Gene Details



VPS35 and homologs in 1 species are found in 59 GeneSets:


- Entrez   - Ensembl   - GeneNetwork   - STRING   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 6743 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human GO 32 Genes GS200607: GO:0042147 retrograde transport, endosome to Golgi
Expand Tier I Human 7 Genes GS173729: HP:0002322 Resting tremor
Expand Tier I Human GO 1745 Genes GS210579: GO:0051649 establishment of localization in cell
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 1692 Genes GS203755: GO:0016265 death
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human GO 1965 Genes GS210586: GO:0051641 cellular localization
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier III Human 3028 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human GO 1690 Genes GS194905: GO:0008219 cell death
Expand Tier I Human GO 2364 Genes GS207365: GO:0005829 cytosol
Expand Tier I Human GO 140 Genes GS195505: GO:0016197 endosomal transport
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 4134 Genes GS200341: GO:0051179 localization
Expand Tier I Human GO 1123 Genes GS196794: GO:0046907 intracellular transport
Expand Tier I Human CTD 1151 Genes GS121437: Fluorouracil interacting genes (MeSH:D005472) in CTD
Expand Tier I Human GO 3364 Genes GS194459: GO:0051234 establishment of localization
Expand Tier I Human CTD 2787 Genes GS123332: 7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide interacting genes (MeSH:D015123) in CTD
Expand Tier I Human 38 Genes GS173459: HP:0001300 Parkinsonism
Expand Tier I Human 122 Genes GS173242: HP:0001337 Tremor
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier III Human 2273 Genes GS137413: Supplementary Table 2. CNA Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 19 Genes GS176120: HP:0002374 Diminished movement
Expand Tier I Human 12 Genes GS176911: HP:0002172 Postural instability
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 1555 Genes GS201869: GO:0008104 protein localization
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 73 Genes GS175408: HP:0002071 Abnormality of extrapyramidal motor function
Expand Tier I Human CTD 238 Genes GS121381: fumonisin B1 interacting genes (MeSH:C056933) in CTD
Expand Tier I Human CTD 768 Genes GS123769: 2-(1'H-indolo-3'-carbonyl)thiazole-4-carboxylic acid methyl ester interacting genes (MeSH:C548651) in CTD
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 938 Genes GS194065: GO:0016192 vesicle-mediated transport
Expand Tier I Human GO 1820 Genes GS205820: GO:0033036 macromolecule localization
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human GO 559 Genes GS208092: GO:0005768 endosome
Expand Tier I Human 27 Genes GS176808: HP:0002067 Bradykinesia
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human GO 1228 Genes GS199113: GO:0015031 protein transport
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human CTD 5081 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human GO 1266 Genes GS197769: GO:0045184 establishment of protein localization
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 1925 Genes GS201025: GO:0071702 organic substance transport
Expand Tier I Human 40 Genes GS175194: HP:0002063 Rigidity
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 10 Genes GS176235: HP:0002304 Akinesia
Expand Tier I Human GO 3310 Genes GS209452: GO:0006810 transport
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance