Previous symbols: CD114. Aliases: GCSFR, G-CSF-R.
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 |
|---|---|---|
| Severe Congenital Neutropenia 1, Autosomal Dominant | somatic driver somatic partial loss of function |
mechanism: Acquisition of Somatic CSF3R Mutations; Clonal Evolution to Myelodysplasia and Acute Myeloid Leukaemia
|
| Severe Congenital Neutropenia 7, Autosomal Recessive | causative germline loss of function |
mechanism: Biallelic Loss-of-Function CSF3R Variants
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.