EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   3.4.24.59 | Muscle Hypotonia |
27799064 |
MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death. |
unassigned |
0 |
| 3.4.24.59 | Myopia |
21640322 |
Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population. |
causal interaction
unassigned |
3
0 |
| 3.4.24.59 | Myopia |
31300455 |
Association of the ZC3H11B, ZFHX1B and SNTB1 genes with myopia of different severities. |
unassigned |
0 |
| 3.4.24.59 | Myopia |
31604699 |
Genotype-phenotype correlation and interaction of 4q25, 15q14 and MIPEP variants with myopia in southern Chinese population. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
2
1
1
0 |
| 3.4.24.59 | Neurodegenerative Diseases |
10783257 |
Functional and genomic analysis of the human mitochondrial intermediate peptidase, a putative protein partner of frataxin. |
causal interaction
diagnostic usage
unassigned |
2
3
0 |
