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GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
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Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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GALAXY
MCAW
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GRable
Guidelines
MIRAGE
sperm associated antigen 1
Summary
- Gene Symbol
-
- SPAG1
- Aliases
-
- CILD28
- CT140
- DNAAF13
- FLJ32920
- HSD-3.8
- SP75
- TPIS
- dynein axonemal assembly factor 13
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cytoplasm
- Fertilization
- GTP-binding
- Hydrolase
- Kartagener syndrome
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Repeat
- TPR repeat
- Proteins
| UniProt | Protein Name |
|---|---|
| Q07617 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| single fertilization | ||
| protein stabilization | ||
| axonemal dynein complex assembly |
GO Hierarchy
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| GTP binding | ||
| hydrolase activity |
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Sperm-associated antigen 1
- Functional Category
-
- C: Energy production and conversion
- I: Lipid transport and metabolism
- Q: Secondary metabolites biosynthesis, transport and catabolism
| InterPro |
|---|
| RNA-polymerase II-associated protein 3-like, C-terminal domain |
| Tetratricopeptide repeat |
| Tetratricopeptide-like helical domain superfamily |
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:0110607 | primary ciliary dyskinesia 28 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000119 | Abnormality of the genitourinary system |
| HP:0000238 | Hydrocephalus |
| HP:0000365 | Hearing impairment |
| HP:0000389 | Chronic otitis media |
| HP:0000403 | Recurrent otitis media |
| HP:0000405 | Conductive hearing impairment |
| HP:0000510 | Rod-cone dystrophy |
| HP:0000750 | Delayed speech and language development |
| HP:0000924 | Abnormality of the skeletal system |
| Disease ID | Disease Name |
|---|---|
| OMIM:615505 |
|
| ORPHA:244 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
