abnormal cell cytoskeleton morphology_Pou1f1<dw>/Pou1f1<dw>

http://metadb.riken.jp/0020378NSPou1f1dwPou1f1dwPou1f1dw

abnormal cell cytoskeleton morphology_Pou1f1<dw>/Pou1f1<dw>

表現型アノテーション

MGI marker

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

• POU domain, class 1, transcription factor 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:97588

遺伝子型

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

• Pou1f1<dw>/Pou1f1<dw>

アレルシンボル

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

• Pou1f1<dw>

遺伝的背景

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

• Not Specified

MP annotation

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

• http://purl.obolibrary.org/obo/MP_0020378

文献

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

• Mirna. Mustapha, et.al., Deafness and permanently reduced potassium channel gene expression and function in hypothyroid Pit1dw mutants., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2009, 29
  http://rdf.ncbi.nlm.nih.gov/pubmed/19176829