demyelination_Pmp22<Tr-1H>/Pmp22<+>

http://metadb.riken.jp/0000921IBALBcAnNCrlC3HHeNPmp22Tr1HPmp22Pmp22Tr1HPmp22

demyelination_Pmp22<Tr-1H>/Pmp22<+>

表現型アノテーション

MGI marker

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

• peripheral myelin protein 22
  http://metadb.riken.jp/db/mgi_rdf/MGI:97631

遺伝子型

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

• Pmp22<Tr-1H>/Pmp22<+>

アレルシンボル

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

• Pmp22<Tr-1H>|Pmp22<+>

遺伝的背景

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

• involves: BALB/cAnNCrl * C3H/HeN

MP annotation

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

• demyelination
  http://purl.obolibrary.org/obo/MP_0000921

文献

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

• P M. Nolan, et.al., A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse., Nature genetics, 2000, 25
  http://rdf.ncbi.nlm.nih.gov/pubmed/10932191
• Adrian M. Isaacs, et.al., Identification of a new Pmp22 mouse mutant and trafficking analysis of a Pmp22 allelic series suggesting that protein aggregates may be protective in Pmp22-associated peripheral neuropathy., Molecular and cellular neurosciences, 2002, 21
  http://rdf.ncbi.nlm.nih.gov/pubmed/12359155