abnormal respiration_Phox2b<tm2Jbr>/Phox2b<+>

http://metadb.riken.jp/0001943I129S2SvPasC57BL6Phox2btm2JbrPhox2bPhox2bPhox2btm2Jbr

abnormal respiration_Phox2b<tm2Jbr>/Phox2b<+>

表現型アノテーション

MGI marker

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

• paired-like homeobox 2b
  http://metadb.riken.jp/db/mgi_rdf/MGI:1100882

遺伝子型

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

• Phox2b<tm2Jbr>/Phox2b<+>

アレルシンボル

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

• Phox2b<+>|Phox2b<tm2Jbr>

遺伝的背景

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

• involves: 129S2/SvPas * C57BL/6

MP annotation

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

• abnormal respiration
  http://purl.obolibrary.org/obo/MP_0001943

文献

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

• Véronique. Dubreuil, et.al., A human mutation in Phox2b causes lack of CO2 chemosensitivity, fatal central apnea, and specific loss of parafacial neurons., Proceedings of the National Academy of Sciences of the United States of America, 2008, 105
  http://rdf.ncbi.nlm.nih.gov/pubmed/18198276