01
Congenital Amaurosis of Retinal Origin
congenital amaurosis of retinal origin
congenital amaurosis of retinal origin
- Entity Type
- Targets
- Relation Groups
- 4
- Relation Preview
- 25
Basic Information
Grouped by core information, identifiers, and descriptions.
Core Information
- Gene Symbol
- CLTB
- Protein Name
- clathrin light chain B
- Gene Type
- protein-coding
- Chromosome
- 5
- Map Location
- 5q35.2
Identifiers
- Entrez ID
- 1212
- Ensembl ID
- ENSG00000175416
- UniProt ID
- No data
- HGNC ID
- No data
- 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 disease8 Diseases
02
03
04
05
06
07
08