Elisabetta. Ferretti, et.al., Hypomorphic mutation of the TALE gene Prep1 (pKnox1) causes a major reduction of Pbx and Meis proteins and a pleiotropic embryonic phenotype., Molecular and cellular biology, 2006, 26

http://rdf.ncbi.nlm.nih.gov/pubmed/16847320

Elisabetta. Ferretti, et.al., Hypomorphic mutation of the TALE gene Prep1 (pKnox1) causes a major reduction of Pbx and Meis proteins and a pleiotropic embryonic phenotype., Molecular and cellular biology, 2006, 26

pubmed

allele

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

• Pknox1<tm1Ngc>
  http://metadb.riken.jp/db/mgi_rdf/MGI:4459452

表現型アノテーション

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

• abnormal retinal pigment epithelium morphology_Pknox1<Gt(OST71835)Lex>/Pknox1<Gt(OST71835)Lex>
  http://metadb.riken.jp/0005201B6129S5Pknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835Lex
• increased nucleated erythrocyte cell number_Pknox1<Gt(OST71835)Lex>/Pknox1<Gt(OST71835)Lex>
  http://metadb.riken.jp/0009395B6129S5Pknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835Lex
• pallor_Pknox1<Gt(OST71835)Lex>/Pknox1<Gt(OST71835)Lex>
  http://metadb.riken.jp/0003717B6129S5Pknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835Lex
• edema_Pknox1<Gt(OST71835)Lex>/Pknox1<Gt(OST71835)Lex>
  http://metadb.riken.jp/0001785B6129S5Pknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835Lex
• abnormal erythropoiesis_Pknox1<Gt(OST71835)Lex>/Pknox1<Gt(OST71835)Lex>
  http://metadb.riken.jp/0000245B6129S5Pknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835Lex
• abnormal eye morphology_Pknox1<Gt(OST71835)Lex>/Pknox1<Gt(OST71835)Lex>
  http://metadb.riken.jp/0002092B6129S5Pknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835Lex
• hemorrhage_Pknox1<Gt(OST71835)Lex>/Pknox1<Gt(OST71835)Lex>
  http://metadb.riken.jp/0001914B6129S5Pknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835Lex
• decreased hematocrit_Pknox1<Gt(OST71835)Lex>/Pknox1<Gt(OST71835)Lex>
  http://metadb.riken.jp/0000208B6129S5Pknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835Lex
• decreased fetal size_Pknox1<Gt(OST71835)Lex>/Pknox1<Gt(OST71835)Lex>
  http://metadb.riken.jp/0004200B6129S5Pknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835Lex
• abnormal prenatal growth/weight/body size_Pknox1<Gt(OST71835)Lex>/Pknox1<Gt(OST71835)Lex>
  http://metadb.riken.jp/0004196B6129S5Pknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835Lex
• perinatal lethality, complete penetrance_Pknox1<Gt(OST71835)Lex>/Pknox1<Gt(OST71835)Lex>
  http://metadb.riken.jp/0011089B6129S5Pknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835Lex
• anemia_Pknox1<Gt(OST71835)Lex>/Pknox1<Gt(OST71835)Lex>
  http://metadb.riken.jp/0001577B6129S5Pknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835Lex
• decreased erythroid progenitor cell number_Pknox1<Gt(OST71835)Lex>/Pknox1<Gt(OST71835)Lex>
  http://metadb.riken.jp/0008973B6129S5Pknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835Lex
• small lens_Pknox1<Gt(OST71835)Lex>/Pknox1<Gt(OST71835)Lex>
  http://metadb.riken.jp/0001306B6129S5Pknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835Lex
• embryonic lethality between implantation and somite formation, complete penetrance_Pknox1<tm1Ngc>/Pknox1<tm1Ngc>
  http://metadb.riken.jp/0011096NSPknox1tm1NgcPknox1tm1NgcPknox1tm1Ngc
• abnormal retinal neuronal layer morphology_Pknox1<Gt(OST71835)Lex>/Pknox1<Gt(OST71835)Lex>
  http://metadb.riken.jp/0006069B6129S5Pknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835Lex
• abnormal eye development_Pknox1<Gt(OST71835)Lex>/Pknox1<Gt(OST71835)Lex>
  http://metadb.riken.jp/0001286B6129S5Pknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835Lex
• decreased angiogenesis_Pknox1<Gt(OST71835)Lex>/Pknox1<Gt(OST71835)Lex>
  http://metadb.riken.jp/0005602B6129S5Pknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835Lex
• abnormal liver development_Pknox1<Gt(OST71835)Lex>/Pknox1<Gt(OST71835)Lex>
  http://metadb.riken.jp/0000596B6129S5Pknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835LexPknox1GtOST71835Lex

class

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

• Pknox1<tm1Ngc>
  http://metadb.riken.jp/db/mgi_rdf/MGI:4459452

トランスクリプトームデータ

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

• CD27748
  http://metadb.riken.jp/db/BrainTx/TranscriptomeData/CD27748
• CD40246
  http://metadb.riken.jp/db/BrainTx/TranscriptomeData/CD40246