1,130 results for setd1b

Setd1b

(Rattus norvegicus)
Gene
Name: SET domain containing 1B, histone lysine methyltransferase
Synonyms: histone-lysine N-methyltransferase SETD1B, SET domain containing 1B, LOC100359816, rCG21620-like
Source: RGD:2323325
Biotype: protein coding gene
Symbol: Setd1b (Rno)
Symbol: Setd1b
Gene Synopsis: Orthologous to human SETD1B (SET domain containing 1B, histone lysine methyltransferase); PARTICIPATES
Automated Gene Synopsis: Orthologous to human SETD1B (SET domain containing 1B, histone lysine methyltransferase).
Synonyms: histone-lysine N-methyltransferase SETD1B
Strict Orthology Symbols: setd1b

Setd1b

(Mus musculus)
Gene
Name: SET domain containing 1B
Synonyms: mKIAA1076, KMT2G, BC035291, MGC:39035, AA516740, cDNA sequence BC035291, expressed sequence AA516740
Source: MGI:2652820
Biotype: protein coding gene
Symbol: Setd1b (Mmu)
Symbol: Setd1b
Automated Gene Synopsis: Orthologous to human SETD1B (SET domain containing 1B, histone lysine methyltransferase).
Strict Orthology Symbols: setd1b
Alleles: Setd1b (Mmu)...Setd1b (Mmu)...Setd1b (Mmu)...Setd1b (Mmu)...Setd1b (Mmu)

SETD1B

(Homo sapiens)
Gene
Name: SET domain containing 1B, histone lysine methyltransferase
Synonyms: FLJ20803, hSET1B, Set1B, KMT2G, histone-lysine N-methyltransferase SETD1B, SET domain containing 1B, lysine N-methyltransferase 2G, IDDSELD, SET domain-containing protein 1B, KIAA1076
Source: HGNC:29187
Biotype: protein coding gene
Symbol: SETD1B (Hsa)
Symbol: SETD1B
Synonyms: histone-lysine N-methyltransferase SETD1B
Strict Orthology Symbols: setd1b

setd1b

(Xenopus tropicalis)
Gene
Name: SET domain containing 1B
Synonyms: setd1b, SET domain containing 1B
Source: Xenbase:XB-GENE-5842344
Biotype: gene
Symbol: setd1b (Xtr)
Symbol: setd1b
Automated Gene Synopsis: Orthologous to human SETD1B (SET domain containing 1B, histone lysine methyltransferase).
Synonyms: setd1b...setd1b...setd1b
Strict Orthology Symbols: Setd1b...setd1b.L...SETD1B...setd1ba...setd1bb

setd1bb

(Danio rerio)
Gene
Name: SET domain containing 1B, histone lysine methyltransferase b
Synonyms: Not Available
Source: ZFIN:ZDB-GENE-080522-1
Biotype: protein coding gene
Symbol: setd1bb (Dre)
Automated Gene Synopsis: Orthologous to human SETD1B (SET domain containing 1B, histone lysine methyltransferase).
Strict Orthology Symbols: setd1b
Symbol: setd1bb

setd1ba

(Danio rerio)
Gene
Name: SET domain containing 1B, histone lysine methyltransferase a
Synonyms: si:dkey-237o15.4, im:7156157
Source: ZFIN:ZDB-GENE-050309-289
Biotype: protein coding gene
Symbol: setd1ba (Dre)
Automated Gene Synopsis: Orthologous to human SETD1B (SET domain containing 1B, histone lysine methyltransferase).
Strict Orthology Symbols: setd1b
Symbol: setd1ba

setd1b.S

(Xenopus laevis)
Gene
Name: SET domain containing 1B
Synonyms: SET domain containing 1B, setd1b.S
Source: Xenbase:XB-GENE-5842376
Biotype: gene
Symbol: setd1b.S (Xla)
Automated Gene Synopsis: Orthologous to human SETD1B (SET domain containing 1B, histone lysine methyltransferase).
Strict Orthology Symbols: setd1b
Symbol: setd1b.S

setd1b.L

(Xenopus laevis)
Gene
Name: SET domain containing 1B
Synonyms: SET domain containing 1B, setd1b.L
Source: Xenbase:XB-GENE-17346666
Biotype: gene
Symbol: setd1b.L (Xla)
Automated Gene Synopsis: Orthologous to human SETD1B (SET domain containing 1B, histone lysine methyltransferase).
Strict Orthology Symbols: setd1b
Symbol: setd1b.L

Setd1btm2.2(IMPC)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:7861524
Genes: Setd1b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Setd1b (Mmu)
Genes: Setd1b (Mmu)
Symbol: Setd1btm2.2(IMPC)Wtsi

Setd1btm1.3Afst

(Mus musculus)
Allele/Variant
Source: MGI:5568945
Genes: Setd1b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Setd1b (Mmu)
Genes: Setd1b (Mmu)
Symbol: Setd1btm1.3Afst

Setd1bem1Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7766659
Genes: Setd1b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Setd1b (Mmu)
Genes: Setd1b (Mmu)
Symbol: Setd1bem1Smoc

Setd1bem2Cya

(Mus musculus)
Allele/Variant
Source: MGI:7586446
Genes: Setd1b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Setd1b (Mmu)
Genes: Setd1b (Mmu)
Symbol: Setd1bem2Cya

Setd1btm1.2Afst

(Mus musculus)
Allele/Variant
Source: MGI:5568944
Genes: Setd1b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Setd1b (Mmu)
Genes: Setd1b (Mmu)
Symbol: Setd1btm1.2Afst

Setd1bem4Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7305976
Genes: Setd1b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Setd1b (Mmu)
Genes: Setd1b (Mmu)
Symbol: Setd1bem4Gpt

Setd1btm1Afst

(Mus musculus)
Allele/Variant
Source: MGI:5568942
Genes: Setd1b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Setd1b (Mmu)
Genes: Setd1b (Mmu)
Symbol: Setd1btm1Afst

Setd1btm1.1Afst

(Mus musculus)
Allele/Variant
Source: MGI:5568943
Genes: Setd1b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Setd1b (Mmu)
Genes: Setd1b (Mmu)
Symbol: Setd1btm1.1Afst

Id: MGI:5568955
Synonyms: Not Available
Symbol: Setd1b/Setd1b [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 (Mmu)
Genes: Setd1b (Mmu)
Alleles: Setd1b (Mmu)
Name: Setd1b/Setd1b [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6

Id: MGI:5568956
Synonyms: Not Available
Symbol: Setd1b/Setd1b [background:] involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6
Genes: Setd1b (Mmu)
Alleles: Setd1b (Mmu)
Name: Setd1b/Setd1b [background:] involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6

set-2

(Caenorhabditis elegans)
Gene
Name: SET (trithorax/polycomb) domain containing 2
Synonyms: CELE_C26E6.9, C26E6.9
Source: WB:WBGene00004782
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human SETD1A (SET domain containing 1A, histone lysine methyltransferase) and SETD1B (
Strict Orthology Symbols: setd1b

Set1

(Drosophila melanogaster)
Gene
Name: SET domain containing 1
Synonyms: lethal 5, aaf45425 Dm, dset1, dSet-1, l5, l(3)h5, SET1, SetD1, SET domain-containing 1, CG17395, lethal5, CG17396, CG40351, dSET1, set1, dSet1, SETD1
Source: FB:FBgn0040022
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human SETD1A (SET domain containing 1A, histone lysine methyltransferase) and SETD1B (
Strict Orthology Symbols: setd1b

SET1

(Saccharomyces cerevisiae)
Gene
Name: SET domain-containing
Synonyms: KMT2, YHR119W, YTX1
Source: SGD:S000001161
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human SETD1A (SET domain containing 1A, histone lysine methyltransferase) and SETD1B (
Strict Orthology Symbols: setd1b

Setd1a

(Rattus norvegicus)
Gene
Name: SET domain containing 1A, histone lysine methyltransferase
Synonyms: histone-lysine N-methyltransferase SETD1A, LOC309001, SET domain containing 1A, SET domain containing 1B, Setd1b, RGD1311624, similar to KIAA0339 protein
Source: RGD:1311624
Biotype: protein coding gene
Synonyms: Setd1b...Setd1b

Source: DOID:0070417
Definition: A autosomal dominant intellectual developmental disorder characterized by developmental delay associated with mild to moderately impaired intellectual development or learning difficulties, behavioral or psychiatric abnormalities, and delayed speech and language acquisition that has_material_basis_in heterozygous mutation in the SETD1A gene on chromosome 16p11.
Genes: SETD1B (Hsa)...setd1bb (Dre)...Setd1b (Mmu)...setd1b (Xtr)...Setd1b (Rno)

Source: GO:0140999
Synonyms:
  • histone H3-K4 trimethylation
  • histone H3K4 trimethylase activity
Branch: molecular function
Genes: Setd1b (Mmu)...SETD1B (Hsa)...setd1ba (Dre)...Setd1b (Rno)

Source: GO:0042800
Synonyms:
  • histone H3 lysine 4-specific methyltransferase activity
  • histone H3K4 methylase activity
Branch: molecular function
Genes: Setd1b (Mmu)...setd1bb (Dre)...SETD1B (Hsa)...setd1ba (Dre)...Setd1b (Rno)

Source: GO:0048188
Synonyms:
  • COMPASS complex
  • Set1/COMPASS complex
Branch: cellular component
Genes: Setd1b (Mmu)...setd1bb (Dre)...SETD1B (Hsa)...setd1ba (Dre)...Setd1b (Rno)
Definition: Spp1p, Bre2p, and the trithorax-related Set1p; in mammals it contains the catalytic subunit (SETD1A or SETD1B

Source: GO:0140945
Synonyms:
  • histone H3K4 monomethylase activity
  • histone H4-K4 methylation
Branch: molecular function
Genes: Setd1b (Mmu)...SETD1B (Hsa)

High-Throughput (HTP) Dataset Index metadata provided by MGI
ID: ArrayExpress:GSE185182
Tags: baseline
Summary: Histone 3 lysine 4 methylation (H3K4me) is mediated by six different lysine methyltransferases. Amongst these enzymes SET domain containing 1b (SETD1B) has been linked to syndromic intellectual disability but its role in the postnatal brain has not been studied yet. Here we employ mice that lack Setd1b from excitatory neurons of the postnatal forebrain and combine neuron-specific ChIP-seq and RNA-seq approaches to elucidate its role in neuronal gene expression. We observe that SETD1B controls the expression of genes with a broad H3K4me3 peak at their promoters that represent neuronal enriched genes linked to learning and memory function. Comparative analysis to corresponding data from conditional Kmt2a and Kmt2b knockout mice suggests that this function is specific to SETD1B. Moreover, postnatal loss of Setd1b leads to severe learning impairment, suggesting that SETD1B-mediated regulation of H3K4me levels in postnatal neurons is critical for cognitive function. Single nuclei RNA sequencing from hippocampus of wildtype young mice.
Symbol: Postnatal SETD1B is essential for learning and the regulation of neuronal plasticity genes [WT scRNA-seq
Name: Postnatal SETD1B is essential for learning and the regulation of neuronal plasticity genes [WT scRNA-seq

High-Throughput (HTP) Dataset Index metadata provided by MGI
ID: ArrayExpress:GSE180326
Tags: WT vs. mutant, anatomical structure, genotype
Summary: We have analyzed changes in histone 3 lysine 4 methylation (H3K4me3 and H3K4me1), histone acetylation (H3K9ac and H3K27ac) and gene expression resulting from Setd1b knockdown in adult hippocampal CA neurons in mice. We implemented Cre/loxP-mediated conditional knockout strategy in order to knockdown this histone methyltransferase in excitatory forebrain neurons in adult mice. Examination of H3K4me3, H3K4me1, H3K9ac and H3K27ac levels, and gene expression in hippocampal CA neurons of adult Setd1b cKO mice.
Symbol: Postnatal SETD1B is essential for learning and the regulation of neuronal plasticity genes
Name: Postnatal SETD1B is essential for learning and the regulation of neuronal plasticity genes

High-Throughput (HTP) Dataset Index metadata provided by MGI
ID: ArrayExpress:GSE167984
Tags: WT vs. mutant, genotype
Summary: Histone 3 lysine 4 trimethylation (H3K4me3) is an epigenetic mark found at active gene promoters and CpG islands. H3K4me3 is essential for mammalian development, yet mechanisms underlying its genomic targeting are poorly understood. H3K4me3 methyltransferases SETD1B and MLL2 are essential for oogenesis. We investigated changes in H3K4me3 in Setd1b conditional knockout (cKO) GV oocytes using ultra-low input ChIP-seq, in complement to DNA methylation and gene expression analysis. Setd1b cKO oocytes showed a redistribution of H3K4me3, with a marked loss at active gene promoters associated with downregulated gene expression. Remarkably, many regions gained H3K4me3 in Setd1b cKOs, in particular those that were DNA hypomethylated, transcriptionally inactive and CpG-rich. All of these are hallmarks of MLL2 targets; thus, loss of SETD1B appears to enable enhanced MLL2 activity. Our work reveals two distinct, complementary mechanisms of genomic targeting of H3K4me3 in oogenesis, with SETD1B linked to transcriptional activity and MLL2 to CpG content. Single GV oocytes were collected from females with an oocyte conditional deletion of Setd1b using Gdf9-cre (Setd1b cKO) and females carrying floxed Setd1b (Setd1b WT) for single cell RNA-seq for four and three biological replicates, respectively.
Symbol: Loss of SETD1B results in the redistribution of genomic H3K4me3 in the oocyte [RNA-seq]
Name: Loss of SETD1B results in the redistribution of genomic H3K4me3 in the oocyte [RNA-seq]

Source: GO:0035097
Synonyms: Not Available
Branch: cellular component
Genes: Setd1b (Mmu)...SETD1B (Hsa)...Setd1b (Rno)

High-Throughput (HTP) Dataset Index metadata provided by MGI
ID: ArrayExpress:GSE85360
Tags: WT vs. mutant, genotype
Summary: Germ cell development involves major reprogramming of the epigenome to prime the zygote for totipotency. Histone 3 lysine 4 (H3K4) methylations are universal epigenetic marks mediated in mammals by six H3K4 methyltransferases related to fly Trithorax, including two yeast Set1 orthologs: Setd1a and Setd1b. Whereas Setd1a plays no role in oogenesis, we report that Setd1b deficiency causes female sterility. Oocyte specific Gdf9iCre conditional knockout (Setd1bGdf9cKO) ovaries develop through all stages however follicular loss accumulated with age and unfertilized metaphase II (MII) oocytes exhibited irregularities of the zona pellucida and meiotic spindle. Most Setd1bGdf9cKO zygotes remained in the pronuclear stage and displayed polyspermy in the perivitelline space. Expression profiling of Setd1bGdf9cKO MII oocytes revealed (i) that Setd1b promotes the expression of the major oocyte transcription factors including Obox1, 2, 5, 7, Meis2 and Sall4; and (ii) two-times more up- than downregulated mRNAs suggesting that Setd1b also promotes the expression of negative regulators of oocyte development with multiple Zfp-KRAB factors implicated. Together, these findings indicate that Setd1b serves as maternal effect gene through regulation of the oocyte gene expression program. Oocyte RNA profiling for Setd1bGdf9cKO and control mice
Symbol: The histone 3 lysine 4 methyltransferase Setd1b is a maternal effect gene required for the oogenic gene
Name: The histone 3 lysine 4 methyltransferase Setd1b is a maternal effect gene required for the oogenic gene

Source: GO:0140938
Synonyms:
  • histone H3 methylase activity
  • histone H3 methylation
Branch: molecular function
Genes: SETD1B (Hsa)

Gene Ontology
Source: GO:0032259
Synonyms: Not Available
Branch: biological process
Genes: setd1ba (Dre)...SETD1B (Hsa)...Setd1b (Mmu)...Setd1b (Rno)...setd1bb (Dre)

Source: GO:0002244
Synonyms:
  • haematopoietic progenitor cell differentiation
  • haemopoietic progenitor cell differentiation
Branch: biological process
Genes: setd1ba (Dre)

Gene Ontology
Source: GO:0016607
Synonyms:
  • nuclear speckle
  • nuclear speckles
Branch: cellular component
Genes: setd1ba (Dre)...SETD1B (Hsa)...Setd1b (Mmu)...Setd1b (Rno)

linc-setd1ba

(Danio rerio)
Gene
Name: linc RNA setd1ba
Synonyms: linc-setd1
Source: ZFIN:ZDB-LINCRNAG-170627-10
Biotype: lincRNA gene

Source: GO:0008168
Synonyms:
  • methylase
Branch: molecular function
Genes: setd1ba (Dre)...SETD1B (Hsa)...setd1bb (Dre)

Source: GO:0006325
Synonyms:
  • DNA replication-independent chromatin assembly
  • DNA replication-independent chromatin organization
Branch: biological process
Genes: setd1ba (Dre)...SETD1B (Hsa)...setd1bb (Dre)

Gene Ontology
Source: GO:0005694
Synonyms:
  • chromatid
  • interphase chromosome
Branch: cellular component
Genes: setd1ba (Dre)...SETD1B (Hsa)...Setd1b (Mmu)...Setd1b (Rno)

linc.setd1ba

(Danio rerio)
Gene
Name: lincRNA upstream of setd1ba
Synonyms: si:ch211-265m20.8, lnc_setd1ba
Source: ZFIN:ZDB-LINCRNAG-091204-41
Biotype: lincRNA gene

Allele/Variant
Source: rs182923294
Genes: SETD1B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:121810440C>T
Gene Synonyms: histone-lysine N-methyltransferase SETD1B

Allele/Variant
Source: rs1875984956
Genes: SETD1B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:121810614C>T
Gene Synonyms: histone-lysine N-methyltransferase SETD1B

Allele/Variant
Source: NC_000012.12:g.121810665C>T
Genes: SETD1B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:121810665C>T
Gene Synonyms: histone-lysine N-methyltransferase SETD1B

Allele/Variant
Source: rs1426898475
Genes: SETD1B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:121809966G>A
Gene Synonyms: histone-lysine N-methyltransferase SETD1B

Allele/Variant
Source: rs1300558177
Genes: SETD1B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:121810017G>A
Gene Synonyms: histone-lysine N-methyltransferase SETD1B

Allele/Variant
Source: rs375525174
Genes: SETD1B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:121810039G>T
Gene Synonyms: histone-lysine N-methyltransferase SETD1B

Allele/Variant
Source: NC_000012.12:g.121814367C>G
Genes: SETD1B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:121814367C>G
Gene Synonyms: histone-lysine N-methyltransferase SETD1B

Allele/Variant
Source: rs996821667
Genes: SETD1B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:121814426G>A
Gene Synonyms: histone-lysine N-methyltransferase SETD1B

Allele/Variant
Source: rs756951883
Genes: SETD1B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:121814522C>T
Gene Synonyms: histone-lysine N-methyltransferase SETD1B