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BMPR1B

bone morphogenetic protein receptor type 1B

HCNC Approved Symbol
BMPR1B (HGNC:1077)
Genomic Coordinates
4:94,757,955 - 95,158,450 (4q22.3)
Synonyms
ALK6, CDw293
Disease Associations
This gene is associated with the following 3 diseases in OMIM.

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the BMPR1B gene.

Frequently observed phenotypes

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

No Results
BMPR1B - Gene browser | 3billion