SAR1A

secretion associated Ras related GTPase 1A

2 disorders 1 modifier 1 no genetic record 10q22.1 gene with protein product

HGNC:10534 Monarch NCBI Gene 56681 ENSG00000079332 UniProt Q9NR31 OMIM 607691

Previous symbols: SARA1. Aliases: SAR1, Sara.

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.

Disorder	Relationship	Where the gene appears
Chylomicron Retention Disease	modifier unknown
Nemaline Myopathy	no genetic record	mechanism: Ubiquitin-Proteasome Pathway Dysregulation (KLHL40)

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