Brain Transcriptome Database (BrainTx)
トランスクリプトームデータ
CD00881
http://metadb.riken.jp/db/BrainTx/TranscriptomeData/CD00881
CD00881(トランスクリプトームデータ)
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CD00881
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
Tbl2
遺伝子名
http://metadb.riken.jp/db/BrainTx/geneName
transducin (beta)-like 2
別名
http://metadb.riken.jp/db/BrainTx/alt_name
transducin beta-like protein 2
transducin (beta)-like 2
別名略称
http://metadb.riken.jp/db/BrainTx/alt_symbol
C76179
WS-bTRP
NCBI遺伝子
http://metadb.riken.jp/db/BrainTx/NCBIGene
https://www.ncbi.nlm.nih.gov/gene/27368
MGI遺伝子
http://metadb.riken.jp/db/BrainTx/mgiGene
transducin (beta)-like 2
http://metadb.riken.jp/db/mgi_rdf/MGI:1351652
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_013763
Ensembl 遺伝子
http://metadb.riken.jp/db/BrainTx/ensemblGene
http://asia.ensembl.org/Mus_musculus/Gene/Summary?g=ENSMUSG00000005374
UniGene 遺伝子
http://metadb.riken.jp/db/BrainTx/uniGene
https://www.ncbi.nlm.nih.gov/unigene/?term=Mm.441276
https://www.ncbi.nlm.nih.gov/unigene/?term=Mm.36746
OMIM ID
http://metadb.riken.jp/db/BrainTx/omim
https://www.omim.org/entry/603434?search=603434&highlight=605842
PubMed ID (PMID)
http://rdf.ncbi.nlm.nih.gov/pubmed/
Doug. Stryke, et.al., BayGenomics: a resource of insertional mutations in mouse embryonic stem cells., Nucleic acids research, 2003, 31
http://rdf.ncbi.nlm.nih.gov/pubmed/12520002
L A. Pérez Jurado, et.al., TBL2, a novel transducin family member in the WBS deletion: characterization of the complete sequence, genomic structure, transcriptional variants and the mouse ortholog., Cytogenetics and cell genetics, 1999, 86
http://rdf.ncbi.nlm.nih.gov/pubmed/10575226
M C. Valero, et.al., Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s)., Genomics, 2000, 69
http://rdf.ncbi.nlm.nih.gov/pubmed/11013070
O. de Luis, et.al., WBSCR14, a putative transcription factor gene deleted in Williams-Beuren syndrome: complete characterisation of the human gene and the mouse ortholog., European journal of human genetics : EJHG, 2000, 8
http://rdf.ncbi.nlm.nih.gov/pubmed/10780788
Graciana. Diez-Roux, et.al., A high-resolution anatomical atlas of the transcriptome in the mouse embryo., PLoS biology, 2011, 9
http://rdf.ncbi.nlm.nih.gov/pubmed/21267068
Gilda. Cobellis, et.al., Tagging genes with cassette-exchange sites., Nucleic acids research, 2005, 33
http://rdf.ncbi.nlm.nih.gov/pubmed/15741177
Udaya. DeSilva, et.al., Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome., Genome research, 2002, 12
http://rdf.ncbi.nlm.nih.gov/pubmed/11779826
Gene Ontology
http://metadb.riken.jp/db/BrainTx/golink
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
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