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GlyTouCan
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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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GALAXY
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Guidelines
MIRAGE
assembly factor for spindle microtubules
Summary
- Gene Symbol
-
- ASPM
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Calmodulin-binding
- Coiled coil
- Cytoplasm
- Cytoskeleton
- Disease variant
- Intellectual disability
- Mitosis
- Nucleus
- Phosphoprotein
- Primary microcephaly
- Proteomics identification
- Reference proteome
- Repeat
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| oogenesis | ||
| developmental growth | ||
| regulation of meiotic cell cycle | ||
| spindle localization | ||
| maintenance of centrosome location |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| microtubule minus-end | ||
| meiotic spindle | ||
| mitotic spindle pole |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| calmodulin binding |
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Abnormal spindle-like microcephaly-associated protein -like protein
- Functional Category
-
- G: Carbohydrate transport and metabolism
- K: Transcription
- O: Posttranslational modification, protein turnover, chaperones
| Gene Ontology |
|---|
| calmodulin binding |
| establishment of meiotic spindle localization |
| InterPro |
|---|
| CH domain superfamily |
| Calponin homology domain |
| IQ motif, EF-hand binding site |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0070280 | primary autosomal recessive microcephaly 5 | |
| DOID:0070296 | primary autosomal recessive microcephaly |
