no abnormal phenotype detected_Rlim<tm1.2Inba>/Y

http://metadb.riken.jp/0002169I129S1Sv129X1SvJC57BL6FVBRlimtm12InbaYRlimtm12Inba

no abnormal phenotype detected_Rlim<tm1.2Inba>/Y

表現型アノテーション

MGI marker

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

• ring finger protein, LIM domain interacting
  http://metadb.riken.jp/db/mgi_rdf/MGI:1342291

遺伝子型

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

• Rlim<tm1.2Inba>/Y

アレルシンボル

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

• Rlim<tm1.2Inba>

遺伝的背景

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

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

• Jongdae. Shin, et.al., Maternal Rnf12/RLIM is required for imprinted X-chromosome inactivation in mice., Nature, 2010, 467
  http://rdf.ncbi.nlm.nih.gov/pubmed/20962847