UniProt | Protein Name |
---|---|
Q15067 |
|
GO Term | Evidence Code | PMID |
---|---|---|
very long-chain fatty acid metabolic process | ||
very long-chain fatty acid beta-oxidation | ||
fatty acid oxidation | ||
generation of precursor metabolites and energy | ||
prostaglandin 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:0070516 | Mitchell syndrome | |
DOID:0080199 | colorectal carcinoma | |
DOID:0110462 | autosomal recessive nonsyndromic deafness 101 | |
DOID:0110463 | autosomal recessive nonsyndromic deafness 102 | |
DOID:0110464 | autosomal recessive nonsyndromic deafness 103 | |
DOID:0110465 | autosomal recessive nonsyndromic deafness 104 | |
DOID:0110466 | obsolete autosomal recessive nonsyndromic deafness 105 | |
DOID:0110467 | autosomal recessive nonsyndromic deafness 12 | |
DOID:0110468 | autosomal recessive nonsyndromic deafness 13 | |
DOID:0110469 | autosomal recessive nonsyndromic deafness 14 |
HPO ID | HPO Term |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000007 | Autosomal recessive inheritance |
HP:0000248 | Brachycephaly |
HP:0000286 | Epicanthus |
HP:0000316 | Hypertelorism |
HP:0000369 | Low-set ears |
HP:0000407 | Sensorineural hearing impairment |
HP:0000431 | Wide nasal bridge |
HP:0000486 | Strabismus |
HP:0000510 | Rod-cone dystrophy |
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
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024