Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55647
Gene name Gene Name - the full gene name approved by the HGNC.
RAB20, member RAS oncogene family
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RAB20
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
13
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
13q34
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1282366 hsa-miR-1299 CLIP-seq
MIRT1282367 hsa-miR-3148 CLIP-seq
MIRT1282368 hsa-miR-3166 CLIP-seq
MIRT1282369 hsa-miR-3665 CLIP-seq
MIRT1282370 hsa-miR-4771 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0003924 Function GTPase activity IBA
GO:0003924 Function GTPase activity IEA
GO:0005525 Function GTP binding IEA
GO:0005769 Component Early endosome IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q9NX57
Protein name Ras-related protein Rab-20 (EC 3.6.5.2)
Protein function The small GTPases Rab are key regulators of intracellular membrane trafficking, from the formation of transport vesicles to their fusion with membranes. Rabs cycle between an inactive GDP-bound form and an active GTP-bound form that is able to r
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00071 Ras 7 202 Ras family Domain
Tissue specificity TISSUE SPECIFICITY: Low or absent expression in normal pancreas and stronger expression in 15 of 18 exocrine pancreatic adenocarcinomas (at protein level). {ECO:0000269|PubMed:16613320}.
Sequence
Sequence length 234
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    RAB geranylgeranylation
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Biliary Atresia Biliary atresia N/A N/A GWAS
Hypothyroidism Hypothyroidism N/A N/A GWAS
Oligodendroglioma Oligodendroglioma N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Adenoma Associate 21102417
Aneuploidy Associate 21102417
Carcinoma Hepatocellular Inhibit 34401050
Carotid Stenosis Associate 31589004
HIV Infections Associate 33692804
Leukemia B Cell Associate 32138279
Leukemia Biphenotypic Acute Associate 32138279
Myelodysplastic Syndromes Associate 15147372
Neoplasm Metastasis Associate 34401050
Neoplasms Associate 21102417