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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
fukutin
Summary
- Gene Symbol
-
- FKTN
- Aliases
-
- LGMD2M
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Cardiomyopathy
- Congenital muscular dystrophy
- Cytoplasm
- Disease variant
- Dystroglycanopathy
- Glycoprotein
- Golgi apparatus
- Limb-girdle muscular dystrophy
- Lissencephaly
- Nucleus
- Reference proteome
- Signal-anchor
- Transferase
- Transmembrane helix
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein glycosylation | ||
| negative regulation of JNK cascade | ||
| protein O-linked mannosylation |
GO Hierarchy
biological process
metabolic process [inference]
biological regulation [inference]
regulation of biological process [inference]
regulation of metabolic process [inference]
regulation of signaling [inference]
negative regulation of biological process [inference]
regulation of response to stimulus [inference]
regulation of cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleus | ||
| endoplasmic reticulum | ||
| cis-Golgi network | ||
| extracellular space |
|
|
| Golgi apparatus |
GO Hierarchy
GlycoGene Database (GGDB)
- GGDB ID
- gg187
- Gene Symbol
-
- FKTN
- Orthologous Gene
| Species | Protein | mRNA |
|---|---|---|
| Rattus norvegicus | XP_342839 | XM_342838 |
| Caenorhabditis elegans | NP_497236 | NM_064835 |
| Mus musculus | NP_647470 | NM_139309 |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060771 | obsolete dextro-looped transposition of the great arteries 1 | |
| DOID:0060772 | multiple types of congenital heart defects 6 | |
| DOID:0060807 | syndromic X-linked intellectual disability Najm type | |
| DOID:0060823 | syndromic X-linked intellectual disability 94 | |
| DOID:0060857 | septooptic dysplasia | |
| DOID:0070247 | autosomal dominant Emery-Dreifuss muscular dystrophy 2 | |
| DOID:0080033 | craniometaphyseal dysplasia | |
| DOID:0080092 | myofibrillar myopathy 1 | |
| DOID:0080094 | myofibrillar myopathy 3 | |
| DOID:0080102 | congenital myopathy 4A |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002355 | Difficulty walking |
| HP:0002359 | Frequent falls |
| HP:0002365 | Hypoplasia of the brainstem |
| HP:0002435 | Meningocele |
| HP:0002438 | Cerebellar malformation |
| HP:0002500 | Abnormal cerebral white matter morphology |
| HP:0002536 | Abnormal cortical gyration |
| HP:0002650 | Scoliosis |
| HP:0002751 | Kyphoscoliosis |
| HP:0002803 | Congenital contracture |
| Disease ID | Disease Name |
|---|---|
| ORPHA:370980 |
|
| ORPHA:154 |
|
| ORPHA:899 |
|
| OMIM:613152 |
|
| ORPHA:272 |
|
| OMIM:236670 |
|
| OMIM:253800 |
|
| OMIM:611588 |
|
| ORPHA:588 |
|
| OMIM:611615 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 173469 | WB:WBGene00020307 | ||
| 188207 | WB:WBGene00011554 | ||
| 189104 | WB:WBGene00020924 | ||
| 189107 | WB:WBGene00020927 | ||
| 189504 | WB:WBGene00021249 | ||
| 100006345 | ZFIN:ZDB-GENE-070410-96 | DANRE35456 | |
| 108259698 | ICTPU23339 | ||
| 113582820 | ELEEL30070 | ||
| 115160178 | SALTR70125 | ||
| 115531894 | GADMO24802 |
