Set domain containing 1b

SETD1B
Available structures PDB Human UniProt search: PDBe RCSB List of PDB id codes 3UVO, 4ES0
Identifiers
Aliases	SETD1B, KMT2G, Set1B, SET domain containing 1B, SET domain containing 1B, histone lysine methyltransferase, IDDSELD
External IDs	OMIM: 611055 HomoloGene: 137311 GeneCards: SETD1B
Gene location (Human) Chr. Chromosome 12 (human) Band 12q24.31 Start 121,804,009 bp End 121,832,656 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in hair follicle parietal pleura cardia visceral pleura urethra nipple saphenous vein germinal epithelium seminal vesicula pylorus n/a More reference expression data BioGPS n/a
Gene ontology Molecular function nucleic acid binding methyltransferase activity transferase activity protein binding histone methyltransferase activity (H3-K4 specific) RNA binding histone-lysine N-methyltransferase activity Cellular component histone methyltransferase complex nuclear speck nucleus chromosome nucleoplasm cytosol Set1C/COMPASS complex Biological process methylation regulation of transcription, DNA-templated transcription, DNA-templated histone H3-K4 methylation chromatin organization Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 23067 n/a Ensembl ENSG00000139718 n/a UniProt Q9UPS6 n/a RefSeq (mRNA) NM_015048 NM_001353345 n/a RefSeq (protein) NP_001340274 n/a Location (UCSC) Chr 12: 121.8 – 121.83 Mb n/a PubMed search n/a
Wikidata
View/Edit Human

SET domain containing 1B is a protein that in humans is encoded by the SETD1B gene.

Function

SET1B is a component of a histone methyltransferase complex that produces trimethylated histone H3 at Lys4 (Lee et al., 2007 [PubMed 17355966]).[supplied by OMIM, Mar 2008].

Further reading

• Lee JH, Skalnik DG (2012). "Rbm15-Mkl1 interacts with the Setd1b histone H3-Lys4 methyltransferase via a SPOC domain that is required for cytokine-independent proliferation". PLOS ONE. 7 (8): e42965. Bibcode:2012PLoSO...742965L. doi:10.1371/journal.pone.0042965. PMC 3424240. PMID 22927943.
• Choi YJ, Oh HR, Choi MR, Gwak M, An CH, Chung YJ, Yoo NJ, Lee SH (2014). "Frameshift mutation of a histone methylation-related gene SETD1B and its regional heterogeneity in gastric and colorectal cancers with high microsatellite instability". Hum. Pathol. 45 (8): 1674–81. doi:10.1016/j.humpath.2014.04.013. PMID 24925220.
• Labonne JD, Lee KH, Iwase S, Kong IK, Diamond MP, Layman LC, Kim CH, Kim HG (2016). "An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability". Hum. Genet. 135 (7): 757–71. doi:10.1007/s00439-016-1668-4. PMID 27106595. S2CID 3760488.
• Kranz, Andrea; Anastassiadis, Konstantinos (2020). "The role of SETD1A and SETD1B in development and disease". Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1863 (8): 194578. doi:10.1016/j.bbagrm.2020.194578. ISSN 1874-9399. PMID 32389824. S2CID 218585660.
• Brici, David; Zhang, Qinyu; Reinhardt, Susanne; Dahl, Andreas; Hartmann, Hella; Schmidt, Kerstin; Goveas, Neha; Huang, Jiahao; Gahurova, Lenka; Kelsey, Gavin; Anastassiadis, Konstantinos; Stewart, A. Francis; Kranz, Andrea (2017). "The histone 3 lysine 4 methyltransferase Setd1b is a maternal effect gene required for the oogenic gene expression program". Development. 144 (14): 2606–2617. doi:10.1242/dev.143347. ISSN 1477-9129. PMID 28619824.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.