Proteins/UNIPROT:Q86VQ0

LCA5

ProteinUNIPROT:Q86VQ0

Involved in intraflagellar protein (IFT) transport in photoreceptor cilia. Plays a role in the ciliary transport of photoreceptors outer segment proteins..

Function from UniProtKB (Q86VQ0), read 2026-09-23. CC BY 4.0.

Curated compounds routed: 0

What the reference databases state

GenCC submitters' classifications

4 rows

LCA5-related retinopathy has a germline basis in LCA5DiseaseGenCC HGNC:31923|MONDO:0100445Inferred only
Leber congenital amaurosis has a germline basis in LCA5DiseaseGenCC HGNC:31923|MONDO:0018998Inferred only
Leber congenital amaurosis 5 has a germline basis in LCA5DiseaseGenCC HGNC:31923|MONDO:0011473Inferred only
severe early-childhood-onset retinal dystrophy has a germline basis in LCA5DiseaseGenCC HGNC:31923|MONDO:0009549Inferred only

Statements

7 statements

7 statements · 2 reference databases · Subject: LCA5 · Sources: Hetionet, WikiPathways

Order

LCA5 covaries with DNHD1ProteinHetionet hetionet:covaries:144132-167691Inferred only
HEATR4 covaries with LCA5ProteinHetionet hetionet:covaries:167691-399671Inferred only
RTL4 covaries with LCA5ProteinHetionet hetionet:covaries:167691-340595Inferred only
SRPK2 interacts with LCA5ProteinHetionet hetionet:interacts:167691-6733Inferred only
LCA5 participates in Bardet Biedl syndromePathwayWikiPathways WP5234Inferred only
LCA5 participates in Ciliary landscapePathwayWikiPathways WP4352Inferred only
LCA5 participates in CiliopathiesPathwayWikiPathways WP4803Inferred only

Other names

3 names

Resolves to: LCA5

Also called: C6orf152Leber congenital amaurosis 5 proteinLebercilin

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