abnormal joint mobility_Lpin1<20884>/Lpin1<20884>

http://metadb.riken.jp/0008069IC57BL6JLpin120884Lpin120884Lpin120884

abnormal joint mobility_Lpin1<20884>/Lpin1<20884>

表現型アノテーション

MGI marker

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

• lipin 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1891340

遺伝子型

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

• Lpin1<20884>/Lpin1<20884>

アレルシンボル

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

• Lpin1<20884>

遺伝的背景

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

• involves: C57BL/6J

MP annotation

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

• abnormal joint mobility
  http://purl.obolibrary.org/obo/MP_0008069

文献

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

• Darlene S. Douglas, et.al., Concurrent Lpin1 and Nrcam mouse mutations result in severe peripheral neuropathy with transitory hindlimb paralysis., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2009, 29
  http://rdf.ncbi.nlm.nih.gov/pubmed/19793967