spontaneous chromosome breakage_Fancg<tm1Faw>/Fancg<tm1Faw>

http://metadb.riken.jp/0004029I129P2OlaHsdFVBNFancgtm1FawFancgtm1FawFancgtm1Faw

spontaneous chromosome breakage_Fancg<tm1Faw>/Fancg<tm1Faw>

表現型アノテーション

MGI marker

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

• Fanconi anemia, complementation group G
  http://metadb.riken.jp/db/mgi_rdf/MGI:1926471

遺伝子型

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

• Fancg<tm1Faw>/Fancg<tm1Faw>

アレルシンボル

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

• Fancg<tm1Faw>

遺伝的背景

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

• involves: 129P2/OlaHsd * FVB/N

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

• Mireille. Koomen, et.al., Reduced fertility and hypersensitivity to mitomycin C characterize Fancg/Xrcc9 null mice., Human molecular genetics, 2002, 11
  http://rdf.ncbi.nlm.nih.gov/pubmed/11823446