GO Term | Evidence Code | PMID |
---|---|---|
cellular response to glucose stimulus |
GO Term | Evidence Code | PMID |
---|---|---|
kinase activity | ||
1-phosphatidylinositol-3-kinase activity | ||
insulin receptor substrate binding | ||
protein serine/threonine kinase activity | ||
protein serine kinase activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050431 | arrhythmogenic right ventricular cardiomyopathy | |
DOID:0050457 | Sertoli cell-only syndrome | |
DOID:0050458 | juvenile myelomonocytic leukemia | |
DOID:0050469 | Costello syndrome | |
DOID:0050486 | exanthem | |
DOID:0050523 | adult T-cell leukemia/lymphoma | |
DOID:0050535 | exudative vitreoretinopathy | |
DOID:0050569 | Seckel syndrome | |
DOID:0050572 | cone-rod dystrophy | |
DOID:0050589 | inflammatory bowel disease |
HPO ID | HPO Term |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000020 | Urinary incontinence |
HP:0000034 | Hydrocele testis |
HP:0000036 | Abnormal penis morphology |
HP:0000044 | Hypogonadotropic hypogonadism |
HP:0000077 | Abnormality of the kidney |
HP:0000089 | Renal hypoplasia |
HP:0000098 | Tall stature |
HP:0000105 | Enlarged kidney |
HP:0000130 | Abnormality of the uterus |
Disease ID | Disease Name |
---|---|
OMIM:615108 |
|
OMIM:613659 |
|
ORPHA:276280 |
|
OMIM:612918 |
|
OMIM:619538 |
|
ORPHA:221061 |
|
ORPHA:201 |
|
ORPHA:60040 |
|
OMIM:114550 |
|
OMIM:182000 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
109520494 | HIPCM13754 | ||
115057907 | ECHNA32252 | ||
115405185 | SALFA33362 | ||
113483286 | ATHCN11299 | ||
103396148 | CYNSE18659 | ||
105806240 | PROCO02280 | ||
103738596 | NANGA16955 | ||
116448589 | CORMO00552 | ||
103266233 | CARSF18361 | ||
115611164 | STRHB11620 |
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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