The domain within your query sequence starts at position 102 and ends at position 295; the E-value for the Lebercilin domain shown below is 4.8e-71.



PFAM accession number:PF15619
Interpro abstract (IPR028933):

This entry represents a domain found in lebercilin (LCA5) and lebercilin like proteins. LCA5 might be involved in minus end-directed microtubule transport [ (PUBMED:17546029) ]. Defects in LCA5 are the cause of Leber congenital amaurosis type 5 (LCA5). LCA designates a clinically and genetically heterogeneous group of childhood retinal degenerations, generally inherited in an autosomal recessive manner. LCA represents the most common genetic cause of congenital visual impairment in infants and children [ (PUBMED:18000884) (PUBMED:17546029) (PUBMED:18334959) ].

This is a PFAM domain. For full annotation and more information, please see the PFAM entry Lebercilin