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Repository for lectin-assisted multimodality data
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MIRAGE
heterogeneous nuclear ribonucleoprotein H2
Summary
- Gene Symbol
-
- HNRNPH2
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Direct protein sequencing
- Disease variant
- Intellectual disability
- Isopeptide bond
- Methylation
- Nucleus
- Phosphoprotein
- Proteomics identification
- RNA-binding
- Reference proteome
- Repeat
- Ribonucleoprotein
- Ubl conjugation
- Proteins
| UniProt | Protein Name |
|---|---|
| A0A384MDT2 |
|
| P55795 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| regulation of RNA splicing |
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| cytosol |
|
|
| membrane |
|
|
| ribonucleoprotein complex |
|
|
| ribonucleoprotein complex |
|
|
| ribonucleoprotein complex |
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleic acid binding |
|
|
| RNA binding |
|
|
| RNA binding |
|
|
| RNA binding |
|
|
| RNA binding |
|
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0070538 | syndromic X-linked intellectual developmental disorder bain type |
Ortholog
| Species | Gene ID | Alliance of Genome Resources |
|---|---|---|
| 56258 | MGI:1201779 |
