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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
fukutin related protein
Summary
- Gene Symbol
-
- FKRP
- Aliases
-
- FKTR
- LGMD2I
- MDC1C
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Cardiomyopathy
- Cell membrane
- Congenital muscular dystrophy
- Cytoplasm
- Disease variant
- Disulfide bond
- Dystroglycanopathy
- Endoplasmic reticulum
- Glycoprotein
- Golgi apparatus
- Limb-girdle muscular dystrophy
- Lissencephaly
- Magnesium
- Metal-binding
- Reference proteome
- Secreted
- Signal-anchor
- Transferase
- Transmembrane helix
- Zinc
- Proteins
| UniProt | Protein Name |
|---|---|
| Q9H9S5 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| reproductive process | ||
| muscle contraction | ||
| protein processing |
GO Hierarchy
- oxygen metabolic process
- lipid metabolic process
- oxygen metabolic process
- localization of cell
- reproductive process
biological process
metabolic process [inference]
nitrogen compound metabolic process [inference]
cellular nitrogen compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
cellular nitrogen compound catabolic process [inference]
catabolic process [inference]
cellular metabolic process [inference]
cellular aromatic compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
aromatic compound catabolic process [inference]
phosphorus metabolic process [inference]
phosphate-containing compound metabolic process [inference]
organophosphate metabolic process [inference]
cellular nitrogen compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
cellular nitrogen compound catabolic process [inference]
cellular catabolic process [inference]
heterocycle metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
heterocycle catabolic process [inference]
primary metabolic process [inference]
small molecule metabolic process [inference]
organic substance metabolic process [inference]
organophosphate metabolic process [inference]
organic cyclic compound metabolic process [inference]
organonitrogen compound metabolic process [inference]
organic substance catabolic process [inference]
cellular process [inference]
cellular metabolic process [inference]
cellular aromatic compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
aromatic compound catabolic process [inference]
phosphorus metabolic process [inference]
phosphate-containing compound metabolic process [inference]
organophosphate metabolic process [inference]
cellular nitrogen compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
cellular nitrogen compound catabolic process [inference]
cellular catabolic process [inference]
heterocycle metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
heterocycle catabolic process [inference]
developmental process [inference]
response to stimulus [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| cytosol | ||
| extracellular space | ||
| sarcolemma | ||
| Golgi apparatus | ||
| skeletal muscle myofibril |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| dystroglycan binding | ||
| laminin binding | ||
| metal ion binding | ||
| protein binding | ||
| phosphotransferase activity, for other substituted phosphate groups |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
GlycoGene Database (GGDB)
- GGDB ID
- gg188
- Gene Symbol
-
- FKRP
- Orthologous Gene
| Species | Protein | mRNA |
|---|---|---|
| Rattus norvegicus | NP_001020849 | NM_001025678 |
| Drosophila melanogaster | NP_611531 | NM_137687 |
| Mus musculus | NP_775606 | NM_173430 |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110304 | autosomal dominant limb-girdle muscular dystrophy type 2 | |
| DOID:0110305 | autosomal dominant limb-girdle muscular dystrophy type 1 | |
| DOID:0110306 | autosomal dominant limb-girdle muscular dystrophy type 3 | |
| DOID:0110423 | dilated cardiomyopathy 1C | |
| DOID:0110424 | dilated cardiomyopathy 1CC | |
| DOID:0110425 | dilated cardiomyopathy 1A | |
| DOID:0110426 | dilated cardiomyopathy 1D | |
| DOID:0110427 | dilated cardiomyopathy 1V | |
| DOID:0110428 | dilated cardiomyopathy 1AA | |
| DOID:0110429 | dilated cardiomyopathy 1H |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000028 | Cryptorchidism |
| HP:0000050 | Hypoplastic male external genitalia |
| HP:0000054 | Micropenis |
| HP:0000110 | Renal dysplasia |
| HP:0000158 | Macroglossia |
| HP:0000175 | Cleft palate |
| HP:0000176 | Submucous cleft hard palate |
| HP:0000193 | Bifid uvula |
| HP:0000204 | Cleft upper lip |
| Disease ID | Disease Name |
|---|---|
| ORPHA:370980 |
|
| ORPHA:34515 |
|
| OMIM:606612 |
|
| ORPHA:899 |
|
| ORPHA:370968 |
|
| OMIM:236670 |
|
| ORPHA:370959 |
|
| OMIM:607155 |
|
| OMIM:613153 |
|
| ORPHA:588 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 101150963 | GORGO14904 | ||
| 746394 | PANTR18735 | ||
| 100939505 | PONAB14386 | ||
| 484426 | CANLF00895 | ||
| 123778747 | URSAM31048 | ||
| 101672499 | MUSPF06982 | ||
| 101099604 | FELCA34586 | ||
| 122207710 | PANLE29028 | ||
| 117309102 | TURTR03465 | ||
| 118884528 | BALMU16334 |
