Brain Transcriptome Database (BrainTx)
トランスクリプトームデータ
CD00609
http://metadb.riken.jp/db/BrainTx/TranscriptomeData/CD00609
CD00609(トランスクリプトームデータ)
ダウンロード
SPARQL
足あと
問い合わせ
URI表示モード
CD00609
トランスクリプトームデータ
遺伝子シンボル
http://metadb.riken.jp/db/BrainTx/geneSymbol
Ubr2
遺伝子名
http://metadb.riken.jp/db/BrainTx/geneName
ubiquitin protein ligase E3 component n-recognin 2
別名
http://metadb.riken.jp/db/BrainTx/alt_name
N-recognin-2
ubiquitin-protein ligase E3-alpha-2
ubiquitin-protein ligase E3-alpha-II
E3 ubiquitin-protein ligase UBR2
ubiquitin ligase E3 alpha-II
ubiquitin protein ligase E3 component n-recognin 2
別名略称
http://metadb.riken.jp/db/BrainTx/alt_symbol
E130209G04Rik
AI462103
mKIAA0349
9930021A08Rik
ENSMUSG00000043296
AW540746
NCBI遺伝子
http://metadb.riken.jp/db/BrainTx/NCBIGene
https://www.ncbi.nlm.nih.gov/gene/224826
MGI遺伝子
http://metadb.riken.jp/db/BrainTx/mgiGene
ubiquitin protein ligase E3 component n-recognin 2
http://metadb.riken.jp/db/mgi_rdf/MGI:1861099
BrainTx遺伝子
http://metadb.riken.jp/db/BrainTx/brainTxGene
脳発現画像
http://metadb.riken.jp/db/BrainTx/brainExpressionImage
時系列発現 (小脳)
http://metadb.riken.jp/db/BrainTx/brainExpression
脳発現特異性/組織別発現
http://metadb.riken.jp/db/BrainTx/brainSpecificity
BrainTx遺伝子カテゴリー
http://metadb.riken.jp/db/BrainTx/brainTxGeneCategory
NCBI Accession Number
http://metadb.riken.jp/db/BrainTx/NCBIAccessionNumber
https://www.ncbi.nlm.nih.gov/nuccore/NM_146078
https://www.ncbi.nlm.nih.gov/nuccore/NM_001177374
Ensembl 遺伝子
http://metadb.riken.jp/db/BrainTx/ensemblGene
http://asia.ensembl.org/Mus_musculus/Gene/Summary?g=ENSMUSG00000023977
UniGene 遺伝子
http://metadb.riken.jp/db/BrainTx/uniGene
https://www.ncbi.nlm.nih.gov/unigene/?term=Mm.28234
OMIM ID
http://metadb.riken.jp/db/BrainTx/omim
https://www.omim.org/entry/603434?search=603434&highlight=609134
PubMed ID (PMID)
http://rdf.ncbi.nlm.nih.gov/pubmed/
Yan. Ouyang, et.al., Loss of Ubr2, an E3 ubiquitin ligase, leads to chromosome fragility and impaired homologous recombinational repair., Mutation research, 2006, 596
http://rdf.ncbi.nlm.nih.gov/pubmed/16488448
Noriko. Okazaki, et.al., Prediction of the coding sequences of mouse homologues of KIAA gene: II. The complete nucleotide sequences of 400 mouse KIAA-homologous cDNAs identified by screening of terminal sequences of cDNA clones randomly sampled from size-fractionated libraries., DNA research : an international journal for rapid publication of reports on genes and genomes, 2003, 10
http://rdf.ncbi.nlm.nih.gov/pubmed/12693553
Y T. Kwon, et.al., Altered activity, social behavior, and spatial memory in mice lacking the NTAN1p amidase and the asparagine branch of the N-end rule pathway., Molecular and cellular biology, 2000, 20
http://rdf.ncbi.nlm.nih.gov/pubmed/10805755
Jee Young. An, et.al., UBR2 mediates transcriptional silencing during spermatogenesis via histone ubiquitination., Proceedings of the National Academy of Sciences of the United States of America, 2010, 107
http://rdf.ncbi.nlm.nih.gov/pubmed/20080676
Y T. Kwon, et.al., Construction and analysis of mouse strains lacking the ubiquitin ligase UBR1 (E3alpha) of the N-end rule pathway., Molecular and cellular biology, 2001, 21
http://rdf.ncbi.nlm.nih.gov/pubmed/11689692
Jee Young. An, et.al., Impaired neurogenesis and cardiovascular development in mice lacking the E3 ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway., Proceedings of the National Academy of Sciences of the United States of America, 2006, 103
http://rdf.ncbi.nlm.nih.gov/pubmed/16606826
Keith S. Kwak, et.al., Regulation of protein catabolism by muscle-specific and cytokine-inducible ubiquitin ligase E3alpha-II during cancer cachexia., Cancer research, 2004, 64
http://rdf.ncbi.nlm.nih.gov/pubmed/15548684
Martin. Zenker, et.al., Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome)., Nature genetics, 2005, 37
http://rdf.ncbi.nlm.nih.gov/pubmed/16311597
Yong Tae. Kwon, et.al., Female lethality and apoptosis of spermatocytes in mice lacking the UBR2 ubiquitin ligase of the N-end rule pathway., Molecular and cellular biology, 2003, 23
http://rdf.ncbi.nlm.nih.gov/pubmed/14585983
Gene Ontology
http://metadb.riken.jp/db/BrainTx/golink
chromatin silencing
http://purl.obolibrary.org/obo/GO_0006342
ligase activity
http://purl.obolibrary.org/obo/GO_0016874
cellular response to leucine
http://purl.obolibrary.org/obo/GO_0071233
spermatogenesis
http://purl.obolibrary.org/obo/GO_0007283
plasma membrane
http://purl.obolibrary.org/obo/GO_0005886
histone H2A ubiquitination
http://purl.obolibrary.org/obo/GO_0033522
chromatin
http://purl.obolibrary.org/obo/GO_0000785
metal ion binding
http://purl.obolibrary.org/obo/GO_0046872
zinc ion binding
http://purl.obolibrary.org/obo/GO_0008270
nucleus
http://purl.obolibrary.org/obo/GO_0005634
negative regulation of TOR signaling
http://purl.obolibrary.org/obo/GO_0032007
ubiquitin-dependent protein catabolic process
http://purl.obolibrary.org/obo/GO_0006511
leucine binding
http://purl.obolibrary.org/obo/GO_0070728
protein binding
http://purl.obolibrary.org/obo/GO_0005515
male meiosis I
http://purl.obolibrary.org/obo/GO_0007141
protein catabolic process
http://purl.obolibrary.org/obo/GO_0030163
ubiquitin ligase complex
http://purl.obolibrary.org/obo/GO_0000151
InterPro ID
http://metadb.riken.jp/db/BrainTx/interPro
KEGG Pathway ID
http://metadb.riken.jp/db/BrainTx/keggPathwayID
KEGG Pathway 名称
http://metadb.riken.jp/db/BrainTx/keggPathwayName
お問い合わせ
システムのお問い合わせ
画像
足跡