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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:5419 | schizophrenia | |
| DOID:5672 | large intestine cancer | |
| DOID:5842 | testis seminoma | |
| DOID:5844 | myocardial infarction | |
| DOID:5854 | silent myocardial infarction | |
| DOID:591 | phobic disorder | |
| DOID:631 | fibromyalgia | |
| DOID:65 | connective tissue disease | |
| DOID:6713 | cerebrovascular disease | |
| DOID:684 | hepatocellular carcinoma |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0012153 | Hypotriglyceridemia |
| HP:0012795 | Abnormal optic disc morphology |
| 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 |
|---|---|---|---|
| 113483310 | ATHCN11435 | ||
| 105808100 | PROCO00885 | ||
| 853116 | SGD:S000003434 | ||
| 109065111 | CYPCA69525 | ||
| 109101880 | CYPCA40526 | ||
| 103738517 | NANGA17719 | ||
| 116448767 | CORMO00556 | ||
| 115612331 | STRHB11759 |
