abnormal enamel rod pattern_Amelx<Rgsc888>/Amelx<+>

http://metadb.riken.jp/0002649IC57BL6JJclDBA2JAmelxRgsc888AmelxAmelxRgsc888Amelx

abnormal enamel rod pattern_Amelx<Rgsc888>/Amelx<+>

表現型アノテーション

MGI marker

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

• amelogenin, X-linked
  http://metadb.riken.jp/db/mgi_rdf/MGI:88005

遺伝子型

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

• Amelx<Rgsc888>/Amelx<+>

アレルシンボル

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

• Amelx<Rgsc888>|Amelx<+>

遺伝的背景

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

• involves: C57BL/6JJcl * DBA/2J

MP annotation

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

• abnormal enamel rod pattern
  http://purl.obolibrary.org/obo/MP_0002649

文献

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

• Martin J. Barron, et.al., A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta., Human molecular genetics, 2010, 19
  http://rdf.ncbi.nlm.nih.gov/pubmed/20067920