UniProt | Protein Name |
---|---|
Q9P212 |
|
B7ZM61 |
|
A0A8I5KXT2 |
|
GO Term | Evidence Code | PMID |
---|---|---|
G protein-coupled receptor signaling pathway | ||
diacylglycerol biosynthetic process | ||
release of sequestered calcium ion into cytosol | ||
positive regulation of lamellipodium assembly | ||
phospholipase C-activating G protein-coupled receptor signaling pathway |
GO Term | Evidence Code | PMID |
---|---|---|
cytosol | ||
plasma membrane | ||
lamellipodium | ||
Golgi membrane |
GO Term | Evidence Code | PMID |
---|---|---|
small GTPase binding | ||
guanyl-nucleotide exchange factor activity |
|
|
enzyme binding | ||
phospholipase C activity | ||
metal ion binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050453 | lissencephaly | |
DOID:0050540 | Charcot-Marie-Tooth disease type 3 | |
DOID:0050865 | tongue squamous cell carcinoma | |
DOID:0050908 | myelodysplastic syndrome | |
DOID:0060402 | chromosome 17p13.1 deletion syndrome | |
DOID:0060469 | Miller-Dieker lissencephaly syndrome | |
DOID:0060600 | obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum | |
DOID:0060843 | hereditary neuropathy with liability to pressure palsies | |
DOID:0080199 | colorectal carcinoma | |
DOID:0080379 | nephrotic syndrome type 2 |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000093 | Proteinuria |
HP:0000097 | Focal segmental glomerulosclerosis |
HP:0000100 | Nephrotic syndrome |
HP:0000707 | Abnormality of the nervous system |
HP:0000737 | Irritability |
HP:0000969 | Edema |
HP:0001945 | Fever |
HP:0001967 | Diffuse mesangial sclerosis |
HP:0002027 | Abdominal pain |
Disease ID | Disease Name |
---|---|
ORPHA:656 |
|
OMIM:610725 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100992707 | PANPA05196 | ||
450620 | PANTR01195 | ||
100444145 | PONAB01350 | ||
486808 | CANLF11321 | ||
112913979 | VULVU00630 | ||
101689486 | MUSPF14792 | ||
101088695 | FELCA27297 | ||
101338810 | TURTR12620 | ||
100677444 | LOXAF15588 | ||
100061676 | HORSE17765 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024