H. Yanagisawa, et.al., Dual genetic pathways of endothelin-mediated intercellular signaling revealed by targeted disruption of endothelin converting enzyme-1 gene., Development (Cambridge, England), 1998, 125

http://rdf.ncbi.nlm.nih.gov/pubmed/9449665

H. Yanagisawa, et.al., Dual genetic pathways of endothelin-mediated intercellular signaling revealed by targeted disruption of endothelin converting enzyme-1 gene., Development (Cambridge, England), 1998, 125

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

トランスクリプトームデータ

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

• CD14251
  http://metadb.riken.jp/db/BrainTx/TranscriptomeData/CD14251

allele

http://purl.org/net/cito/citesAsAuthority

• Ece1<tm1Reh>
  http://metadb.riken.jp/db/mgi_rdf/MGI:2158947

表現型アノテーション

http://purl.org/net/cito/citesAsAuthority

• abnormal epidermal melanocyte morphology_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0009388I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• abnormal choroid melanocyte morphology_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0010191I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• abnormal artery morphology_Ednra<tm1Ywa>/Ednra<tm1Ywa>,Ednrb<tm1Ywa>/Ednrb<tm1Ywa>
  http://metadb.riken.jp/0002191I129SSvEvEdnratm1YwaEdnratm1YwaEdnrbtm1YwaEdnrbtm1YwaEdnratm1YwaEdnrbtm1Ywa
• palatine bone hypoplasia_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0004475I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• abnormal squamosal bone morphology_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0004423I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• thyroid hypoplasia_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0003499I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• absent enteric neurons_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0001048I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• embryonic lethality during organogenesis, incomplete penetrance_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0011108I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• absent middle ear ossicles_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0000040I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• abnormal styloid process morphology_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0008023I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• abnormal submandibular duct morphology_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0009525I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• absent tympanic ring_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0003138I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• absent incus_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0004318I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• hydrops fetalis_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0002192I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• absent stapes_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0004204I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• enlarged heart_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0000274I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• parathyroid hypoplasia_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0003494I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• absent right subclavian artery_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0010486I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• absent tongue_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0009905I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• overriding aortic valve_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0000273I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• absent Meckel's cartilage_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0004439I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• double outlet right ventricle_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0000284I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• embryonic lethality during organogenesis, incomplete penetrance_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0011108I129S6SvEvTacEce1tm1RehEce1tm1RehEce1tm1Reh
• absent sublingual duct_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0010720I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• abnormal skeleton morphology_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0005508I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• mandible hypoplasia_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0000460I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• pericardial effusion_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0005312I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• decreased atrioventricular cushion size_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0000301I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• ventricular septal defect_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0010402I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• neonatal lethality, complete penetrance_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0011087I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• interrupted aortic arch_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0004157I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• persistent cervical thymus_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0010722I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• pericardial effusion_Ednra<tm1Ywa>/Ednra<tm1Ywa>,Ednrb<tm1Ywa>/Ednrb<tm1Ywa>
  http://metadb.riken.jp/0005312I129SSvEvEdnratm1YwaEdnratm1YwaEdnrbtm1YwaEdnrbtm1YwaEdnratm1YwaEdnrbtm1Ywa
• prenatal lethality_Ednra<tm1Ywa>/Ednra<tm1Ywa>,Ednrb<tm1Ywa>/Ednrb<tm1Ywa>
  http://metadb.riken.jp/0002080I129SSvEvEdnratm1YwaEdnratm1YwaEdnrbtm1YwaEdnrbtm1YwaEdnratm1YwaEdnrbtm1Ywa
• alisphenoid bone hypoplasia_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0004460I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• absent external auditory canal_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0009707I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• abnormal Harderian gland pigmentation_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0003798I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• abnormal vasodilation_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0001613I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh
• absent malleus_Ece1<tm1Reh>/Ece1<tm1Reh>
  http://metadb.riken.jp/0004319I129S6SvEvTacC57BL6Ece1tm1RehEce1tm1RehEce1tm1Reh

article

http://www.w3.org/2000/01/rdf-schema#seeAlso

• [Blank]

BRC マウスの系統

http://purl.org/net/cito/citesAsAuthority

• B6;129-Ece1<tm1Reh>
  http://metadb.riken.jp/db/rikenbrc_mouse/RBRC06166

表現型アノテーション

http://purl.org/net/cito/citesAsAuthority

• absent Meckel's cartilage in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009168
• absent tympanic ring in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009158
• interrupted aortic arch in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009162
• abnormal melanocyte morphology in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1014616
• neonatal lethality, complete penetrance in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009191
• absent sublingual duct in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009189
• absent incus in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009165
• ventricular septal defect in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009183
• decreased atrioventricular cushion size in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009152
• absent tongue in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009181
• abnormal styloid process morphology in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009176
• palatine bone hypoplasia in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009170
• hydrops fetalis in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009157
• enlarged heart in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009151
• abnormal thymus morphology in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1014615
• persistent cervical thymus in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009190
• temporal bone squamous part hypoplasia in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1019896
• absent malleus in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009166
• alisphenoid bone hypoplasia in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009169
• thyroid hypoplasia in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009160
• absent middle ear ossicles in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009150
• small mandible in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1019126
• absent right subclavian artery in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009187
• abnormal vasodilation in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009155
• absent external auditory canal in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009179
• abnormal temporal bone squamous part morphology in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009167
• absent enteric neurons in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009154
• absent stapes in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009164
• abnormal choroid pigmentation in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1014618
• abnormal submandibular duct morphology in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009178
• abnormal choroid melanocyte morphology in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009182
• abnormal Harderian gland pigmentation in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009161
• abnormal skeleton morphology in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009172
• parathyroid hypoplasia in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009159
• mandible hypoplasia in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009153
• absent salivary gland in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1014614
• pericardial effusion in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009171
• abnormal epidermal melanocyte morphology in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009177
• small thyroid gland in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1014617
• embryonic lethality during organogenesis, incomplete penetrance in RBRC06166
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1009192

article

http://www.w3.org/2000/01/rdf-schema#seeAlso

• [Blank]