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BEND6 (BEN Domain Containing 6) is a Protein Coding gene. Diseases associated with BEND6 include Carpenter Syndrome 1. Among its related pathways are Notch Signaling Pathway (WikiPathways). Gene Ontology (GO) annotations related to this gene include chromatin binding.
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0003682 | chromatin binding | IEA | -- |
GO:0003714 | transcription corepressor activity | IGI | 23571214 |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005634 | nucleus | IEA | -- |
SuperPathway | Contained pathways | ||
---|---|---|---|
1 | Notch Signaling Pathway (WikiPathways) |
Symbol | External ID(s) | Details |
---|---|---|
RBPJ |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0007399 | nervous system development | IEA | -- |
GO:0045666 | positive regulation of neuron differentiation | IEA | -- |
GO:0045746 | negative regulation of Notch signaling pathway | IEA | -- |
GO:1903507 | negative regulation of nucleic acid-templated transcription | IEA | -- |
ExUns: | 1 | ^ | 2a | · | 2b | ^ | 3a | · | 3b | ^ | 4 | ^ | 5 | ^ | 6 | ^ | 7 | ^ | 8a | · | 8b | ^ | 9 | ^ | 10 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SP1: | |||||||||||||||||||||||||
SP2: | - | - | - | ||||||||||||||||||||||
SP3: | - | - | - | ||||||||||||||||||||||
SP4: |
This gene was present in the common ancestor of chordates.
Organism | Taxonomy | Gene | Similarity | Type | Details |
---|---|---|---|---|---|
Chimpanzee (Pan troglodytes) |
Mammalia | BEND6 30 31 |
|
OneToOne | |
Dog (Canis familiaris) |
Mammalia | BEND6 30 31 |
|
OneToOne | |
Cow (Bos Taurus) |
Mammalia | BEND6 30 31 |
|
OneToOne | |
Rat (Rattus norvegicus) |
Mammalia | Bend6 30 |
|
||
Mouse (Mus musculus) |
Mammalia | Bend6 30 17 31 |
|
OneToOne | |
Oppossum (Monodelphis domestica) |
Mammalia | BEND6 31 |
|
OneToOne | |
Chicken (Gallus gallus) |
Aves | BEND6 30 31 |
|
OneToOne |
Variant ID | Type | Subtype | PubMed ID |
---|---|---|---|
dgv3319n106 | CNV | deletion | 24896259 |
nsv1073562 | CNV | deletion | 25765185 |
nsv970124 | CNV | duplication | 23825009 |
Disorder | Aliases | PubMed IDs |
---|---|---|
carpenter syndrome 1 |
|
|