NSD2 Chromosome 4
Nuclear receptor binding SET domain protein 2
Upload your DNA to see your personal genotypes for variants in NSD2.
What This Gene Does
This gene encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene maps to the 165 kb WHS critical region and has also been involved in the chromosomal translocation t(4;14)(p16.3;q32.3) in multiple myelomas. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. Some transcript variants are nonsense-mediated mRNA (NMD) decay candidates, hence not represented as reference sequences. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"PHD finger proteins|Histone lysine methyltransferases|PWWP domain containing|SET domain containing"
Locus Type
gene with protein product
Location
4p16.3
Ensembl
ENSG00000109685
Associated Conditions (14)
Inborn genetic diseases
Rauch-Steindl syndrome
Lymphoma
Neurodevelopmental delay
13 conditions
Medulloblastoma WNT activated
Precursor B-cell acute lymphoblastic leukemia
Syndromic intellectual disability
NSD2-related disorder
Wolf-Hirschhorn like syndrome
4p partial monosomy syndrome
Global developmental delay
NSD2-associated disorder
atypical Wolf-Hirschhorn syndrome
Key Variants
RS1035199365
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1047838051
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS140468997
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS142100377
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS142278631
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS144335923
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS144714547
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS201252361
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS201619712
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS2108804497
Conflicting classifications of pathogenicity
Health Risk
RS2109035117
Conflicting classifications of pathogenicity
Rauch-Steindl syndrome, Rauch-Steindl syndrome
Health Risk
RS2474342362
Conflicting classifications of pathogenicity
Inborn genetic diseases, Rauch-Steindl syndrome, Inborn genetic diseases
Health Risk
All Variants (76)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS1035199365 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS1047838051 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS140468997 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS142100377 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS142278631 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS144335923 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS144714547 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS201252361 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS201619712 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS2108804497 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS2109035117 | Health Risk | Conflicting classifications of pathogenicity | Rauch-Steindl syndrome, Rauch-Steindl syndrome |
| RS2474342362 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Rauch-Steindl syndrome, Inborn genetic diseases |
| RS370127436 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS371529672 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS535066596 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS753120179 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS757383616 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS757846841 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS762870190 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS763851539 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS763969166 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS764506321 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS766736390 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS766759466 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS771867435 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS772470710 | Health Risk | Conflicting classifications of pathogenicity | Lymphoma, Neurodevelopmental delay, 13 conditions |
| RS1440755101 | Health Risk | Likely pathogenic | Rauch-Steindl syndrome, Rauch-Steindl syndrome |
| RS1553872623 | Health Risk | Likely pathogenic | Syndromic intellectual disability, Syndromic intellectual disability |
| RS1577434780 | Health Risk | Likely pathogenic | NSD2-related disorder, NSD2-related disorder |
| RS1719727262 | Health Risk | Likely pathogenic | — |
| RS1726909627 | Health Risk | Likely pathogenic | Rauch-Steindl syndrome, Rauch-Steindl syndrome, Rauch-Steindl syndrome |
| RS2108805626 | Health Risk | Likely pathogenic | Rauch-Steindl syndrome, Rauch-Steindl syndrome |
| RS2108950399 | Health Risk | Likely pathogenic | Rauch-Steindl syndrome, Rauch-Steindl syndrome |
| RS2108958731 | Health Risk | Likely pathogenic | Wolf-Hirschhorn like syndrome, Wolf-Hirschhorn like syndrome |
| RS2108976771 | Health Risk | Likely pathogenic | Rauch-Steindl syndrome, Rauch-Steindl syndrome |
| RS2109020533 | Health Risk | Likely pathogenic | — |
| RS2474331632 | Health Risk | Likely pathogenic | 4p partial monosomy syndrome, 4p partial monosomy syndrome |
| RS2474340489 | Health Risk | Likely pathogenic | NSD2-related disorder, NSD2-related disorder |
| RS2474512303 | Health Risk | Likely pathogenic | — |
| RS2474621465 | Health Risk | Likely pathogenic | Rauch-Steindl syndrome, Rauch-Steindl syndrome |
| RS2474622067 | Health Risk | Likely pathogenic | Inborn genetic diseases, Inborn genetic diseases |
| RS2474746861 | Health Risk | Likely pathogenic | Rauch-Steindl syndrome, Rauch-Steindl syndrome |
| RS2474762078 | Health Risk | Likely pathogenic | Rauch-Steindl syndrome, Rauch-Steindl syndrome |
| RS2474781315 | Health Risk | Likely pathogenic | Rauch-Steindl syndrome, Rauch-Steindl syndrome |
| RS1267410871 | Health Risk | Pathogenic | — |
| RS1553873247 | Health Risk | Pathogenic | 4p partial monosomy syndrome, Global developmental delay, Neurodevelopmental delay |
| RS1560602800 | Health Risk | Pathogenic | Wolf-Hirschhorn like syndrome, 4p partial monosomy syndrome, Wolf-Hirschhorn like syndrome |
| RS1560635105 | Health Risk | Pathogenic | Wolf-Hirschhorn like syndrome, 4p partial monosomy syndrome, Wolf-Hirschhorn like syndrome |
| RS1560696317 | Health Risk | Pathogenic | Wolf-Hirschhorn like syndrome, 4p partial monosomy syndrome, Wolf-Hirschhorn like syndrome |
| RS1577484648 | Health Risk | Pathogenic | Rauch-Steindl syndrome, Rauch-Steindl syndrome, Rauch-Steindl syndrome |