Gene Name | deafness, autosomal dominant 5 | |
Image | No pdb structure | |
Gene Ontology Annotations | Cellular Component | |
Molecular Function | ||
Biological Process | ||
Pathways | ||
Drugs | ||
Diseases | ||
GWAS | ||
Protein-protein Interactions | 1 interactors: PTN | |
Entrez ID | 1687 | |
HPRD ID | 02996 | |
Ensembl ID | ENSG00000105928 | |
Uniprot IDs | A4FVA8 O60443 | |
PDB IDs | ||
Enriched GO Terms of Interacting Partners? | ||
Tagcloud ? | abundance
adulthood
cochlea
constant
day
deafness
developing
dramatically
e15
embryonic
highest
imply
mature
morphogenesis
mrna
orthologues
p15
p3
p45
particularly
persisted
points
postnatal
radioactive
rt
tecta
tectorial
throughout
transcribed
|