neonatal lethality, incomplete penetrance_Syne1<tm1.1Mcn>/Syne1<tm1.1Mcn>

http://metadb.riken.jp/0011088I129S4SvJae129S6SvEvTacC57BLSyne1tm11McnSyne1tm11McnSyne1tm11Mcn

neonatal lethality, incomplete penetrance_Syne1<tm1.1Mcn>/Syne1<tm1.1Mcn>

表現型アノテーション

MGI marker

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

• spectrin repeat containing, nuclear envelope 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1927152

遺伝子型

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

• Syne1<tm1.1Mcn>/Syne1<tm1.1Mcn>

アレルシンボル

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

• Syne1<tm1.1Mcn>

遺伝的背景

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

• involves: 129S4/SvJae * 129S6/SvEvTac * C57BL

MP annotation

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

• partial neonatal lethality
  http://purl.obolibrary.org/obo/MP_0011088

文献

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

• Megan J. Puckelwartz, et.al., Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice., Human molecular genetics, 2009, 18
  http://rdf.ncbi.nlm.nih.gov/pubmed/19008300