CD18777

http://metadb.riken.jp/db/BrainTx/TranscriptomeData/CD18777

CD18777

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

• Dfna5

遺伝子名

http://metadb.riken.jp/db/BrainTx/geneName

• deafness, autosomal dominant 5 (human)

別名

http://metadb.riken.jp/db/BrainTx/alt_name

• deafness, autosomal dominant 5 (human)
• deafness, autosomal dominant 5 homolog
• nonsyndromic hearing impairment protein
• non-syndromic hearing impairment protein 5 homolog

別名略称

http://metadb.riken.jp/db/BrainTx/alt_symbol

• Fin15
• EG14210
• 4932441K13Rik
• Dfna5h
• 2310037D07Rik

NCBI遺伝子

http://metadb.riken.jp/db/BrainTx/NCBIGene

• https://www.ncbi.nlm.nih.gov/gene/54722

MGI遺伝子

http://metadb.riken.jp/db/BrainTx/mgiGene

• deafness, autosomal dominant 5 (human)
  http://metadb.riken.jp/db/mgi_rdf/MGI:1889850

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_018769

Ensembl 遺伝子

http://metadb.riken.jp/db/BrainTx/ensemblGene

• http://asia.ensembl.org/Mus_musculus/Gene/Summary?g=ENSMUSG00000029821

UniGene 遺伝子

http://metadb.riken.jp/db/BrainTx/uniGene

• https://www.ncbi.nlm.nih.gov/unigene/?term=Mm.248361

OMIM ID

http://metadb.riken.jp/db/BrainTx/omim

• https://www.omim.org/entry/603434?search=603434&highlight=608798

PubMed ID (PMID)

http://rdf.ncbi.nlm.nih.gov/pubmed/

• Lut. Van Laer, et.al., Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cells., Neurobiology of disease, 2005, 19
  http://rdf.ncbi.nlm.nih.gov/pubmed/16023581
• M A. Guthridge, et.al., Induction of expression of growth-related genes by FGF-4 in mouse fibroblasts., Oncogene, 1996, 12
  http://rdf.ncbi.nlm.nih.gov/pubmed/8649829
• Sedigheh. Delmaghani, et.al., Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy., Nature genetics, 2006, 38
  http://rdf.ncbi.nlm.nih.gov/pubmed/16804542
• Y. Maeda, et.al., Quantification of TECTA and DFNA5 expression in the developing mouse cochlea., Neuroreport, 2001, 12
  http://rdf.ncbi.nlm.nih.gov/pubmed/11711860
• L. Van Laer, et.al., Nonsyndromic hearing impairment is associated with a mutation in DFNA5., Nature genetics, 1998, 20
  http://rdf.ncbi.nlm.nih.gov/pubmed/9771715
• Susan. Magdaleno, et.al., BGEM: an in situ hybridization database of gene expression in the embryonic and adult mouse nervous system., PLoS biology, 2006, 4
  http://rdf.ncbi.nlm.nih.gov/pubmed/16602821
• Karen. Vrijens, et.al., Characterization of the murine Dfna5 promoter and regulatory regions., Gene, 2009, 432
  http://rdf.ncbi.nlm.nih.gov/pubmed/19095048
• 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
• Yoshiko. Masuda, et.al., The potential role of DFNA5, a hearing impairment gene, in p53-mediated cellular response to DNA damage., Journal of human genetics, 2006, 51
  http://rdf.ncbi.nlm.nih.gov/pubmed/16897187

Gene Ontology

http://metadb.riken.jp/db/BrainTx/golink

• inner ear receptor cell differentiation
  http://purl.obolibrary.org/obo/GO_0060113
• sensory perception of sound
  http://purl.obolibrary.org/obo/GO_0007605

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