no abnormal phenotype detected_Prrx2<tm1Mjk>/Prrx2<tm1Mjk>

http://metadb.riken.jp/0002169NSPrrx2tm1MjkPrrx2tm1MjkPrrx2tm1Mjk

no abnormal phenotype detected_Prrx2<tm1Mjk>/Prrx2<tm1Mjk>

表現型アノテーション

MGI marker

http://metadb.riken.jp/db/mgi_rdf/variant_of

• paired related homeobox 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:98218

遺伝子型

http://metadb.riken.jp/db/mgi_rdf/allele_composition

• Prrx2<tm1Mjk>/Prrx2<tm1Mjk>

アレルシンボル

http://metadb.riken.jp/db/mgi_rdf/allele_symbol

• Prrx2<tm1Mjk>

遺伝的背景

http://metadb.riken.jp/db/mgi_rdf/genetic_background

• Not Specified

MP annotation

http://metadb.riken.jp/db/bioresource_schema/brs_indicatesPhenotype

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• M F. Lu, et.al., prx-1 functions cooperatively with another paired-related homeobox gene, prx-2, to maintain cell fates within the craniofacial mesenchyme., Development (Cambridge, England), 1999, 126
  http://rdf.ncbi.nlm.nih.gov/pubmed/9876178
• M. Bergwerff, et.al., Loss of function of the Prx1 and Prx2 homeobox genes alters architecture of the great elastic arteries and ductus arteriosus., Virchows Archiv : an international journal of pathology, 2000, 436
  http://rdf.ncbi.nlm.nih.gov/pubmed/10664157