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:0110805 | hereditary spastic paraplegia 53 | |
DOID:0110806 | hereditary spastic paraplegia 54 | |
DOID:0110807 | hereditary spastic paraplegia 55 | |
DOID:0110808 | hereditary spastic paraplegia 56 | |
DOID:0110809 | hereditary spastic paraplegia 57 | |
DOID:0110810 | hereditary spastic paraplegia 5A | |
DOID:0110811 | hereditary spastic paraplegia 6 | |
DOID:0110812 | hereditary spastic paraplegia 61 | |
DOID:0110813 | hereditary spastic paraplegia 62 | |
DOID:0110814 | hereditary spastic paraplegia 63 |
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 |
---|---|---|---|
101590171 | OCTDE23673 | ||
100028028 | MONDO35982 | ||
114030882 | VOMUR30213 | ||
105867318 | MICMU07290 | ||
100949201 | OTOGA01197 | ||
101065574 | TAKRU38243 | ||
102020500 | CHILA24756 | ||
105707107 | AOTNA39726 | ||
101034097 | SAIBB38855 | ||
101969264 | ICTTR08590 |
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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