Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10048
Gene name Gene Name - the full gene name approved by the HGNC.
RAN binding protein 9
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RANBP9
Synonyms (NCBI Gene) Gene synonyms aliases
BPM-L, BPM90, RANBPM, RanBP7
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p23
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a protein that binds RAN, a small GTP binding protein belonging to the RAS superfamily that is essential for the translocation of RNA and proteins through the nuclear pore complex. The protein encoded by this gene has also been shown to
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT027298 hsa-miR-101-3p Sequencing 20371350
MIRT048208 hsa-miR-196a-5p CLASH 23622248
MIRT053411 hsa-miR-591 Microarray 23807165
MIRT1289709 hsa-miR-101 CLIP-seq
MIRT1289710 hsa-miR-1200 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000151 Component Ubiquitin ligase complex IDA 29911972
GO:0000165 Process MAPK cascade TAS
GO:0005515 Function Protein binding IPI 12220523, 12421467, 12812986, 14500717, 15381419, 16478441, 18555800, 18710924, 19788913, 20580816, 21382349, 23840749, 31413325, 32814053
GO:0005634 Component Nucleus IDA 12220523, 15381419, 17467196
GO:0005654 Component Nucleoplasm IDA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
603854 13727 ENSG00000010017
Protein
UniProt ID Q96S59
Protein name Ran-binding protein 9 (RanBP9) (BPM-L) (BPM90) (Ran-binding protein M) (RanBPM) (RanBP7)
Protein function May act as scaffolding protein, and as adapter protein to couple membrane receptors to intracellular signaling pathways (Probable). Acts as a mediator of cell spreading and actin cytoskeleton rearrangement (PubMed:18710924). Core component of th
PDB 5JI7 , 5JI9 , 5JIU , 7NSC
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00622 SPRY 214 332 SPRY domain Family
PF08513 LisH 367 393 LisH Domain
PF10607 CLTH 403 711 CTLH/CRA C-terminal to LisH motif domain Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitously expressed, with highest levels in testes, placenta, heart, and muscle, and lowest levels in lung. Within the brain, expressed predominantly by neurons in the gray matter of cortex, the granular layer of cerebellum and the
Sequence
Sequence length 729
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    L1CAM interactions
RAF/MAP kinase cascade
MET activates RAS signaling
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
25482375
Unknown
Disease term Disease name Evidence References Source
Breast cancer Breast cancer Importantly, breast cancer patients bearing PRC2 LOF mutations displayed significantly worse prognosis compared with PRC2 wild-type patients GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 12421467
Breast Neoplasms Stimulate 34875851
Carcinogenesis Associate 23118896
HAIR AN syndrome Associate 26943034
Inflammation Associate 12421467
Larva Migrans Associate 26919101
Lung Neoplasms Associate 26943034
Neoplasms Associate 12421467, 34875851
Neurodegenerative Diseases Associate 32217127
Prostatic Neoplasms Associate 12361945