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
RS878853111 Health Risk Likely pathogenic
RS1006906224 Health Risk Pathogenic Sotos syndrome, Sotos syndrome
RS1057518175 Health Risk Pathogenic
RS1057518184 Health Risk Pathogenic
RS1057520339 Health Risk Pathogenic Acute myeloid leukemia, Sotos syndrome, Acute myeloid leukemia
RS1057520581 Health Risk Pathogenic Sotos syndrome, Sotos syndrome
RS1057520620 Health Risk Pathogenic
RS1057520671 Health Risk Pathogenic
RS1057520710 Health Risk Pathogenic
RS1060501490 Health Risk Pathogenic Beckwith-Wiedemann syndrome, Sotos syndrome, Beckwith-Wiedemann syndrome
RS1060501492 Health Risk Pathogenic Beckwith-Wiedemann syndrome, Sotos syndrome, Beckwith-Wiedemann syndrome
RS1060501493 Health Risk Pathogenic Sotos syndrome, Sotos syndrome
RS1060501494 Health Risk Pathogenic
RS1060501497 Health Risk Pathogenic Beckwith-Wiedemann syndrome, Sotos syndrome, Beckwith-Wiedemann syndrome
RS1064793218 Health Risk Pathogenic
RS1064793336 Health Risk Pathogenic
RS1064793361 Health Risk Pathogenic
RS1064793616 Health Risk Pathogenic
RS1064793705 Health Risk Pathogenic
RS1064793843 Health Risk Pathogenic
RS1064794033 Health Risk Pathogenic
RS1064794051 Health Risk Pathogenic Beckwith-Wiedemann syndrome, Sotos syndrome, Beckwith-Wiedemann syndrome
RS1064795734 Health Risk Pathogenic
RS1064796081 Health Risk Pathogenic
RS1064796114 Health Risk Pathogenic
RS1064796161 Health Risk Pathogenic
RS1064796184 Health Risk Pathogenic
RS1064796222 Health Risk Pathogenic
RS1131691754 Health Risk Pathogenic Inborn genetic diseases, Sotos syndrome, Inborn genetic diseases
RS1131692328 Health Risk Pathogenic Sotos syndrome, Sotos syndrome
RS121908067 Health Risk Pathogenic Sotos syndrome, Squamous cell lung carcinoma, Sotos syndrome
RS121908068 Health Risk Pathogenic Sotos syndrome, Sotos syndrome
RS121908069 Health Risk Pathogenic Sotos syndrome, Sotos syndrome
RS121908070 Health Risk Pathogenic Sotos syndrome, Sotos syndrome
RS1270264665 Health Risk Pathogenic
RS1286331975 Health Risk Pathogenic Sotos syndrome, Sotos syndrome
RS1310684026 Health Risk Pathogenic Sotos syndrome, Sotos syndrome
RS1481136060 Health Risk Pathogenic Sotos syndrome, Sotos syndrome
RS1554185405 Health Risk Pathogenic
RS1554189042 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1554189131 Health Risk Pathogenic Beckwith-Wiedemann syndrome, Beckwith-Wiedemann syndrome
RS1554189269 Health Risk Pathogenic
RS1554189482 Health Risk Pathogenic Sotos syndrome, Sotos syndrome
RS1554189490 Health Risk Pathogenic Beckwith-Wiedemann syndrome, Sotos syndrome, Beckwith-Wiedemann syndrome
RS1554189512 Health Risk Pathogenic Beckwith-Wiedemann syndrome, Sotos syndrome, Beckwith-Wiedemann syndrome
RS1554189720 Health Risk Pathogenic Neurodevelopmental delay, Neurodevelopmental delay
RS1554189871 Health Risk Pathogenic
RS1554189879 Health Risk Pathogenic
RS1554189941 Health Risk Pathogenic Sotos syndrome, Sotos syndrome
RS1554190214 Health Risk Pathogenic Beckwith-Wiedemann syndrome, Sotos syndrome, Beckwith-Wiedemann syndrome
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