UniProt | Protein Name |
---|---|
A0A384NL00 |
|
P11413 |
|
GO Term | Evidence Code | PMID |
---|---|---|
NADPH regeneration | ||
substantia nigra development | ||
negative regulation of cell growth involved in cardiac muscle cell development | ||
lipid metabolic process | ||
regulation of neuron apoptotic process |
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:0070123 | congenital nongoitrous hypothyroidism 4 | |
DOID:0070124 | congenital nongoitrous hypothyroidism 2 | |
DOID:0070125 | congenital nongoitrous hypothyroidism 5 | |
DOID:0070126 | congenital nongoitrous hypothyroidism 1 | |
DOID:0070127 | congenital nongoitrous hypothyroidism 3 | |
DOID:0070128 | congenital nongoitrous hypothyroidism 6 | |
DOID:0070195 | X-linked chronic granulomatous disease | |
DOID:0070322 | childhood hepatocellular carcinoma | |
DOID:0070328 | adult hepatocellular carcinoma | |
DOID:0080144 | childhood acute lymphocytic leukemia |
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 |
---|---|---|---|
100073461 | ORNAN23587 | ||
100388810 | CALJA48297 | ||
105579745 | CERAT45795 | ||
102117021 | MACFA45489 | ||
105467964 | MACNE46030 | ||
105534279 | MANLE40389 | ||
101145237 | GORGO44111 | ||
100985592 | PANPA42399 | ||
743041 | PANTR47160 | ||
100449143 | PONAB37197 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024