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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
phosphate cytidylyltransferase 1A, choline
Summary
- Gene Symbol
-
- PCYT1A
- Aliases
-
- CCTalpha
- CT
- CTP:phosphocholine cytidylyltransferase-alpha
- CTPCT
- choline-phosphate cytidylyltransferase alpha
- phosphate cytidylyltransferase 1, choline, alpha isoform
- phosphorylcholine transferase alpha
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Acetylation
- Coiled coil
- Cone-rod dystrophy
- Congenital generalized lipodystrophy
- Cytoplasm
- Diabetes mellitus
- Disease variant
- Dwarfism
- Endoplasmic reticulum
- Membrane
- Nucleotidyltransferase
- Nucleus
- Phospholipid biosynthesis
- Phosphoprotein
- Reference proteome
- Repeat
- Ubl conjugation
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| CDP-choline pathway | ||
| phosphatidylcholine biosynthetic process |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleus | ||
| glycogen granule | ||
| nuclear envelope | ||
| endoplasmic reticulum | ||
| cytosol |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| choline-phosphate cytidylyltransferase activity | ||
| protein homodimerization activity | ||
| molecular function inhibitor activity | ||
| phosphatidylcholine binding | ||
| protein binding |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050959 | spinocerebellar ataxia type 8 | |
| DOID:0060000 | infective endocarditis | |
| DOID:0060041 | autism spectrum disorder | |
| DOID:0060224 | atrial fibrillation | |
| DOID:0060249 | scoliosis | |
| DOID:0060326 | myelomeningocele | |
| DOID:0060597 | atypical chronic myeloid leukemia, BCR-ABL1 negative | |
| DOID:0060688 | arteriovenous malformations of the brain | |
| DOID:0080001 | bone disease | |
| DOID:0080016 | spina bifida |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0004374 | Hemiplegia/hemiparesis |
| HP:0004565 | Severe platyspondyly |
| HP:0005054 | Metaphyseal spurs |
| HP:0005930 | Abnormal epiphysis morphology |
| HP:0006487 | Bowing of the long bones |
| HP:0006817 | Aplasia/Hypoplasia of the cerebellar vermis |
| HP:0007401 | Macular atrophy |
| HP:0007663 | Reduced visual acuity |
| HP:0007688 | Undetectable light- and dark-adapted electroretinogram |
| HP:0007703 | Abnormality of retinal pigmentation |
| Disease ID | Disease Name |
|---|---|
| ORPHA:65 |
|
| ORPHA:85167 |
|
| OMIM:608940 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP001277
- Gene Name
- phosphate cytidylyltransferase 1, choline, alpha
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 108264716 | ICTPU27974 | ||
| 108267677 | ICTPU32341 | ||
| 113570084 | ELEEL09046 | ||
| 113576956 | ELEEL18988 | ||
| 115156767 | SALTR61658 | ||
| 115169928 | SALTR41693 | ||
| 115205839 | SALTR109694 | ||
| 101157809 | ORYLA06823 | ||
| 100691229 | ORENI29119 | ||
| 115572478 | SPAAU38777 |
