absent corpus callosum_Tubb2b<brdp>/Tubb2b<brdp>

http://metadb.riken.jp/0002196IAJFVBTubb2bbrdpTubb2bbrdpTubb2bbrdp

absent corpus callosum_Tubb2b<brdp>/Tubb2b<brdp>

表現型アノテーション

MGI marker

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

• tubulin, beta 2B class IIB
  http://metadb.riken.jp/db/mgi_rdf/MGI:1920960

遺伝子型

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

• Tubb2b<brdp>/Tubb2b<brdp>

アレルシンボル

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

• Tubb2b<brdp>

遺伝的背景

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

• involves: A/J * FVB

MP annotation

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

• absent corpus callosum
  http://purl.obolibrary.org/obo/MP_0002196

文献

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

• R W. Stottmann, et.al., A mutation in Tubb2b, a human polymicrogyria gene, leads to lethality and abnormal cortical development in the mouse., Human molecular genetics, 2013, 22
  http://rdf.ncbi.nlm.nih.gov/pubmed/23727838