01
Abnormal isoelectric focusing of serum transferrin
abnormal isoelectric focusing of serum transferrin
abnormal isoelectric focusing of serum transferrin
- Entity Type
- Targets
- Relation Groups
- 2
- Relation Preview
- 14
Basic Information
Grouped by core information, identifiers, and descriptions.
Core Information
- Gene Symbol
- COG1
- 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
- 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
Clubfoot, Congenital, With Or Without Deficiency Of Long Bones And/Or Mirror-Image Polydactyly
clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly
clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly
03
Congenital Disorder of Glycosylation, Type 2G
congenital disorder of glycosylation, type 2g
congenital disorder of glycosylation, type 2g
04
Congenital Disorder Of Glycosylation, Type Iig
congenital disorder of glycosylation, type iig
congenital disorder of glycosylation, type iig
05
Congenital Disorder of Glycosylation, Type In
congenital disorder of glycosylation, type in
congenital disorder of glycosylation, type in
06
Congenital Disorders of Glycosylation
congenital disorders of glycosylation
congenital disorders of glycosylation
07
08