UniProt | Protein Name |
---|---|
O75787 |
|
GO Term | Evidence Code | PMID |
---|---|---|
endosomal lumen acidification |
|
GO Term | Evidence Code | PMID |
---|---|---|
autophagosome membrane | ||
clathrin-coated vesicle membrane | ||
vacuolar proton-transporting V-type ATPase, V0 domain | ||
external side of plasma membrane | ||
axon |
GO Term | Evidence Code | PMID |
---|---|---|
signaling receptor activity | ||
protein binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050156 | idiopathic pulmonary fibrosis | |
DOID:0050571 | congenital disorder of glycosylation type II | |
DOID:0050678 | Blau syndrome | |
DOID:0050848 | obstructive sleep apnea | |
DOID:0060135 | apraxia | |
DOID:0060224 | atrial fibrillation | |
DOID:0060249 | scoliosis | |
DOID:0060262 | gallbladder disease | |
DOID:0060309 | syndromic X-linked intellectual disability | |
DOID:0060318 | acute promyelocytic leukemia |
HPO ID | HPO Term |
---|---|
HP:0004313 | Decreased circulating antibody level |
HP:0006801 | Hyperactive deep tendon reflexes |
HP:0006956 | Lateral ventricle dilatation |
HP:0007076 | Extrapyramidal muscular rigidity |
HP:0007082 | Dilated third ventricle |
HP:0010527 | Astereognosis |
HP:0010529 | Echolalia |
HP:0010819 | Atonic seizure |
HP:0011448 | Ankle clonus |
HP:0011812 | Agraphesthesia |
Disease ID | Disease Name |
---|---|
ORPHA:363654 |
|
OMIM:300911 |
|
OMIM:301045 |
|
OMIM:300423 |
|
ORPHA:93952 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100541439 | MELGA01337 | ||
100082327 | ORNAN09879 | ||
100935292 | SARHA09442 | ||
100394594 | CALJA47971 | ||
105595612 | CERAT35055 | ||
101925193 | MACFA44073 | ||
705048 | MACMU47488 | ||
105499913 | MACNE32264 | ||
101018086 | PAPAN43178 | ||
101125474 | GORGO43785 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024