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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
PRKCSH beta subunit of glucosidase II
Summary
- Gene Symbol
-
- PRKCSH
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Calcium
- Coiled coil
- Direct protein sequencing
- Disease variant
- Disulfide bond
- Endoplasmic reticulum
- Glycoprotein
- Metal-binding
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Repeat
- Signal
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| N-glycan processing | ||
| liver development | ||
| intracellular signal transduction |
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum lumen | ||
| intracellular membrane-bounded organelle | ||
| endoplasmic reticulum | ||
| glucosidase II complex |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein kinase C binding | ||
| calcium ion binding | ||
| transmembrane transporter binding | ||
| phosphoprotein 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
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:1837 | diabetic ketoacidosis | |
| DOID:0050770 | polycystic liver disease | |
| DOID:0050778 | Meckel syndrome | |
| DOID:0050990 | episodic ataxia type 2 | |
| DOID:0050997 | cerebellar ataxia, mental retardation and dysequlibrium syndrome | |
| DOID:0060178 | familial hemiplegic migraine | |
| DOID:0060262 | gallbladder disease | |
| DOID:0110741 | type 1 diabetes mellitus 2 | |
| DOID:0110742 | type 1 diabetes mellitus 3 | |
| DOID:0110743 | type 1 diabetes mellitus 4 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000107 | Renal cyst |
| HP:0001541 | Ascites |
| HP:0001732 | Abnormality of the pancreas |
| HP:0002020 | Gastroesophageal reflux |
| HP:0002027 | Abdominal pain |
| HP:0002086 | Abnormality of the respiratory system |
| HP:0002093 | Respiratory insufficiency |
| HP:0002094 | Dyspnea |
| HP:0002239 | Gastrointestinal hemorrhage |
| Disease ID | Disease Name |
|---|---|
| ORPHA:2924 |
|
| OMIM:174050 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 174515 | WB:WBGene00014249 | ||
| 35056 | FB:FBgn0032643 | ||
| 394028 | ZFIN:ZDB-GENE-040426-770 | DANRE31792 | |
| 108257446 | ICTPU18832 | ||
| 113588197 | ELEEL41003 | ||
| 106601057 | SALSA22656 | ||
| 106607221 | SALSA34372 | ||
| 115171233 | SALTR92826 | ||
| 115199086 | SALTR25129 | ||
| 115530043 | GADMO40814 |
