Gene:
GRN
granulin

PharmGKB contains no dosing guidelines for this . To report known genotype-based dosing guidelines, or if you are interested in developing guidelines, click here.

PharmGKB has no annotated drug labels with pharmacogenomic information for this . If you know of a drug label with PGx, send us a message.

PharmGKB contains no Clinical Variants that meet the highest level of criteria.

Disclaimer: The PharmGKB's clinical annotations reflect expert consensus based on clinical evidence and peer-reviewed literature available at the time they are written and are intended only to assist clinicians in decision-making and to identify questions for further research. New evidence may have emerged since the time an annotation was submitted to the PharmGKB. The annotations are limited in scope and are not applicable to interventions or diseases that are not specifically identified.

The annotations do not account for individual variations among patients, and cannot be considered inclusive of all proper methods of care or exclusive of other treatments. It remains the responsibility of the health-care provider to determine the best course of treatment for a patient. Adherence to any guideline is voluntary, with the ultimate determination regarding its application to be made solely by the clinician and the patient. PharmGKB assumes no responsibility for any injury or damage to persons or property arising out of or related to any use of the PharmGKB clinical annotations, or for any errors or omissions.

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This is a non-comprehensive list of genetic tests with pharmacogenetics relevance, typically submitted by the manufacturer and manually curated by PharmGKB. The information listed is provided for educational purposes only and does not constitute an endorsement of any listed test or manufacturer.

A more complete listing of genetic tests is found at the Genetic Testing Registry (GTR).

PGx Test Variants Assayed Related Drugs?

Overview

Alternate Names:  progranulin
Alternate Symbols:  CLN11; PCDGF; PGRN
PharmGKB Accession Id: PA28998

Details

Cytogenetic Location: chr17 : q21.32 - q21.31
GP mRNA Boundary: chr17 : 42422491 - 42430470
GP Gene Boundary: chr17 : 42412491 - 42433470
Strand: plus
The mRNA boundaries are calculated using the gene's default feature set from NCBI, mapped onto the UCSC Golden Path. PharmGKB sets gene boundaries by expanding the mRNA boundaries by no less than 10,000 bases upstream (5') and 3,000 bases downstream (3') to allow for potential regulatory regions.

LinkOuts

Entrez Gene:
2896
OMIM:
138945
607485
UCSC Genome Browser:
NM_002087
RefSeq RNA:
NM_002087
RefSeq Protein:
NP_002078
RefSeq DNA:
AC_000060
AC_000149
NC_000017
NG_007886
NT_010783
NW_001838437
NW_926839
UniProtKB:
GRN_HUMAN (P28799)
Ensembl:
ENSG00000030582
GenAtlas:
GRN
GeneCard:
GRN
MutDB:
GRN
ALFRED:
LO218339A
HuGE:
GRN
Comparative Toxicogenomics Database:
2896
ModBase:
P28799
HumanCyc Gene:
HS00479
HGNC:
4601

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