MAPKBP1 Chromosome 15
Mitogen-activated protein kinase binding protein 1
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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
RS139378790
Conflicting classifications of pathogenicity
Inborn genetic diseases, MAPKBP1-related disorder, Inborn genetic diseases
Health Risk
RS141214790
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS142880448
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS143368521
Conflicting classifications of pathogenicity
Inborn genetic diseases, MAPKBP1-related disorder, Inborn genetic diseases
Health Risk
RS147620917
Conflicting classifications of pathogenicity
MAPKBP1-related disorder, Nephronophthisis 20, MAPKBP1-related disorder
Health Risk
RS150009369
Conflicting classifications of pathogenicity
Inborn genetic diseases, MAPKBP1-related disorder, Inborn genetic diseases
Health Risk
RS199906537
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS201725344
Conflicting classifications of pathogenicity
Health Risk
RS2152083811
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS546384224
Conflicting classifications of pathogenicity
Nephronophthisis 20, Nephronophthisis 20
Health Risk
RS577983461
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1219418471
Likely pathogenic
MAPKBP1-related disorder, MAPKBP1-related disorder
Health Risk
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 |