Jump to:
loading...| Preferred Name |
Imprinting Gene |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C54401 |
| code |
C54401 |
| DEFINITION |
A gene that does not exhibit equal expression of both alleles due to repression or inactivation, resulting in the genetic non-equivalence of mammalian paternal and maternal genomes. |
| DesignNote |
Several severe human genetic disorders are associated with imprinted genes such as Beckwith-Wiedemann, Prader-Willi and Angelman syndromes. |
| FULL_SYN |
Imprinting Gene Imprinted Gene |
| label |
Imprinting Gene |
| Legacy Concept Name |
Imprinting_Gene |
| Preferred_Name |
Imprinting Gene |
| prefixIRI |
Thesaurus:C54401 |
| prefLabel |
Imprinting Gene |
| Semantic_Type |
Gene or Genome |
| UMLS_CUI |
C1708477 |
| subClassOf |
Create New Mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| There are currently no mappings for this class. | |||