no abnormal phenotype detected_Tsc2<tm2.1Djk>/Tsc2<tm2.1Djk>

http://metadb.riken.jp/0002169I129S4SvJaeC57BL6Tsc2tm21DjkTsc2tm21DjkTsc2tm21Djk

no abnormal phenotype detected_Tsc2<tm2.1Djk>/Tsc2<tm2.1Djk>

表現型アノテーション

MGI marker

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

• tuberous sclerosis 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:102548

遺伝子型

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

• Tsc2<tm2.1Djk>/Tsc2<tm2.1Djk>

アレルシンボル

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

• Tsc2<tm2.1Djk>

遺伝的背景

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

• involves: 129S4/SvJae * C57BL/6

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

• Kristen. Pollizzi, et.al., A hypomorphic allele of Tsc2 highlights the role of TSC1/TSC2 in signaling to AKT and models mild human TSC2 alleles., Human molecular genetics, 2009, 18
  http://rdf.ncbi.nlm.nih.gov/pubmed/19357198