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MIRAGE
zinc finger CCCH-type containing 14
Summary
- Gene Symbol
-
- ZC3H14
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Acetylation
- Alternative splicing
- Cytoplasm
- Disease variant
- Intellectual disability
- Isopeptide bond
- Nucleus
- Phosphoprotein
- Proteomics identification
- RNA-binding
- Reference proteome
- Repeat
- Spermatogenesis
- Ubl conjugation
- Zinc-finger
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| spermatogenesis | ||
| regulation of mRNA stability | ||
| mRNA stabilization | ||
| spliceosome-depend formation of circular RNA |
GO Hierarchy
biological process
metabolic process [inference]
cellular process [inference]
biological regulation [inference]
regulation of biological process [inference]
regulation of metabolic process [inference]
regulation of biosynthetic process [inference]
negative regulation of metabolic process [inference]
regulation of cellular metabolic process [inference]
regulation of nitrogen compound metabolic process [inference]
regulation of macromolecule metabolic process [inference]
positive regulation of biological process [inference]
negative regulation of biological process [inference]
regulation of cellular process [inference]
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| RNA binding | ||
| mRNA 3'-UTR binding | ||
| protein binding | ||
| poly(A) binding | ||
| poly(A) binding |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Zinc finger CCCH domain-containing protein 14
- Functional Category
-
- M: Cell wall/membrane/envelope biogenesis
- Q: Secondary metabolites biosynthesis, transport and catabolism
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| metal ion binding |
| negative regulation of mRNA polyadenylation |
| poly(A) binding |
| regulation of mRNA stability |
| InterPro |
|---|
| Nuclear polyadenylated RNA-binding protein Nab2/ZC3H14 |
| Zinc finger, CCCH-type |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0081217 | autosomal recessive intellectual developmental disorder 56 |
