malocclusion_Mecp2<tm1Pplt>/0

http://metadb.riken.jp/0000120I129S1Sv129X1SvJC3HHeSnMecp2tm1Pplt0Mecp2tm1Pplt

malocclusion_Mecp2<tm1Pplt>/0

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<tm1Pplt>/0

アレルシンボル

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

• Mecp2<tm1Pplt>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ * C3H/HeSn

MP annotation

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

• malocclusion
  http://purl.obolibrary.org/obo/MP_0000120

文献

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

• Gregory J. Pelka, et.al., Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of mice., Brain : a journal of neurology, 2006, 129
  http://rdf.ncbi.nlm.nih.gov/pubmed/16467389