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Repository for lectin-assisted multimodality data
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MIRAGE
Dmx like 2
Summary
- Gene Symbol
-
- DMXL2
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Coiled coil
- Cytoplasmic vesicle
- Diabetes mellitus
- Direct protein sequencing
- Disease variant
- Epilepsy
- Hypogonadotropic hypogonadism
- Membrane
- Neuropathy
- Non-syndromic deafness
- Phosphoprotein
- Reference proteome
- Repeat
- Synapse
- WD repeat
- Proteins
| UniProt | Protein Name |
|---|---|
| Q8TDJ6 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| vacuolar acidification |
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular space | ||
| synaptic vesicle | ||
| synaptic vesicle membrane | ||
| RAVE complex | ||
| neuronal dense core vesicle |
| GO Term | Evidence Code | PMID |
|---|---|---|
| small GTPase binding |
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Dmx-like protein
- Functional Category
-
- E: Amino acid transport and metabolism
- G: Carbohydrate transport and metabolism
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| vacuolar acidification |
| InterPro |
|---|
| RAVE complex protein Rav1 C-terminal |
| WD40 repeat |
| WD40-repeat-containing domain superfamily |
| WD40/YVTN repeat-like-containing domain superfamily |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080267 | autosomal dominant nonsyndromic deafness 71 | |
| DOID:0112217 | developmental and epileptic encephalopathy 81 |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 1657 | SGD:S000003794 | ||
| 23312 | Xenbase:XB-GENE-1004082 | ||
| 235380 | Xenbase:XB-GENE-1004082 | MOUSE61132 | |
| 315676 | RATNO40794 | ||
| 378958 | DANRE13690 | ||
| 453436 | PANTR10319 | ||
| 478306 | CANLF12516 | ||
| 693954 | MACMU42984 | ||
| 782535 | BOVIN01342 | ||
| 100026227 | MONDO04341 |
