no abnormal phenotype detected_Aldh1a3<tm1Pcn>/Aldh1a3<tm1Pcn>

http://metadb.riken.jp/0002169I129SvC57BL6Aldh1a3tm1PcnAldh1a3tm1PcnAldh1a3tm1Pcn

no abnormal phenotype detected_Aldh1a3<tm1Pcn>/Aldh1a3<tm1Pcn>

表現型アノテーション

MGI marker

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

• aldehyde dehydrogenase family 1, subfamily A3
  http://metadb.riken.jp/db/mgi_rdf/MGI:1861722

遺伝子型

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

• Aldh1a3<tm1Pcn>/Aldh1a3<tm1Pcn>

アレルシンボル

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

• Aldh1a3<tm1Pcn>

遺伝的背景

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

• involves: 129/Sv * C57BL/6

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• Valérie. Dupé, et.al., A newborn lethal defect due to inactivation of retinaldehyde dehydrogenase type 3 is prevented by maternal retinoic acid treatment., Proceedings of the National Academy of Sciences of the United States of America, 2003, 100
  http://rdf.ncbi.nlm.nih.gov/pubmed/14623956