hindlimb paralysis_Myh4<arl>/Myh4<arl>

http://metadb.riken.jp/0000755IC3HHeHC57BL6JMyh4arlMyh4arlMyh4arl

hindlimb paralysis_Myh4<arl>/Myh4<arl>

表現型アノテーション

MGI marker

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

• myosin, heavy polypeptide 4, skeletal muscle
  http://metadb.riken.jp/db/mgi_rdf/MGI:1339713

遺伝子型

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

• Myh4<arl>/Myh4<arl>

アレルシンボル

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

• Myh4<arl>

遺伝的背景

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

• involves: C3H/HeH * C57BL/6J

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

• Ramakrishna. Kurapati, et.al., Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIb., Human molecular genetics, 2012, 21
  http://rdf.ncbi.nlm.nih.gov/pubmed/22199023