UniProt | Protein Name |
---|---|
P48651 |
|
GO Term | Evidence Code | PMID |
---|---|---|
phosphatidylserine biosynthetic process |
GO Term | Evidence Code | PMID |
---|---|---|
L-serine-phosphatidylethanolamine phosphatidyltransferase activity | ||
transferase activity |
|
|
L-serine-phosphatidylcholine phosphatidyltransferase activity |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050429 | Hailey-Hailey disease | |
DOID:0060249 | scoliosis | |
DOID:0060320 | inguinal hernia | |
DOID:0060467 | humeroradial synostosis | |
DOID:0060762 | restrictive dermopathy | |
DOID:0060862 | mal de Meleda | |
DOID:0070129 | autosomal recessive cutis laxa type IID | |
DOID:0070130 | autosomal dominant cutis laxa 1 | |
DOID:0070131 | autosomal dominant cutis laxa 3 | |
DOID:0070132 | autosomal recessive cutis laxa type IIIA |
HPO ID | HPO Term |
---|---|
HP:0001511 | Intrauterine growth retardation |
HP:0001545 | Anteriorly placed anus |
HP:0001582 | Redundant skin |
HP:0001804 | Hypoplastic fingernail |
HP:0001812 | Hyperconvex fingernails |
HP:0002007 | Frontal bossing |
HP:0002119 | Ventriculomegaly |
HP:0002120 | Cerebral cortical atrophy |
HP:0002342 | Intellectual disability, moderate |
HP:0002650 | Scoliosis |
Disease ID | Disease Name |
---|---|
ORPHA:2658 |
|
OMIM:151050 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
112931317 | VULVU02806 | ||
123797862 | URSAM04144 | ||
100468000 | AILME11006 | ||
101679721 | MUSPF06489 | ||
101091087 | FELCA37821 | ||
122210485 | PANLE18534 | ||
118883673 | BALMU01449 | ||
100670511 | LOXAF16431 | ||
100059691 | HORSE42402 | ||
100156809 | PIGXX23115 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024