Table Neurological functions | ||||
---|---|---|---|---|
Disease | Diseases or Functions Annotation | p-value | Molecules | Proteins |
T1DM | Dysmyelination | 3,90E-05 | ARHGEF6↓, CNP↓, NADK2↓, PSAP↑, SLC25A12↓ | 5 |
Leukodystrophy | 2,28E-04 | ARHGEF6↓, CNP↓, NADK2↓, PSAP↑ | 4 | |
Abnormal brain myelination | 1,28E-03 | CNP↓, PSAP↑, SLC25A12↓ | 3 | |
Hereditary myelin disorder | 1,61E-03 | ARHGEF6↓, NADK2↓, PSAP↑ | 3 | |
Hypomyelination of brain | 6,41E-03 | CNP↓, SLC25A12↓ | 2 | |
Alzheimer disease | 6,85E-03 | APOA2↓, APOC1↓, APOC3↓, C1R↓, CNP↓, GLRX↓, GSK3B↓, PON1↓, PSAP↑, SELENBP1↓ | 10 | |
Quantity of Ca2 + | 2,16E-02 | APOC3↓, CD59↑, F2RL3↑, ITPR1↓ | 4 | |
Outgrowth of neurites | 3,60E-02 | GSK3B↓, PSAP↑ | 2 | |
Movement Disorders | 4,67E-02 | AP1S1↓, ARHGEF7↓, CNP↓, CSTB↓, CYTH1↑, GSK3B↓, ITPR1↓, PON1↓, PSAP↑, SEC11A↓, STMN1↓ | 11 | |
MS | Quantity of Ca2 + | 2,01E-02 | CD59↑, CXCR4↑, ORM1↑ | 3 |
Formation of focal adhesions | 2,25E-02 | SLC9A1, STMN1↓ | 2 |