UniProt | Protein Name |
---|---|
Q15067 |
|
GO Term | Evidence Code | PMID |
---|---|---|
hydrogen peroxide biosynthetic process | ||
fatty acid beta-oxidation using acyl-CoA oxidase | ||
spermatogenesis | ||
fatty acid catabolic process | ||
lipid metabolic process |
GO Term | Evidence Code | PMID |
---|---|---|
cytosol |
|
|
membrane | ||
peroxisome | ||
peroxisomal membrane | ||
peroxisomal matrix |
|
GO Term | Evidence Code | PMID |
---|---|---|
flavin adenine dinucleotide binding | ||
protein homodimerization activity | ||
fatty acid binding | ||
acyl-CoA oxidase activity | ||
PDZ domain binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0014667 | disease of metabolism | |
DOID:0050564 | autosomal dominant nonsyndromic deafness | |
DOID:0050565 | autosomal recessive nonsyndromic deafness | |
DOID:0050566 | X-linked nonsyndromic deafness | |
DOID:0050572 | cone-rod dystrophy | |
DOID:0050591 | tooth agenesis | |
DOID:0050797 | peroxisomal acyl-CoA oxidase deficiency | |
DOID:0060058 | lymphoma | |
DOID:0060690 | autosomal dominant auditory neuropathy 1 | |
DOID:0060823 | syndromic X-linked intellectual disability 94 |
HPO ID | HPO Term |
---|---|
HP:0001250 | Seizure |
HP:0001252 | Hypotonia |
HP:0001263 | Global developmental delay |
HP:0001276 | Hypertonia |
HP:0001288 | Gait disturbance |
HP:0001298 | Encephalopathy |
HP:0001319 | Neonatal hypotonia |
HP:0001332 | Dystonia |
HP:0001344 | Absent speech |
HP:0001347 | Hyperreflexia |
Disease ID | Disease Name |
---|---|
ORPHA:2971 |
|
OMIM:264470 |
|
OMIM:618960 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
173162 | WB:WBGene00008564 | ||
173163 | WB:WBGene00008565 | ||
173164 | WB:WBGene00008567 | ||
176353 | WB:WBGene00008167 | ||
181668 | WB:WBGene00010336 | ||
184167 | WB:WBGene00008566 | ||
31641 | FB:FBgn0029924 | ||
37028 | FB:FBgn0027572 | ||
37445 | FB:FBgn0034628 | ||
37446 | FB:FBgn0034629 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: August 19, 2024