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HNRNPA2B1

heterogeneous nuclear ribonucleoprotein A2/B1

HCNC Approved Symbol
HNRNPA2B1 (HGNC:5033)
Genomic Coordinates
7:26,189,927 - 26,200,746 (7p15.2)
Synonyms
HNRNPA2, HNRNPB1, HNRPA2B1
Disease Associations
This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the HNRNPA2B1 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Progressive muscle weakness
 1 (100.0%)
Respiratory insufficiency due to muscle weakness
 1 (100.0%)
Right bundle branch block
 1 (100.0%)
HNRNPA2B1 - Gene browser | 3billion