abnormal rod electrophysiology_Slc24a1<tm1Xen>/Slc24a1<tm1Xen>

http://metadb.riken.jp/0004021IC57BL6Slc24a1tm1XenSlc24a1tm1XenSlc24a1tm1Xen

abnormal rod electrophysiology_Slc24a1<tm1Xen>/Slc24a1<tm1Xen>

表現型アノテーション

MGI marker

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

• solute carrier family 24 (sodium/potassium/calcium exchanger), member 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:2384871

遺伝子型

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

• Slc24a1<tm1Xen>/Slc24a1<tm1Xen>

アレルシンボル

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

• Slc24a1<tm1Xen>

遺伝的背景

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

• involves: C57BL/6

MP annotation

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

• abnormal rod electrophysiology
  http://purl.obolibrary.org/obo/MP_0004021

文献

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

• Frans. Vinberg, et.al., A new mouse model for stationary night blindness with mutant Slc24a1 explains the pathophysiology of the associated human disease., Human molecular genetics, 2015, 24
  http://rdf.ncbi.nlm.nih.gov/pubmed/26246500