abnormal retina morphology_Elovl4<tm1Sie>/Elovl4<+>

http://metadb.riken.jp/0001325I129P2OlaHsdC57BL6Elovl4tm1SieElovl4Elovl4tm1SieElovl4

abnormal retina morphology_Elovl4<tm1Sie>/Elovl4<+>

表現型アノテーション

MGI marker

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

• elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 4
  http://metadb.riken.jp/db/mgi_rdf/MGI:1933331

遺伝子型

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

• Elovl4<tm1Sie>/Elovl4<+>

アレルシンボル

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

• Elovl4<tm1Sie>|Elovl4<+>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6

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

• Dorit. Raz-Prag, et.al., Haploinsufficiency is not the key mechanism of pathogenesis in a heterozygous Elovl4 knockout mouse model of STGD3 disease., Investigative ophthalmology & visual science, 2006, 47
  http://rdf.ncbi.nlm.nih.gov/pubmed/16877435