abnormal muscle contractility_Tnnt1<tm1.2Jin>/Tnnt1<tm1.2Jin>

http://metadb.riken.jp/0005620I129P2OlaHsdC57BL6Tnnt1tm12JinTnnt1tm12JinTnnt1tm12Jin

abnormal muscle contractility_Tnnt1<tm1.2Jin>/Tnnt1<tm1.2Jin>

表現型アノテーション

MGI marker

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

• troponin T1, skeletal, slow
  http://metadb.riken.jp/db/mgi_rdf/MGI:1333868

遺伝子型

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

• Tnnt1<tm1.2Jin>/Tnnt1<tm1.2Jin>

アレルシンボル

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

• Tnnt1<tm1.2Jin>

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

• abnormal muscle contractility
  http://purl.obolibrary.org/obo/MP_0005620

文献

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

• Bin. Wei, et.al., Deficiency of slow skeletal muscle troponin T causes atrophy of type I slow fibres and decreases tolerance to fatigue., The Journal of physiology, 2014, 592
  http://rdf.ncbi.nlm.nih.gov/pubmed/24445317