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KLF13 belongs to a family of transcription factors that contain 3 classical zinc finger DNA-binding domains consisting of a zinc atom tetrahedrally coordinated by 2 cysteines and 2 histidines (C2H2 motif). These transcription factors bind to GC-rich sequences and related GT and CACCC boxes (Scohy et al., 2000 [PubMed 11087666]).[supplied by OMIM, Mar 2008]
KLF13 (Kruppel Like Factor 13) is a Protein Coding gene. Diseases associated with KLF13 include Chromosome 15Q13.3 Deletion Syndrome. Gene Ontology (GO) annotations related to this gene include nucleic acid binding. An important paralog of this gene is KLF16.
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0000978 | RNA polymerase II proximal promoter sequence-specific DNA binding | IEA | -- |
GO:0000981 | DNA-binding transcription factor activity, RNA polymerase II-specific | NAS | 19274049 |
GO:0001228 | DNA-binding transcription activator activity, RNA polymerase II-specific | IEA | -- |
GO:0003676 | nucleic acid binding | IEA | -- |
GO:0003677 | DNA binding | IEA | -- |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005634 | nucleus | IBA | 21873635 |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0006357 | regulation of transcription by RNA polymerase II | IBA,IEA | 21873635 |
GO:0006366 | transcription by RNA polymerase II | TAS | 10023774 |
GO:0008285 | negative regulation of cell proliferation | IEA | -- |
GO:0045647 | negative regulation of erythrocyte differentiation | IEA | -- |
GO:0045944 | positive regulation of transcription by RNA polymerase II | IEA | -- |
Name | Status | Disease Links | Group | Role | Mechanism of Action | Clinical Trials |
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Name | Synonyms | Role | CAS Number | PubChem IDs | PubMed IDs |
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This gene was present in the common ancestor of animals.
Organism | Taxonomy | Gene | Similarity | Type | Details |
---|---|---|---|---|---|
chimpanzee (Pan troglodytes) |
Mammalia | KLF13 33 32 |
|
OneToOne | |
dog (Canis familiaris) |
Mammalia | KLF13 33 |
|
OneToOne | |
rat (Rattus norvegicus) |
Mammalia | Klf13 32 |
|
||
cow (Bos Taurus) |
Mammalia | KLF13 32 |
|
||
mouse (Mus musculus) |
Mammalia | Klf13 17 33 32 |
|
||
oppossum (Monodelphis domestica) |
Mammalia | KLF13 33 |
|
OneToOne | |
chicken (Gallus gallus) |
Aves | KLF13 33 32 |
|
OneToOne | |
lizard (Anolis carolinensis) |
Reptilia | KLF13 33 |
|
OneToOne | |
tropical clawed frog (Silurana tropicalis) |
Amphibia | klf13 32 |
|
||
zebrafish (Danio rerio) |
Actinopterygii | klf13 33 32 |
|
OneToOne | |
wufi22b08 32 |
|
||||
fruit fly (Drosophila melanogaster) |
Insecta | EP2237 34 |
|
|
|
worm (Caenorhabditis elegans) |
Secernentea | Y40B1A.4 34 |
|
|
|
sea squirt (Ciona savignyi) |
Ascidiacea | CSA.7373 33 |
|
OneToMany |
SNP ID | Clin | Chr 15 pos | Variation | AA Info | Type |
---|---|---|---|---|---|
rs1000023945 | -- | 31,399,542(+) | A/G | genic_downstream_transcript_variant, intron_variant | |
rs1000063088 | -- | 31,355,646(+) | G/A | intron_variant | |
rs1000076300 | -- | 31,399,308(+) | A/T | genic_downstream_transcript_variant, intron_variant | |
rs1000078509 | -- | 31,353,167(+) | T/C | intron_variant | |
rs1000086185 | -- | 31,361,271(+) | G/C | intron_variant |
Variant ID | Type | Subtype | PubMed ID |
---|---|---|---|
dgv4429n54 | CNV | loss | 21841781 |
dgv4430n54 | CNV | loss | 21841781 |
dgv4431n54 | CNV | gain+loss | 21841781 |
dgv4432n54 | CNV | gain | 21841781 |
dgv4433n54 | CNV | gain | 21841781 |
dgv4434n54 | CNV | loss | 21841781 |
esv29856 | CNV | loss | 19812545 |
esv34100 | CNV | loss | 18971310 |
esv3636052 | CNV | gain | 21293372 |
nsv1070262 | CNV | deletion | 25765185 |
nsv456747 | CNV | loss | 19166990 |
nsv456748 | CNV | loss | 19166990 |
nsv511044 | OTHER | inversion | 20534489 |
nsv516681 | CNV | loss | 19592680 |
nsv568772 | CNV | loss | 21841781 |
nsv568773 | CNV | loss | 21841781 |
nsv568774 | CNV | gain | 21841781 |
nsv568777 | CNV | gain+loss | 21841781 |
nsv568781 | CNV | gain+loss | 21841781 |
nsv568799 | CNV | gain | 21841781 |
nsv568801 | CNV | loss | 21841781 |
nsv827280 | CNV | gain | 20364138 |
Disorder | Aliases | PubMed IDs |
---|---|---|
chromosome 15q13.3 deletion syndrome |
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