decreased retinal cone cell number_Syne2<cpfl8>/Syne2<cpfl8>

http://metadb.riken.jp/0008446B6CgSyne2cpfl8Syne2cpfl8Syne2cpfl8Syne2cpfl8

decreased retinal cone cell number_Syne2<cpfl8>/Syne2<cpfl8>

表現型アノテーション

MGI marker

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

• spectrin repeat containing, nuclear envelope 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:2449316

遺伝子型

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

• Syne2<cpfl8>/Syne2<cpfl8>

アレルシンボル

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

• Syne2<cpfl8>

遺伝的背景

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

• B6.Cg-Syne2<cpfl8>

MP annotation

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

• decreased retinal cone cell number
  http://purl.obolibrary.org/obo/MP_0008446

文献

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

• Dennis M. Maddox, et.al., A Mutation in Syne2 Causes Early Retinal Defects in Photoreceptors, Secondary Neurons, and Müller Glia., Investigative ophthalmology & visual science, 2015, 56
  http://rdf.ncbi.nlm.nih.gov/pubmed/26066746