UniProt | Protein Name |
---|---|
O60931 |
|
I3L4A9 |
|
A0A0S2Z3K3 |
|
A0A0S2Z3I9 |
|
GO Term | Evidence Code | PMID |
---|---|---|
renal glucose absorption | ||
proton transmembrane transport | ||
ATP metabolic process | ||
renal water absorption | ||
negative regulation of hydrogen peroxide biosynthetic process |
GO Term | Evidence Code | PMID |
---|---|---|
intracellular membrane-bounded organelle | ||
melanosome | ||
plasma membrane | ||
lysosomal membrane | ||
early endosome |
DO ID | Disease Name | Source |
---|---|---|
DOID:0014667 | disease of metabolism | |
DOID:0050336 | hypophosphatemia | |
DOID:0050572 | cone-rod dystrophy | |
DOID:0060891 | Parkinson's disease 19A | |
DOID:0060895 | Parkinson's disease 4 | |
DOID:0060896 | Parkinson's disease 23 | |
DOID:0080001 | bone disease | |
DOID:0080348 | Alzheimer's disease 1 | |
DOID:0110035 | Alzheimer's disease 2 | |
DOID:0110037 | Alzheimer's disease 5 |
HPO ID | HPO Term |
---|---|
HP:0001508 | Failure to thrive |
HP:0001510 | Growth delay |
HP:0001531 | Failure to thrive in infancy |
HP:0001738 | Exocrine pancreatic insufficiency |
HP:0001744 | Splenomegaly |
HP:0001824 | Weight loss |
HP:0001941 | Acidosis |
HP:0001942 | Metabolic acidosis |
HP:0001944 | Dehydration |
HP:0001959 | Polydipsia |
Disease ID | Disease Name |
---|---|
OMIM:219800 |
|
ORPHA:411629 |
|
OMIM:219900 |
|
ORPHA:411641 |
|
ORPHA:411634 |
|
OMIM:219750 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
101976099 | ICTTR01178 | ||
101613890 | JACJA24478 | ||
118318033 | SCOMX04957 | ||
102419464 | MYOLU16052 | ||
117012753 | RHIFE08316 | ||
100223329 | TAEGU07728 | ||
103242158 | CHLSB05097 | ||
108523097 | RHIBE33705 | ||
104677236 | RHIRO28276 | ||
100592953 | NOMLE15938 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024