UniProt | Protein Name |
---|---|
P32004 |
|
GO Term | Evidence Code | PMID |
---|---|---|
axon development | ||
cell migration | ||
nervous system development |
|
|
synapse organization | ||
chemotaxis |
|
GO Term | Evidence Code | PMID |
---|---|---|
axon guidance receptor activity | ||
protein binding | ||
protein domain specific binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050156 | idiopathic pulmonary fibrosis | |
DOID:0050328 | congenital hypothyroidism | |
DOID:0050387 | nonpapillary renal cell carcinoma | |
DOID:0050425 | restless legs syndrome | |
DOID:0050445 | X-linked dominant hypophosphatemic rickets | |
DOID:0050589 | inflammatory bowel disease | |
DOID:0050635 | alternating hemiplegia of childhood | |
DOID:0050771 | pheochromocytoma | |
DOID:0050819 | obsolete Matthew-Wood syndrome | |
DOID:0050865 | tongue squamous cell carcinoma |
HPO ID | HPO Term |
---|---|
HP:0000218 | High palate |
HP:0000238 | Hydrocephalus |
HP:0000252 | Microcephaly |
HP:0000256 | Macrocephaly |
HP:0000280 | Coarse facial features |
HP:0000486 | Strabismus |
HP:0000639 | Nystagmus |
HP:0000750 | Delayed speech and language development |
HP:0001181 | Adducted thumb |
HP:0001188 | Hand clenching |
Disease ID | Disease Name |
---|---|
ORPHA:306617 |
|
ORPHA:2182 |
|
OMIM:304100 |
|
ORPHA:1497 |
|
OMIM:303350 |
|
OMIM:307000 |
|
ORPHA:2466 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
177078 | WB:WBGene00002243 | ||
31792 | FB:FBgn0264975 | ||
30634 | ZFIN:ZDB-GENE-990415-10 | DANRE24007 | |
30656 | ZFIN:ZDB-GENE-980526-512 | ||
108276290 | ICTPU08109 | ||
106572712 | SALSA79509 | ||
115168850 | SALTR75714 | ||
101166379 | ORYLA15726 | ||
115584934 | SPAAU52848 | ||
373742 | Xenbase:XB-GENE-5914737 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
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Last updated: August 19, 2024