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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
phosphatidylinositol glycan anchor biosynthesis class P
Summary
- Gene Symbol
-
- PIGP
- Aliases
-
- DCRC
- DSRC
- phosphatidylinositol-n-acetylglucosaminyltranferase subunit P
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Direct protein sequencing
- Disease variant
- Epilepsy
- GPI-anchor biosynthesis
- Reference proteome
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| P57054 |
|
Gene Ontology (GO)
GO Hierarchy
biological process
metabolic process [inference]
cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum | ||
| endoplasmic reticulum membrane | ||
| glycosylphosphatidylinositol-N-acetylglucosaminyltransferase (GPI-GnT) complex |
| GO Term | Evidence Code | PMID |
|---|---|---|
| phosphatidylinositol N-acetylglucosaminyltransferase activity | ||
| protein binding |
GO Hierarchy
GlycoGene Database (GGDB)
- GGDB ID
- gg217
- Gene Symbol
-
- PIGP
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110096 | short-rib thoracic dysplasia 14 with polydactyly | |
| DOID:0110213 | isolated cleft palate | |
| DOID:10283 | prostate cancer | |
| DOID:10286 | prostate carcinoma | |
| DOID:1059 | intellectual disability | |
| DOID:10907 | microcephaly | |
| DOID:11832 | visual epilepsy | |
| DOID:13515 | tuberous sclerosis | |
| DOID:14250 | Down syndrome | |
| DOID:14323 | Marfan syndrome |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001537 | Umbilical hernia |
| HP:0001629 | Ventricular septal defect |
| HP:0002069 | Bilateral tonic-clonic seizure |
| HP:0002079 | Hypoplasia of the corpus callosum |
| HP:0002121 | Generalized non-motor (absence) seizure |
| HP:0002131 | Episodic ataxia |
| HP:0002169 | Clonus |
| HP:0002187 | Intellectual disability, profound |
| HP:0002353 | EEG abnormality |
| HP:0002360 | Sleep abnormality |
| Disease ID | Disease Name |
|---|---|
| ORPHA:1934 |
|
| OMIM:617599 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP000186
- Gene Name
- phosphatidylinositol glycan anchor biosynthesis, class P
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 100394113 | CALJA22508 | ||
| 105575425 | CERAT16355 | ||
| 105472655 | MACNE05375 | ||
| 101010550 | PAPAN28562 | ||
| 101138365 | GORGO23081 | ||
| 100978727 | PANPA23032 | ||
| 473990 | PANTR25661 | ||
| 100174471 | PONAB21467 | ||
| 478413 | CANLF12867 | ||
| 112911376 | VULVU37639 |
