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:0000316 | Hypertelorism |
HP:0000337 | Broad forehead |
HP:0000347 | Micrognathia |
HP:0000400 | Macrotia |
HP:0000407 | Sensorineural hearing impairment |
HP:0000452 | Choanal stenosis |
HP:0000453 | Choanal atresia |
HP:0000614 | Abnormal nasolacrimal system morphology |
HP:0000682 | Abnormal dental enamel morphology |
HP:0000885 | Broad ribs |
Disease ID | Disease Name |
---|---|
ORPHA:2658 |
|
OMIM:151050 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
779154 | Xenbase:XB-GENE-6252982 | ||
108719355 | Xenbase:XB-GENE-17346603 | ||
100145636 | Xenbase:XB-GENE-6455449 | ||
101949650 | CHRPI06136 | ||
109320622 | CROPO00391 | ||
113439889 | PSETE11646 | ||
101804047 | ANAPP09534 | ||
100073865 | ORNAN20660 | ||
100413392 | CALJA14154 | ||
105586505 | CERAT23436 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024