Gene Gene information from NCBI Gene database.
Entrez ID 29098
Gene name RAN guanine nucleotide release factor
Gene symbol RANGRF
Synonyms (NCBI Gene)
HSPC165HSPC236MOG1RANGNRF
Chromosome 17
Chromosome location 17p13.1
Summary This gene encodes a protein that has been shown to function as a guanine nucleotide release factor in mouse and to regulate the expression and function of the Nav1.5 cardiac sodium channel in human. Alternative splicing results in multiple transcript vari
miRNA miRNA information provided by mirtarbase database.
6
miRTarBase ID miRNA Experiments Reference
MIRT1289828 hsa-miR-2355-5p CLIP-seq
MIRT1289829 hsa-miR-3661 CLIP-seq
MIRT1289830 hsa-miR-4751 CLIP-seq
MIRT1289831 hsa-miR-492 CLIP-seq
MIRT1289832 hsa-miR-631 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
54
GO ID Ontology Definition Evidence Reference
GO:0002027 Process Regulation of heart rate TAS 21621375
GO:0003254 Process Regulation of membrane depolarization IEA
GO:0003254 Process Regulation of membrane depolarization IMP 23420830
GO:0005085 Function Guanyl-nucleotide exchange factor activity IBA
GO:0005085 Function Guanyl-nucleotide exchange factor activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607954 17679 ENSG00000108961
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9HD47
Protein name Ran guanine nucleotide release factor (RanGNRF) (Ran-binding protein MOG1)
Protein function May regulate the intracellular trafficking of RAN (PubMed:11290418). Promotes guanine nucleotide release from RAN and inhibits binding of new GTP by preventing the binding of the RAN guanine nucleotide exchange factor RCC1 (PubMed:29040603). Reg
PDB 5YFG
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04603 Mog1 7 145 Ran-interacting Mog1 protein Domain
Tissue specificity TISSUE SPECIFICITY: Isoform 1 and isoform 2 are ubiquitously expressed (PubMed:11290418). Detected in heart and brain (PubMed:21621375). {ECO:0000269|PubMed:11290418, ECO:0000269|PubMed:21621375}.
Sequence
Sequence length 186
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Phase 0 - rapid depolarisation
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
135
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cardiac arrhythmia Uncertain significance; Likely benign; Benign; Conflicting classifications of pathogenicity rs150856064, rs767541224, rs1380032341, rs200615633, rs1247874145, rs769218673, rs755244411, rs771333875, rs548428743, rs774053920, rs755816071, rs2151609934, rs140016697, rs140312984, rs2151611212
View all (109 more)
RCV001841208
RCV001841207
RCV001841210
RCV001841204
RCV001841212
RCV001841211
RCV001841214
RCV001842034
RCV001842032
RCV001842029
RCV001842031
RCV001842040
RCV001842045
RCV001842052
RCV001842049
RCV001842046
RCV001842048
RCV002046512
RCV001995316
RCV001901691
RCV001935473
RCV002055768
RCV001842432
RCV001926693
RCV001899184
RCV001874969
RCV001964616
RCV002013717
RCV002037401
RCV001971948
RCV001890009
RCV001909093
RCV001963187
RCV002098764
RCV002146391
RCV002212158
RCV002167340
RCV002215229
RCV002095360
RCV002197117
RCV002098339
RCV002147603
RCV002162496
RCV002162498
RCV002169656
RCV002171035
RCV003089175
RCV003074404
RCV003058975
RCV003077441
RCV001842510
RCV001842511
RCV001852051
RCV003079660
RCV003076211
RCV003088203
RCV003073452
RCV002620184
RCV002607629
RCV003108177
RCV002583202
RCV002594275
RCV002654220
RCV002700950
RCV002746655
RCV002771042
RCV002837996
RCV002846679
RCV002918291
RCV002933653
RCV002949066
RCV003008328
RCV003011776
RCV003033970
RCV003046265
RCV003755000
RCV001842999
RCV001843039
RCV001843040
RCV003592769
RCV003592776
RCV003592731
RCV003592733
RCV003592792
RCV003592921
RCV003591233
RCV003591153
RCV003755181
RCV003755283
RCV003755380
RCV003755496
RCV003755715
RCV003756012
RCV003756202
RCV003756436
RCV003756541
RCV003826053
RCV003834476
RCV003850216
RCV003862091
RCV003858717
RCV003851869
RCV003870511
RCV001841322
RCV002062459
RCV002063640
RCV001841338
RCV001841336
RCV002061665
RCV005090830
RCV001841345
RCV001841344
RCV005091226
RCV001841484
RCV003754880
RCV001841850
RCV001842003
RCV001841982
RCV001841986
RCV001842005
RCV002544523
RCV001842593
RCV001842596
RCV001842597
RCV001842590
RCV001841186
RCV001841187
RCV001841185
RCV001841190
RCV001841202
Glioma susceptibility 1 Uncertain significance rs200615633 RCV005911017
RANGRF-related disorder Likely benign rs548428743, rs746275946 RCV003946140
RCV003911271
Thyroid cancer, nonmedullary, 1 Likely benign rs200354447 RCV005896598
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Arrhythmias Cardiac Associate 28796037
Brugada Syndrome Associate 26173111, 30282806, 31627867
Focal Nodular Hyperplasia Stimulate 27600827
Growth Disorders Associate 27600827
Hyperparathyroidism Secondary Associate 27600827