UniProt | Protein Name |
---|---|
A0A384NL00 |
|
P11413 |
|
GO Term | Evidence Code | PMID |
---|---|---|
cellular response to oxidative stress | ||
cholesterol biosynthetic process | ||
positive regulation of calcium ion transmembrane transport via high voltage-gated calcium channel | ||
erythrocyte maturation | ||
glutathione metabolic process |
GO Term | Evidence Code | PMID |
---|---|---|
cytoplasmic side of plasma membrane | ||
extracellular exosome |
GO Term | Evidence Code | PMID |
---|---|---|
glucose binding | ||
protein homodimerization activity | ||
glucose-6-phosphate dehydrogenase activity | ||
protein binding | ||
NADP binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0060357 | chylomicron retention disease | |
DOID:0060359 | Sakati-Nyhan syndrome | |
DOID:0060380 | orofaciodigital syndrome X | |
DOID:0060474 | familial erythrocytosis 2 | |
DOID:0060597 | atypical chronic myeloid leukemia, BCR-ABL1 negative | |
DOID:0060599 | Nance-Horan syndrome | |
DOID:0060703 | Muenke Syndrome | |
DOID:0060891 | Parkinson's disease 19A | |
DOID:0060895 | Parkinson's disease 4 | |
DOID:0060896 | Parkinson's disease 23 |
HPO ID | HPO Term |
---|---|
HP:0000952 | Jaundice |
HP:0000980 | Pallor |
HP:0001423 | X-linked dominant inheritance |
HP:0001744 | Splenomegaly |
HP:0001923 | Reticulocytosis |
HP:0001945 | Fever |
HP:0001974 | Leukocytosis |
HP:0002027 | Abdominal pain |
HP:0003577 | Congenital onset |
HP:0003593 | Infantile onset |
Disease ID | Disease Name |
---|---|
OMIM:300908 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
101955556 | ICTTR08614 | ||
103147817 | POEFO14124 | ||
101594346 | JACJA24194 | ||
102437266 | MYOLU04214 | ||
117020782 | RHIFE17743 | ||
103232833 | CHLSB18914 | ||
108518782 | RHIBE40860 | ||
104667047 | RHIRO43461 | ||
114587310 | PODMU24709 | ||
107594489 | SINGR06921 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024