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2024-04-19 23:21:43, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001127582 1461 bp mRNA linear PRI 02-JUN-2013
DEFINITION Homo sapiens inhibitor of growth family, member 4 (ING4),
transcript variant 9, mRNA.
ACCESSION NM_001127582
VERSION NM_001127582.1 GI:189083820
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 1461)
AUTHORS Zeng,Z.L., Li,F.J., Gao,F., Sun,D.S. and Yao,L.
TITLE Upregulation of miR-650 is correlated with down-regulation of ING4
and progression of hepatocellular carcinoma
JOURNAL J Surg Oncol 107 (2), 105-110 (2013)
PUBMED 22767438
REMARK GeneRIF: Data suggested that miR-650 is correlated with the
pathogenesis of hepatocellular carcinoma (HCC) and is involved in
the HCC tumorigenesis process by inhibiting the expression of ING4.
REFERENCE 2 (bases 1 to 1461)
AUTHORS Lou,C., Jiang,S., Guo,X. and Dong,X.S.
TITLE ING4 is negatively correlated with microvessel density in colon
cancer
JOURNAL Tumour Biol. 33 (6), 2357-2364 (2012)
PUBMED 23055189
REMARK GeneRIF: Loss of ING4 expression is associated with lymphatic
metastasis in colon cancer.
REFERENCE 3 (bases 1 to 1461)
AUTHORS Zhang,L., Wang,Y., Zhang,F., Wang,Y. and Zhang,Q.
TITLE Correlation between tumor suppressor inhibitor of growth family
member 4 expression and microvessel density in breast cancer
JOURNAL Hum. Pathol. 43 (10), 1611-1617 (2012)
PUBMED 22436625
REMARK GeneRIF: Inhibitor of growth 4 may represent an important biomarker
for assessing the severity of breast cancer
REFERENCE 4 (bases 1 to 1461)
AUTHORS Tzouvelekis,A., Ntolios,P., Karameris,A., Koutsopoulos,A.,
Boglou,P., Koulelidis,A., Archontogeorgis,K., Zacharis,G.,
Drakopanagiotakis,F., Steiropoulos,P., Anevlavis,S.,
Polychronopoulos,V., Mikroulis,D. and Bouros,D.
TITLE Expression of hypoxia-inducible factor (HIF)-1a-vascular
endothelial growth factor (VEGF)-inhibitory growth factor (ING)-4-
axis in sarcoidosis patients
JOURNAL BMC Res Notes 5, 654 (2012)
PUBMED 23181555
REMARK GeneRIF: Report up-regulation of ING4 expression in sarcoid
granulomas.
Publication Status: Online-Only
REFERENCE 5 (bases 1 to 1461)
AUTHORS Byron,S.A., Min,E., Thal,T.S., Hostetter,G., Watanabe,A.T.,
Azorsa,D.O., Little,T.H., Tapia,C. and Kim,S.
TITLE Negative regulation of NF-kappaB by the ING4 tumor suppressor in
breast cancer
JOURNAL PLoS ONE 7 (10), E46823 (2012)
PUBMED 23056468
REMARK GeneRIF: ING4 negatively regulates NF-kappaB in breast cancer
REFERENCE 6 (bases 1 to 1461)
AUTHORS Raho,G., Miranda,C., Tamborini,E., Pierotti,M.A. and Greco,A.
TITLE Detection of novel mRNA splice variants of human ING4 tumor
suppressor gene
JOURNAL Oncogene 26 (36), 5247-5257 (2007)
PUBMED 17325660
REMARK GeneRIF: data suggest that alternative splicing could modulate the
activity of ING4 tumor suppressor protein
REFERENCE 7 (bases 1 to 1461)
AUTHORS Zhang,X., Xu,L.S., Wang,Z.Q., Wang,K.S., Li,N., Cheng,Z.H.,
Huang,S.Z., Wei,D.Z. and Han,Z.G.
TITLE ING4 induces G2/M cell cycle arrest and enhances the
chemosensitivity to DNA-damage agents in HepG2 cells
JOURNAL FEBS Lett. 570 (1-3), 7-12 (2004)
PUBMED 15251430
REMARK GeneRIF: ING4 induces G2/M cell cycle arrest and enhances the
chemosensitivity to DNA-damage agents in HepG2 cells
REFERENCE 8 (bases 1 to 1461)
AUTHORS Garkavtsev,I., Kozin,S.V., Chernova,O., Xu,L., Winkler,F.,
Brown,E., Barnett,G.H. and Jain,R.K.
TITLE The candidate tumour suppressor protein ING4 regulates brain tumour
growth and angiogenesis
JOURNAL Nature 428 (6980), 328-332 (2004)
PUBMED 15029197
REMARK GeneRIF: In mice, xenografts of human glioblastoma U87MG, which has
decreased expression of ING4, grow significantly faster and have
higher vascular volume fractions than control tumours
REFERENCE 9 (bases 1 to 1461)
AUTHORS Shiseki,M., Nagashima,M., Pedeux,R.M., Kitahama-Shiseki,M.,
Miura,K., Okamura,S., Onogi,H., Higashimoto,Y., Appella,E.,
Yokota,J. and Harris,C.C.
TITLE p29ING4 and p28ING5 bind to p53 and p300, and enhance p53 activity
JOURNAL Cancer Res. 63 (10), 2373-2378 (2003)
PUBMED 12750254
REMARK GeneRIF: p29ING4 and p28ING5 may be significant modulators of p53
function.
REFERENCE 10 (bases 1 to 1461)
AUTHORS Hu,R.M., Han,Z.G., Song,H.D., Peng,Y.D., Huang,Q.H., Ren,S.X.,
Gu,Y.J., Huang,C.H., Li,Y.B., Jiang,C.L., Fu,G., Zhang,Q.H.,
Gu,B.W., Dai,M., Mao,Y.F., Gao,G.F., Rong,R., Ye,M., Zhou,J.,
Xu,S.H., Gu,J., Shi,J.X., Jin,W.R., Zhang,C.K., Wu,T.M.,
Huang,G.Y., Chen,Z., Chen,M.D. and Chen,J.L.
TITLE Gene expression profiling in the human
hypothalamus-pituitary-adrenal axis and full-length cDNA cloning
JOURNAL Proc. Natl. Acad. Sci. U.S.A. 97 (17), 9543-9548 (2000)
PUBMED 10931946
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from BP303219.1, AF156552.1 and
AW614868.1.
Summary: This gene encodes a tumor suppressor protein that contains
a PHD-finger, which is a common motif in proteins involved in
chromatin remodeling. This protein can bind TP53 and EP300/p300, a
component of the histone acetyl transferase complex, suggesting its
involvement in the TP53-dependent regulatory pathway. Multiple
alternatively spliced transcript variants have been observed that
encode distinct proteins. [provided by RefSeq, Jul 2008].
Transcript Variant: This variant (9) represents the longest
transcript and it encodes the longest protein (isoform 9). Another
name for this variant is ING4_v1.
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 :: AF156552.1, AF110645.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025084 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-24 BP303219.1 1-24
25-1395 AF156552.1 1-1371
1396-1461 AW614868.1 1-66 c
FEATURES Location/Qualifiers
source 1..1461
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="12"
/map="12p13.31"
gene 1..1461
/gene="ING4"
/gene_synonym="my036; p29ING4"
/note="inhibitor of growth family, member 4"
/db_xref="GeneID:51147"
/db_xref="HGNC:19423"
/db_xref="MIM:608524"
exon 1..78
/gene="ING4"
/gene_synonym="my036; p29ING4"
/inference="alignment:Splign:1.39.8"
variation complement(6)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="c"
/replace="t"
/db_xref="dbSNP:374390006"
variation complement(26)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="c"
/replace="t"
/db_xref="dbSNP:199768855"
CDS 42..791
/gene="ING4"
/gene_synonym="my036; p29ING4"
/note="isoform 9 is encoded by transcript variant 9;
candidate tumor suppressor p33 ING1 homolog; brain my036
protein; inhibitor of growth protein 4"
/codon_start=1
/product="inhibitor of growth protein 4 isoform 9"
/protein_id="NP_001121054.1"
/db_xref="GI:189083821"
/db_xref="CCDS:CCDS44813.1"
/db_xref="GeneID:51147"
/db_xref="HGNC:19423"
/db_xref="MIM:608524"
/translation="
MAAGMYLEHYLDSIENLPFELQRNFQLMRDLDQRTEDLKAEIDKLATEYMSSARSLSSEEKLALLKQIQEAYGKCKEFGDDKVQLAMQTYEMVDKHIRRLDTDLARFEADLKEKQIESSDYDSSSSKGKKKGRTQKEKKAARARSKGKNSDEEAPKTAQKKLKLVRTSPEYGMPSVTFGSVHPSDVLDMPVDPNEPTYCLCHQVSYGEMIGCDNPDCSIEWFHFACVGLTTKPRGKWFCPRCSQERKKK
"
misc_feature 54..362
/gene="ING4"
/gene_synonym="my036; p29ING4"
/note="Inhibitor of growth proteins N-terminal
histone-binding; Region: ING; pfam12998"
/db_xref="CDD:205182"
misc_feature 60..776
/gene="ING4"
/gene_synonym="my036; p29ING4"
/note="Chromatin remodeling protein, contains PhD zinc
finger [Chromatin structure and dynamics]; Region: TNG2;
COG5034"
/db_xref="CDD:34639"
misc_feature 375..377
/gene="ING4"
/gene_synonym="my036; p29ING4"
/experiment="experimental evidence, no additional details
recorded"
/note="N6-acetyllysine; propagated from
UniProtKB/Swiss-Prot (Q9UNL4.1); acetylation site"
misc_feature 420..485
/gene="ING4"
/gene_synonym="my036; p29ING4"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9UNL4.1);
Region: Bipartite nuclear localization signal"
misc_feature 420..422
/gene="ING4"
/gene_synonym="my036; p29ING4"
/experiment="experimental evidence, no additional details
recorded"
/note="N6-acetyllysine; propagated from
UniProtKB/Swiss-Prot (Q9UNL4.1); acetylation site"
misc_feature 426..428
/gene="ING4"
/gene_synonym="my036; p29ING4"
/experiment="experimental evidence, no additional details
recorded"
/note="N6-acetyllysine; propagated from
UniProtKB/Swiss-Prot (Q9UNL4.1); acetylation site"
misc_feature 438..440
/gene="ING4"
/gene_synonym="my036; p29ING4"
/experiment="experimental evidence, no additional details
recorded"
/note="Citrulline; propagated from UniProtKB/Swiss-Prot
(Q9UNL4.1); modified site"
misc_feature 477..479
/gene="ING4"
/gene_synonym="my036; p29ING4"
/experiment="experimental evidence, no additional details
recorded"
/note="N6-acetyllysine; propagated from
UniProtKB/Swiss-Prot (Q9UNL4.1); acetylation site"
misc_feature 483..485
/gene="ING4"
/gene_synonym="my036; p29ING4"
/experiment="experimental evidence, no additional details
recorded"
/note="N6-acetyllysine; propagated from
UniProtKB/Swiss-Prot (Q9UNL4.1); acetylation site"
misc_feature 507..509
/gene="ING4"
/gene_synonym="my036; p29ING4"
/experiment="experimental evidence, no additional details
recorded"
/note="N6-acetyllysine; propagated from
UniProtKB/Swiss-Prot (Q9UNL4.1); acetylation site"
misc_feature 537..539
/gene="ING4"
/gene_synonym="my036; p29ING4"
/experiment="experimental evidence, no additional details
recorded"
/note="Citrulline; propagated from UniProtKB/Swiss-Prot
(Q9UNL4.1); modified site"
misc_feature 633..776
/gene="ING4"
/gene_synonym="my036; p29ING4"
/note="PHD-finger; Region: PHD; pfam00628"
/db_xref="CDD:201356"
variation complement(50)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="g"
/db_xref="dbSNP:147493061"
variation complement(56)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="g"
/db_xref="dbSNP:190900185"
variation complement(68)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="c"
/replace="t"
/db_xref="dbSNP:143202414"
variation complement(70)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="t"
/db_xref="dbSNP:371180258"
variation complement(78)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="t"
/db_xref="dbSNP:376965069"
exon 79..150
/gene="ING4"
/gene_synonym="my036; p29ING4"
/inference="alignment:Splign:1.39.8"
variation complement(117)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="c"
/replace="g"
/db_xref="dbSNP:140970573"
exon 151..317
/gene="ING4"
/gene_synonym="my036; p29ING4"
/inference="alignment:Splign:1.39.8"
variation complement(199)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="c"
/replace="t"
/db_xref="dbSNP:144340616"
variation complement(202)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="g"
/db_xref="dbSNP:371595694"
variation complement(213)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="c"
/replace="t"
/db_xref="dbSNP:139185675"
variation complement(224)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="c"
/db_xref="dbSNP:201959427"
exon 318..432
/gene="ING4"
/gene_synonym="my036; p29ING4"
/inference="alignment:Splign:1.39.8"
variation 367
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="c"
/db_xref="dbSNP:193921122"
variation complement(397)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="g"
/db_xref="dbSNP:11551179"
variation complement(403)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="g"
/db_xref="dbSNP:374543463"
exon 433..541
/gene="ING4"
/gene_synonym="my036; p29ING4"
/inference="alignment:Splign:1.39.8"
variation complement(439)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="g"
/db_xref="dbSNP:374663258"
variation complement(466)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="g"
/db_xref="dbSNP:371095155"
variation complement(472)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="g"
/db_xref="dbSNP:149630308"
variation complement(476)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="c"
/replace="t"
/db_xref="dbSNP:117012163"
variation complement(491)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="g"
/db_xref="dbSNP:201626425"
variation complement(501)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="g"
/db_xref="dbSNP:150080565"
variation complement(534)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="g"
/db_xref="dbSNP:186742663"
variation complement(535)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="g"
/replace="t"
/db_xref="dbSNP:113932069"
variation complement(541)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="c"
/replace="t"
/db_xref="dbSNP:142380796"
exon 542..689
/gene="ING4"
/gene_synonym="my036; p29ING4"
/inference="alignment:Splign:1.39.8"
variation complement(557)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="g"
/replace="t"
/db_xref="dbSNP:371654809"
variation complement(563)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="c"
/replace="t"
/db_xref="dbSNP:146347929"
variation complement(645..646)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace=""
/replace="g"
/db_xref="dbSNP:11426491"
variation complement(650)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="g"
/replace="t"
/db_xref="dbSNP:369007352"
variation complement(681)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="g"
/db_xref="dbSNP:201257362"
variation complement(689)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="c"
/replace="t"
/db_xref="dbSNP:77283008"
exon 690..751
/gene="ING4"
/gene_synonym="my036; p29ING4"
/inference="alignment:Splign:1.39.8"
variation complement(695)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="c"
/replace="t"
/db_xref="dbSNP:371902029"
variation complement(698)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="c"
/replace="t"
/db_xref="dbSNP:140339044"
variation complement(720)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="g"
/db_xref="dbSNP:139075674"
exon 752..1448
/gene="ING4"
/gene_synonym="my036; p29ING4"
/inference="alignment:Splign:1.39.8"
STS 774..1420
/gene="ING4"
/gene_synonym="my036; p29ING4"
/standard_name="ING4_9672"
/db_xref="UniSTS:468482"
variation complement(777)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="c"
/replace="t"
/db_xref="dbSNP:199800012"
variation complement(785)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="g"
/db_xref="dbSNP:76327967"
variation complement(843)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="t"
/db_xref="dbSNP:369960359"
variation complement(863)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="g"
/db_xref="dbSNP:373140860"
STS 1034..1308
/gene="ING4"
/gene_synonym="my036; p29ING4"
/standard_name="WI-19753"
/db_xref="UniSTS:66995"
variation complement(1059)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="g"
/db_xref="dbSNP:76290581"
STS 1091..1320
/gene="ING4"
/gene_synonym="my036; p29ING4"
/standard_name="RH11183"
/db_xref="UniSTS:66445"
variation complement(1094)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="c"
/db_xref="dbSNP:184942338"
STS 1107..1364
/gene="ING4"
/gene_synonym="my036; p29ING4"
/standard_name="A001T24"
/db_xref="UniSTS:59161"
STS 1107..1364
/gene="ING4"
/gene_synonym="my036; p29ING4"
/standard_name="G19629"
/db_xref="UniSTS:59160"
variation complement(1158)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="c"
/replace="g"
/db_xref="dbSNP:114082659"
variation complement(1182)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="t"
/db_xref="dbSNP:150675992"
variation complement(1214)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="a"
/replace="g"
/db_xref="dbSNP:14542"
variation complement(1218)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="c"
/replace="t"
/db_xref="dbSNP:145532274"
variation complement(1258)
/gene="ING4"
/gene_synonym="my036; p29ING4"
/replace="c"
/replace="g"
/db_xref="dbSNP:376640690"
polyA_signal 1376..1381
/gene="ING4"
/gene_synonym="my036; p29ING4"
polyA_site 1395
/gene="ING4"
/gene_synonym="my036; p29ING4"
ORIGIN
acttccggggcggatcggaagttgctttgttttgcttcgagatggctgcggggatgtatttggaacattatctggacagtattgaaaaccttccctttgaattacagagaaactttcagctcatgagggacctagaccaaagaacagaggacctgaaggctgaaattgacaagttggccactgagtatatgagtagtgcccgcagcctgagctccgaggaaaaattggcccttctcaaacagatccaggaagcctatggcaagtgcaaggaatttggtgacgacaaggtgcagcttgccatgcagacctatgagatggtggacaaacacattcggcggctggacacagacctggcccgttttgaggctgatctcaaggagaaacagattgagtcaagtgactatgacagctcttccagcaaaggcaaaaagaaaggccggactcaaaaggagaagaaagctgctcgtgctcgttccaaagggaaaaactcggatgaagaagcccccaagactgcccagaagaagttaaagctcgtgcgcacaagtcctgagtatgggatgccctcagtgacctttggcagtgtccacccctctgatgtgttggatatgcctgtggatcccaacgaacccacctattgcctttgtcaccaggtctcctatggagagatgattggctgtgacaaccctgattgttccattgagtggttccattttgcctgtgtggggctgacaaccaagcctcgggggaaatggttttgcccacgctgctcccaagaacggaagaagaaatagataagggccttggattccaacacagtttcttccacatcccctgacttgggctagtgggcagaggaatgcctgtgctggggccaggggttcagggaggagtggatggcacagtgctgtcatcccttctcctcccctctccccactcccggtgctgaggctgcatcagaccctggtagggaggggtgccgcagccactaacggtatgtgctctccttcagccctctcccttcggagggacgtggtcttgcccactgtccttttgcctccatgctgaggtcggtgctgtatttcagagggagggtccttttcattctccttgctttgtatttaaggactggggcatagcatgggggcagtcccccagacctcttcattccccctcctgtggtgagggctaggtgtgatcaacacttttcttctccattcccttcctgcttttttcatggtgggggatccaccaggtcatctaggctctggccctagttgaaggggcaccccttcctctgtgccaagaggattcatcctgggagagggggcaaggtggaatgcagataactcacatgtaaaaggaacttgggtaggtaaataaaagctatacatgttggcctgctgtgtttattgtagagacactgttttagtaaacatgctgagcattcaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:51147 -> Molecular function: GO:0003713 [transcription coactivator activity] evidence: IDA
GeneID:51147 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:51147 -> Molecular function: GO:0008270 [zinc ion binding] evidence: IEA
GeneID:51147 -> Molecular function: GO:0035064 [methylated histone residue binding] evidence: IDA
GeneID:51147 -> Biological process: GO:0006260 [DNA replication] evidence: IDA
GeneID:51147 -> Biological process: GO:0006473 [protein acetylation] evidence: IDA
GeneID:51147 -> Biological process: GO:0006915 [apoptotic process] evidence: IDA
GeneID:51147 -> Biological process: GO:0006978 [DNA damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediator] evidence: IDA
GeneID:51147 -> Biological process: GO:0007050 [cell cycle arrest] evidence: IDA
GeneID:51147 -> Biological process: GO:0008285 [negative regulation of cell proliferation] evidence: IDA
GeneID:51147 -> Biological process: GO:0043065 [positive regulation of apoptotic process] evidence: IDA
GeneID:51147 -> Biological process: GO:0043966 [histone H3 acetylation] evidence: IDA
GeneID:51147 -> Biological process: GO:0043981 [histone H4-K5 acetylation] evidence: IDA
GeneID:51147 -> Biological process: GO:0043982 [histone H4-K8 acetylation] evidence: IDA
GeneID:51147 -> Biological process: GO:0043983 [histone H4-K12 acetylation] evidence: IDA
GeneID:51147 -> Biological process: GO:0043984 [histone H4-K16 acetylation] evidence: IDA
GeneID:51147 -> Biological process: GO:0045892 [negative regulation of transcription, DNA-dependent] evidence: IDA
GeneID:51147 -> Biological process: GO:0045926 [negative regulation of growth] evidence: IDA
GeneID:51147 -> Cellular component: GO:0000123 [histone acetyltransferase complex] evidence: IDA
GeneID:51147 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
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