Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
285282
Gene name Gene Name - the full gene name approved by the HGNC.
RAB, member of RAS oncogene family like 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RABL3
Synonyms (NCBI Gene) Gene synonyms aliases
PNCA5
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3q13.33
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs200612497 G>T Risk-factor Coding sequence variant, non coding transcript variant, stop gained
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT029456 hsa-miR-26b-5p Microarray 19088304
MIRT612626 hsa-miR-362-3p HITS-CLIP 19536157
MIRT612625 hsa-miR-329-3p HITS-CLIP 19536157
MIRT612624 hsa-miR-8485 HITS-CLIP 19536157
MIRT612623 hsa-miR-6729-3p HITS-CLIP 19536157
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:0001779 Process Natural killer cell differentiation IEA
GO:0001779 Process Natural killer cell differentiation ISS
GO:0003924 Function GTPase activity IBA
GO:0005515 Function Protein binding IPI 31406347
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
618542 18072 ENSG00000144840
Protein
UniProt ID Q5HYI8
Protein name Rab-like protein 3
Protein function Required for KRAS signaling regulation and modulation of cell proliferation (PubMed:31406347). Regulator of KRAS prenylation, and probably prenylation of other small GTPases (PubMed:31406347). Required for lymphocyte development and function (By
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF08477 Roc 8 132 Domain
Sequence
MASLDRVKVLVLGDSGVGKSSLVHLLCQNQVLGNPSWTVGCSVDVRVHDYKEGTPEEKTY
YIELWDVGGSVGSASSVKSTRAVFYNSVNGIIFVHDLTNKKSSQNLRRWSLEALNRDLVP
TGVLVTNGDYDQ
EQFADNQIPLLVIGTKLDQIHETKRHEVLTRTAFLAEDFNPEEINLDC
TNPRYLAAGSSNAVKLSRFFDKVIEKRYFLREGNQIPGFPDRKRFGAGTLKSLHYD
Sequence length 236
Interactions View interactions
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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
Pancreatic cancer Pancreatic cancer, susceptibility to, 5, pancreatic cancer, susceptibility to, 5 N/A N/A ClinVar, GenCC
Pancreatic Carcinoma familial pancreatic carcinoma N/A N/A GenCC
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Hepatocellular Stimulate 28443498
Carcinoma Non Small Cell Lung Associate 27164297
Lung Neoplasms Stimulate 27164297
Lymphatic Metastasis Stimulate 28443498
Mouth Neoplasms Associate 31748878
Neoplasms Associate 28443498
Neoplasms Stimulate 31748878
Pancreatic Neoplasms Stimulate 33724601
Squamous Cell Carcinoma of Head and Neck Associate 31748878
Thrombosis Stimulate 28443498