Aliases: SRm300, SRL300, KIAA0324, Cwc21.
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 |
|---|---|---|
| Familial Nonmedullary Thyroid Carcinoma | susceptibility germline |
mechanism: Inherited Non-Syndromic Susceptibility in Thyroid Follicular Cells
|
| Intellectual Developmental Disorder, Autosomal Dominant 72 | causative de novo loss of function |
mechanism: SRRM2 Haploinsufficiency
dataset: geo:GSE299937
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.