P J. Kozel, et.al., Balance and hearing deficits in mice with a null mutation in the gene encoding plasma membrane Ca2+-ATPase isoform 2., The Journal of biological chemistry, 1998, 273

http://rdf.ncbi.nlm.nih.gov/pubmed/9668038

P J. Kozel, et.al., Balance and hearing deficits in mice with a null mutation in the gene encoding plasma membrane Ca2+-ATPase isoform 2., The Journal of biological chemistry, 1998, 273

pubmed

allele

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

• Atp2b2<tm1Ges>
  http://metadb.riken.jp/db/mgi_rdf/MGI:1857876

表現型アノテーション

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

• absent tunnel of Corti_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0003151I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• impaired righting response_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0001523I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• decreased body weight_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0001262I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• abnormal inner ear morphology_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0000026I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• abnormal reflex_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0001961I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• absent cochlear hair cells_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0004405I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• ataxia_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0001393I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• increased or absent threshold for auditory brainstem response_Atp2b2<tm1Ges>/Atp2b2<+>
  http://metadb.riken.jp/0011967I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2Atp2b2tm1GesAtp2b2
• increased Purkinje cell number_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0000879I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• increased or absent threshold for auditory brainstem response_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0011967I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• decreased cochlear hair cell number_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0004408I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• absent organ of Corti supporting cells_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0004301I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• abnormal organ of Corti morphology_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0000042I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• absent pillar cells_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0004312I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• decreased organ of Corti supporting cell number_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0004497I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• absent otoliths_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0002978I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• deafness_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0001967I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• abnormal organ of Corti morphology_Atp2b2<tm1Ges>/Atp2b2<+>
  http://metadb.riken.jp/0000042I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2Atp2b2tm1GesAtp2b2
• abnormal cochlear nerve morphology_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0004716I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• abnormal cerebellum morphology_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0000849I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• impaired hearing_Atp2b2<tm1Ges>/Atp2b2<+>
  http://metadb.riken.jp/0006325I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2Atp2b2tm1GesAtp2b2
• abnormal gait_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0001406I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• impaired balance_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0001525I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• sensorineural hearing loss_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0004740I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• thin cerebellar molecular layer_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0000890I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• abnormal inner ear vestibule morphology_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0000034I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges
• abnormal cerebellar granule cell morphology_Atp2b2<tm1Ges>/Atp2b2<tm1Ges>
  http://metadb.riken.jp/0004098I129Sv129X1SvJBlackSwissAtp2b2tm1GesAtp2b2tm1GesAtp2b2tm1Ges

class

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

• Atp2b2<tm1Ges>
  http://metadb.riken.jp/db/mgi_rdf/MGI:1857876

article

http://www.w3.org/2000/01/rdf-schema#seeAlso

• [Blank]

BRC マウスの系統

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

• FVB.Cg-Atp2b2<tm1Ges>
  http://metadb.riken.jp/db/rikenbrc_mouse/RBRC04709

表現型アノテーション

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

• decreased cochlear hair cell number in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011958
• abnormal reflex in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011949
• absent tunnel of Corti in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011952
• abnormal inner ear vestibule morphology in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011938
• decreased organ of Corti supporting cell number in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011962
• abnormal cochlear nerve morphology in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011965
• impaired balance in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011948
• abnormal gait in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011946
• absent otoliths in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011951
• increased Purkinje cell number in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011942
• ataxia in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011945
• absent cochlear hair cells in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011957
• impaired righting response in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011947
• deafness in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011950
• abnormal organ of Corti morphology in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011939
• decreased body weight in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011944
• thin cerebellar molecular layer in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011943
• absent organ of Corti supporting cells in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011955
• sensorineural hearing loss in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011968
• abnormal inner ear morphology in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011937
• impaired hearing in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011970
• abnormal cerebellum morphology in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011941
• abnormal cerebellar granule cell morphology in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011953
• absent pillar cells in RBRC04709
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1011956

article

http://www.w3.org/2000/01/rdf-schema#seeAlso

• [Blank]