NSD1
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Homo sapiens |
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NSD1 is differentially expressed in 246 experiments: 123 organism parts: testis, bone marrow, ... (121 more);, 158 disease states: normal, breast carcinoma, ... (156 more);, 65 cell types 343 cell lines 34 compound treatments and 70 other conditions. |
| Synonyms |
FLJ22263, STO, ARA267, KMT3B |
| Orthologs |
NSD1
(Gallus gallus)
nsd1b
(Danio rerio)
Nsd1
(Rattus norvegicus)
Nsd1
(Mus musculus)
NSD1
(Bos taurus)
nsd1a
(Danio rerio)
nsd1
(Xenopus laevis)
NSD1
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology ID |
GO:0008168, GO:0003682, GO:0008270, GO:0003714, GO:0003712, GO:0010452, GO:0016571, GO:0016568, GO:0016922, GO:0016740, GO:0042799, GO:0005515, GO:0005694, GO:0005634, GO:0000122, GO:0046872, GO:0018024, GO:0046975, GO:0042054, GO:0045893, GO:0042974, GO:0050681, GO:0001702, GO:0046965, GO:0046966, GO:0030331, GO:0034770 |
| Gene Ontology Term |
histone H3-K36 methylation, histone methyltransferase activity (H4-K20 specific), ligand-dependent nuclear receptor binding, protein binding, histone methylation, transcription corepressor activity, histone methyltransferase activity (H3-K36 specific), metal ion binding, methyltransferase activity, transcription cofactor activity, nucleus, chromatin binding, transferase activity, chromosome, chromatin modification, histone methyltransferase activity, negative regulation of transcription from RNA polymerase II promoter, positive regulation of transcription, DNA-dependent, histone-lysine N-methyltransferase activity, zinc ion binding, androgen receptor binding, retinoid X receptor binding, gastrulation with mouth forming second, estrogen receptor binding, thyroid hormone receptor binding, retinoic acid receptor binding, histone H4-K20 methylation |
| InterPro ID |
IPR001214, IPR019787, IPR000313, IPR001965, IPR006560, IPR003616 |
| InterPro Term |
Znf_PHD-finger, AWS, Znf_PHD, Post-SET_dom, PWWP, SET_dom |
| Ensembl Family Description |
HISTONE LYSINE N METHYLTRANSFERASE EC_2.1.1.43 NUCLEAR SET DOMAIN CONTAINING WOLF HIRSCHHORN SYNDROME CANDIDATE 1 |
| Ensembl Family |
ENSFM00250000000687 |
| RefSeq ID |
NP_758859, NP_071900, NM_022455, NM_172349 |
| EMBL-Bank ID |
AK026066, AF380302, AK055187, AF395588, AC146507, AF322907, AY049721, AL832983, AC008570, AC027314, AK056667, AK025916 |
| UniProt Accession |
Q96L73, Q96DQ7, Q9H6B5, Q9H6H8, Q96MN8, D6RA58, D6RA90, D6RE14, D6RBP3, D6RBV9, D6RG26, Q658U6 |
| Entrez Gene ID |
64324 |
| Ensembl Protein ID |
ENSP00000425120, ENSP00000422996, ENSP00000424096, ENSP00000424024, ENSP00000348031, ENSP00000364499, ENSP00000426428, ENSP00000346111, ENSP00000395929, ENSP00000343209, ENSP00000423982, ENSP00000423372, ENSP00000354310, ENSP00000423048 |
| Description |
nuclear receptor binding SET domain protein 1 [Source:HGNC Symbol;Acc:14234] |
| Gene-Disease Assocation |
WEAVER SYNDROME, SOTOS SYNDROME, LEUKEMIA, ACUTE MYELOID; AML, BECKWITH-WIEDEMANN SYNDROME; BWS |
| UniGene ID |
Hs.106861 |
| Ensembl Gene ID |
ENSG00000165671 |
| HGNC Symbol |
NSD1 |
| Ensembl Transcript ID |
ENST00000355783, ENST00000505395, ENST00000503056, ENST00000513736, ENST00000511258, ENST00000375350, ENST00000512992, ENST00000347982, ENST00000508896, ENST00000510954, ENST00000508029, ENST00000354179, ENST00000504457, ENST00000515735, ENST00000361032, ENST00000439151 |
| Design Element |
42193_r_at, 49812_at, 79236_at, ENST00000510954, g11967992_3p_at, 235760_at, 243612_at, 92098_at, ENST00000354179, ENST00000512992, ENST00000361032, Hs.106861.0.S1_3p_at, ENST00000505395, ENST00000511258, ENST00000504457, ENST00000347982, ENST00000513736, ENST00000503056, 48066_at, 85782_at, ENST00000508029, ENST00000355783, ENST00000508896, gnf1h07490_at, 225654_at, ENST00000515735, ENST00000439151, 68705_at, ENST00000375350, 219084_at, Hs.98802.0.A1_3p_at |
| Search EB-eye |
ENSG00000165671
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