cataract_Sprtn<tm1Yjm>/Sprtn<tm1Yjm>

http://metadb.riken.jp/0001304I129SSvEvC57BL6Sprtntm1YjmSprtntm1YjmSprtntm1Yjm

cataract_Sprtn<tm1Yjm>/Sprtn<tm1Yjm>

表現型アノテーション

MGI marker

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

• SprT-like N-terminal domain
  http://metadb.riken.jp/db/mgi_rdf/MGI:2685351

遺伝子型

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

• Sprtn<tm1Yjm>/Sprtn<tm1Yjm>

アレルシンボル

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

• Sprtn<tm1Yjm>

遺伝的背景

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

• involves: 129S/SvEv * C57BL/6

MP annotation

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

• cataracts
  http://purl.obolibrary.org/obo/MP_0001304

文献

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

• Reeja S. Maskey, et.al., Spartan deficiency causes genomic instability and progeroid phenotypes., Nature communications, 2014, 5
  http://rdf.ncbi.nlm.nih.gov/pubmed/25501849