GO Term | Evidence Code | PMID |
---|---|---|
glycosphingolipid catabolic process | ||
response to Thyroglobulin triiodothyronine | ||
carbohydrate metabolic process | ||
response to cortisone | ||
galactose catabolic process |
GO Term | Evidence Code | PMID |
---|---|---|
intracellular membrane-bounded organelle | ||
extracellular region | ||
cytoplasm | ||
vacuole | ||
Golgi apparatus |
GO Term | Evidence Code | PMID |
---|---|---|
protein homodimerization activity | ||
galactoside binding | ||
beta-galactosidase activity | ||
protein binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0060584 | Noonan syndrome 6 | |
DOID:0060585 | Noonan syndrome 7 | |
DOID:0060586 | Noonan syndrome 8 | |
DOID:0060587 | Noonan syndrome 9 | |
DOID:0060588 | Noonan syndrome 10 | |
DOID:0060608 | microcephalic osteodysplastic primordial dwarfism type I | |
DOID:0060609 | microcephalic osteodysplastic primordial dwarfism type II | |
DOID:0060644 | chondrodysplasia-pseudohermaphroditism syndrome | |
DOID:0060764 | autosomal recessive Robinow syndrome | |
DOID:0060765 | autosomal dominant Robinow syndrome 2 |
HPO ID | HPO Term |
---|---|
HP:0001251 | Ataxia |
HP:0001252 | Hypotonia |
HP:0001256 | Intellectual disability, mild |
HP:0001257 | Spasticity |
HP:0001260 | Dysarthria |
HP:0001263 | Global developmental delay |
HP:0001276 | Hypertonia |
HP:0001288 | Gait disturbance |
HP:0001290 | Generalized hypotonia |
HP:0001332 | Dystonia |
Disease ID | Disease Name |
---|---|
ORPHA:79255 |
|
OMIM:230600 |
|
OMIM:230500 |
|
OMIM:230650 |
|
OMIM:253010 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
114032505 | VOMUR19701 | ||
113880962 | BOBOX09266 | ||
100951714 | OTOGA18820 | ||
102016922 | CHILA06220 | ||
110209145 | PHACI27627 | ||
101961768 | ICTTR03724 | ||
118312046 | SCOMX30886 | ||
102440059 | MYOLU04308 | ||
117036756 | RHIFE15993 | ||
100226450 | TAEGU18385 |
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
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024