embryonic growth retardation_Opa1<M1Bewi>/Opa1<M1Bewi>

http://metadb.riken.jp/0003984IC3HeBFeJC57BL6Opa1M1BewiOpa1M1BewiOpa1M1Bewi

embryonic growth retardation_Opa1<M1Bewi>/Opa1<M1Bewi>

表現型アノテーション

MGI marker

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

• OPA1, mitochondrial dynamin like GTPase
  http://metadb.riken.jp/db/mgi_rdf/MGI:1921393

遺伝子型

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

• Opa1<M1Bewi>/Opa1<M1Bewi>

アレルシンボル

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

• Opa1<M1Bewi>

遺伝的背景

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

• involves: C3HeB/FeJ * C57BL/6

MP annotation

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

• embryonic growth retardation
  http://purl.obolibrary.org/obo/MP_0003984

文献

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

• Marcel V. Alavi, et.al., A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophy., Brain : a journal of neurology, 2007, 130
  http://rdf.ncbi.nlm.nih.gov/pubmed/17314202