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PharmGKB contains no Clinical Variants that meet the highest level of criteria.
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|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|
UCSC has a Genome Browser that you can use to view PharmGKB annotations for this gene in context with many other sources of information.View on UCSC Browser
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:
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- RefSeq RNA:
- RefSeq Protein:
- RefSeq DNA: