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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?|
|Alternate Names:||Four-and-a-half LIM domains 1; LIM protein SLIMMER|
|Alternate Symbols: ||FHL1B; FLH1A; KYO-T; MGC111107; SLIM1; XMPMA; bA535K18.1|
|PharmGKB Accession Id:||PA28141|
|Cytogenetic Location:||chrX : q26.3 - q26.3|
|GP mRNA Boundary†:||chrX : 135228861 - 135293518|
|GP Gene Boundary†:||chrX : 135218861 - 135296518|
Publications related to FHL1: 3
The following icons indicate that data of a certain type is available:
- DG Dosing Guideline information is available
- DL Drug Label information is available
- CA High-level Clinical Annotation is available
- VA Variant Annotation is available
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- PW Pathway is available
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||An X-linked myopathy with postural muscle atrophy and generalized hypertrophy, termed XMPMA, is caused by mutations in FHL1. American journal of human genetics. 2008. Windpassinger Christian, et al.|
||X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1. American journal of human genetics. 2008. Quinzii Catarina M, et al.|
||Classification, subtype discovery, and prediction of outcome in pediatric acute lymphoblastic leukemia by gene expression profiling. Cancer cell. 2002. Yeoh Eng-Juh, et al.|
- Entrez Gene:
- UCSC Genome Browser:
- RefSeq RNA:
- RefSeq Protein:
- RefSeq DNA: