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RBFA (Ribosome Binding Factor A) is a Protein Coding gene. Diseases associated with RBFA include Autosomal Dominant Non-Syndromic Intellectual Disability 1 and Autosomal Dominant Non-Syndromic Intellectual Disability.
GeneHancer (GH) Identifier | GH Type | GH Score |
GH Sources | Gene Association Score | Total Score | TSS distance (kb) | Number of Genes Away | Size (kb) | Transcription Factor Binding Sites |
Gene Targets |
---|---|---|---|---|---|---|---|---|---|---|
GH18J080032 | Promoter/Enhancer | 2 | EPDnew Ensembl ENCODE CraniofacialAtlas | 612.1 | +0.0 | 12 | 4 | SP1 HNRNPL CREB1 CTCF TEAD4 TFE3 IKZF1 NFKBIZ ZNF692 POLR2A | TXNL4A RBFA ENSG00000267127 lnc-PQLC1-1 RBFADN ENSG00000267251 ADNP2 HSBP1L1 SLC66A2 | |
GH18J080044 | Promoter | 0.6 | EPDnew | 600.4 | +9.9 | 9879 | 0.1 | FOXA2 KDM1A ARID3A | RBFA ADNP2 HSBP1L1 SLC66A2 RBFADN ENSG00000267127 | |
GH18J080037 | Promoter | 0.4 | EPDnew | 600.7 | +3.0 | 2985 | 0.1 | REST | RBFA ADNP2 HSBP1L1 SLC66A2 ENSG00000267127 RBFADN | |
GH18J080038 | Promoter | 0.3 | EPDnew | 600.7 | +4.2 | 4211 | 0.1 | RBFA ADNP2 HSBP1L1 SLC66A2 ENSG00000267127 RBFADN | ||
GH18J080042 | Promoter | 0.3 | EPDnew | 600.4 | +7.7 | 7704 | 0.1 | RBFA HSBP1L1 SLC66A2 RBFADN ENSG00000267127 ADNP2 |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0003674 | molecular_function | ND | -- |
GO:0005515 | protein binding | IPI | 25416956 |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005575 | cellular_component | ND | -- |
GO:0005739 | mitochondrion | IEA | -- |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0006364 | rRNA processing | IEA | -- |
GO:0008150 | biological_process | ND | -- |
ExUns: | 1a | · | 1b | · | 1c | ^ | 2 | ^ | 3a | · | 3b | · | 3c | ^ | 4 | ^ | 5 | ^ | 6 | ^ | 7a | · | 7b |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SP1: | - | ||||||||||||||||||||||
SP2: | - | - | |||||||||||||||||||||
SP3: | - | ||||||||||||||||||||||
SP4: |
This gene was present in the common ancestor of animals.
Organism | Taxonomy | Gene | Similarity | Type | Details |
---|---|---|---|---|---|
Chimpanzee (Pan troglodytes) |
Mammalia | RBFA 30 31 |
|
OneToOne | |
Cow (Bos Taurus) |
Mammalia | RBFA 30 31 |
|
OneToOne | |
Rat (Rattus norvegicus) |
Mammalia | Rbfa 30 |
|
||
Mouse (Mus musculus) |
Mammalia | Rbfa 30 17 31 |
|
OneToOne | |
Dog (Canis familiaris) |
Mammalia | RBFA 30 31 |
|
OneToOne | |
Oppossum (Monodelphis domestica) |
Mammalia | RBFA 31 |
|
OneToOne | |
Platypus (Ornithorhynchus anatinus) |
Mammalia | RBFA 31 |
|
OneToOne | |
Chicken (Gallus gallus) |
Aves | RBFA 30 31 |
|
OneToOne | |
Lizard (Anolis carolinensis) |
Reptilia | RBFA 31 |
|
OneToOne | |
Zebrafish (Danio rerio) |
Actinopterygii | rbfa 30 31 |
|
OneToOne | |
Fruit Fly (Drosophila melanogaster) |
Insecta | CG15916 31 |
|
OneToOne |
Variant ID | Type | Subtype | PubMed ID |
---|---|---|---|
dgv3412n100 | CNV | gain | 25217958 |
dgv3413n100 | CNV | gain | 25217958 |
esv28269 | CNV | gain | 19812545 |
esv3643326 | CNV | loss | 21293372 |
esv3643328 | CNV | loss | 21293372 |
nsv1061450 | CNV | gain | 25217958 |
nsv1065902 | CNV | gain | 25217958 |
nsv1072826 | CNV | deletion | 25765185 |
nsv428359 | CNV | gain | 18775914 |
nsv470437 | CNV | loss | 18288195 |
nsv577958 | CNV | gain | 21841781 |
Disorder | Aliases | PubMed IDs |
---|---|---|
autosomal dominant non-syndromic intellectual disability 1 |
|
|
autosomal dominant non-syndromic intellectual disability |
|
|