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ALG14

ALG14 UDP-N-acetylglucosaminyltransferase subunit

HCNC Approved Symbol
ALG14 (HGNC:28287)
Genomic Coordinates
1:94,974,405 - 95,072,951 (1p21.3)
Synonyms
MGC19780
Disease Associations
This gene is associated with the following 3 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Myasthenic syndrome, congenital, 15, without tubular aggregates
616227AR
Intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies
619031AR
Myopathy, epilepsy, and progressive cerebral atrophy
619036AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the ALG14 gene.

Frequently observed phenotypes

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

No Results