NSD1: Difference between revisions
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{{Infobox | |||
| name = | {{Infobox gene | ||
| image = | | name = NSD1 | ||
| caption = | | image = <!-- Image removed --> | ||
| symbol = | | caption = <!-- Image caption removed --> | ||
| | | symbol = NSD1 | ||
| alt_symbols = KMT3B, SOTOS, SOTOS1 | |||
| EntrezGene = 64324 | |||
| HGNCid = 7999 | |||
| OMIM = 606681 | |||
| RefSeq = NM_022455 | |||
| UniProt = Q96L73 | |||
| chromosome = 5 | |||
| arm = q | |||
| band = 35 | |||
}} | }} | ||
''' | '''NSD1''' (Nuclear receptor-binding SET domain protein 1) is a [[gene]] that encodes a [[histone methyltransferase]] involved in the regulation of [[chromatin]] structure and [[gene expression]]. NSD1 is located on [[chromosome 5]] at the 5q35 region. | ||
==Function== | == Function == | ||
NSD1 is a member of the [[SET domain]]-containing family of proteins, which are known to play a role in [[epigenetic]] regulation. The protein encoded by NSD1 is involved in the methylation of [[histone]] H3 at lysine 36 (H3K36), a modification associated with active [[transcription]]. | |||
== Clinical significance == | |||
Mutations in the NSD1 gene are associated with [[Sotos syndrome]], a disorder characterized by [[overgrowth]], advanced [[bone age]], and distinctive facial features. NSD1 mutations can also be involved in other [[developmental disorders]] and have been implicated in certain types of [[cancer]]. | |||
=== Sotos syndrome === | |||
Sotos syndrome, also known as cerebral gigantism, is an [[autosomal dominant]] condition. It is characterized by excessive physical growth during the first years of life, [[macrocephaly]], and [[learning disabilities]]. | |||
=== Cancer === | |||
Alterations in NSD1 have been observed in various [[cancers]], including [[acute myeloid leukemia]] (AML) and [[neuroblastoma]]. NSD1 can act as an [[oncogene]] or a [[tumor suppressor gene]] depending on the context. | |||
== | == Interactions == | ||
NSD1 interacts with several other proteins and factors involved in [[transcriptional regulation]], including nuclear receptors and other chromatin-modifying enzymes. | |||
== | == See also == | ||
* [[Histone methylation]] | |||
* [[Epigenetics]] | |||
* [[Chromatin remodeling]] | |||
== | == References == | ||
<references /> | |||
== External links == | |||
* [https://www.ncbi.nlm.nih.gov/gene/64324 NSD1 gene - NCBI] | |||
* [https://ghr.nlm.nih.gov/gene/NSD1 NSD1 - Genetics Home Reference] | |||
[[Category: | {{Genes on human chromosome 5}} | ||
[[Category: | [[Category:Genes on human chromosome 5]] | ||
[[Category: | [[Category:Epigenetics]] | ||
[[Category:Histone-modifying enzymes]] | |||
[[Category:Oncogenes]] | |||
[[Category:Tumor suppressor genes]] | |||
Latest revision as of 20:32, 30 December 2024
| Symbol | NSD1 |
|---|---|
| HGNC ID | 7999 |
| Alternative symbols | – |
| Entrez Gene | 64324 |
| OMIM | 606681 |
| RefSeq | NM_022455 |
| UniProt | Q96L73 |
| Chromosome | 5q35 |
| Locus supplementary data | – |
NSD1 (Nuclear receptor-binding SET domain protein 1) is a gene that encodes a histone methyltransferase involved in the regulation of chromatin structure and gene expression. NSD1 is located on chromosome 5 at the 5q35 region.
Function[edit]
NSD1 is a member of the SET domain-containing family of proteins, which are known to play a role in epigenetic regulation. The protein encoded by NSD1 is involved in the methylation of histone H3 at lysine 36 (H3K36), a modification associated with active transcription.
Clinical significance[edit]
Mutations in the NSD1 gene are associated with Sotos syndrome, a disorder characterized by overgrowth, advanced bone age, and distinctive facial features. NSD1 mutations can also be involved in other developmental disorders and have been implicated in certain types of cancer.
Sotos syndrome[edit]
Sotos syndrome, also known as cerebral gigantism, is an autosomal dominant condition. It is characterized by excessive physical growth during the first years of life, macrocephaly, and learning disabilities.
Cancer[edit]
Alterations in NSD1 have been observed in various cancers, including acute myeloid leukemia (AML) and neuroblastoma. NSD1 can act as an oncogene or a tumor suppressor gene depending on the context.
Interactions[edit]
NSD1 interacts with several other proteins and factors involved in transcriptional regulation, including nuclear receptors and other chromatin-modifying enzymes.
See also[edit]
References[edit]
<references />
External links[edit]
| Genes on human chromosome 5 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|
This human genetics related article is a stub.
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