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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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GALAXY
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GRable
Guidelines
MIRAGE
grainyhead like transcription factor 2
Summary
- Gene Symbol
-
- GRHL2
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Activator
- Alternative splicing
- Corneal dystrophy
- DNA-binding
- Disease variant
- Dwarfism
- Ectodermal dysplasia
- Membrane
- Non-syndromic deafness
- Nucleus
- Reference proteome
- Transcription regulation
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| bicellular tight junction assembly | ||
| cell junction assembly | ||
| multicellular organism growth | ||
| anterior neural tube closure | ||
| face development |
GO Hierarchy
biological process
developmental process [inference]
biological regulation [inference]
regulation of biological process [inference]
regulation of metabolic process [inference]
regulation of biosynthetic process [inference]
positive regulation of metabolic process [inference]
regulation of cellular metabolic process [inference]
regulation of nitrogen compound metabolic process [inference]
regulation of macromolecule metabolic process [inference]
regulation of primary metabolic process [inference]
positive regulation of biological process [inference]
regulation of cellular process [inference]
regulation of cellular metabolic process [inference]
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| DNA-binding transcription factor binding | ||
| RNA polymerase II cis-regulatory region sequence-specific DNA binding | ||
| protein binding | ||
| intronic transcription regulatory region sequence-specific DNA binding | ||
| DNA-binding transcription activator activity |
GO Hierarchy
molecular function
binding [inference]
organic cyclic compound binding [inference]
nucleic acid binding [inference]
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050564 | autosomal dominant nonsyndromic deafness | |
| DOID:0080669 | posterior polymorphous corneal dystrophy 4 | |
| DOID:0110557 | autosomal dominant nonsyndromic deafness 28 |
