abnormal gait_Mpz<tm1Msch>/Mpz<tm1Msch>

http://metadb.riken.jp/0001406I129S7SvEvBrdMpztm1MschMpztm1MschMpztm1Msch

abnormal gait_Mpz<tm1Msch>/Mpz<tm1Msch>

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<tm1Msch>

アレルシンボル

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

• Mpz<tm1Msch>

遺伝的背景

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

• involves: 129S7/SvEvBrd

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

• K P. Giese, et.al., Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons., Cell, 1992, 71
  http://rdf.ncbi.nlm.nih.gov/pubmed/1384988