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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Repository for lectin-assisted multimodality data
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Guidelines
MIRAGE
actin gamma 1
Summary
- Gene Symbol
-
- ACTG1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- ATP-binding
- Acetylation
- Cytoskeleton
- Direct protein sequencing
- Disease variant
- Hydrolase
- Intellectual disability
- Isopeptide bond
- Methylation
- Non-syndromic deafness
- Oxidation
- Proteomics identification
- Reference proteome
- Proteins
| UniProt | Protein Name |
|---|---|
| P63261 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| angiogenesis |
|
|
| morphogenesis of a polarized epithelium |
|
|
| cytoskeleton organization |
|
|
| axonogenesis |
|
|
| positive regulation of gene expression |
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular region |
|
|
| obsolete extracellular space |
|
|
| nucleus |
|
|
| cytoplasm |
|
|
| cytosol |
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| structural constituent of cytoskeleton |
|
|
| structural constituent of cytoskeleton |
|
|
| protein binding |
|
|
| profilin binding |
|
|
| ATP binding |
|
|
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Actin
- Functional Category
-
- J: Translation, ribosomal structure and biogenesis
- O: Posttranslational modification, protein turnover, chaperones
- T: Signal transduction mechanisms
| InterPro |
|---|
| ATPase, nucleotide binding domain |
| Actin family |
| Actin/actin-like conserved site |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0081113 | Baraitser-Winter syndrome 2 | |
| DOID:0110550 | autosomal dominant nonsyndromic deafness 20 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000072 | Hydroureter |
| HP:0000126 | Hydronephrosis |
| HP:0000154 | Wide mouth |
| HP:0000202 | Orofacial cleft |
| HP:0000219 | Thin upper lip vermilion |
| HP:0000233 | Thin vermilion border |
| HP:0000239 | Large fontanelles |
| HP:0000243 | Trigonocephaly |
| HP:0000252 | Microcephaly |
| Disease ID | Disease Name |
|---|---|
| OMIM:604717 |
|
| ORPHA:2995 |
|
| OMIM:614583 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
