SH3D19 wt Allele

Preferred Label : SH3D19 wt Allele;

NCIt synonyms : SH3 Domain Containing 19 wt Allele; MGC105136; MGC118913; MGC118910; EBP; MGC118911; SH3P19; DKFZp434D0215; MGC118912; Kryn; EVE1; EEN Binding Protein Gene;

NCIt definition : Human SH3D19 wild-type allele is located in the vicinity of 4q31.3 and is approximately 108 kb in length. This allele, which encodes SH3 domain-containing protein 19, plays a role in both protein-protein interactions and protein localization to the plasma membrane. A translocation involving this gene and the RUNX1 gene may be associated with acute myeloid leukemia.;

GenBank Accession Number : BX647422;

Details

Origin ID

C98006;

UMLS CUI

C3273758;

OMIM relation
- Sh3 domain protein 19 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_plays_role_in_process
- Intracellular Transport [NCIt concept]
- Ligand Binding [NCIt concept]
- Regulated Intramembrane Proteolysis [NCIt concept]
- Subcellular Protein Targeting [NCIt concept]
- Transport Process [NCIt concept]

Keyword's position in hierarchy(ies) :

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