MAPKBP1 Chromosome 15

Mitogen-activated protein kinase binding protein 1
22 variants 22 Health Risk

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What This Gene Does
This gene encodes a scaffold protein that regulates the JNK (c-Jun N-terminal kinase) and NOD2 (nucleotide-binding oligomerization domain-containing protein 2) signaling pathways. The encoded protein interacts with another related JNK pathway scaffold protein, WDR62, via a conserved dimerization domain, and enhances JNK signaling. This protein may play a role in bacterial immunity by binding to the NOD2 receptor and negatively regulating downstream antibacterial and pro-inflammatory signaling. Mutations in this gene that impair cellular localization of the encoded protein cause a form of nephronophthisis, an autosomal-recessive kidney disorder, in human patients. [provided by RefSeq, May 2017]
Gene Info
Gene Group
WD repeat domain containing
Locus Type
gene with protein product
Location
15q15.1
Ensembl
ENSG00000137802
Associated Conditions (3)
Inborn genetic diseases
MAPKBP1-related disorder
Nephronophthisis 20
Key Variants
All Variants (22)
RSID Category Clinical Significance Conditions
RS139378790 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, MAPKBP1-related disorder, Inborn genetic diseases
RS141214790 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS142880448 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS143368521 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, MAPKBP1-related disorder, Inborn genetic diseases
RS147620917 Health Risk Conflicting classifications of pathogenicity MAPKBP1-related disorder, Nephronophthisis 20, MAPKBP1-related disorder
RS150009369 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, MAPKBP1-related disorder, Inborn genetic diseases
RS199906537 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS201725344 Health Risk Conflicting classifications of pathogenicity
RS2152083811 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS546384224 Health Risk Conflicting classifications of pathogenicity Nephronophthisis 20, Nephronophthisis 20
RS577983461 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1219418471 Health Risk Likely pathogenic MAPKBP1-related disorder, MAPKBP1-related disorder
RS1301664794 Health Risk Likely pathogenic
RS1596088812 Health Risk Likely pathogenic Nephronophthisis 20, Nephronophthisis 20
RS2551103543 Health Risk Likely pathogenic Nephronophthisis 20, Nephronophthisis 20
RS1057519303 Health Risk Pathogenic Nephronophthisis 20, Nephronophthisis 20
RS1057519304 Health Risk Pathogenic Nephronophthisis 20, Nephronophthisis 20
RS1057519305 Health Risk Pathogenic Nephronophthisis 20, Nephronophthisis 20
RS1057519306 Health Risk Pathogenic Nephronophthisis 20, Nephronophthisis 20
RS202001274 Health Risk Pathogenic Nephronophthisis 20, Nephronophthisis 20
RS752616462 Health Risk Pathogenic Nephronophthisis 20, Nephronophthisis 20
RS2152080114 Health Risk Pathogenic/Likely pathogenic Nephronophthisis 20, MAPKBP1-related disorder, Nephronophthisis 20
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