no abnormal phenotype detected_Tg(MECP2*G273X/GFP)#Hzo/0

http://metadb.riken.jp/0002169I129P2OlaHsdFVBTgMECP2G273XGFPHzo0TgMECP2G273XGFPHzo

no abnormal phenotype detected_Tg(MECP2*G273X/GFP)#Hzo/0

表現型アノテーション

MGI marker

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

• transgene insertion, Huda Y Zoghbi
  http://metadb.riken.jp/db/mgi_rdf/MGI:5491037

遺伝子型

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

• Tg(MECP2*G273X/GFP)#Hzo/0

アレルシンボル

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

• Tg(MECP2*G273X/GFP)#Hzo

遺伝的背景

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

• involves: 129P2/OlaHsd * FVB

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

• Steven Andrew. Baker, et.al., An AT-hook domain in MeCP2 determines the clinical course of Rett syndrome and related disorders., Cell, 2013, 152
  http://rdf.ncbi.nlm.nih.gov/pubmed/23452848