abnormal parietal bone morphology_Gja1<tm1Kdr>/Gja1<tm1Kdr>

http://metadb.riken.jp/0000109I129S1Sv129X1SvJC57BLGja1tm1KdrGja1tm1KdrGja1tm1Kdr

abnormal parietal bone morphology_Gja1<tm1Kdr>/Gja1<tm1Kdr>

表現型アノテーション

MGI marker

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

• gap junction protein, alpha 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:95713

遺伝子型

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

• Gja1<tm1Kdr>/Gja1<tm1Kdr>

アレルシンボル

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

• Gja1<tm1Kdr>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ * C57BL

MP annotation

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

• abnormal parietal bone morphology
  http://purl.obolibrary.org/obo/MP_0000109

文献

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

• F. Lecanda, et.al., Connexin43 deficiency causes delayed ossification, craniofacial abnormalities, and osteoblast dysfunction., The Journal of cell biology, 2000, 151
  http://rdf.ncbi.nlm.nih.gov/pubmed/11076975