UniProt | Protein Name |
---|---|
Q7Z449 |
|
GO Term | Evidence Code | PMID |
---|---|---|
cytochrome metabolic process |
|
|
omega-hydroxylase P450 pathway | ||
organic acid metabolic process | ||
xenobiotic metabolic process |
GO Term | Evidence Code | PMID |
---|---|---|
intracellular membrane-bounded organelle | ||
mitochondrial inner membrane | ||
cytoplasm | ||
endoplasmic reticulum membrane |
|
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0110763 | hereditary spastic paraplegia 10 | |
DOID:0110764 | hereditary spastic paraplegia 11 | |
DOID:0110765 | hereditary spastic paraplegia 12 | |
DOID:0110766 | hereditary spastic paraplegia 13 | |
DOID:0110767 | hereditary spastic paraplegia 14 | |
DOID:0110768 | hereditary spastic paraplegia 15 | |
DOID:0110769 | hereditary spastic paraplegia 16 | |
DOID:0110770 | hereditary spastic paraplegia 17 | |
DOID:0110771 | hereditary spastic paraplegia 18 | |
DOID:0110772 | hereditary spastic paraplegia 19 |
HPO ID | HPO Term |
---|---|
HP:0002395 | Lower limb hyperreflexia |
HP:0002453 | Abnormal globus pallidus morphology |
HP:0002500 | Abnormal cerebral white matter morphology |
HP:0003477 | Peripheral axonal neuropathy |
HP:0003487 | Babinski sign |
HP:0003577 | Congenital onset |
HP:0003593 | Infantile onset |
HP:0003621 | Juvenile onset |
HP:0007350 | Hyperreflexia in upper limbs |
HP:0011463 | Childhood onset |
Disease ID | Disease Name |
---|---|
ORPHA:320411 |
|
OMIM:615030 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
105706268 | AOTNA12189 | ||
110218598 | PHACI00984 | ||
101048855 | SAIBB15884 | ||
101973126 | ICTTR17083 | ||
101614371 | JACJA23602 | ||
118311847 | SCOMX30847 | ||
102440622 | MYOLU09995 | ||
117022557 | RHIFE18696 | ||
100229295 | TAEGU24465 | ||
103236086 | CHLSB16588 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024