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SP7

Sp7 transcription factor

HCNC Approved Symbol
SP7 (HGNC:17321)
Genomic Coordinates
12:53,326,575 - 53,344,793 (12q13.13)
Synonyms
osterix, OSX
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Osteogenesis imperfecta, type XII
613849AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SP7 gene.

Frequently observed phenotypes

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

No Results