microphthalmia_Gja8<Lop10>/Gja8<tm1Scr>

http://metadb.riken.jp/0001297I129S4SvJaeAKRJBALBcJC57BL6JGja8Lop10Gja8tm1ScrGja8Lop10Gja8tm1Scr

microphthalmia_Gja8<Lop10>/Gja8<tm1Scr>

表現型アノテーション

MGI marker

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

• gap junction protein, alpha 8
  http://metadb.riken.jp/db/mgi_rdf/MGI:99953

遺伝子型

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

• Gja8<Lop10>/Gja8<tm1Scr>

アレルシンボル

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

• Gja8<Lop10>|Gja8<tm1Scr>

遺伝的背景

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

• involves: 129S4/SvJae * AKR/J * BALB/cJ * C57BL/6J

MP annotation

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

• microphthalmia
  http://purl.obolibrary.org/obo/MP_0001297

文献

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

• Bo. Chang, et.al., A Gja8 (Cx50) point mutation causes an alteration of alpha 3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice., Human molecular genetics, 2002, 11
  http://rdf.ncbi.nlm.nih.gov/pubmed/11875045