|
|
RAB27A |
RAB27A, member RAS oncogene family |
- Insulin processing
- Neutrophil degranulation
- RAB geranylgeranylation
- RAB GEFs exchange GTP for GDP on RABs
- Regulation of MITF-M-dependent genes involved in pigmentation
|
|
- Other phagocyte defects, including the following eight diseases: Chediak-Higashi syndrome; Griscelli syndrome, type 1 (GS1); Griscelli syndrome, type 2 (GS2); Griscelli syndrome, type 3 (GS3); beta-actin deficiency; Neutrophil-specific granule deficiency; Myeloperoxidase deficiency; Glucose 6-phosphate dehydrogenase deficiency; Shwachman syndrome
|
|
|
RAB28 |
RAB28, member RAS oncogene family |
|
|
|
|
|
RAB2B |
RAB2B, member RAS oncogene family |
|
|
|
|
|
RAB35 |
RAB35, member RAS oncogene family |
- TBC/RABGAPs
- RAB geranylgeranylation
- RAB GEFs exchange GTP for GDP on RABs
|
|
|
|
|
RAB38 |
RAB38, member RAS oncogene family |
- RAB geranylgeranylation
- RAB GEFs exchange GTP for GDP on RABs
|
|
|
|
|
RAB39A |
RAB39A, member RAS oncogene family |
- Intra-Golgi traffic
- RAB geranylgeranylation
- RAB GEFs exchange GTP for GDP on RABs
|
|
|
|
|
RAB3A |
RAB3A, member RAS oncogene family |
- Serotonin Neurotransmitter Release Cycle
- Norepinephrine Neurotransmitter Release Cycle
- Glutamate Neurotransmitter Release Cycle
- Dopamine Neurotransmitter Release Cycle
- Acetylcholine Neurotransmitter Release Cycle
- Neutrophil degranulation
- RAB geranylgeranylation
- RAB GEFs exchange GTP for GDP on RABs
- GABA synthesis, release, reuptake and degradation
- Sensory processing of sound by inner hair cells of the cochlea
|
|
|
|
|
RAB3D |
RAB3D, member RAS oncogene family |
- Neutrophil degranulation
- RAB geranylgeranylation
|
|
|
|
|
RAB40B |
RAB40B, member RAS oncogene family |
|
|
|
|
|
RAB43 |
RAB43, member RAS oncogene family |
- Retrograde transport at the Trans-Golgi-Network
- RAB geranylgeranylation
|
|
|
|
|
RAB5C |
RAB5C, member RAS oncogene family |
- Golgi Associated Vesicle Biogenesis
- Neutrophil degranulation
- TBC/RABGAPs
- Clathrin-mediated endocytosis
- RAB geranylgeranylation
- RAB GEFs exchange GTP for GDP on RABs
- Respiratory syncytial virus (RSV) attachment and entry
|
|
|
|
|
RAB7B |
RAB7B, member RAS oncogene family |
- TBC/RABGAPs
- RAB geranylgeranylation
- RAB GEFs exchange GTP for GDP on RABs
|
|
|
|
|
RAB8B |
RAB8B, member RAS oncogene family |
- TBC/RABGAPs
- RAB geranylgeranylation
- RAB GEFs exchange GTP for GDP on RABs
|
- Phosphoaminophosphonic acid guanylate ester
- Guanosine-5'-Diphosphate
|
|
|
|
RABL3 |
RAB, member of RAS oncogene family like 3 |
|
|
|
|
|
RAD51AP1 |
RAD51 associated protein 1 |
- HDR through Homologous Recombination (HRR)
- Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA)
- Resolution of D-loop Structures through Holliday Junction Intermediates
- Homologous DNA Pairing and Strand Exchange
- Defective homologous recombination repair (HRR) due to BRCA1 loss of function
- Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function
- Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function
- Impaired BRCA2 binding to PALB2
|
|
|
|
|
RAD51C |
RAD51 paralog C |
- HDR through Homologous Recombination (HRR)
- Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA)
- Resolution of D-loop Structures through Holliday Junction Intermediates
- Homologous DNA Pairing and Strand Exchange
- Presynaptic phase of homologous DNA pairing and strand exchange
- Meiotic recombination
- Defective homologous recombination repair (HRR) due to BRCA1 loss of function
- Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function
- Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function
- Impaired BRCA2 binding to PALB2
- Factors involved in megakaryocyte development and platelet production
|
|
|
|
|
RAG1 |
recombination activating 1 |
- Interleukin-7 signaling
- MAPK6/MAPK4 signaling
|
|
- Combined immunodeficiencies (CIDs), including the following nine diseases: X-linked hyper IgM syndrome; CD40 deficiency hyper IgM syndrome; Purine nucleoside phosphorylase (PNP) deficiency; Omenn syndrome; MHC deficiency (HLA-class I); MHC deficiency (HLA-class II); Zap-70 deficiency; p56 Lck deficiency; CD8 deficiency
- T-B-Severe combined immunodeficiencies (SCIDs), including the following four diseases: Adenosine deaminase (ADA) deficiency; Recombinase activating gene (RAG) deficiencies; Artemis deficiency; Reticular dysgenesis
|
|
|
RAI2 |
retinoic acid induced 2 |
|
|
|
|
|
RALGPS1 |
Ral GEF with PH domain and SH3 binding motif 1 |
|
|
|
|
|
RAP1B |
RAP1B, member of RAS oncogene family |
- Integrin signaling
- GRB2:SOS provides linkage to MAPK signaling for Integrins
- p130Cas linkage to MAPK signaling for integrins
- Rap1 signalling
- MAP2K and MAPK activation
- Neutrophil degranulation
- Signaling by moderate kinase activity BRAF mutants
- Signaling by high-kinase activity BRAF mutants
- Signaling by BRAF and RAF1 fusions
- Paradoxical activation of RAF signaling by kinase inactive BRAF
- MET activates RAP1 and RAC1
- Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation
- Signaling downstream of RAS mutants
- Signaling by RAF1 mutants
|
|
|