myopathy_Fhl1<tm1.1Mihi>/Y

http://metadb.riken.jp/0000751IC57BL6JFhl1tm11MihiYFhl1tm11Mihi

myopathy_Fhl1<tm1.1Mihi>/Y

表現型アノテーション

MGI marker

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

• four and a half LIM domains 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1298387

遺伝子型

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

• Fhl1<tm1.1Mihi>/Y

アレルシンボル

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

• Fhl1<tm1.1Mihi>

遺伝的背景

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

• involves: C57BL/6J

MP annotation

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

• myopathy
  http://purl.obolibrary.org/obo/MP_0000751

文献

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

• Valentina. Emmanuele, et.al., Fhl1 W122S causes loss of protein function and late-onset mild myopathy., Human molecular genetics, 2015, 24
  http://rdf.ncbi.nlm.nih.gov/pubmed/25274776