abnormal social investigation_Mecp2<tm1.1Dhy>/Y

http://metadb.riken.jp/0001360C57BL6NMecp2tm11DhyMecp2tm11DhyYMecp2tm11Dhy

abnormal social investigation_Mecp2<tm1.1Dhy>/Y

表現型アノテーション

MGI marker

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

• methyl CpG binding protein 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:99918

遺伝子型

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

• Mecp2<tm1.1Dhy>/Y

アレルシンボル

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

• Mecp2<tm1.1Dhy>

遺伝的背景

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

• C57BL/6N-Mecp2<tm1.1Dhy>

MP annotation

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

• abnormal social investigation
  http://purl.obolibrary.org/obo/MP_0001360

文献

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

• Dag H. Yasui, et.al., Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome., Human molecular genetics, 2014, 23
  http://rdf.ncbi.nlm.nih.gov/pubmed/24352790