SPRED1 Chromosome 15

Sprouty related EVH1 domain containing 1
178 variants 178 Health Risk

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What This Gene Does
The protein encoded by this gene is a member of the Sprouty family of proteins and is phosphorylated by tyrosine kinase in response to several growth factors. The encoded protein can act as a homodimer or as a heterodimer with SPRED2 to regulate activation of the MAP kinase cascade. Defects in this gene are a cause of neurofibromatosis type 1-like syndrome (NFLS). [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"Protein phosphatase 1 regulatory subunits|Sprouty related EVH1 domain containing "
Locus Type
gene with protein product
Location
15q14
Ensembl
ENSG00000166068
Associated Conditions (12)
Legius syndrome
Noonan syndrome and Noonan-related syndrome
Cardiovascular phenotype
SPRED1-related disorder
Noonan syndrome
Neurofibromatosis
type 1
Neurodevelopmental delay
Inborn genetic diseases
See cases
Incidental Discovery
Male infertility with spermatogenesis disorder
Key Variants
RS114636635
Conflicting classifications of pathogenicity
Legius syndrome, Noonan syndrome and Noonan-related syndrome, Cardiovascular phenotype
Health Risk
RS115440602
Conflicting classifications of pathogenicity
Legius syndrome, Cardiovascular phenotype, Legius syndrome
Health Risk
RS1241478218
Conflicting classifications of pathogenicity
Legius syndrome, Cardiovascular phenotype, Legius syndrome
Health Risk
RS1255579349
Conflicting classifications of pathogenicity
Legius syndrome, Cardiovascular phenotype, Legius syndrome
Health Risk
RS1270752951
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Legius syndrome, Cardiovascular phenotype
Health Risk
RS138553244
Conflicting classifications of pathogenicity
Legius syndrome, Noonan syndrome and Noonan-related syndrome, SPRED1-related disorder
Health Risk
RS1427402192
Conflicting classifications of pathogenicity
Legius syndrome, Cardiovascular phenotype, Legius syndrome
Health Risk
RS142928983
Conflicting classifications of pathogenicity
Legius syndrome, Legius syndrome
Health Risk
RS1442783307
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Cardiovascular phenotype
Health Risk
RS146702985
Conflicting classifications of pathogenicity
Legius syndrome, Noonan syndrome and Noonan-related syndrome, Cardiovascular phenotype
Health Risk
RS147204964
Conflicting classifications of pathogenicity
Legius syndrome, Noonan syndrome and Noonan-related syndrome, Cardiovascular phenotype
Health Risk
RS147474792
Conflicting classifications of pathogenicity
Legius syndrome, Noonan syndrome and Noonan-related syndrome, Cardiovascular phenotype
Health Risk
All Variants (178)
RSID Category Clinical Significance Conditions
RS114636635 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Noonan syndrome and Noonan-related syndrome, Cardiovascular phenotype
RS115440602 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS1241478218 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS1255579349 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS1270752951 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Legius syndrome, Cardiovascular phenotype
RS138553244 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Noonan syndrome and Noonan-related syndrome, SPRED1-related disorder
RS1427402192 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS142928983 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Legius syndrome
RS1442783307 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiovascular phenotype
RS146702985 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Noonan syndrome and Noonan-related syndrome, Cardiovascular phenotype
RS147204964 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Noonan syndrome and Noonan-related syndrome, Cardiovascular phenotype
RS147474792 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Noonan syndrome and Noonan-related syndrome, Cardiovascular phenotype
RS147547509 Health Risk Conflicting classifications of pathogenicity
RS1555391042 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Legius syndrome
RS1566877075 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Noonan syndrome, Legius syndrome
RS186366365 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Legius syndrome
RS1888489281 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Legius syndrome, Cardiovascular phenotype
RS1888490204 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS200338097 Health Risk Conflicting classifications of pathogenicity
RS200871227 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS200974459 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS201933663 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS368307475 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Legius syndrome
RS369150309 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Legius syndrome
RS369492789 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS369711772 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Noonan syndrome and Noonan-related syndrome, Cardiovascular phenotype
RS372791883 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Noonan syndrome and Noonan-related syndrome, Cardiovascular phenotype
RS373477920 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS376527959 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Noonan syndrome and Noonan-related syndrome, Cardiovascular phenotype
RS532147114 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS537477031 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Legius syndrome
RS541556786 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Legius syndrome
RS566065329 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Legius syndrome
RS573603750 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS574232846 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Legius syndrome
RS750686148 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Legius syndrome
RS751923342 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS752656697 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Legius syndrome
RS758087535 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS760132893 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS761001792 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS761473300 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Legius syndrome
RS762633609 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS762735151 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS764823722 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Legius syndrome, SPRED1-related disorder
RS765788978 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Legius syndrome
RS765841849 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS766431294 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Cardiovascular phenotype, Legius syndrome
RS766814966 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Legius syndrome
RS768937237 Health Risk Conflicting classifications of pathogenicity Legius syndrome, Noonan syndrome and Noonan-related syndrome, Cardiovascular phenotype
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