retinal photoreceptor degeneration_Mfsd8<tm1a(EUCOMM)Hmgu>/Mfsd8<tm1a(EUCOMM)Hmgu>

http://metadb.riken.jp/0008450IC57BL6NMfsd8tm1aEUCOMMHmguMfsd8tm1aEUCOMMHmguMfsd8tm1aEUCOMMHmgu

retinal photoreceptor degeneration_Mfsd8<tm1a(EUCOMM)Hmgu>/Mfsd8<tm1a(EUCOMM)Hmgu>

表現型アノテーション

MGI marker

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

• major facilitator superfamily domain containing 8
  http://metadb.riken.jp/db/mgi_rdf/MGI:1919425

遺伝子型

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

• Mfsd8<tm1a(EUCOMM)Hmgu>/Mfsd8<tm1a(EUCOMM)Hmgu>

アレルシンボル

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

• Mfsd8<tm1a(EUCOMM)Hmgu>

遺伝的背景

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

• involves: C57BL/6N

MP annotation

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

• retinal photoreceptor degeneration
  http://purl.obolibrary.org/obo/MP_0008450

文献

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

• Markus. Damme, et.al., Gene disruption of Mfsd8 in mice provides the first animal model for CLN7 disease., Neurobiology of disease, 2014, 65
  http://rdf.ncbi.nlm.nih.gov/pubmed/24423645