increased cellular sensitivity to ionizing radiation_Atm<tm1Led>/Atm<tm1Led>

http://metadb.riken.jp/0004227I129S6SvEvTacBlackSwissAtmtm1LedAtmtm1LedAtmtm1Led

increased cellular sensitivity to ionizing radiation_Atm<tm1Led>/Atm<tm1Led>

表現型アノテーション

MGI marker

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

• ataxia telangiectasia mutated
  http://metadb.riken.jp/db/mgi_rdf/MGI:107202

遺伝子型

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

• Atm<tm1Led>/Atm<tm1Led>

アレルシンボル

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

• Atm<tm1Led>

遺伝的背景

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

• involves: 129S6/SvEvTac * Black Swiss

MP annotation

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

• increased cellular sensitivity to ionizing radiation
  http://purl.obolibrary.org/obo/MP_0004227

文献

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

• K. Spring, et.al., Atm knock-in mice harboring an in-frame deletion corresponding to the human ATM 7636del9 common mutation exhibit a variant phenotype., Cancer research, 2001, 61
  http://rdf.ncbi.nlm.nih.gov/pubmed/11389091