NSD1 Chromosome 5

Nuclear receptor binding SET domain protein 1
709 variants 709 Health Risk

Upload your DNA to see your personal genotypes for variants in NSD1.

What This Gene Does
This gene encodes a protein containing a SET domain, 2 LXXLL motifs, 3 nuclear translocation signals (NLSs), 4 plant homeodomain (PHD) finger regions, and a proline-rich region. The encoded protein enhances androgen receptor (AR) transactivation, and this enhancement can be increased further in the presence of other androgen receptor associated coregulators. This protein may act as a nucleus-localized, basic transcriptional factor and also as a bifunctional transcriptional regulator. Mutations of this gene have been associated with Sotos syndrome and Weaver syndrome. One version of childhood acute myeloid leukemia is the result of a cryptic translocation with the breakpoints occurring within nuclear receptor-binding Su-var, enhancer of zeste, and trithorax domain protein 1 on chromosome 5 and nucleoporin, 98-kd on chromosome 11. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Sep 2018]
Gene Info
Gene Group
"PHD finger proteins|Histone lysine methyltransferases|PWWP domain containing|SET domain containing"
Locus Type
gene with protein product
Location
5q35.3
Ensembl
ENSG00000165671
Associated Conditions (21)
Inborn genetic diseases
Sotos syndrome
Acute myeloid leukemia
NSD1-related disorder
See cases
Holoprosencephaly 2
Thyroid cancer
nonmedullary
1
Beckwith-Wiedemann syndrome
Intellectual disability
Hereditary cancer
Neurodevelopmental disorder
Squamous cell lung carcinoma
Neurodevelopmental delay
Non-immune hydrops fetalis
Squamous cell carcinoma of the head and neck
Neoplasm
Marfanoid habitus and intellectual disability
9 conditions
+1 more conditions
Key Variants
All Variants (709)
RSID Category Clinical Significance Conditions
RS111638717 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Sotos syndrome, Inborn genetic diseases
RS113856002 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Sotos syndrome, Inborn genetic diseases
RS1159759744 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1189702665 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1210587929 Health Risk Conflicting classifications of pathogenicity Sotos syndrome, Sotos syndrome
RS1215568879 Health Risk Conflicting classifications of pathogenicity Sotos syndrome, Sotos syndrome
RS1233891472 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1237230298 Health Risk Conflicting classifications of pathogenicity
RS1251583221 Health Risk Conflicting classifications of pathogenicity Sotos syndrome, Sotos syndrome
RS1264350592 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1299908416 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1341121356 Health Risk Conflicting classifications of pathogenicity
RS1341227088 Health Risk Conflicting classifications of pathogenicity Sotos syndrome, Sotos syndrome
RS1358404983 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Sotos syndrome, Inborn genetic diseases
RS137993153 Health Risk Conflicting classifications of pathogenicity Sotos syndrome, Sotos syndrome
RS1388409083 Health Risk Conflicting classifications of pathogenicity Sotos syndrome, Sotos syndrome
RS1397377820 Health Risk Conflicting classifications of pathogenicity Sotos syndrome, Sotos syndrome
RS140583358 Health Risk Conflicting classifications of pathogenicity Sotos syndrome, Acute myeloid leukemia, Inborn genetic diseases
RS1406037834 Health Risk Conflicting classifications of pathogenicity Sotos syndrome, Inborn genetic diseases, Sotos syndrome
RS140815139 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Sotos syndrome, NSD1-related disorder
RS140839289 Health Risk Conflicting classifications of pathogenicity
RS141014337 Health Risk Conflicting classifications of pathogenicity NSD1-related disorder, NSD1-related disorder
RS141065357 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Sotos syndrome, Inborn genetic diseases
RS1416255762 Health Risk Conflicting classifications of pathogenicity Sotos syndrome, Sotos syndrome
RS1417236940 Health Risk Conflicting classifications of pathogenicity NSD1-related disorder, Inborn genetic diseases, NSD1-related disorder
RS141911573 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Sotos syndrome, Inborn genetic diseases
RS142023792 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Sotos syndrome, Inborn genetic diseases
RS142544192 Health Risk Conflicting classifications of pathogenicity
RS142657029 Health Risk Conflicting classifications of pathogenicity Sotos syndrome, Inborn genetic diseases, Sotos syndrome
RS142703625 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Sotos syndrome, Inborn genetic diseases
RS143406017 Health Risk Conflicting classifications of pathogenicity Sotos syndrome, Sotos syndrome
RS143571876 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Sotos syndrome, Inborn genetic diseases
RS143585233 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Sotos syndrome, NSD1-related disorder
RS144257298 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Sotos syndrome, NSD1-related disorder
RS144524958 Health Risk Conflicting classifications of pathogenicity Sotos syndrome, Sotos syndrome
RS144937234 Health Risk Conflicting classifications of pathogenicity Sotos syndrome, Sotos syndrome
RS1454813710 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1460187564 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Sotos syndrome, Inborn genetic diseases
RS147033795 Health Risk Conflicting classifications of pathogenicity Sotos syndrome, Sotos syndrome
RS147146776 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Sotos syndrome, NSD1-related disorder
RS147235302 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Sotos syndrome, NSD1-related disorder
RS147592452 Health Risk Conflicting classifications of pathogenicity See cases, See cases
RS1488271424 Health Risk Conflicting classifications of pathogenicity Sotos syndrome, Sotos syndrome
RS150296373 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Sotos syndrome, NSD1-related disorder
RS150854966 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Sotos syndrome, Inborn genetic diseases
RS150920473 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Sotos syndrome, Inborn genetic diseases
RS150977055 Health Risk Conflicting classifications of pathogenicity Sotos syndrome, Inborn genetic diseases, Sotos syndrome
RS151165525 Health Risk Conflicting classifications of pathogenicity
RS1554199383 Health Risk Conflicting classifications of pathogenicity
RS1554200207 Health Risk Conflicting classifications of pathogenicity Sotos syndrome, Sotos syndrome
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