Gene:
HPS4
Hermansky-Pudlak syndrome 4

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:  None
Alternate Symbols:  KIAA1667; LE
PharmGKB Accession Id: PA29434

Details

Cytogenetic Location: chr22 : q12.3 - q12.1
GP mRNA Boundary: chr22 : 26847446 - 26879820
GP Gene Boundary: chr22 : 26844446 - 26889820
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.

Publications related to HPS4: 1

No Dosing Guideline available No Drug Label available No Clinical Annotation available No Variant Annotation available No VIP available No VIP available
Classification of pediatric acute lymphoblastic leukemia by gene expression profiling. Blood. 2003. Ross Mary E, et al. PubMed

LinkOuts

Entrez Gene:
89781
OMIM:
203300
606682
UCSC Genome Browser:
NM_022081
RefSeq RNA:
NM_022081
NM_152841
RefSeq Protein:
NP_071364
NP_690054
RefSeq DNA:
AC_000065
AC_000154
NC_000022
NG_009763
NT_011520
NW_001838745
NW_927628
UniProtKB:
HPS4_HUMAN (Q9NQG7)
Ensembl:
ENSG00000100099
GenAtlas:
HPS4
GeneCard:
HPS4
MutDB:
HPS4
ALFRED:
LO144196Z
HuGE:
HPS4
Comparative Toxicogenomics Database:
89781
ModBase:
Q9NQG7
HumanCyc Gene:
HS12385
HGNC:
15844

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