polydactyly_Ift88<tm1Rpw>/Ift88<tm1Rpw>

http://metadb.riken.jp/0000562I129SvIft88tm1RpwIft88tm1RpwIft88tm1Rpw

polydactyly_Ift88<tm1Rpw>/Ift88<tm1Rpw>

表現型アノテーション

MGI marker

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

• intraflagellar transport 88
  http://metadb.riken.jp/db/mgi_rdf/MGI:98715

遺伝子型

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

• Ift88<tm1Rpw>/Ift88<tm1Rpw>

アレルシンボル

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

• Ift88<tm1Rpw>

遺伝的背景

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

• involves: 129/Sv

MP annotation

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

• polydactyly
  http://purl.obolibrary.org/obo/MP_0000562

文献

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

• Qihong. Zhang, et.al., Loss of the Tg737 protein results in skeletal patterning defects., Developmental dynamics : an official publication of the American Association of Anatomists, 2003, 227
  http://rdf.ncbi.nlm.nih.gov/pubmed/12701101