01
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3
multiple congenital anomalies-hypotonia-seizures syndrome 3
multiple congenital anomalies-hypotonia-seizures syndrome 3
- Entity Type
- Targets
- Relation Groups
- 2
- Relation Preview
- 6
Basic Information
Grouped by core information, identifiers, and descriptions.
Core Information
- Gene Symbol
- MIR6812
- Protein Name
- No data
- Gene Type
- No data
- Chromosome
- No data
- Map Location
- No data
Identifiers
- Entrez ID
- No data
- Ensembl ID
- No data
- UniProt ID
- No data
- HGNC ID
- 50116.0
- PDB ID
- No data
Description and Extensions
- Description
- No data
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Related Diseases
target disease2 Diseases
02
Paroxysmal Nocturnal Hemoglobinuria 2
paroxysmal nocturnal hemoglobinuria 2
paroxysmal nocturnal hemoglobinuria 2