abnormal gait_Mpz<tm1Msch>/Mpz<+>

http://metadb.riken.jp/0001406I129S7SvEvBrdC57BL6Mpztm1MschMpzMpztm1MschMpz

abnormal gait_Mpz<tm1Msch>/Mpz<+>

表現型アノテーション

MGI marker

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

• myelin protein zero
  http://metadb.riken.jp/db/mgi_rdf/MGI:103177

遺伝子型

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

• Mpz<tm1Msch>/Mpz<+>

アレルシンボル

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

• Mpz<tm1Msch>|Mpz<+>

遺伝的背景

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

• involves: 129S7/SvEvBrd * C57BL/6

MP annotation

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

• abnormal gait
  http://purl.obolibrary.org/obo/MP_0001406

文献

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

• Katsuichi. Miyamoto, et.al., Heterozygous null mutation of myelin P0 protein enhances susceptibility to autoimmune neuritis targeting P0 peptide., European journal of immunology, 2003, 33
  http://rdf.ncbi.nlm.nih.gov/pubmed/12616486