no abnormal phenotype detected_Lrsam1<Gt(RRK239)Byg>/Lrsam1<Gt(RRK239)Byg>

http://metadb.riken.jp/0002169I129P2OlaHsdLrsam1GtRRK239BygLrsam1GtRRK239BygLrsam1GtRRK239Byg

no abnormal phenotype detected_Lrsam1<Gt(RRK239)Byg>/Lrsam1<Gt(RRK239)Byg>

表現型アノテーション

MGI marker

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

• leucine rich repeat and sterile alpha motif containing 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:2684789

遺伝子型

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

• Lrsam1<Gt(RRK239)Byg>/Lrsam1<Gt(RRK239)Byg>

アレルシンボル

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

• Lrsam1<Gt(RRK239)Byg>

遺伝的背景

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

• involves: 129P2/OlaHsd

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• Laurent P. Bogdanik, et.al., Loss of the E3 ubiquitin ligase LRSAM1 sensitizes peripheral axons to degeneration in a mouse model of Charcot-Marie-Tooth disease., Disease models & mechanisms, 2013, 6
  http://rdf.ncbi.nlm.nih.gov/pubmed/23519028