NSD1 Chromosome 5

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

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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
RS587784197 Health Risk Pathogenic/Likely pathogenic Sotos syndrome, Sotos syndrome
RS587784200 Health Risk Pathogenic/Likely pathogenic Sotos syndrome, Sotos syndrome
RS587784206 Health Risk Pathogenic/Likely pathogenic Sotos syndrome, Sotos syndrome
RS587784208 Health Risk Pathogenic/Likely pathogenic Sotos syndrome, Sotos syndrome
RS587784219 Health Risk Pathogenic/Likely pathogenic Sotos syndrome, Sotos syndrome
RS755758018 Health Risk Pathogenic/Likely pathogenic
RS797045825 Health Risk Pathogenic/Likely pathogenic Inborn genetic diseases, Sotos syndrome, Inborn genetic diseases
RS863224905 Health Risk Pathogenic/Likely pathogenic Sotos syndrome, Sotos syndrome
RS886041219 Health Risk Pathogenic/Likely pathogenic Sotos syndrome, NSD1-related disorder, Sotos syndrome
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