Gene Gene information from NCBI Gene database.
Entrez ID 8934
Gene name RAB29, member RAS oncogene family
Gene symbol RAB29
Synonyms (NCBI Gene)
RAB7LRAB7L1
Chromosome 1
Chromosome location 1q32.1
miRNA miRNA information provided by mirtarbase database.
2
miRTarBase ID miRNA Experiments Reference
MIRT741809 hsa-miR-548c-3p HITS-CLIP 23824327
MIRT741810 hsa-miR-711 HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
63
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IEA
GO:0000166 Function Nucleotide binding IEA
GO:0001921 Process Positive regulation of receptor recycling IMP 26021297
GO:0003924 Function GTPase activity IBA
GO:0003924 Function GTPase activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
603949 9789 ENSG00000117280
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O14966
Protein name Ras-related protein Rab-7L1 (Rab-7-like protein 1) (Ras-related protein Rab-29)
Protein function The small GTPases Rab are key regulators in vesicle trafficking (PubMed:24788816). Essential for maintaining the integrity of the endosome-trans-Golgi network structure (By similarity). Together with LRRK2, plays a role in the retrograde traffic
PDB 6HH2 , 8FO2 , 8FO8 , 8FO9
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00071 Ras 9 175 Ras family Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. {ECO:0000269|PubMed:24788816}.
Sequence
Sequence length 203
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    RAB geranylgeranylation
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
RAB29-related disorder Benign rs41302139 RCV003907259
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Atherosclerosis Associate 34167169
Drug Related Side Effects and Adverse Reactions Associate 29177506
Fibrosis Associate 36142381
Heart Failure Associate 34167169
Inflammation Associate 36142381
Neurodegenerative Diseases Associate 37454237
Parkinson Disease Associate 20683486, 25966061, 29177506, 33436766, 33523105, 34040254, 36116551, 37454237, 40053464