A M. Robertson, et.al., Comparison of a new pmp22 transgenic mouse line with other mouse models and human patients with CMT1A., Journal of anatomy, 2002, 200

http://rdf.ncbi.nlm.nih.gov/pubmed/12090404

A M. Robertson, et.al., Comparison of a new pmp22 transgenic mouse line with other mouse models and human patients with CMT1A., Journal of anatomy, 2002, 200

pubmed

allele

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

• Tg(Pmp22)My41Clh
  http://metadb.riken.jp/db/mgi_rdf/MGI:2183742

表現型アノテーション

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

• abnormal submucous nerve plexus morphology_Tg(Pmp22)My41Clh/0
  http://metadb.riken.jp/0010800IC57BL6JCBACaTgPmp22My41Clh0TgPmp22My41Clh
• decreased myelin sheath thickness_Tg(PMP22)C22Clh/0
  http://metadb.riken.jp/0011731IC57BL6JCBACaTgPMP22C22Clh0TgPMP22C22Clh
• dysmyelination_Pmp22<Tr-J>/?
  http://metadb.riken.jp/0013438IC57BL6JPmp22TrJPmp22TrJ
• axon degeneration_Pmp22<Tr-J>/?
  http://metadb.riken.jp/0005405IC57BL6JPmp22TrJPmp22TrJ
• increased Schwann cell number_Pmp22<Tr-J>/?
  http://metadb.riken.jp/0010742IC57BL6JPmp22TrJPmp22TrJ
• male infertility_Tg(Pmp22)My41Clh/0
  http://metadb.riken.jp/0001925IC57BL6JCBACaTgPmp22My41Clh0TgPmp22My41Clh
• decreased myelin sheath thickness_Pmp22<Tr-J>/?
  http://metadb.riken.jp/0011731IC57BL6JPmp22TrJPmp22TrJ
• weakness_Tg(Pmp22)My41Clh/0
  http://metadb.riken.jp/0000746IC57BL6JCBACaTgPmp22My41Clh0TgPmp22My41Clh
• abnormal gait_Tg(Pmp22)My41Clh/0
  http://metadb.riken.jp/0001406IC57BL6JCBACaTgPmp22My41Clh0TgPmp22My41Clh
• dysmyelination_Tg(Pmp22)My41Clh/0
  http://metadb.riken.jp/0013438IC57BL6JCBACaTgPmp22My41Clh0TgPmp22My41Clh
• premature death_Tg(Pmp22)My41Clh/0
  http://metadb.riken.jp/0002083IC57BL6JCBACaTgPmp22My41Clh0TgPmp22My41Clh
• abnormal submucous nerve plexus morphology_Tg(PMP22)C22Clh/0
  http://metadb.riken.jp/0010800IC57BL6JCBACaTgPMP22C22Clh0TgPMP22C22Clh
• decreased myelin sheath thickness_Tg(Pmp22)My41Clh/0
  http://metadb.riken.jp/0011731IC57BL6JCBACaTgPmp22My41Clh0TgPmp22My41Clh
• axon degeneration_Tg(Pmp22)My41Clh/0
  http://metadb.riken.jp/0005405IC57BL6JCBACaTgPmp22My41Clh0TgPmp22My41Clh
• dysmyelination_Tg(PMP22)C22Clh/0
  http://metadb.riken.jp/0013438IC57BL6JCBACaTgPMP22C22Clh0TgPMP22C22Clh
• increased Schwann cell number_Tg(Pmp22)My41Clh/0
  http://metadb.riken.jp/0010742IC57BL6JCBACaTgPmp22My41Clh0TgPmp22My41Clh
• increased Schwann cell number_Tg(PMP22)C22Clh/0
  http://metadb.riken.jp/0010742IC57BL6JCBACaTgPMP22C22Clh0TgPMP22C22Clh
• abnormal myelination_Tg(Pmp22)My41Clh/0
  http://metadb.riken.jp/0000920IC57BL6JCBACaTgPmp22My41Clh0TgPmp22My41Clh
• demyelination_Tg(Pmp22)My41Clh/0
  http://metadb.riken.jp/0000921IC57BL6JCBACaTgPmp22My41Clh0TgPmp22My41Clh
• reduced female fertility_Tg(Pmp22)My41Clh/0
  http://metadb.riken.jp/0001923IC57BL6JCBACaTgPmp22My41Clh0TgPmp22My41Clh
• abnormal myelination_Tg(PMP22)C22Clh/0
  http://metadb.riken.jp/0000920IC57BL6JCBACaTgPMP22C22Clh0TgPMP22C22Clh

class

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

• Tg(Pmp22)My41Clh
  http://metadb.riken.jp/db/mgi_rdf/MGI:2183742