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TRIM64 (Tripartite Motif Containing 64) is a Protein Coding gene. Diseases associated with TRIM64 include Septooptic Dysplasia. An important paralog of this gene is TRIM64B.
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005515 | protein binding | IEA | -- |
GO:0008270 | zinc ion binding | IEA | -- |
GO:0046872 | metal ion binding | IEA | -- |
GO:0061630 | ubiquitin protein ligase activity | IBA | 21873635 |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005737 | cytoplasm | IBA | 21873635 |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0010468 | regulation of gene expression | IBA | 21873635 |
GO:0016567 | protein ubiquitination | IBA | 21873635 |
GO:0045087 | innate immune response | IBA | 21873635 |
This gene was present in the common ancestor of human and chimp.
Organism | Taxonomy | Gene | Similarity | Type | Details |
---|---|---|---|---|---|
Chimpanzee (Pan troglodytes) |
Mammalia | TRIM64B 30 |
|
Variant ID | Type | Subtype | PubMed ID |
---|---|---|---|
esv2759849 | CNV | gain+loss | 17122850 |
esv3579832 | CNV | loss | 25503493 |
esv3579993 | CNV | gain | 25503493 |
esv3892056 | CNV | gain+loss | 25118596 |
esv3892060 | CNV | gain | 25118596 |
nsv1036092 | CNV | loss | 25217958 |
nsv1070473 | CNV | deletion | 25765185 |
nsv1133000 | OTHER | inversion | 24896259 |
nsv1136137 | CNV | deletion | 24896259 |
nsv469862 | CNV | gain | 16826518 |
nsv508646 | CNV | deletion | 20534489 |
nsv7222 | OTHER | inversion | 18451855 |
nsv819015 | CNV | loss | 19587683 |
nsv832225 | CNV | gain | 17160897 |
nsv8858 | CNV | gain+loss | 18304495 |
nsv972060 | CNV | duplication | 23825009 |
Disorder | Aliases | PubMed IDs |
---|---|---|
septooptic dysplasia |
|
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