abnormal imprinting_Kcnq1ot1<tm2.1Ckan>/Kcnq1ot1<+>,Meox2<tm1(cre)Sor>/Meox2<+>

http://metadb.riken.jp/0003787I129S1Sv129S4SvJaeSor129X1SvJC57BL6SD7Kcnq1ot1tm21CkanKcnq1ot1Meox2tm1creSorMeox2Kcnq1ot1Meox2Kcnq1ot1tm21CkanMeox2tm1creSor

abnormal imprinting_Kcnq1ot1<tm2.1Ckan>/Kcnq1ot1<+>,Meox2<tm1(cre)Sor>/Meox2<+>

表現型アノテーション

MGI marker

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

• mesenchyme homeobox 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:103219
• KCNQ1 overlapping transcript 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1926855

遺伝子型

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

• Kcnq1ot1<tm2.1Ckan>/Kcnq1ot1<+>,Meox2<tm1(cre)Sor>/Meox2<+>

アレルシンボル

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

• Kcnq1ot1<+>|Meox2<+>|Kcnq1ot1<tm2.1Ckan>|Meox2<tm1(cre)Sor>

遺伝的背景

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

• involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * SD7

MP annotation

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

• abnormal imprinting
  http://purl.obolibrary.org/obo/MP_0003787

文献

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

• Faizaan. Mohammad, et.al., Long noncoding RNA-mediated maintenance of DNA methylation and transcriptional gene silencing., Development (Cambridge, England), 2012, 139
  http://rdf.ncbi.nlm.nih.gov/pubmed/22721776