EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
3.1.1.29 | Bacterial Infections |
22509481 |
Crystal structure of peptidyl-tRNA hydrolase from mycobacterium smegmatis reveals novel features related to enzyme dynamics. |
unassigned |
0 |
3.1.1.29 | Carcinoma |
29328466 |
Knockdown of immature colon carcinoma transcript 1 induces suppression of proliferation, S-phase arrest and apoptosis in leukemia cells. |
unassigned |
0 |
3.1.1.29 | Colonic Neoplasms |
31257922 |
High ANKZF1 expression is associated with poor overall survival and recurrence-free survival in colon cancer. |
causal interaction diagnostic usage ongoing research therapeutic application |
4 4 2 1 |
3.1.1.29 | Colorectal Neoplasms |
31257922 |
High ANKZF1 expression is associated with poor overall survival and recurrence-free survival in colon cancer. |
causal interaction diagnostic usage ongoing research therapeutic application |
4 4 2 1 |
3.1.1.29 | Infections |
16849786 |
Peptidyl-tRNA hydrolase and its critical role in protein biosynthesis. |
unassigned |
0 |
3.1.1.29 | Intellectual Disability |
27753167 |
PTRHD1 (C2orf79) mutations lead to autosomal-recessive intellectual disability and parkinsonism. |
causal interaction unassigned |
4 0 |
3.1.1.29 | Intellectual Disability |
29143421 |
PTRHD1 and possibly ADORA1 mutations contribute to Parkinsonism with intellectual disability. |
unassigned |
0 |
3.1.1.29 | Intellectual Disability |
30398675 |
PTRHD1 Loss-of-function mutation in an african family with juvenile-onset Parkinsonism and intellectual disability. |
causal interaction unassigned |
1 0 |
3.1.1.29 | Intellectual Disability |
33004232 |
Lack of PTRHD1 mutation in patients with young-onset and familial Parkinson's disease in a Taiwanese population. |
causal interaction unassigned |
3 0 |
3.1.1.29 | Lyme Disease |
8635758 |
Microbial genes homologous to the peptidyl-tRNA hydrolase-encoding gene of Escherichia coli. |
unassigned |
0 |