abnormal gait_Rab18<m1Hongc>/Rab18<m1Hongc>

http://metadb.riken.jp/0001406C57BL6JRab18m1HongcRab18m1HongcRab18m1HongcRab18m1Hongc

abnormal gait_Rab18<m1Hongc>/Rab18<m1Hongc>

表現型アノテーション

MGI marker

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

• RAB18, member RAS oncogene family
  http://metadb.riken.jp/db/mgi_rdf/MGI:102790

遺伝子型

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

• Rab18<m1Hongc>/Rab18<m1Hongc>

アレルシンボル

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

• Rab18<m1Hongc>

遺伝的背景

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

• C57BL/6J-Rab18<m1Hongc>

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

• Chih-Ya. Cheng, et.al., ENU mutagenesis identifies mice modeling Warburg Micro Syndrome with sensory axon degeneration caused by a deletion in Rab18., Experimental neurology, 2015, 267
  http://rdf.ncbi.nlm.nih.gov/pubmed/25779931