GO Term | Evidence Code | PMID |
---|---|---|
angiogenesis | ||
natural killer cell chemotaxis |
|
|
neutrophil extravasation |
|
|
phosphatidylinositol phosphate biosynthetic process | ||
positive regulation of cytosolic calcium ion concentration |
GO Term | Evidence Code | PMID |
---|---|---|
kinase activity | ||
ephrin receptor binding | ||
1-phosphatidylinositol-3-kinase activity | ||
protein serine/threonine kinase activity | ||
protein serine kinase activity |
DO ID | Disease Name | Source |
---|---|---|
DOID:0080548 | Noonan syndrome with multiple lentigines 1 | |
DOID:0090018 | autosomal dominant familial periodic fever | |
DOID:0090021 | split hand-foot malformation 1 | |
DOID:0090053 | episodic kinesigenic dyskinesia 1 | |
DOID:0090103 | Huntington's disease-like 1 | |
DOID:0090104 | Huntington's disease-like 2 | |
DOID:0110035 | Alzheimer's disease 2 | |
DOID:0110037 | Alzheimer's disease 5 | |
DOID:0110038 | Alzheimer's disease 6 | |
DOID:0110039 | Alzheimer's disease 7 |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000010 | Recurrent urinary tract infections |
HP:0000403 | Recurrent otitis media |
HP:0000964 | Eczematoid dermatitis |
HP:0001252 | Hypotonia |
HP:0001433 | Hepatosplenomegaly |
HP:0001581 | Recurrent skin infections |
HP:0001742 | Nasal congestion |
HP:0001744 | Splenomegaly |
HP:0001873 | Thrombocytopenia |
Disease ID | Disease Name |
---|---|
OMIM:619802 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115036690 | ECHNA41811 | ||
115403926 | SALFA10000 | ||
113490925 | ATHCN05581 | ||
105815179 | PROCO05914 | ||
109060929 | CYPCA63285 | ||
109064199 | CYPCA33330 | ||
103732179 | NANGA02072 | ||
116442892 | CORMO19998 | ||
103252973 | CARSF17749 | ||
115605592 | STRHB21515 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024