phospholipase D family member 3
| UniProt | Protein Name |
|---|---|
| Q8IV08 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| immune system process |
|
|
| lipid metabolic process |
|
|
| inflammatory response |
|
|
| myotube differentiation |
|
|
| negative regulation of toll-like receptor 9 signaling pathway |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| Golgi membrane |
|
|
| Golgi membrane |
|
|
| lysosome |
|
|
| lysosome |
|
|
| lysosomal membrane |
|
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| catalytic activity |
|
|
| 5'-3' RNA exonuclease activity |
|
|
| D-type glycerophospholipase activity |
|
|
| protein binding |
|
|
| acyltransferase activity, transferring groups other than amino-acyl groups |
|
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080288 | spinocerebellar ataxia 46 |
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000514 | Slow saccadic eye movements |
| HP:0000639 | Nystagmus |
| HP:0001260 | Dysarthria |
| HP:0001272 | Cerebellar atrophy |
| HP:0001310 | Dysmetria |
| HP:0002066 | Gait ataxia |
| HP:0002070 | Limb ataxia |
| HP:0002403 | Positive Romberg sign |
| HP:0003390 | Sensory axonal neuropathy |
| Disease ID | Disease Name |
|---|---|
| OMIM:617770 |
|
| Species | Gene ID | Alliance of Genome Resources |
|---|---|---|
| 18807 | MGI:1333782 | |
| 361527 | RGD:1308248 | |
| 179105 | WB:WBGene00017316 | |
| 398831 | Xenbase:XB-GENE-1006830 | |
| 496432 | Xenbase:XB-GENE-1006824 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
GlyCosmos Portal v4.5.0
Last updated: April 6, 2026