SETD5 Chromosome 3

SET domain containing 5
274 variants 274 Health Risk

Upload your DNA to see your personal genotypes for variants in SETD5.

What This Gene Does
This function of this gene has yet to be determined but based on sequence similarity to other SET domain proteins it may function as a histone methyltransferase. Mutations in this gene have been associated with an autosomal dominant form of intellectual disability. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2017]
Gene Info
Gene Group
"SET domain containing|Putative lysine methyltransferases"
Locus Type
gene with protein product
Location
3p25.3
Ensembl
ENSG00000168137
Associated Conditions (22)
Inborn genetic diseases
SETD5-related disorder
Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
Neurodevelopmental disorder
Intellectual disability
Moyamoya angiopathy with developmental delay
See cases
Polymicrogyria
Chromatinopathy
Neurodevelopmental delay
Rare genetic intellectual disability
Developmental disorder
Neurodevelopmental abnormality
Cleft palate
Cleft lip
KBG syndrome
Autism spectrum disorder
Cornelia de Lange-like syndrome
Global developmental delay
Heart
+2 more conditions
Key Variants
RS1002403677
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1049067352
Conflicting classifications of pathogenicity
Health Risk
RS1052957698
Conflicting classifications of pathogenicity
Health Risk
RS1165727019
Conflicting classifications of pathogenicity
Inborn genetic diseases, SETD5-related disorder, Inborn genetic diseases
Health Risk
RS1202232628
Conflicting classifications of pathogenicity
Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
Health Risk
RS1270531724
Conflicting classifications of pathogenicity
Health Risk
RS1301522020
Conflicting classifications of pathogenicity
Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
Health Risk
RS1335595318
Conflicting classifications of pathogenicity
Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
Health Risk
RS1349032508
Conflicting classifications of pathogenicity
Inborn genetic diseases, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Inborn genetic diseases
Health Risk
RS1412309993
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1434450419
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1438851980
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
All Variants (274)
RSID Category Clinical Significance Conditions
RS1553635477 Health Risk Pathogenic Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
RS1553638715 Health Risk Pathogenic
RS1553638877 Health Risk Pathogenic
RS1559427364 Health Risk Pathogenic Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, SETD5-related disorder, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
RS1559439258 Health Risk Pathogenic
RS1559451052 Health Risk Pathogenic Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
RS1575427309 Health Risk Pathogenic
RS1575466399 Health Risk Pathogenic Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
RS1575466995 Health Risk Pathogenic
RS1575467870 Health Risk Pathogenic
RS1575472601 Health Risk Pathogenic
RS1575472646 Health Risk Pathogenic
RS1575475545 Health Risk Pathogenic
RS1575475764 Health Risk Pathogenic Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
RS2040265772 Health Risk Pathogenic
RS2040365404 Health Risk Pathogenic Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
RS2041147607 Health Risk Pathogenic Intellectual disability, Intellectual disability
RS2041149106 Health Risk Pathogenic
RS2041310524 Health Risk Pathogenic
RS2041311648 Health Risk Pathogenic
RS2041316219 Health Risk Pathogenic Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
RS2041380175 Health Risk Pathogenic
RS2041797086 Health Risk Pathogenic Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Inborn genetic diseases, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
RS2041850053 Health Risk Pathogenic Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
RS2041850171 Health Risk Pathogenic Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Neurodevelopmental abnormality, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
RS2041854606 Health Risk Pathogenic
RS2041856807 Health Risk Pathogenic Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
RS2042109833 Health Risk Pathogenic Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
RS2042123799 Health Risk Pathogenic Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
RS2042128326 Health Risk Pathogenic Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
RS2042181751 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2042190198 Health Risk Pathogenic
RS2042191502 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2042206485 Health Risk Pathogenic
RS2042262374 Health Risk Pathogenic Cleft palate, Intellectual disability, Cleft lip
RS2042266753 Health Risk Pathogenic
RS2042271732 Health Risk Pathogenic KBG syndrome, KBG syndrome
RS2042899128 Health Risk Pathogenic
RS2042902664 Health Risk Pathogenic Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
RS2044336029 Health Risk Pathogenic Autism spectrum disorder, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Autism spectrum disorder
RS2044345693 Health Risk Pathogenic
RS2045177486 Health Risk Pathogenic Cornelia de Lange-like syndrome, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Developmental disorder
RS2045187265 Health Risk Pathogenic Neurodevelopmental abnormality, Neurodevelopmental abnormality
RS2045208860 Health Risk Pathogenic
RS2045779618 Health Risk Pathogenic Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
RS2125111250 Health Risk Pathogenic Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
RS2125111475 Health Risk Pathogenic Neurodevelopmental disorder, Neurodevelopmental disorder
RS2125171543 Health Risk Pathogenic
RS2125187131 Health Risk Pathogenic
RS2125187619 Health Risk Pathogenic Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency, Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
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