dbSNP:182977132"
variation 1292
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="g"
/db_xref="dbSNP:14852"
variation 1313
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="c"
/db_xref="dbSNP:1051083"
variation 1344
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
/replace="a"
/replace="g"
/db_xref="dbSNP:4151410"
polyA_signal 1361..1366
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
polyA_site 1383
/gene="MNAT1"
/gene_synonym="CAP35; MAT1; RNF66; TFB3"
ORIGIN
gcgaagggaccgtctctgccaagcgcctgttggtaggaacctgcttggtcgcgtctgagggggcttgtaggtggctctggctgaaacaggcgcctgcgagagtctgtaggagggaaaccgccatggacgatcagggttgccctcggtgtaagaccaccaaatatcggaacccctccttgaagctgatggtgaatgtgtgcggacacactctctgtgaaagttgtgtagatttactgtttgtgagaggagctggaaactgccctgagtgtggtactccactcagaaagagcaacttcagggtacaactctttgaagatcccactgttgacaaggaggttgagatcaggaaaaaagtgctaaagatatacaataaaagggaagaagattttcctagtctaagagaatacaatgatttcttggaagaagtggaagaaattgttttcaacttgaccaacaatgtggatttggacaacaccaaaaagaaaatggagatataccaaaaggaaaacaaagatgttattcagaaaaataaattaaagctgactcgagaacaggaagaactggaagaagctttagaagtggaacgacaggaaaatgaacaaagaagattatttatacaaaaagaagaacaactgcagcagattctaaaaaggaagaataagcaggcttttttagatgagctggagagttctgatctccctgttgctctgcttttggctcagcataaagatagatctacccaattagaaatgcaacttgagaaacccaaacctgtaaaaccagtgacgttttccacaggcatcaaaatgggtcaacatatttcactggcacctattcacaagcttgaagaagctctgtatgaataccagccactgcagatagagacatatggaccacatgttcctgagcttgagatgctaggaagacttgggtatttaaaccatgtcagagctgcctcaccacaggaccttgctggaggctatacttcttctcttgcttgtcacagagcactacaggatgcattcagtgggcttttctggcagcccagttaaccatttataagatttggaccttggagctgaaccagggagctagcaaaagtaaagcagacttataaaattatagctatgtgcagctgcacaacacagtccttccactagcagctgtgttaaagtatttataaggagaaaatttcagaactaagttgagtaatataggggatatatatttgtgaaaaataatttttacttatatttttcagaggatttgacacgataagcctcatctgatggaagagaggaataaataattcacctatatgtgtttgaggttgtgacagacttataaaatctttttaaaaaataaagctataatttatattaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:4331 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:4331 -> Molecular function: GO:0008094 [DNA-dependent ATPase activity] evidence: IDA
GeneID:4331 -> Molecular function: GO:0008270 [zinc ion binding] evidence: IEA
GeneID:4331 -> Molecular function: GO:0008353 [RNA polymerase II carboxy-terminal domain kinase activity] evidence: IDA
GeneID:4331 -> Molecular function: GO:0047485 [protein N-terminus binding] evidence: IPI
GeneID:4331 -> Biological process: GO:0000079 [regulation of cyclin-dependent protein serine/threonine kinase activity] evidence: TAS
GeneID:4331 -> Biological process: GO:0000082 [G1/S transition of mitotic cell cycle] evidence: TAS
GeneID:4331 -> Biological process: GO:0000086 [G2/M transition of mitotic cell cycle] evidence: TAS
GeneID:4331 -> Biological process: GO:0000278 [mitotic cell cycle] evidence: TAS
GeneID:4331 -> Biological process: GO:0000718 [nucleotide-excision repair, DNA damage removal] evidence: TAS
GeneID:4331 -> Biological process: GO:0006281 [DNA repair] evidence: TAS
GeneID:4331 -> Biological process: GO:0006283 [transcription-coupled nucleotide-excision repair] evidence: TAS
GeneID:4331 -> Biological process: GO:0006289 [nucleotide-excision repair] evidence: TAS
GeneID:4331 -> Biological process: GO:0006357 [regulation of transcription from RNA polymerase II promoter] evidence: IDA
GeneID:4331 -> Biological process: GO:0006360 [transcription from RNA polymerase I promoter] evidence: TAS
GeneID:4331 -> Biological process: GO:0006361 [transcription initiation from RNA polymerase I promoter] evidence: TAS
GeneID:4331 -> Biological process: GO:0006362 [transcription elongation from RNA polymerase I promoter] evidence: TAS
GeneID:4331 -> Biological process: GO:0006363 [termination of RNA polymerase I transcription] evidence: TAS
GeneID:4331 -> Biological process: GO:0006366 [transcription from RNA polymerase II promoter] evidence: IDA
GeneID:4331 -> Biological process: GO:0006366 [transcription from RNA polymerase II promoter] evidence: TAS
GeneID:4331 -> Biological process: GO:0006367 [transcription initiation from RNA polymerase II promoter] evidence: TAS
GeneID:4331 -> Biological process: GO:0006368 [transcription elongation from RNA polymerase II promoter] evidence: TAS
GeneID:4331 -> Biological process: GO:0006370 [7-methylguanosine mRNA capping] evidence: TAS
GeneID:4331 -> Biological process: GO:0006461 [protein complex assembly] evidence: TAS
GeneID:4331 -> Biological process: GO:0006915 [apoptotic process] evidence: IEA
GeneID:4331 -> Biological process: GO:0007512 [adult heart development] evidence: IEA
GeneID:4331 -> Biological process: GO:0008283 [cell proliferation] evidence: TAS
GeneID:4331 -> Biological process: GO:0010467 [gene expression] evidence: TAS
GeneID:4331 -> Biological process: GO:0016032 [viral process] evidence: TAS
GeneID:4331 -> Biological process: GO:0021591 [ventricular system development] evidence: IEA
GeneID:4331 -> Biological process: GO:0043066 [negative regulation of apoptotic process] evidence: IEA
GeneID:4331 -> Biological process: GO:0044236 [multicellular organismal metabolic process] evidence: IEA
GeneID:4331 -> Biological process: GO:0045944 [positive regulation of transcription from RNA polymerase II promoter] evidence: IDA
GeneID:4331 -> Biological process: GO:0045944 [positive regulation of transcription from RNA polymerase II promoter] evidence: IMP
GeneID:4331 -> Biological process: GO:0048661 [positive regulation of smooth muscle cell proliferation] evidence: IEA
GeneID:4331 -> Biological process: GO:0050434 [positive regulation of viral transcription] evidence: TAS
GeneID:4331 -> Biological process: GO:0051592 [response to calcium ion] evidence: IEA
GeneID:4331 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
GeneID:4331 -> Cellular component: GO:0005654 [nucleoplasm] evidence: TAS
GeneID:4331 -> Cellular component: GO:0005675 [holo TFIIH complex] evidence: IDA
GeneID:4331 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
GeneID:4331 -> Cellular component: GO:0043231 [intracellular membrane-bounded organelle] evidence: IDA
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DBCLS
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