no abnormal phenotype detected_Prrx2<tm1Hubr>/Prrx2<tm1Hubr>

http://metadb.riken.jp/0002169I129P2OlaHsdFVBPrrx2tm1HubrPrrx2tm1HubrPrrx2tm1Hubr

no abnormal phenotype detected_Prrx2<tm1Hubr>/Prrx2<tm1Hubr>

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<tm1Hubr>/Prrx2<tm1Hubr>

アレルシンボル

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

• Prrx2<tm1Hubr>

遺伝的背景

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

• involves: 129P2/OlaHsd * FVB

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

• D. ten Berge, et.al., Prx1 and Prx2 in skeletogenesis: roles in the craniofacial region, inner ear and limbs., Development (Cambridge, England), 1998, 125
  http://rdf.ncbi.nlm.nih.gov/pubmed/9729491