Gene:
GLRA1
glycine receptor, alpha 1

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.

? = Mouse-over for quick help

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:  STHE; startle disease/hyperekplexia; stiff person syndrome
Alternate Symbols:  None
PharmGKB Accession Id: PA28727

Details

Cytogenetic Location: chr5 : q32 - q33.1
GP mRNA Boundary: chr5 : 151202074 - 151304397
GP Gene Boundary: chr5 : 151199074 - 151314397
Strand: minus
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:
2741
OMIM:
138491
149400
UCSC Genome Browser:
NM_000171
RefSeq RNA:
NM_000171
NM_001146040
RefSeq Protein:
NP_000162
NP_001139512
RefSeq DNA:
AC_000048
AC_000137
NC_000005
NG_011764
NT_029289
NW_001838953
NW_922784
UniProtKB:
GLRA1_HUMAN (P23415)
Ensembl:
ENSG00000145888
GenAtlas:
GLRA1
GeneCard:
GLRA1
MutDB:
GLRA1
ALFRED:
LO006775Z
HuGE:
GLRA1
Comparative Toxicogenomics Database:
2741
ModBase:
P23415
HumanCyc Gene:
HS07298
IUPHAR Receptor:
α1 (423)
HGNC:
4326

Common Searches