no abnormal phenotype detected_Nmnat2<Gt(EUCE0262a08)Hmgu>/Nmnat2<Gt(RRF238)Byg>

http://metadb.riken.jp/0002169I129P2OlaHsdC57BL6JNmnat2GtEUCE0262a08HmguNmnat2GtRRF238BygNmnat2GtRRF238BygNmnat2GtEUCE0262a08Hmgu

no abnormal phenotype detected_Nmnat2<Gt(EUCE0262a08)Hmgu>/Nmnat2<Gt(RRF238)Byg>

表現型アノテーション

MGI marker

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

• 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(RRF238)Byg>

アレルシンボル

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

• Nmnat2<Gt(RRF238)Byg>|Nmnat2<Gt(EUCE0262a08)Hmgu>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6J

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