GO Term | Evidence Code | PMID |
---|---|---|
axon ensheathment | ||
cell adhesion involved in heart morphogenesis | ||
presynaptic membrane assembly | ||
cell-cell junction organization | ||
dorsal closure |
GO Term | Evidence Code | PMID |
---|---|---|
plasma membrane | ||
pleated septate junction | ||
presynaptic active zone | ||
synapse |
Gene Ontology |
---|
lysine biosynthetic process via aminoadipic acid |
magnesium ion binding |
Location | References |
---|---|
DO ID | Disease Name | Source |
---|---|---|
DOID:0060041 | autism spectrum disorder | |
DOID:0060244 | specific language impairment | |
DOID:0060308 | autosomal recessive intellectual developmental disorder | |
DOID:0060488 | Pitt-Hopkins syndrome | |
DOID:0060558 | lethal congenital contracture syndrome | |
DOID:0090130 | cortical dysplasia-focal epilepsy syndrome | |
DOID:1059 | intellectual disability | |
DOID:11257 | social phobia | |
DOID:11832 | visual epilepsy | |
DOID:12849 | autistic disorder |
Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|---|
8506 | HGNC:8011 | |||
26047 | HGNC:13830 | |||
53321 | MGI:1858201 | |||
66797 | MGI:1914047 | |||
79937 | HGNC:13834 | |||
84008 | RGD:70902 | |||
85445 | HGNC:18747 | |||
129684 | HGNC:18748 | |||
170571 | MGI:2183572 | |||
178167 | WB:WBGene00003772 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: December 9, 2024