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NPR2

natriuretic peptide receptor 2

HCNC Approved Symbol
NPR2 (HGNC:7944)
Genomic Coordinates
9:35,791,591 - 35,809,731 (9p13.3)
Synonyms
GUCY2B, ANPb, GC-B, ANPRB, NPRB, AMDM
Disease Associations
This gene is associated with the following 3 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Acromesomelic dysplasia 1, Maroteaux type
602875AR
Epiphyseal chondrodysplasia, Miura type
615923AD
Short stature with nonspecific skeletal abnormalities
616255AD

Diagnosed Cases

17Patients

In total, 17 patients were diagnosed with a variant in the NPR2 gene.

Frequently observed phenotypes

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

Skeletal dysplasia
 6 (35.3%)
Disproportionate short stature
 4 (23.5%)
Disproportionate dwarfism
 3 (17.6%)
Abnormal vertebral bodies
 
2 (11.8%)
Brachydactyly
 
2 (11.8%)