dystrophic muscle_Tln2<tm2Crit>/Tln2<tm2Crit>

http://metadb.riken.jp/0000752I129P2OlaHsdC57BL6Tln2tm2CritTln2tm2CritTln2tm2Crit

dystrophic muscle_Tln2<tm2Crit>/Tln2<tm2Crit>

表現型アノテーション

MGI marker

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

• talin 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1917799

遺伝子型

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

• Tln2<tm2Crit>/Tln2<tm2Crit>

アレルシンボル

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

• Tln2<tm2Crit>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6

MP annotation

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

• dystrophic muscle
  http://purl.obolibrary.org/obo/MP_0000752

文献

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

• Emmanuel. Debrand, et.al., Mice carrying a complete deletion of the talin2 coding sequence are viable and fertile., Biochemical and biophysical research communications, 2012, 426
  http://rdf.ncbi.nlm.nih.gov/pubmed/22925892