Tissue expression
Cell line expression
Protein structure
LCA5
Lebercilin LCA5C6orf152
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]
Top validated antibodies |
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Proteintech Group | ![]() |
4 references | Polyclonal |
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antibodies-online | ![]() |
2 references | Polyclonal |
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Atlas Antibodies | ![]() |
Polyclonal |
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Novus Biologicals | ![]() |
Polyclonal |
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Invitrogen Antibodies | ![]() |
Polyclonal |
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