PKD1L1 Chromosome 7

Polycystin 1 like 1, transient receptor potential channel interacting
78 variants 78 Health Risk

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What This Gene Does
This gene encodes a member of the polycystin protein family containing 11 transmembrane domains, a receptor for egg jelly (REJ) domain, and a polycystin-1, lipoxygenase, alpha-toxin (PLAT) domain. The encoded protein may play a role in the male reproductive system. Alternative splice variants have been described but their biological nature has not been determined. [provided by RefSeq, Jul 2008]
Associated Conditions (8)
PKD1L1-related disorder
Inborn genetic diseases
Heterotaxy
visceral
8
autosomal
Situs inversus
Visceral heterotaxy
Key Variants
All Variants (78)
RSID Category Clinical Significance Conditions
RS10274334 Health Risk Conflicting classifications of pathogenicity
RS111983425 Health Risk Conflicting classifications of pathogenicity PKD1L1-related disorder, PKD1L1-related disorder
RS116988549 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS139293796 Health Risk Conflicting classifications of pathogenicity
RS139651403 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, PKD1L1-related disorder, Inborn genetic diseases
RS139858574 Health Risk Conflicting classifications of pathogenicity
RS140064044 Health Risk Conflicting classifications of pathogenicity Heterotaxy, visceral, 8
RS141015632 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS141074403 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, PKD1L1-related disorder, Inborn genetic diseases
RS141425680 Health Risk Conflicting classifications of pathogenicity PKD1L1-related disorder, PKD1L1-related disorder
RS141685583 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, PKD1L1-related disorder, Inborn genetic diseases
RS142048596 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, PKD1L1-related disorder, Inborn genetic diseases
RS143597419 Health Risk Conflicting classifications of pathogenicity Heterotaxy, visceral, 8
RS144104914 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS145827073 Health Risk Conflicting classifications of pathogenicity Heterotaxy, visceral, 8
RS146513154 Health Risk Conflicting classifications of pathogenicity PKD1L1-related disorder, Inborn genetic diseases, PKD1L1-related disorder
RS147141584 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS148549783 Health Risk Conflicting classifications of pathogenicity PKD1L1-related disorder, Inborn genetic diseases, PKD1L1-related disorder
RS149025049 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, PKD1L1-related disorder, Inborn genetic diseases
RS150679968 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, PKD1L1-related disorder, Inborn genetic diseases
RS189308323 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS370329516 Health Risk Conflicting classifications of pathogenicity PKD1L1-related disorder, Inborn genetic diseases, PKD1L1-related disorder
RS372682154 Health Risk Conflicting classifications of pathogenicity Heterotaxy, visceral, 8
RS544774439 Health Risk Conflicting classifications of pathogenicity PKD1L1-related disorder, Heterotaxy, visceral
RS544795414 Health Risk Conflicting classifications of pathogenicity Heterotaxy, visceral, 8
RS750052718 Health Risk Conflicting classifications of pathogenicity PKD1L1-related disorder, Inborn genetic diseases, PKD1L1-related disorder
RS751408049 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS752496736 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS765195623 Health Risk Conflicting classifications of pathogenicity Heterotaxy, visceral, 8
RS886037834 Health Risk Conflicting classifications of pathogenicity Situs inversus, Heterotaxy, visceral
RS953044138 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1007145713 Health Risk Likely pathogenic PKD1L1-related disorder, PKD1L1-related disorder
RS1368668141 Health Risk Likely pathogenic Situs inversus, Situs inversus
RS1453356354 Health Risk Likely pathogenic
RS1463074700 Health Risk Likely pathogenic PKD1L1-related disorder, PKD1L1-related disorder
RS1562988323 Health Risk Likely pathogenic PKD1L1-related disorder, PKD1L1-related disorder
RS1786877657 Health Risk Likely pathogenic Heterotaxy, visceral, 8
RS1787156507 Health Risk Likely pathogenic PKD1L1-related disorder, PKD1L1-related disorder
RS1787715929 Health Risk Likely pathogenic PKD1L1-related disorder, PKD1L1-related disorder
RS1787768161 Health Risk Likely pathogenic
RS199776435 Health Risk Likely pathogenic PKD1L1-related disorder, PKD1L1-related disorder
RS200518403 Health Risk Likely pathogenic Heterotaxy, visceral, 8
RS2128738625 Health Risk Likely pathogenic Heterotaxy, Heterotaxy
RS2128741114 Health Risk Likely pathogenic Heterotaxy, visceral, 8
RS2483884719 Health Risk Likely pathogenic Heterotaxy, visceral, 8
RS2483942654 Health Risk Likely pathogenic Heterotaxy, visceral, 8
RS2484009005 Health Risk Likely pathogenic
RS2484009393 Health Risk Likely pathogenic
RS2484097162 Health Risk Likely pathogenic PKD1L1-related disorder, PKD1L1-related disorder
RS765198326 Health Risk Likely pathogenic
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