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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q16518: Variant p.Pro363Thr

Retinoid isomerohydrolase
Gene: RPE65
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Variant information Variant position: help 363 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LP/P [Disclaimer] The variants are classified into three categories: LP/P, LB/B and US.
  • LP/P: likely pathogenic or pathogenic.
  • LB/B: likely benign or benign.
  • US: uncertain significance

Residue change: help From Proline (P) to Threonine (T) at position 363 (P363T, p.Pro363Thr). Indicates the amino acid change of the variant. The one-letter and three-letter codes for amino acids used in UniProtKB/Swiss-Prot are those adopted by the commission on Biochemical Nomenclature of the IUPAC-IUB.
Physico-chemical properties: help Change from medium size and hydrophobic (P) to medium size and polar (T) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -1 The score within a Blosum matrix for the corresponding wild-type to variant amino acid change. The log-odds score measures the logarithm for the ratio of the likelihood of two amino acids appearing by chance. The Blosum62 substitution matrix is used. This substitution matrix contains scores for all possible exchanges of one amino acid with another:
  • Lowest score: -4 (low probability of substitution).
  • Highest score: 11 (high probability of substitution).
More information can be found on the following page

Variant description: help In LCA2. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 363 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 533 The length of the canonical sequence.
Location on the sequence: help LANLRENWEEVKKNARKAPQ P EVRRYVLPLNIDKADTGKNL The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: help The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human                         LANLRENWEEVKKNARKAPQPEVRRYVLPLNIDKADTGKNL

                              LANLRENWEEVKKNARKAPQPEVRRYVLPLNIDKADTGKNL

Mouse                         LANLRENWEEVKRNAMKAPQPEVRRYVLPLTIDKVDTGRNL

Rat                           LANLRENWEEVKRNAMKAPQPEVRRYVLPLTIDKADTGRNL

Bovine                        LANLRENWEEVKKNARKAPQPEVRRYVLPLNIDKADTGKNL

Chicken                       LANLRANWDEVKKQAEKAPQPEARRYVLPLRIDKADTGKNL

Sequence annotation in neighborhood: help The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:
  • Type: the type of sequence feature.
  • Positions: endpoints of the sequence feature.
  • Description: contains additional information about the feature.
TypePositionsDescription
Chain 2 – 533 Retinoid isomerohydrolase



Literature citations
Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy.
Gu S.M.; Thompson D.A.; Srikumari C.R.; Lorenz B.; Finckh U.; Nicoletti A.; Murthy K.R.; Rathmann M.; Kumaramanickavel G.; Denton M.J.; Gal A.;
Nat. Genet. 17:194-197(1997)
Cited for: VARIANT LCA2 THR-363; Different functional outcome of RetGC1 and RPE65 gene mutations in Leber congenital amaurosis.
Perrault I.; Rozet J.-M.; Ghazi I.; Leowski C.; Bonnemaison M.; Gerber S.; Ducroq D.; Cabot A.; Souied E.; Dufier J.-L.; Munnich A.; Kaplan J.;
Am. J. Hum. Genet. 64:1225-1228(1999)
Cited for: VARIANTS LCA2 TYR-330; THR-363 AND VAL-434; Leber congenital amaurosis: comprehensive survey of the genetic heterogeneity, refinement of the clinical definition, and genotype-phenotype correlations as a strategy for molecular diagnosis.
Hanein S.; Perrault I.; Gerber S.; Tanguy G.; Barbet F.; Ducroq D.; Calvas P.; Dollfus H.; Hamel C.; Lopponen T.; Munier F.; Santos L.; Shalev S.; Zafeiriou D.; Dufier J.-L.; Munnich A.; Rozet J.-M.; Kaplan J.;
Hum. Mutat. 23:306-317(2004)
Cited for: VARIANTS LCA2 GLN-44; ASP-148; ASN-182; TYR-330; THR-363; VAL-434 AND ASP-473;
Disclaimer: Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.