FERMT1 Chromosome 20

FERM domain containing kindlin 1
51 variants 51 Health Risk

Upload your DNA to see your personal genotypes for variants in FERMT1.

What This Gene Does
This gene encodes a member of the fermitin family, and contains a FERM domain and a pleckstrin homology domain. The encoded protein is involved in integrin signaling and linkage of the actin cytoskeleton to the extracellular matrix. Mutations in this gene have been linked to Kindler syndrome. [provided by RefSeq, Dec 2009]
Gene Info
Gene Group
"Fermitins|Pleckstrin homology domain containing|FERM domain containing"
Locus Type
gene with protein product
Location
20p12.3
Ensembl
ENSG00000101311
Associated Conditions (4)
Kindler syndrome
Inborn genetic diseases
FERMT1-related disorder
Abnormality of the skin
Key Variants
All Variants (51)
RSID Category Clinical Significance Conditions
RS138986656 Health Risk Conflicting classifications of pathogenicity Kindler syndrome, Kindler syndrome
RS142825013 Health Risk Conflicting classifications of pathogenicity Kindler syndrome, Inborn genetic diseases, Kindler syndrome
RS150528781 Health Risk Conflicting classifications of pathogenicity Kindler syndrome, Kindler syndrome
RS184046854 Health Risk Conflicting classifications of pathogenicity Kindler syndrome, Kindler syndrome
RS201694674 Health Risk Conflicting classifications of pathogenicity Kindler syndrome, FERMT1-related disorder, Kindler syndrome
RS2232078 Health Risk Conflicting classifications of pathogenicity Kindler syndrome, Kindler syndrome
RS550863008 Health Risk Conflicting classifications of pathogenicity Kindler syndrome, Kindler syndrome
RS570732725 Health Risk Conflicting classifications of pathogenicity Kindler syndrome, FERMT1-related disorder, Kindler syndrome
RS6053893 Health Risk Conflicting classifications of pathogenicity Kindler syndrome, FERMT1-related disorder, Kindler syndrome
RS749711628 Health Risk Conflicting classifications of pathogenicity Kindler syndrome, Kindler syndrome
RS751558324 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS754424986 Health Risk Conflicting classifications of pathogenicity Kindler syndrome, Kindler syndrome
RS759081971 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS760256639 Health Risk Conflicting classifications of pathogenicity Kindler syndrome, Kindler syndrome
RS774007627 Health Risk Conflicting classifications of pathogenicity Kindler syndrome, Kindler syndrome
RS775613961 Health Risk Conflicting classifications of pathogenicity Kindler syndrome, Kindler syndrome
RS1172664527 Health Risk Likely pathogenic
RS1324272731 Health Risk Likely pathogenic
RS1983207985 Health Risk Likely pathogenic Kindler syndrome, Kindler syndrome
RS2514701114 Health Risk Likely pathogenic
RS869312723 Health Risk Likely pathogenic Kindler syndrome, Kindler syndrome
RS869312726 Health Risk Likely pathogenic Abnormality of the skin, Abnormality of the skin
RS869312731 Health Risk Likely pathogenic Kindler syndrome, Kindler syndrome
RS943430432 Health Risk Likely pathogenic
RS1064793979 Health Risk Pathogenic Kindler syndrome, Kindler syndrome
RS121918292 Health Risk Pathogenic Kindler syndrome, Kindler syndrome
RS121918293 Health Risk Pathogenic Kindler syndrome, FERMT1-related disorder, Kindler syndrome
RS121918294 Health Risk Pathogenic Kindler syndrome, Kindler syndrome
RS1318979798 Health Risk Pathogenic
RS139252668 Health Risk Pathogenic
RS1411462678 Health Risk Pathogenic Kindler syndrome, Kindler syndrome
RS146180696 Health Risk Pathogenic Kindler syndrome, FERMT1-related disorder, Kindler syndrome
RS1568654138 Health Risk Pathogenic Kindler syndrome, Kindler syndrome
RS1568664492 Health Risk Pathogenic Kindler syndrome, Kindler syndrome
RS1982142302 Health Risk Pathogenic Kindler syndrome, Kindler syndrome
RS1982268239 Health Risk Pathogenic Kindler syndrome, Kindler syndrome
RS1983080839 Health Risk Pathogenic Kindler syndrome, Kindler syndrome
RS2123105057 Health Risk Pathogenic
RS2123118335 Health Risk Pathogenic Kindler syndrome, Kindler syndrome
RS2123140877 Health Risk Pathogenic
RS2514703437 Health Risk Pathogenic
RS2514723064 Health Risk Pathogenic
RS2514723164 Health Risk Pathogenic
RS748240859 Health Risk Pathogenic Kindler syndrome, FERMT1-related disorder, Kindler syndrome
RS755090824 Health Risk Pathogenic Kindler syndrome, Kindler syndrome
RS761341202 Health Risk Pathogenic
RS765716291 Health Risk Pathogenic Kindler syndrome, Kindler syndrome
RS773429449 Health Risk Pathogenic Kindler syndrome, Kindler syndrome
RS779915885 Health Risk Pathogenic Kindler syndrome, Kindler syndrome
RS869312718 Health Risk Pathogenic Kindler syndrome, Kindler syndrome
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