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MAMMALIAN PHENOTYPE - ANNOTATIONS

The Mouse Adult Gross Anatomy Ontology and Mammalian Phenotype Ontology are downloaded weekly from the Mouse Genome Informatics databases at Jackson Laboratories (ftp://ftp.informatics.jax.org/pub/reports/index.html). For more information about these ontologies, see the MGI Publications Page at http://www.informatics.jax.org/mgihome/other/publications.shtml.

Term:abnormal inner ear morphology
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Accession:MP:0000026 term browser browse the term
Definition:any structural anomaly of any components of the labyrinth, including the semicircular canals, vestibule and cochlea
Synonyms:exact_synonym: inner ear dysplasia
 xref: GO:0042472



show annotations for term's descendants           Sort by:
abnormal cochlear hair cell stereociliary bundle morphology term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Myo7a myosin VIIA IAGP DNA:nonsense mutation:cds RGD PMID:15965244 RGD:1581470 NCBI chr 1:152,342,611...152,414,171
Ensembl chr 1:152,344,448...152,414,157
JBrowse link
G Myo7atnd/Hubr myosin VIIA; ENU induced tornado mutant, Hubr IAGP DNA:nonsense mutation:cds RGD PMID:15965244 RGD:1581470
absent otoliths term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Cyba cytochrome b-245 alpha chain IAGP DNA:deletion:splice junction: RGD PMID:19406829 RGD:11040542 NCBI chr19:50,487,598...50,495,669
Ensembl chr19:50,487,597...50,495,721
JBrowse link
G Cybam1Sdi cytochrome b-245 alpha chain;mutant 1,Sdi IAGP DNA:deletion:splice junction: RGD PMID:19406829 RGD:11040542
thin stria vascularis term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ednrb endothelin receptor type B IAGP RGD PMID:21915282 RGD:6480217 NCBI chr15:80,640,839...80,672,115
Ensembl chr15:80,643,043...80,672,115
JBrowse link
G Ednrbsl endothelin receptor type B, spotting lethal IAGP RGD PMID:21915282 RGD:6480217

Term paths to the root
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Term Annotations click to browse term
  mammalian phenotype 5402
    hearing/vestibular/ear phenotype 23
      abnormal ear morphology 12
        abnormal inner ear morphology 11
          abnormal bony labyrinth + 0
          abnormal cochlea morphology + 7
          abnormal hair cell morphology + 4
          abnormal inner ear canal morphology + 0
          abnormal inner ear development + 0
          abnormal inner ear vestibule morphology + 0
          abnormal internal auditory canal morphology 0
          abnormal membranous labyrinth morphology + 11
          abnormal otic capsule morphology + 0
          abnormal pars superior vestibularis morphology 0
          abnormal round window morphology + 0
          abnormal sulcus ampullaris morphology 0
          abnormal vestibular aqueduct morphology 0
          absent inner ear 0
          inner ear cyst 0
          inner ear hypoplasia 0
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