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:1443 | cerebral degeneration | |
DOID:14524 | senile degeneration of brain | |
DOID:14525 | Reye syndrome | |
DOID:1573 | communicating hydrocephalus | |
DOID:1712 | aortic valve stenosis | |
DOID:1756 | facial nerve disease | |
DOID:1924 | hypogonadism | |
DOID:2732 | Rothmund-Thomson syndrome | |
DOID:3144 | cutis laxa | |
DOID:3891 | placental insufficiency |
HPO ID | HPO Term |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000023 | Inguinal hernia |
HP:0000028 | Cryptorchidism |
HP:0000036 | Abnormal penis morphology |
HP:0000039 | Epispadias |
HP:0000041 | Chordee |
HP:0000047 | Hypospadias |
HP:0000135 | Hypogonadism |
HP:0000154 | Wide mouth |
HP:0000164 | Abnormality of the dentition |
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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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024