abnormal gait_Trpc3<Mwk>/Trpc3<+>

http://metadb.riken.jp/0001406IBALBcAnNC3HHeHTrpc3MwkTrpc3Trpc3MwkTrpc3

abnormal gait_Trpc3<Mwk>/Trpc3<+>

表現型アノテーション

MGI marker

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

• transient receptor potential cation channel, subfamily C, member 3
  http://metadb.riken.jp/db/mgi_rdf/MGI:109526

遺伝子型

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

• Trpc3<Mwk>/Trpc3<+>

アレルシンボル

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

• Trpc3<Mwk>|Trpc3<+>

遺伝的背景

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

• involves: BALB/cAnN * C3H/HeH

MP annotation

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

• abnormal gait
  http://purl.obolibrary.org/obo/MP_0001406

文献

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

• Esther B E. Becker, et.al., A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice., Proceedings of the National Academy of Sciences of the United States of America, 2009, 106
  http://rdf.ncbi.nlm.nih.gov/pubmed/19351902