IMP
Process View
Homo sapiens
8 genes annotated in human
leukodystrophy
DOID:10579
A cerebral degeneration characterized by dysfunction of the white matter of the brain.
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In addition to gene-name show these genes:
Click on a gene's description to view its network relationships with genes known to be involved in "leukodystrophy"
| Name | Description | Probability | Func Analog Organism | |
|---|---|---|---|---|
| PEX14 | peroxisomal biogenesis factor 14 | 0.399 | ||
| CTSD | cathepsin D | 0.299 | ||
| PEX12 | peroxisomal biogenesis factor 12 | 0.200 | ||
| GRN | granulin | 0.182 | ||
| PLD3 | phospholipase D family, member 3 | 0.151 | ||
| PEX19 | peroxisomal biogenesis factor 19 | 0.116 | ||
| CTSA | cathepsin A | 0.105 | ||
| TPP1 | tripeptidyl peptidase I | 0.059 | ||
| OS9 | osteosarcoma amplified 9, endoplasmic reticulum lectin | 0.046 | ||
| GNS | glucosamine (N-acetyl)-6-sulfatase | 0.025 | ||
| GAA | glucosidase, alpha; acid | 0.025 | ||
| NUDT3 | nudix (nucleoside diphosphate linked moiety X)-type motif 3 | 0.021 | ||
| ATP6AP1 | ATPase, H+ transporting, lysosomal accessory protein 1 | 0.018 | ||
| NPC2 | Niemann-Pick disease, type C2 | 0.018 | ||
| APLP2 | amyloid beta (A4) precursor-like protein 2 | 0.015 | ||
| MAN2B1 | mannosidase, alpha, class 2B, member 1 | 0.013 | ||
| CTSB | cathepsin B | 0.013 | ||
| LAMP1 | lysosomal-associated membrane protein 1 | 0.011 | ||
| ZBED1 | zinc finger, BED-type containing 1 | 0.011 | ||
| HLA-A | major histocompatibility complex, class I, A | 0.010 | ||
| HEXB | hexosaminidase B (beta polypeptide) | 0.010 | ||
| FTL | ferritin, light polypeptide | 0.010 | ||
| ARSA | arylsulfatase A | 0.002 | ||
| PLP1 | proteolipid protein 1 | 0.002 | ||
| ASPA | aspartoacylase | 0.002 | ||
| PSAP | prosaposin | 0.002 | ||
| GALC | galactosylceramidase | 0.001 | ||
| PEX5 | peroxisomal biogenesis factor 5 | 0.001 | ||
| GFAP | glial fibrillary acidic protein | 0.001 | ||
| ABCD1 | ATP-binding cassette, sub-family D (ALD), member 1 | 0.001 |