decreased retinal photoreceptor cell number_Cln3<tm1.1Mem>/Cln3<tm1.1Mem>

http://metadb.riken.jp/0001327I129SSvEvCD1Cln3tm11MemCln3tm11MemCln3tm11Mem

decreased retinal photoreceptor cell number_Cln3<tm1.1Mem>/Cln3<tm1.1Mem>

表現型アノテーション

MGI marker

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

• ceroid lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease)
  http://metadb.riken.jp/db/mgi_rdf/MGI:107537

遺伝子型

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

• Cln3<tm1.1Mem>/Cln3<tm1.1Mem>

アレルシンボル

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

• Cln3<tm1.1Mem>

遺伝的背景

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

• involves: 129S/SvEv * CD-1

MP annotation

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

• decreased retinal photoreceptor cell number
  http://purl.obolibrary.org/obo/MP_0001327

文献

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

• Susan L. Cotman, et.al., Cln3(Deltaex7/8) knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth., Human molecular genetics, 2002, 11
  http://rdf.ncbi.nlm.nih.gov/pubmed/12374761