hindlimb paralysis_Lama2<tm1Eeng>/Lama2<tm1Eeng>

http://metadb.riken.jp/0000755I129S1SvBlackSwissFVBNLama2tm1EengLama2tm1EengLama2tm1Eeng

hindlimb paralysis_Lama2<tm1Eeng>/Lama2<tm1Eeng>

表現型アノテーション

MGI marker

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

• laminin, alpha 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:99912

遺伝子型

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

• Lama2<tm1Eeng>/Lama2<tm1Eeng>

アレルシンボル

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

• Lama2<tm1Eeng>

遺伝的背景

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

• involves: 129S1/Sv * Black Swiss * FVB/N

MP annotation

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

• hindlimb paralysis
  http://purl.obolibrary.org/obo/MP_0000755

文献

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

• W. Kuang, et.al., Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models., The Journal of clinical investigation, 1998, 102
  http://rdf.ncbi.nlm.nih.gov/pubmed/9710454