D L. Guris, et.al., Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome., Nature genetics, 2001, 27

http://rdf.ncbi.nlm.nih.gov/pubmed/11242111

D L. Guris, et.al., Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome., Nature genetics, 2001, 27

rdfs:label

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

• D L. Guris, et.al., Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome., Nature genetics, 2001, 27

article

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

• [Blank]
• [Blank]

class

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

• Crkl<tm1Imo>
  http://metadb.riken.jp/db/mgi_rdf/MGI:1931805

表現型アノテーション

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

• aberrant origin of the right subclavian artery_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0010465I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• abnormal thyroid gland development_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0003421I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• abnormal vagus ganglion morphology_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0001100I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• abnormal glossopharyngeal ganglion morphology_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0001096I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• dilated heart right atrium_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0004062I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• decreased cranium height_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0008525I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• abnormal nasal bone morphology_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0000102I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• overriding aortic valve_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0000273I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• otic hypertelorism_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0000025I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• increased cranium width_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0000441I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• abnormal trigeminal ganglion morphology_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0001092I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• abnormal thymus development_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0000704I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• abnormal heart left atrium morphology_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0003923I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• abnormal aortic arch morphology_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0004113I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• abnormal craniofacial morphology_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0000428I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• interrupted aortic arch_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0004157I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• decreased body weight_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0001262I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• double outlet right ventricle_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0000284I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• abnormal cranial ganglia morphology_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0001081I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• lethality throughout fetal growth and development, complete penetrance_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0011099I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• ventricular septal defect_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0010402I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• abnormal parathyroid gland development_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0013573I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• short frontal bone_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0004380I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• ocular hypertelorism_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0001300I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo
• pallor_Crkl<tm1Imo>/Crkl<tm1Imo>
  http://metadb.riken.jp/0003717I129S4SvJaeSorC57BL6JCrkltm1ImoCrkltm1ImoCrkltm1Imo

Class

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

• B6.129S4-Sh2b3<tm1Rmp>/Rbrc
  http://metadb.riken.jp/db/rikenbrc_mouse/RBRC00993
• B6;129S4-Sh2b1<tm1Ayos>/Rbrc
  http://metadb.riken.jp/db/rikenbrc_mouse/RBRC00994

トランスクリプトームデータ

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

• CD19103
  http://metadb.riken.jp/db/BrainTx/TranscriptomeData/CD19103

allele

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

• Crkl<tm1Imo>
  http://metadb.riken.jp/db/mgi_rdf/MGI:1931805

BRC マウスの系統

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

• B6.129S4-Sh2b3<tm1Rmp>/Rbrc
  http://metadb.riken.jp/db/rikenbrc_mouse/RBRC00993
• B6;129S4-Sh2b1<tm1Ayos>/Rbrc
  http://metadb.riken.jp/db/rikenbrc_mouse/RBRC00994