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Nsd3 nuclear receptor binding SET domain protein 3 [ Mus musculus (house mouse) ]

Gene ID: 234135, updated on 27-Nov-2024

Summary

Official Symbol
Nsd3provided by MGI
Official Full Name
nuclear receptor binding SET domain protein 3provided by MGI
Primary source
MGI:MGI:2142581
See related
Ensembl:ENSMUSG00000054823 AllianceGenome:MGI:2142581
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Mus musculus
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Mus; Mus
Also known as
WHISTLE; Whsc1l1; 6720429E03; A530023P05
Summary
This gene encodes a member of the SET domain family of histone lysine N-methyltransferase proteins. This protein methylates histone H3 at lysine residues 4 and 27, which represses gene transcription. It acts in opposition to the histone demethylase Jmjd1c. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2015]
Expression
Ubiquitous expression in placenta adult (RPKM 8.2), CNS E18 (RPKM 5.3) and 28 other tissues See more
Orthologs
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Genomic context

See Nsd3 in Genome Data Viewer
Location:
8 A2; 8 14.17 cM
Exon count:
26
Annotation release Status Assembly Chr Location
RS_2024_02 current GRCm39 (GCF_000001635.27) 8 NC_000074.7 (26091617..26209694)
108.20200622 previous assembly GRCm38.p6 (GCF_000001635.26) 8 NC_000074.6 (25601601..25719667)

Chromosome 8 - NC_000074.7Genomic Context describing neighboring genes Neighboring gene fibroblast growth factor receptor 1 Neighboring gene STARR-seq mESC enhancer starr_20978 Neighboring gene predicted gene 16159 Neighboring gene CapStarr-seq enhancer MGSCv37_chr8:26686963-26687146 Neighboring gene STARR-positive B cell enhancer ABC_E8232 Neighboring gene STARR-positive B cell enhancer ABC_E2860 Neighboring gene leucine zipper-EF-hand containing transmembrane protein 2 Neighboring gene STARR-positive B cell enhancer ABC_E6630 Neighboring gene CapStarr-seq enhancer MGSCv37_chr8:26722454-26722679 Neighboring gene CapStarr-seq enhancer MGSCv37_chr8:26728550-26728737 Neighboring gene predicted gene, 24992 Neighboring gene CapStarr-seq enhancer MGSCv37_chr8:26830817-26831000 Neighboring gene phospholipid phosphatase 5 Neighboring gene DDHD domain containing 2

Genomic regions, transcripts, and products

Expression

  • Project title: Mouse ENCODE transcriptome data
  • Description: RNA profiling data sets generated by the Mouse ENCODE project.
  • BioProject: PRJNA66167
  • Publication: PMID 25409824
  • Analysis date: n/a

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Variation

Alleles

Alleles of this type are documented at Mouse Genome Informatics  (MGI)
  • Endonuclease-mediated (2) 
  • Targeted (4)  1 citation

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Gene Ontology Provided by MGI

Process Evidence Code Pubs
involved_in chromatin remodeling IEA
Inferred from Electronic Annotation
more info
 
involved_in methylation IEA
Inferred from Electronic Annotation
more info
 
acts_upstream_of_or_within negative regulation of DNA-templated transcription IDA
Inferred from Direct Assay
more info
PubMed 
involved_in positive regulation of DNA-templated transcription ISO
Inferred from Sequence Orthology
more info
 
involved_in positive regulation of DNA-templated transcription ISS
Inferred from Sequence or Structural Similarity
more info
 
involved_in regulation of DNA-templated transcription IBA
Inferred from Biological aspect of Ancestor
more info
 
Component Evidence Code Pubs
located_in chromatin IBA
Inferred from Biological aspect of Ancestor
more info
 
located_in chromosome IEA
Inferred from Electronic Annotation
more info
 
is_active_in nucleus IBA
Inferred from Biological aspect of Ancestor
more info
 
located_in nucleus ISO
Inferred from Sequence Orthology
more info
 
located_in nucleus ISS
Inferred from Sequence or Structural Similarity
more info
 

General protein information

Preferred Names
histone-lysine N-methyltransferase NSD3
Names
WHSC1-like protein 1
nuclear SET domain-containing protein 3
wolf-Hirschhorn syndrome candidate 1-like protein 1 homolog
NP_001001735.1
NP_001074738.1
NP_001295410.1
NP_001295411.1

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

mRNA and Protein(s)

  1. NM_001001735.2NP_001001735.1  histone-lysine N-methyltransferase NSD3 isoform 1

    See identical proteins and their annotated locations for NP_001001735.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (1) encodes isoform 1. Variants 1 and 3 encode the same isoform (1).
    Source sequence(s)
    AC156990, AC162367, BC064447
    Consensus CDS
    CCDS40305.1
    UniProtKB/TrEMBL
    A0A1B0GSG3
    Related
    ENSMUSP00000115470.2, ENSMUST00000146919.8
    Conserved Domains (1) summary
    cd05837
    Location:277393
    MSH6_like; The PWWP domain is present in MSH6, a mismatch repair protein homologous to bacterial MutS. The PWWP domain of histone-lysine N-methyltransferase, also known as Nuclear SET domain-containing protein 3, is also included. Mutations in MSH6 have been ...
  2. NM_001081269.2NP_001074738.1  histone-lysine N-methyltransferase NSD3 isoform 2

    See identical proteins and their annotated locations for NP_001074738.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (2) has a shorter 5' UTR, lacks the 3' terminal exon, and contains multiple alternate 3' exons, resulting in a distinct 3' coding region and 3' UTR, compared to variant 1. The encoded isoform (2) has a distinct C-terminus and is longer than isoform 1.
    Source sequence(s)
    AC156990, AC162367
    Consensus CDS
    CCDS52528.1
    UniProtKB/Swiss-Prot
    Q3TDS4, Q3U0L8, Q3V131, Q6P2L6, Q8BJT3
    UniProtKB/TrEMBL
    D3Z357
    Related
    ENSMUSP00000117778.2, ENSMUST00000142395.8
    Conserved Domains (8) summary
    cd05837
    Location:277393
    MSH6_like; The PWWP domain is present in MSH6, a mismatch repair protein homologous to bacterial MutS. The PWWP domain of histone-lysine N-methyltransferase, also known as Nuclear SET domain-containing protein 3, is also included. Mutations in MSH6 have been ...
    cd05838
    Location:9681061
    WHSC1_related; The PWWP domain was first identified in the WHSC1 (Wolf-Hirschhorn syndrome candidate 1) protein, a protein implicated in Wolf-Hirschhorn syndrome (WHS). When translocated, WHSC1 plays a role in lymphoid multiple myeloma (MM) disease, also known as ...
    smart00570
    Location:11041154
    AWS; associated with SET domains
    smart00317
    Location:11551278
    SET; SET (Su(var)3-9, Enhancer-of-zeste, Trithorax) domain
    cd15652
    Location:761807
    PHD2_NSD3; PHD finger 2 found in nuclear SET domain-containing protein 3 (NSD3)
    cd15658
    Location:927962
    PHD4_NSD3; PHD finger 4 found in nuclear SET domain-containing protein 3 (NSD3)
    cd15661
    Location:13321374
    PHD5_NSD3; PHD finger 5 found in nuclear SET domain-containing protein 3 (NSD3)
    cl22851
    Location:808860
    PHD_SF; PHD finger superfamily
  3. NM_001308481.1NP_001295410.1  histone-lysine N-methyltransferase NSD3 isoform 1

    See identical proteins and their annotated locations for NP_001295410.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (3) differs in the 5' UTR compared to variant 1. Variants 1 and 3 encode the same isoform (1).
    Source sequence(s)
    AC156990, AC162367, BB618167, BC064447
    Consensus CDS
    CCDS40305.1
    UniProtKB/TrEMBL
    A0A1B0GSG3
    Related
    ENSMUSP00000117596.2, ENSMUST00000155861.8
    Conserved Domains (1) summary
    cd05837
    Location:277393
    MSH6_like; The PWWP domain is present in MSH6, a mismatch repair protein homologous to bacterial MutS. The PWWP domain of histone-lysine N-methyltransferase, also known as Nuclear SET domain-containing protein 3, is also included. Mutations in MSH6 have been ...
  4. NM_001308482.1NP_001295411.1  histone-lysine N-methyltransferase NSD3 isoform 3

    See identical proteins and their annotated locations for NP_001295411.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (4) lacks two 3' exons and its transcription extends past a splice site used in variant 1, resulting in a distinct 3' coding region and 3' UTR. The encoded isoform (3) has a distinct C-terminus and is shorter than isoform 1.
    Source sequence(s)
    AC156990, BC064447, BP766225
    Consensus CDS
    CCDS85518.1
    UniProtKB/TrEMBL
    A0A1B0GSG3
    Related
    ENSMUSP00000147840.2, ENSMUST00000136107.9
    Conserved Domains (1) summary
    cd05837
    Location:277393
    MSH6_like; The PWWP domain is present in MSH6, a mismatch repair protein homologous to bacterial MutS. The PWWP domain of histone-lysine N-methyltransferase, also known as Nuclear SET domain-containing protein 3, is also included. Mutations in MSH6 have been ...

RefSeqs of Annotated Genomes: GCF_000001635.27-RS_2024_02

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCm39 C57BL/6J

Genomic

  1. NC_000074.7 Reference GRCm39 C57BL/6J

    Range
    26091617..26209694
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)