Disease

Meckel syndrome 6

Definition
A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the CC2D2A gene on chromosome 4p15.32.
Synonyms
  • Meckel-Gruber syndrome, type 6
  • MKS6
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 inMeckel syndrome 6
  • IAGP
Rattus norvegicusis implicated via orthologyMeckel syndrome 6
  • IEA
MGI:6194238
Mus musculusis implicated via orthologyMeckel syndrome 6
  • IEA
MGI:6194238
Xenopus laevisis implicated via orthologyMeckel syndrome 6
  • IEA
MGI:6194238
Danio reriois implicated via orthologyMeckel syndrome 6
  • IEA
MGI:6194238
Drosophila melanogasteris implicated via orthologyMeckel syndrome 6
  • IEA
MGI:6194238
Caenorhabditis elegansis implicated via orthologyMeckel syndrome 6
  • IEA
MGI:6194238
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Associated Alleles

No data available

Associated Models

No data available