no abnormal phenotype detected_Nmnat2<Gt(EUCE0262a08)Hmgu>/Nmnat2<Gt(EUCE0262a08)Hmgu>,Wld<s>/Wld<s>

http://metadb.riken.jp/0002169I129P2OlaHsdC57BL6JC57BL6OlaNmnat2GtEUCE0262a08HmguNmnat2GtEUCE0262a08HmguWldsWldsNmnat2GtEUCE0262a08HmguWlds

no abnormal phenotype detected_Nmnat2<Gt(EUCE0262a08)Hmgu>/Nmnat2<Gt(EUCE0262a08)Hmgu>,Wld<s>/Wld<s>

表現型アノテーション

MGI marker

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

• wallerian degeneration
  http://metadb.riken.jp/db/mgi_rdf/MGI:98952
• nicotinamide nucleotide adenylyltransferase 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:2444155

遺伝子型

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

• Nmnat2<Gt(EUCE0262a08)Hmgu>/Nmnat2<Gt(EUCE0262a08)Hmgu>,Wld<s>/Wld<s>

アレルシンボル

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

• Nmnat2<Gt(EUCE0262a08)Hmgu>|Wld<s>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6J * C57BL/6Ola

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

• Jonathan. Gilley, et.al., Rescue of peripheral and CNS axon defects in mice lacking NMNAT2., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2013, 33
  http://rdf.ncbi.nlm.nih.gov/pubmed/23946398