retinal degeneration_Pin1<tm1Tuc>/Pin1<tm1Tuc>

http://metadb.riken.jp/0001326I129P2OlaHsdC57BL6Pin1tm1TucPin1tm1TucPin1tm1Tuc

retinal degeneration_Pin1<tm1Tuc>/Pin1<tm1Tuc>

表現型アノテーション

MGI marker

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

• protein (peptidyl-prolyl cis/trans isomerase) NIMA-interacting 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1346036

遺伝子型

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

• Pin1<tm1Tuc>/Pin1<tm1Tuc>

アレルシンボル

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

• Pin1<tm1Tuc>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6

MP annotation

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

• retinal degeneration
  http://purl.obolibrary.org/obo/MP_0001326

文献

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

• Yih-Cherng. Liou, et.al., Loss of Pin1 function in the mouse causes phenotypes resembling cyclin D1-null phenotypes., Proceedings of the National Academy of Sciences of the United States of America, 2002, 99
  http://rdf.ncbi.nlm.nih.gov/pubmed/11805292