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HOXB1

homeobox B1

HCNC Approved Symbol
HOXB1 (HGNC:5111)
Genomic Coordinates
17:48,528,526 - 48,531,011 (17q21.32)
Synonyms
HOX2, HOX2I
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Facial paresis, hereditary congenital, 3
614744AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the HOXB1 gene.

Frequently observed phenotypes

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

No Results