abnormal skin condition_Srebf2<lop13>/Srebf2<lop13>

http://metadb.riken.jp/0001191STOCKSrebf2lop13JSrebf2lop13Srebf2lop13Srebf2lop13

abnormal skin condition_Srebf2<lop13>/Srebf2<lop13>

表現型アノテーション

MGI marker

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

• sterol regulatory element binding factor 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:107585

遺伝子型

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

• Srebf2<lop13>/Srebf2<lop13>

アレルシンボル

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

• Srebf2<lop13>

遺伝的背景

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

• STOCK Srebf2<lop13>/J

MP annotation

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

• abnormal skin condition
  http://purl.obolibrary.org/obo/MP_0001191

文献

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

• Kate M. Merath, et.al., A spontaneous mutation in Srebf2 leads to cataracts and persistent skin wounds in the lens opacity 13 (lop13) mouse., Mammalian genome : official journal of the International Mammalian Genome Society, 2011, 22
  http://rdf.ncbi.nlm.nih.gov/pubmed/21858719