abnormal retina morphology_Fmr1<tm1Cgr>/Y

http://metadb.riken.jp/0001325I129P2OlaHsdC57BL6JFmr1tm1CgrYFmr1tm1Cgr

abnormal retina morphology_Fmr1<tm1Cgr>/Y

表現型アノテーション

MGI marker

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

• fragile X mental retardation syndrome 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:95564

遺伝子型

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

• Fmr1<tm1Cgr>/Y

アレルシンボル

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

• Fmr1<tm1Cgr>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6J

MP annotation

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

• abnormal retina morphology
  http://purl.obolibrary.org/obo/MP_0001325

文献

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

• Rafaëlle. Rossignol, et.al., Visual sensorial impairments in neurodevelopmental disorders: evidence for a retinal phenotype in Fragile X Syndrome., PloS one, 2014, 9
  http://rdf.ncbi.nlm.nih.gov/pubmed/25153086