abnormal retinal neuronal layer morphology_Clcn3<tm1Suc>/Clcn3<tm1Suc>

http://metadb.riken.jp/0006069I129P2OlaHsdC57BL6Clcn3tm1SucClcn3tm1SucClcn3tm1Suc

abnormal retinal neuronal layer morphology_Clcn3<tm1Suc>/Clcn3<tm1Suc>

表現型アノテーション

MGI marker

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

• chloride channel, voltage-sensitive 3
  http://metadb.riken.jp/db/mgi_rdf/MGI:103555

遺伝子型

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

• Clcn3<tm1Suc>/Clcn3<tm1Suc>

アレルシンボル

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

• Clcn3<tm1Suc>

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

• abnormal retinal neuronal layer morphology
  http://purl.obolibrary.org/obo/MP_0006069

文献

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

• Momono. Yoshikawa, et.al., CLC-3 deficiency leads to phenotypes similar to human neuronal ceroid lipofuscinosis., Genes to cells : devoted to molecular & cellular mechanisms, 2002, 7
  http://rdf.ncbi.nlm.nih.gov/pubmed/12059962