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A reference for what the literature reports. Not medical advice.

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Proteins/UNIPROT:O43822

CFAP410

Protein·UNIPROT:O43822

Open in the graph

Plays a role in cilia formation and/or maintenance (By similarity). Plays a role in the regulation of cell morphology and cytoskeletal organization. Involved in DNA damage repair..

Function from UniProtKB (O43822), read 2026-09-23. CC BY 4.0.

Curated compounds routed: 0

What the reference databases state

Inferred

Inferred — not reported by a source. Evidence key

GenCC submitters' classifications

4 rows

amyotrophic lateral sclerosis has a germline basis in CFAP410DiseaseGenCC HGNC:1260|MONDO:0004976Inferred only
axial spondylometaphyseal dysplasia has a germline basis in CFAP410DiseaseGenCC HGNC:1260|MONDO:0011211Inferred only
ciliopathy has a germline basis in CFAP410DiseaseGenCC HGNC:1260|MONDO:0005308Inferred only
cone-rod dystrophy has a germline basis in CFAP410DiseaseGenCC HGNC:1260|MONDO:0015993Inferred only

Statements

5 statements

5 statements · 2 reference databases · Subject: CFAP410 · Sources: Hetionet, WikiPathways

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MROH1 covaries with CFAP410ProteinHetionet hetionet:covaries:727957-755Inferred only
CFAP410 covaries with USP36ProteinHetionet hetionet:covaries:57602-755Inferred only
CFAP410 interacts with UBCProteinHetionet hetionet:interacts:7316-755Inferred only
CFAP410 participates in Bardet Biedl syndromePathwayWikiPathways WP5234Inferred only
CFAP410 participates in CiliopathiesPathwayWikiPathways WP4803Inferred only

Other names

5 names

Resolves to: CFAP410

Also called: C21orf-HUMF09G8.5C21orf2Leucine-rich repeat-containing protein 76LRRC76YF5/A2

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