GO Term | Evidence Code | PMID |
---|---|---|
membrane organization |
|
|
synaptic vesicle uncoating | ||
phosphatidylinositol-3-phosphate biosynthetic process | ||
phosphatidylinositol biosynthetic process |
|
|
learning |
GO Term | Evidence Code | PMID |
---|---|---|
clathrin coat of coated pit | ||
cytosol |
|
|
terminal bouton | ||
presynapse | ||
microtubule |
GO Term | Evidence Code | PMID |
---|---|---|
phosphatidylinositol-3-phosphate phosphatase activity | ||
phosphatidylinositol phosphate 5-phosphatase activity | ||
phosphatidylinositol-3,5-bisphosphate 5-phosphatase activity |
|
|
inositol-1,4,5-trisphosphate 5-phosphatase activity |
|
|
phosphatidylinositol-4-phosphate phosphatase activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050557 | congenital muscular dystrophy | |
DOID:0050572 | cone-rod dystrophy | |
DOID:0050591 | tooth agenesis | |
DOID:0050709 | early infantile epileptic encephalopathy | |
DOID:0050777 | Joubert syndrome | |
DOID:0050841 | focal hand dystonia | |
DOID:0060249 | scoliosis | |
DOID:0060255 | rippling muscle disease 2 | |
DOID:0060260 | ptosis | |
DOID:0060261 | congenital ptosis |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000252 | Microcephaly |
HP:0000338 | Hypomimic face |
HP:0000348 | High forehead |
HP:0000494 | Downslanted palpebral fissures |
HP:0000504 | Abnormality of vision |
HP:0000505 | Visual impairment |
HP:0000508 | Ptosis |
HP:0000546 | Retinal degeneration |
HP:0000551 | Color vision defect |
Disease ID | Disease Name |
---|---|
ORPHA:2828 |
|
ORPHA:391411 |
|
OMIM:617389 |
|
ORPHA:442835 |
|
OMIM:615530 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
178284 | WB:WBGene00006763 | ||
37517 | FB:FBgn0034691 | ||
102367670 | LATCH15231 | ||
337236 | ZFIN:ZDB-GENE-030131-9180 | DANRE00491 | |
113571772 | ELEEL08025 | ||
115204661 | SALTR78206 | ||
100697157 | ORENI03864 | ||
115594749 | SPAAU20565 | ||
100380968 | Xenbase:XB-GENE-956333 | ||
108707879 | Xenbase:XB-GENE-17332541 |
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
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Last updated: August 19, 2024