Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
57139
Gene name Gene Name - the full gene name approved by the HGNC.
Ral guanine nucleotide dissociation stimulator like 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RGL3
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19p13.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT2089933 hsa-miR-1226 CLIP-seq
MIRT2089934 hsa-miR-3670 CLIP-seq
MIRT2089935 hsa-miR-4691-3p CLIP-seq
MIRT2314769 hsa-miR-128 CLIP-seq
MIRT2314770 hsa-miR-1343 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005085 Function Guanyl-nucleotide exchange factor activity IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0007264 Process Small GTPase mediated signal transduction IEA
GO:0031267 Function Small GTPase binding IEA
GO:0043547 Process Positive regulation of GTPase activity IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616743 30282 ENSG00000205517
Protein
UniProt ID Q3MIN7
Protein name Ral guanine nucleotide dissociation stimulator-like 3 (RalGDS-like 3)
Protein function Guanine nucleotide exchange factor (GEF) for Ral-A. Potential effector of GTPase HRas and Ras-related protein M-Ras. Negatively regulates Elk-1-dependent gene induction downstream of HRas and MEKK1 (By similarity).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00618 RasGEF_N 68 174 RasGEF N-terminal motif Domain
PF00617 RasGEF 250 453 RasGEF domain Family
PF00788 RA 613 700 Ras association (RalGDS/AF-6) domain Domain
Sequence
MERTAGKELALAPLQDWGEETEDGAVYSVSLRRQRSQRRSPAEGPGGSQAPSPIANTFLH
YRTSKVRVLRAARLERLVGELVFGDREQDPSFMPAFLATYRTFVPTACLLGFLLPPMPPP
PPPGVEIKKTAVQDLSFNKNLRAVVSVLGSWLQDHPQDFRDPPAHSDLGSVRTF
LGWAAP
GSAEAQKAEKLLEDFLEEAEREQEEEPPQVWTGPPRVAQTSDPDSSEACAEEEEGLMPQG
PQLLDFSVDEVAEQLTLIDLELFSKVRLYECLGSVWSQRDRPGAAGASPTVRATVAQFNT
VTGCVLGSVLGAPGLAAPQRAQRLEKWIRIAQRCRELRNFSSLRAILSALQSNPIYRLKR
SWGAVSREPLSTFRKLSQIFSDENNHLSSREILFQEEATEGSQEEDNTPGSLPSKPPPGP
VPYLGTFLTDLVMLDTALPDMLEGDLINFEKRR
KEWEILARIQQLQRRCQSYTLSPHPPI
LAALHAQNQLTEEQSYRLSRVIEPPAASCPSSPRIRRRISLTKRLSAKLAREKSSSPSGS
PGDPSSPTSSVSPGSPPSSPRSRDAPAGSPPASPGPQGPSTKLPLSLDLPSPRPFALPLG
SPRIPLPAQQSSEARVIRVSIDNDHGNLYRSILLTSQDKAPSVVRRALQKHNVPQPWACD
YQLFQVLPGDRVLLIPDNANVFYAMSPVAPRDFMLRRKEG
TRNTLSVSPS
Sequence length 710
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Hypertension Hypertensive disease rs13306026 27618448, 27618447
Unknown
Disease term Disease name Evidence References Source
Coronary artery disease Coronary artery disease GWAS
Associations from Text Mining
Disease Name Relationship Type References
Glaucoma Associate 36833422
Glaucoma Angle Closure Associate 36833422
Hypertension Associate 37175507
Pre Eclampsia Associate 37285119
Pulmonary Arterial Hypertension Associate 37176017