spontaneous chromosome breakage_Fen1<tm2.1Bhsh>/Fen1<+>

http://metadb.riken.jp/0004029I129S1SvFen1tm21BhshFen1Fen1Fen1tm21Bhsh

spontaneous chromosome breakage_Fen1<tm2.1Bhsh>/Fen1<+>

表現型アノテーション

MGI marker

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

• flap structure specific endonuclease 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:102779

遺伝子型

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

• Fen1<tm2.1Bhsh>/Fen1<+>

アレルシンボル

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

• Fen1<+>|Fen1<tm2.1Bhsh>

遺伝的背景

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

• involves: 129S1/Sv

MP annotation

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

• spontaneous chromosome breakage
  http://purl.obolibrary.org/obo/MP_0004029

文献

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

• L. Chung, et.al., The FEN1 E359K germline mutation disrupts the FEN1-WRN interaction and FEN1 GEN activity, causing aneuploidy-associated cancers., Oncogene, 2015, 34
  http://rdf.ncbi.nlm.nih.gov/pubmed/24608430