UniProt | Protein Name |
---|---|
Q969N2 |
|
GO Term | Evidence Code | PMID |
---|---|---|
neuron differentiation | ||
neuron apoptotic process | ||
attachment of GPI anchor to protein |
GO Term | Evidence Code | PMID |
---|---|---|
endoplasmic reticulum membrane | ||
membrane | ||
GPI-anchor transamidase complex | ||
cytoplasmic vesicle |
GO Term | Evidence Code | PMID |
---|---|---|
protein binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:13250 | diarrhea | |
DOID:0060249 | scoliosis | |
DOID:0060284 | paroxysmal nocturnal hemoglobinuria | |
DOID:0080140 | multiple congenital anomalies-hypotonia-seizures syndrome 3 | |
DOID:10293 | monocular esotropia | |
DOID:10575 | calcium metabolism disease | |
DOID:11476 | osteoporosis | |
DOID:11771 | spontaneous ocular nystagmus | |
DOID:11832 | visual epilepsy | |
DOID:12678 | hypercalcemia |
HPO ID | HPO Term |
---|---|
HP:0002094 | Dyspnea |
HP:0002101 | Abnormal lung lobation |
HP:0002121 | Generalized non-motor (absence) seizure |
HP:0002123 | Generalized myoclonic seizure |
HP:0002150 | Hypercalciuria |
HP:0002155 | Hypertriglyceridemia |
HP:0002263 | Exaggerated cupid's bow |
HP:0002283 | Global brain atrophy |
HP:0002315 | Headache |
HP:0002376 | Developmental regression |
Disease ID | Disease Name |
---|---|
OMIM:615398 |
|
ORPHA:369837 |
|
OMIM:615399 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
179519 | WB:WBGene00008918 | ||
31772 | FB:FBgn0030035 | ||
102349594 | LATCH19871 | ||
556667 | ZFIN:ZDB-GENE-090313-46 | DANRE50251 | |
108276100 | ICTPU07619 | ||
113582246 | ELEEL29749 | ||
105013799 | ESOLU34437 | ||
115168926 | SALTR74822 | ||
103481160 | POERE14098 | ||
102290799 | HAPBU29825 |
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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