no abnormal phenotype detected_Pkdcc<tm1Hssk>/Pkdcc<+>

http://metadb.riken.jp/0002169IC57BL6CBAPkdcctm1HsskPkdccPkdcctm1HsskPkdcc

no abnormal phenotype detected_Pkdcc<tm1Hssk>/Pkdcc<+>

表現型アノテーション

MGI marker

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

• protein kinase domain containing, cytoplasmic
  http://metadb.riken.jp/db/mgi_rdf/MGI:2147077

遺伝子型

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

• Pkdcc<tm1Hssk>/Pkdcc<+>

アレルシンボル

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

• Pkdcc<tm1Hssk>|Pkdcc<+>

遺伝的背景

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

• involves: C57BL/6 * CBA

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

• Yu. Imuta, et.al., Short limbs, cleft palate, and delayed formation of flat proliferative chondrocytes in mice with targeted disruption of a putative protein kinase gene, Pkdcc (AW548124)., Developmental dynamics : an official publication of the American Association of Anatomists, 2009, 238
  http://rdf.ncbi.nlm.nih.gov/pubmed/19097194