The domain within your query sequence starts at position 5 and ends at position 133; the E-value for the RD3 domain shown below is 5.3e-54.
SWVKWPRNYSYKQTRYAGSEVVTKTLLRELKWHLKERERLIHEIENEQKVKKTGVDYNWL RSYQTSHTMIPATEQRQLEVLCSQVQPCQAGTVLSRFRELLAENDVLPWEIVYIFKQVLK DFLSSPARG
RD3 |
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PFAM accession number: | PF14473 |
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Interpro abstract (IPR028092): | In humans, Retinal degeneration protein 3 (RD3) is found preferentially expressed in the retina [ (PUBMED:12914764) ]. Mutations in RD3 causes Leber Congenital Amaurosis type 12,which is a severe dystrophy of the retina, typically becoming evident in the first years of life [ (PUBMED:17186464) ]. |
This is a PFAM domain. For full annotation and more information, please see the PFAM entry RD3