Previous symbols: HNRPA1. Aliases: hnRNP-A1, ALS20.
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 |
|---|---|---|
| Amyotrophic Lateral Sclerosis | causative |
mechanism: RNA-Binding Protein Mislocalization and Stress Granule Dysfunction
subtype: ALS20
scoped to subtype: ALS20
|
| Inclusion body myopathy with Paget disease of bone and frontotemporal dementia | causative |
mechanism: hnRNP prion-like domain fibril assembly; hnRNP recruitment into stress granules and cytoplasmic inclusions
subtype: IBMPFD3
scoped to subtype: IBMPFD3
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.