Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
29098
Gene name Gene Name - the full gene name approved by the HGNC.
RAN guanine nucleotide release factor
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RANGRF
Synonyms (NCBI Gene) Gene synonyms aliases
HSPC165, HSPC236, MOG1, RANGNRF
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17p13.1
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002027 Process Regulation of heart rate TAS 21621375
GO:0003254 Process Regulation of membrane depolarization IDA 18184654
GO:0003254 Process Regulation of membrane depolarization IMP 23420830
GO:0005085 Function Guanyl-nucleotide exchange factor activity ISS
GO:0005634 Component Nucleus HDA 21630459
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
607954 17679 ENSG00000108961
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Atrioventricular block First degree atrioventricular block rs766840243, rs763809932
Brugada syndrome Brugada Syndrome (disorder), Brugada syndrome rs104894718, rs397514252, rs397514446, rs137854613, rs137854601, rs397514449, rs137854604, rs28937318, rs137854611, rs137854612, rs137854615, rs137854618, rs137854620, rs72554632, rs121912776
View all (97 more)
21447824, 23420830, 21621375, 24142675, 18184654, 26903377
Lung adenocarcinoma Adenocarcinoma of lung (disorder) rs28934576, rs121913530, rs397516975, rs587776805, rs121913469, rs121913364, rs121913351, rs121913366, rs397516896, rs397516977, rs397516981, rs397517127, rs121913344, rs727504233, rs121913370
View all (5 more)
27602772
Sick sinus syndrome Sick Sinus Syndrome rs104894488, rs1057519015, rs121908411, rs869025519, rs1057519274, rs794727637, rs1057519275, rs1057519276
Associations from Text Mining
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