skeletal muscle hypertrophy_Mstn<tm1.1Mgs>/Mstn<tm1.1Mgs>

http://metadb.riken.jp/0009461I129S1Sv129X1SvJC57BLFVBNMstntm11MgsMstntm11MgsMstntm11Mgs

skeletal muscle hypertrophy_Mstn<tm1.1Mgs>/Mstn<tm1.1Mgs>

表現型アノテーション

MGI marker

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

• myostatin
  http://metadb.riken.jp/db/mgi_rdf/MGI:95691

遺伝子型

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

• Mstn<tm1.1Mgs>/Mstn<tm1.1Mgs>

アレルシンボル

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

• Mstn<tm1.1Mgs>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ * C57BL * FVB/N

MP annotation

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

• skeletal muscle hypertrophy
  http://purl.obolibrary.org/obo/MP_0009461

文献

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

• Claire. Ploquin, et.al., Lack of myostatin alters intermyofibrillar mitochondria activity, unbalances redox status, and impairs tolerance to chronic repetitive contractions in muscle., American journal of physiology. Endocrinology and metabolism, 2012, 302
  http://rdf.ncbi.nlm.nih.gov/pubmed/22318951