Gene:
MYNN
myoneurin

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

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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:  SBBIZ1; ZBTB31; ZNF902
PharmGKB Accession Id: PA31393

Details

Cytogenetic Location: chr3 : q26.2 - q26.2
GP mRNA Boundary: chr3 : 169490853 - 169507504
GP Gene Boundary: chr3 : 169480853 - 169510504
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:
55892
OMIM:
606042
UCSC Genome Browser:
NM_018657
RefSeq RNA:
NM_001185118
NM_001185119
NM_018657
NR_033702
NR_033703
RefSeq Protein:
NP_001172047
NP_001172048
NP_061127
MutDB:
MYNN
ALFRED:
LO049056Y
HuGE:
MYNN
ModBase:
Q86Z11
HumanCyc Gene:
HS01489
HGNC:
14955

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