Disease

Joubert syndrome 10

Definition
A Joubert syndrome that has_material_basis_in X-linked recessive inheritance of mutation in the OFD1 gene on chromosome Xp22.2.
Synonyms
  • JBTS10
Cross References
Parent Terms
Child Terms
None
Sources of Associations

Associated Genes

Gene
Species
Association
Disease Qualifier
Disease
Evidence
Based On
Source
References
Homo sapiensis implicated inJoubert syndrome 10
  • IAGP
Rattus norvegicusis implicated via orthologyJoubert syndrome 10
  • IEA
MGI:6194238
Mus musculusis implicated via orthologyJoubert syndrome 10
  • IEA
MGI:6194238
Xenopus laevisis implicated via orthologyJoubert syndrome 10
  • IEA
MGI:6194238
Xenopus tropicalisis implicated via orthologyJoubert syndrome 10
  • IEA
MGI:6194238
Xenopus tropicalisis implicated via orthologyJoubert syndrome 10
  • IEA
MGI:6194238
Danio reriois implicated via orthologyJoubert syndrome 10
  • IEA
MGI:6194238
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Associated Alleles

No data available

Associated Models

No data available