abnormal amacrine cell morphology_Plxna2<tm1Hfu>/Plxna2<tm1Hfu>,Sema6a<Gt(KST069)Byg>/Sema6a<Gt(KST069)Byg>

http://metadb.riken.jp/0005240I129P2OlaHsdC57BL6NCrljCBAJNCrljPlxna2tm1HfuPlxna2tm1HfuSema6aGtKST069BygSema6aGtKST069BygPlxna2tm1HfuSema6aGtKST069Byg

abnormal amacrine cell morphology_Plxna2<tm1Hfu>/Plxna2<tm1Hfu>,Sema6a<Gt(KST069)Byg>/Sema6a<Gt(KST069)Byg>

表現型アノテーション

MGI marker

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

• plexin A2
  http://metadb.riken.jp/db/mgi_rdf/MGI:107684
• sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A
  http://metadb.riken.jp/db/mgi_rdf/MGI:1203727

遺伝子型

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

• Plxna2<tm1Hfu>/Plxna2<tm1Hfu>,Sema6a<Gt(KST069)Byg>/Sema6a<Gt(KST069)Byg>

アレルシンボル

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

• Plxna2<tm1Hfu>|Sema6a<Gt(KST069)Byg>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6NCrlj * CBA/JNCrlj

MP annotation

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

• abnormal amacrine cell morphology
  http://purl.obolibrary.org/obo/MP_0005240

文献

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

• Lu O. Sun, et.al., On and off retinal circuit assembly by divergent molecular mechanisms., Science (New York, N.Y.), 2013, 342
  http://rdf.ncbi.nlm.nih.gov/pubmed/24179230