KDM1B (lysine demethylase 1B)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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221656 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Lysine demethylase 1B |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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KDM1B |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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AOF1, C6orf193, LSD2 |
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Chromosome
Chromosome number
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6 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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6p22.3 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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Flavin-dependent histone demethylases, such as KDM1B, regulate histone lysine methylation, an epigenetic mark that regulates gene expression and chromatin function (Karytinos et al., 2009 [PubMed 19407342]).[supplied by OMIM, Oct 2009] |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | |||||||||||||||||||||
| UniProt ID | Q8NB78 | ||||||||||||||||||||
| Protein name | Lysine-specific histone demethylase 2 (EC 1.14.99.66) (Flavin-containing amine oxidase domain-containing protein 1) (Lysine-specific histone demethylase 1B) | ||||||||||||||||||||
| Protein function | Histone demethylase that demethylates 'Lys-4' of histone H3, a specific tag for epigenetic transcriptional activation, thereby acting as a corepressor. Required for de novo DNA methylation of a subset of imprinted genes during oogenesis. Acts by | ||||||||||||||||||||
| PDB | 4FWE , 4FWF , 4FWJ , 4GU0 , 4GU1 , 4GUR , 4GUS , 4GUT , 4GUU , 4HSU , 6R1U , 6R25 , 7XE1 , 7XE2 , 7XE3 | ||||||||||||||||||||
| Family and domains |
Pfam
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| Sequence |
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| Sequence length | 822 | ||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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