Gene

kdm5ba

ID
ZDB-GENE-030131-5379
Name
lysine demethylase 5Ba
Symbol
kdm5ba Nomenclature History
Previous Names
  • id:ibd5050
  • jarid1b
  • jarid1ba
  • wu:fd15c05
Type
protein_coding_gene
Location
Chr: 11 Mapping Details/Browsers
Description
Predicted to enable histone H3K4me/H3K4me2/H3K4me3 demethylase activity. Predicted to be involved in chromatin remodeling and regulation of DNA-templated transcription. Predicted to act upstream of or within chromatin organization. Predicted to be active in chromatin and nucleus. Is expressed in neural rod; paraxial mesoderm; pronephric duct; tail bud; and telencephalon. Human ortholog(s) of this gene implicated in autosomal recessive intellectual developmental disorder 65; breast cancer; and high grade glioma. Orthologous to human KDM5B (lysine demethylase 5B).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
3 figures from 2 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Allele Type Localization Consequence Mutagen Supplier
sa7348Allele with one point mutationUnknownMissenseENU
sa14585Allele with one point mutationUnknownPremature StopENU
sa16159Allele with one point mutationUnknownPremature StopENU
sa21908Allele with one point mutationUnknownPremature StopENU
sa27786Allele with one point mutationUnknownSplice SiteENU
sa31828Allele with one point mutationUnknownPremature StopENU
sa35081Allele with one point mutationUnknownPremature StopENU
sa35082Allele with one point mutationUnknownPremature StopENU
sa38842Allele with one point mutationUnknownPremature StopENU
uab316Allele with one delinsUnknownUnknownCRISPR
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Sequence Targeting Reagents
Targeting Reagent Created Alleles Citations
CRISPR1-kdm5ba (2)
CRISPR2-kdm5ba (2)
MO1-kdm5baN/AHuang et al., 2013
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Human Disease
Associated With kdm5ba Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
autosomal recessive intellectual developmental disorder 65 Alliance Intellectual developmental disorder, autosomal recessive 65 618109
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Associated With kdm5ba Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Conserved_site IPR019786 Zinc finger, PHD-type, conserved site
Domain IPR001606 ARID DNA-binding domain
Domain IPR001965 Zinc finger, PHD-type
Domain IPR003347 JmjC domain
Domain IPR003349 JmjN domain
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Domain Details Per Protein
Protein Additional Resources Length ARID DNA-binding domain ARID DNA-binding domain superfamily JmjC domain JmjN domain Lysine-specific demethylase 5B, first PHD-finger Lysine-specific demethylase 5B, third PHD-finger Lysine-specific demethylase 5, C-terminal helical domain Lysine-specific demethylase-like domain Zinc finger, C5HC2-type Zinc finger, FYVE/PHD-type Zinc finger, PHD-finger Zinc finger, PHD-type Zinc finger, PHD-type, conserved site Zinc finger, RING/FYVE/PHD-type
UniProtKB:A5WUR6 InterPro 1477
UniProtKB:A0A8M9Q713 InterPro 1478
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Transcripts
Genome Browsers
Genome Build: GRCz11Chromosome: 11
Type Name Annotation Method Has Havana Data Length (nt) Analysis
mRNA kdm5ba-201 (1) Ensembl 5,330 nt
mRNA kdm5ba-202 (1) Ensembl 425 nt
mRNA kdm5ba-203 (1) Ensembl 5,677 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 inBACCH211-137O16ZFIN Curated Data
EncodesESTfd15c05
EncodesESTibd5050ZFIN Curated Data
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Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Species Symbol Chromosome Accession # Evidence
HumanKDM5B1
Amino acid sequence comparison (1)
Conserved genome location (synteny) (1)
MouseKdm5b1
Conserved genome location (synteny) (1)
Amino acid sequence comparison (1)
Citations
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