LCA5
gene productC6orf152
This gene encodes a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. Alternatively spliced transcript variants are described. [provided by RefSeq, Oct 2009]
Featured antibodies
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0 references | Polyclonal |
WB
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0 references | Polyclonal |
WB
![]() EL ![]() IHC
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Antibodies
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