HYLS1 Back

hydrolethalus syndrome 1

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of HYLS1

This gene encodes a protein localized to the cytoplasm. Mutations in this gene are associated with hydrolethalus syndrome. Multiple alternatively spliced variants, encoding the same protein, have been identified.

Community Annotation of HYLS1 Add / Edit HYLS1: Annotations

No community annotations yet for HYLS1.
Sort mutations by: Tumor type  Mutation type  Position  
Straightedge cursor Expand

Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

HYLS1 is highly significantly mutated in
(none)
HYLS1 is significantly mutated in
(none)
HYLS1 is near significance in
(none)

Click on a tumor type to see its full list of significant genes.

Data details


Mutation list for HYLS1