Gene ID | Gene Symbol | Description | Source |
---|---|---|---|
37 | ACADVL | acyl-CoA dehydrogenase very long chain | |
1555 | CYP2B6 | cytochrome P450 family 2 subfamily B member 6 | |
1557 | CYP2C19 | cytochrome P450 family 2 subfamily C member 19 | |
1583 | CYP11A1 | cytochrome P450 family 11 subfamily A member 1 | |
1584 | CYP11B1 | cytochrome P450 family 11 subfamily B member 1 | |
1585 | CYP11B2 | cytochrome P450 family 11 subfamily B member 2 | |
1586 | CYP17A1 | cytochrome P450 family 17 subfamily A member 1 | |
1588 | CYP19A1 | cytochrome P450 family 19 subfamily A member 1 | |
1589 | CYP21A2 | cytochrome P450 family 21 subfamily A member 2 | |
2271 | FH | fumarate hydratase |
UniProt ID | Protein Name | Source |
---|---|---|
P49748 | Very long-chain specific acyl-CoA dehydrogenase, mitochondrial | |
Q04760 | Lactoylglutathione lyase | |
Q7LGC8 | Carbohydrate sulfotransferase 3 | |
Q7RTW8 | Otoancorin |
HPO ID | HPO Term |
---|---|
HP:0012112 | Abnormal circulating corticosterone level |
HP:0012244 | Abnormal sex determination |
HP:0100607 | Dysmenorrhea |
HP:0000027 | Azoospermia |
HP:0000808 | Penoscrotal hypospadias |
HP:0000848 | Increased circulating renin level |
HP:0001263 | Global developmental delay |
HP:0001944 | Dehydration |
HP:0001998 | Neonatal hypoglycemia |
HP:0002013 | Vomiting |
Gene ID | Gene Symbol | Description |
---|---|---|
1586 | CYP17A1 | cytochrome P450 family 17 subfamily A member 1 |
3284 | HSD3B2 | hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 |
1584 | CYP11B1 | cytochrome P450 family 11 subfamily B member 1 |
1589 | CYP21A2 | cytochrome P450 family 21 subfamily A member 2 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024