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:0008065 | Aplasia/Hypoplasia of the skin |
HP:0008070 | Sparse hair |
HP:0009773 | Symphalangism affecting the phalanges of the hand |
HP:0009843 | Aplasia/Hypoplasia of the middle phalanges of the hand |
HP:0010554 | Cutaneous finger syndactyly |
HP:0010627 | Anterior pituitary hypoplasia |
HP:0010628 | Facial palsy |
HP:0011001 | Increased bone mineral density |
HP:0011002 | Osteopetrosis |
HP:0011220 | Prominent forehead |
Disease ID | Disease Name |
---|---|
ORPHA:2658 |
|
OMIM:151050 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
109111002 | CYPCA76638 | ||
109111680 | CYPCA108823 | ||
103745843 | NANGA09110 | ||
116453888 | CORMO09228 | ||
103258557 | CARSF13033 | ||
115605249 | STRHB14415 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024