Leber Congenital Amaurosis 17 (LCA17)

Alias:
Lca17
Leber Congenital Amaurosis, Type 17
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Leber Congenital Amaurosis 17, also known as lca17, is related to klippel-feil syndrome 1 and synostoses, tarsal, carpal, and digital. An important gene associated with Leber Congenital Amaurosis 17 is GDF6 (Growth Differentiation Factor 6), and among its related pathways/superpathways are p70S6K Signaling and G-protein signaling RAC1 in cellular process. Affiliated tissues include retina and eye, and related phenotypes are ultra-low vision with retained motion projection and Increased shRNA abundance (Z-score > 2)
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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6
41
3

Medical Symptom

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Gene & Mutation

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Disease Model

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References Literature

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