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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
enolase superfamily member 1
Summary
- Gene Symbol
-
- ENOSF1
- Aliases
-
- FUCD
- HSRTSBETA
- L-fuconate dehydratase
- TYMSAS
- rTS
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Dyskeratosis congenita
- Isomerase
- Lyase
- Magnesium
- Metal-binding
- Mitochondrion
- Phosphoprotein
- Reference proteome
- Ubl conjugation
- Proteins
| UniProt | Protein Name |
|---|---|
| Q7L5Y1 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| amino acid catabolic process | ||
| carbohydrate catabolic process |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| cellular_component | ||
| mitochondrion |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| magnesium ion binding | ||
| L-fuconate dehydratase activity | ||
| hydro-lyase activity | ||
| isomerase activity |
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:0070138 | autosomal recessive cutis laxa type IIIB | |
| DOID:0070140 | autosomal recessive cutis laxa type IIC | |
| DOID:0070141 | autosomal recessive cutis laxa type II classic type | |
| DOID:0070142 | autosomal dominant cutis laxa | |
| DOID:0080199 | colorectal carcinoma | |
| DOID:0080302 | mixed sleep apnea | |
| DOID:0090024 | split hand-foot malformation 1 with sensorineural hearing loss | |
| DOID:10534 | stomach cancer | |
| DOID:1059 | intellectual disability | |
| DOID:11260 | rabies |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 116831985 | CHEAB15697 | ||
| 115061206 | ECHNA38741 | ||
| 105816639 | PROCO08029 |
