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STX3

syntaxin 3

HCNC Approved Symbol
STX3 (HGNC:11438)
Genomic Coordinates
11:59,754,188 - 59,805,878 (11q12.1)
Synonyms
STX3A
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Diarrhea 12, with microvillus atrophy
619445AR
Retinal dystrophy and microvillus inclusion disease
619446AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the STX3 gene.

Frequently observed phenotypes

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

No Results