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:0110047 | Alzheimer's disease 14 | |
DOID:0110048 | Alzheimer's disease 15 | |
DOID:0110938 | autosomal dominant osteopetrosis 2 | |
DOID:0110946 | autosomal recessive osteopetrosis 7 | |
DOID:0111343 | lateral meningocele syndrome | |
DOID:0111507 | Lenz-Majewski hyperostotic dwarfism | |
DOID:10003 | sensorineural hearing loss | |
DOID:1059 | intellectual disability | |
DOID:10652 | Alzheimer's disease | |
DOID:10892 | hypospadias |
HPO ID | HPO Term |
---|---|
HP:0001249 | Intellectual disability |
HP:0001252 | Hypotonia |
HP:0001263 | Global developmental delay |
HP:0001274 | Agenesis of corpus callosum |
HP:0001290 | Generalized hypotonia |
HP:0001328 | Specific learning disability |
HP:0001331 | Absent septum pellucidum |
HP:0001376 | Limitation of joint mobility |
HP:0001382 | Joint hypermobility |
HP:0001508 | Failure to thrive |
Disease ID | Disease Name |
---|---|
ORPHA:2658 |
|
OMIM:151050 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
509819 | BOVIN06164 | ||
102169493 | CAPHI04519 | ||
105982835 | DIPOR02709 | ||
19210 | MGI:1276575 | MOUSE09993 | |
314553 | RGD:1308949 | RATNO37992 | |
101581731 | OCTDE19618 | ||
101708774 | HETGA08289 | ||
102445899 | PELSI09937 | ||
100564978 | ANOCA05410 | ||
103661485 | URSMA06522 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024