preaxial polydactyly_2410089E03Rik<b2b012Clo>/2410089E03Rik<b2b012Clo>

http://metadb.riken.jp/0009743C57BL6J2410089E03Rikb2b012Clo2410089E03Rikb2b012Clo2410089E03Rikb2b012Clo2410089E03Rikb2b012Clo

preaxial polydactyly_2410089E03Rik<b2b012Clo>/2410089E03Rik<b2b012Clo>

表現型アノテーション

MGI marker

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

• RIKEN cDNA 2410089E03 gene
  http://metadb.riken.jp/db/mgi_rdf/MGI:1920942

遺伝子型

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

• 2410089E03Rik<b2b012Clo>/2410089E03Rik<b2b012Clo>

アレルシンボル

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

• 2410089E03Rik<b2b012Clo>

遺伝的背景

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

• C57BL/6J-2410089E03Rik<b2b012Clo>

MP annotation

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

• preaxial polydactyly
  http://purl.obolibrary.org/obo/MP_0009743

文献

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

• Rama Rao. Damerla, et.al., Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies., Human molecular genetics, 2015, 24
  http://rdf.ncbi.nlm.nih.gov/pubmed/25877302