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GRN

granulin precursor

HCNC Approved Symbol
GRN (HGNC:4601)
Genomic Coordinates
17:44,345,302 - 44,353,106 (17q21.31)
Synonyms
PCDGF, PGRN, CLN11
Disease Associations
This gene is associated with the following 3 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Aphasia, primary progressive
607485AD
Ceroid lipofuscinosis, neuronal, 11
614706AR
Frontotemporal lobar degeneration with ubiquitin-positive inclusions
607485AD

Diagnosed Cases

0Patient

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

Frequently observed phenotypes

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

No Results