| RAB35 |
| LOCUS ID | 11021 | ||||||||||
| GENE_SYMBOL | RAB35 | ||||||||||
| GENE NAME | RAB35, member RAS o | ||||||||||
| SYNONYMNS | RAY, H-ray, RAB1C | ||||||||||
| CHROMOSOME | 12 | ||||||||||
| HOMOLOGENE ID | 21361 |
| microRNAs | NA | NA |
| GENE SUMMARY |
|---|
| RAB35 (RAB35, Member RAS Oncogene Family) is a Protein Coding gene. Diseases associated with RAB35 include Familial Renal Oncocytoma and Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, And Seizures Syndrome. Among its related pathways are RAB GEFs exchange GTP for GDP on RABs and TBC/RABGAPs. Gene Ontology (GO) annotations related to this gene include GTP binding and GDP binding. An important paralog of this gene is RAB1A. |
| OBSERVATIONS |
|---|
| Complication | Evidence | PMID |
| Neuropathy | 1. We identified four genes differentially expressed between the two study arms post-treatment, but not pre-treatment: GFRA2 (GDNF family receptor alpha-2), C1QBP (complement C1q binding protein), RAB35 (member of RAS oncogene family) and SYNJ1 (synaptic inositol 1,4,5-trisphosphate 5-phosphatase 1). | 30221321 |