01
Abnormality Of The Cerebral White Matter
abnormality of the cerebral white matter
abnormality of the cerebral white matter
- Entity Type
- Targets
- Relation Groups
- 5
- Relation Preview
- 29
Basic Information
Grouped by core information, identifiers, and descriptions.
Core Information
- Gene Symbol
- CTNS
- Protein Name
- cystinosin, lysosomal cystine transporter
- Gene Type
- protein-coding
- Chromosome
- 17
- Map Location
- 17p13.2
Identifiers
- Entrez ID
- 1497
- Ensembl ID
- ENSG00000040531
- 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
Abnormality of vitamin D metabolism
abnormality of vitamin d metabolism
abnormality of vitamin d metabolism
04
05
06
07
Autosomal dominant hypophosphatemic rickets
autosomal dominant hypophosphatemic rickets
autosomal dominant hypophosphatemic rickets
08