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IQ motif containing N
Summary
- Gene Symbol
-
- IQCN
- Organism
- Homo sapiens (human)
Annotation
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| spermatid development |
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleus | ||
| mitochondrion |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- abnormal spindle-like microcephaly-associated protein
- Functional Category
-
- E: Amino acid transport and metabolism
- G: Carbohydrate transport and metabolism
- T: Signal transduction mechanisms
| InterPro |
|---|
| IQ motif, EF-hand binding site |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0070577 | spermatogenic failure 78 |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 80726 | RGD:7549926 | ||
| 455859 | PANTR17626 | ||
| 637079 | MOUSE60329 | ||
| 100439072 | PONAB15630 | ||
| 100606726 | NOMLE02104 | ||
| 100769749 | CRIGR05655 | ||
| 100963327 | OTOGA06300 | ||
| 100969646 | PANPA19900 | ||
| 101016048 | PAPAN22853 | ||
| 101033982 | SAIBB36269 |
