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ATR

ATR checkpoint kinase
2 disorders 1 no genetic record 1 causative 3q23 gene with protein product
HGNC:882MonarchNCBI Gene 545ENSG00000175054UniProt Q13535OMIM 601215

Aliases: FRP1, SCKL, SCKL1, MEC1.

In the knowledge base · computed from kb/ at build time

Disorders

Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.

DisorderRelationshipWhere the gene appears
Seckel syndrome causative
mechanism: ATR-related DNA damage checkpoint disruption
subtype: SCKL1
scoped to subtype: SCKL1
Parvovirus B19 Infection no genetic record
mechanism: Cell Cycle Arrest and Apoptosis

Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.