FKTN-Related Disorders
Clinical Genetic Test
offered by
GTR Test Accession: Help GTR000569236.1
Last updated in GTR: 2019-10-22
Last annual review date for the lab: 2023-12-27 LinkOut
At a Glance
Walker-Warburg congenital muscular dystrophy; Autosomal recessive limb-girdle muscular dystrophy type 2M; Muscle eye brain disease more...
Genes (1): Help
FKTN (9q31.2)
Molecular Genetics - Sequence analysis of the entire coding region: Next-Generation (NGS)/Massively parallel sequencing (MPS)
Adult patients of reproductive age
Not provided
Not provided
Ordering Information
Offered by: Help
Myriad Genetics, Inc.
View lab's website
Specimen Source: Help
Contact Policy: Help
Post-test email/phone consultation regarding genetic test results and interpretation is provided to patients/families.
Informed consent required: Help
Decline to answer
Pre-test genetic counseling required: Help
Decline to answer
Post-test genetic counseling required: Help
Decline to answer
Recommended fields not provided:
Conditions Help
Total conditions: 4
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 1
Gene Associated Condition Germline or Somatic Allele (Lab-provided) Variant in NCBI
Total methods: 1
Method Category Help
Test method Help
Instrument *
Sequence analysis of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)
* Instrument: Not provided
Clinical Information
Test purpose: Help
Target population: Help
Adult patients of reproductive age
Recommended fields not provided:
Technical Information
Availability: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
>99% sensitivity and specificity for single nucleotide variants and small (<5 bp) insertions and deletions. >75% sensitivity and >99% specificity for large deletions.
Proficiency testing (PT):
Is proficiency testing performed for this test? Help
Recommended fields not provided:
Regulatory Approval
FDA Review: Help
Not provided
NYS CLEP Approval: Help
Number: 8535
Status: Approved
Additional Information

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