Gene

dnmt3bb.1

ID
ZDB-GENE-050314-1
Name
DNA (cytosine-5-)-methyltransferase 3 beta, duplicate b.1
Symbol
dnmt3bb.1 Nomenclature History
Previous Names
  • cb633 (1)
  • dnmt3b1 (1)
  • dnmt3b (1)
  • dnmt4
Type
protein_coding_gene
Location
Chr: 23 Mapping Details/Browsers
Description
Predicted to enable DNA (cytosine-5-)-methyltransferase activity, acting on CpG substrates and DNA binding activity. Acts upstream of or within several processes, including Kupffer's vesicle development; hematopoietic stem cell homeostasis; and negative regulation of gene expression via chromosomal CpG island methylation. Predicted to be active in nucleus. Is expressed in several structures, including digestive system; hematopoietic system; immature eye; mesoderm; and nervous system. Human ortholog(s) of this gene implicated in several diseases, including autoimmune disease (multiple); carcinoma (multiple); facioscapulohumeral muscular dystrophy 4; immunodeficiency-centromeric instability-facial anomalies syndrome 1; and thymoma. Orthologous to human DNMT3B (DNA methyltransferase 3 beta).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
28 figures from 12 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
10 figures from 4 publications
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Allele Type Localization Consequence Mutagen Supplier
b1237Allele with one deletionUnknownPremature StopTALEN
ioz103Allele with one delinsExon 3UnknownCRISPR
la022494TgTransgenic insertionUnknownUnknownDNA
la022495TgTransgenic insertionUnknownUnknownDNA
mk24Allele with one deletionUnknownUnknownTALEN
sa12816Allele with one point mutationUnknownPremature StopENU
sa15458Allele with one point mutationUnknownPremature StopENU
y258Allele with one deletionExon 6Premature StopTALEN
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Sequence Targeting Reagents
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Human Disease
Associated With dnmt3bb.1 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
facioscapulohumeral muscular dystrophy 4 Alliance Facioscapulohumeral muscular dystrophy 4, digenic 619478
immunodeficiency-centromeric instability-facial anomalies syndrome 1 Alliance Immunodeficiency-centromeric instability-facial anomalies syndrome 1 242860
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Associated With dnmt3bb.1 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Active_site IPR018117 DNA methylase, C-5 cytosine-specific, active site
Domain IPR000313 PWWP domain
Domain IPR025766 ADD domain
Domain IPR030488 DNA (cytosine-5)-methyltransferase 3B, ADD domain
Domain IPR040552 DNMT3, cysteine rich ADD domain, GATA1-like zinc finger
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Domain Details Per Protein
Protein Additional Resources Length ADD domain C-5 cytosine methyltransferase DNA (cytosine-5)-methyltransferase 3B, ADD domain DNA methylase, C-5 cytosine-specific, active site DNMT3, ADD domain, PHD zinc finger DNMT3, cysteine rich ADD domain, GATA1-like zinc finger PWWP domain S-adenosyl-L-methionine-dependent methyltransferase superfamily Zinc finger, FYVE/PHD-type
UniProtKB:A0A8M3AY81 InterPro 768
UniProtKB:A0A8M2B8X0 InterPro 813
UniProtKB:A0A8M3AV60 InterPro 753
UniProtKB:Q588C6 InterPro 816
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Transcripts
Genome Browsers
Genome Build: GRCz11Chromosome: 23
Type Name Annotation Method Has Havana Data Length (nt) Analysis
mRNA dnmt3bb.1-201 (1) Ensembl 3,678 nt
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Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
No data available
Marker Relationships
Relationship Marker Type Marker Accession Numbers Citations
Contained inBACDKEY-108P14ZFIN Curated Data
Contained inBACDKEY-210I3ZFIN Curated Data
EncodesESTcb633
EncodesESTIMAGE:7155993Thisse et al., 2004
EncodescDNAMGC:152725ZFIN Curated Data
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Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Species Symbol Chromosome Accession # Evidence
HumanDNMT3B20
Conserved genome location (synteny) (1)
Amino acid sequence comparison (1)
Phylogenetic tree (2)
Citations
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