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LCA5


Official Full Name
lebercilin LCA5
Organism
Homo sapiens
Gene ID
167691
Background
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]
Synonyms
C6orf152

Cat.No. Product Name Price
SHH328783 shRNA set against Human LCA5 (NM_181714.3) Inquiry
SHH328787 shRNA set against Mouse LCA5 (NM_029434.3) Inquiry
SHH328791 shRNA set against Rat LCA5 (NM_001013954.1) Inquiry
Cat.No. Product Name Price
CDFL006852 Mouse Lca5 cDNA Clone(NM_029434.3) Inquiry
CDFR003033 Rat Lca5 cDNA Clone(NM_001013954.1) Inquiry
MiUTR1R-06628 LCA5 miRNA 3'UTR clone Inquiry
MiUTR4H-TG11640 LCA5 miRNA 3'UTR clone Inquiry
CDCB158333 Human LCA5 ORF clone (BC050327) Inquiry
CDCB186000 Rabbit LCA5 ORF clone (XM_008263136.1) Inquiry
CDCR007924 Mouse LCA5 ORF clone(NM_027448.2) Inquiry
CDCR262640 Mouse Lca5 ORF Clone(NM_029434.3) Inquiry
CDCR370109 Rat Lca5 ORF Clone(NM_001013954.1) Inquiry
CDCS418893 Human LCA5 ORF Clone (BC050327) Inquiry
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