abnormal axon morphology_Lmna<tm1Stw>/Lmna<tm1Stw>

http://metadb.riken.jp/0005404I129S1SvLmnatm1StwLmnatm1StwLmnatm1Stw

abnormal axon morphology_Lmna<tm1Stw>/Lmna<tm1Stw>

表現型アノテーション

MGI marker

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

• lamin A
  http://metadb.riken.jp/db/mgi_rdf/MGI:96794

遺伝子型

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

• Lmna<tm1Stw>/Lmna<tm1Stw>

アレルシンボル

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

• Lmna<tm1Stw>

遺伝的背景

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

• involves: 129S1/Sv

MP annotation

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

• abnormal axon morphology
  http://purl.obolibrary.org/obo/MP_0005404

文献

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

• Annachiara. De Sandre-Giovannoli, et.al., Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse., American journal of human genetics, 2002, 70
  http://rdf.ncbi.nlm.nih.gov/pubmed/11799477