Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6014
Gene name Gene Name - the full gene name approved by the HGNC.
Ras like without CAAX 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RIT2
Synonyms (NCBI Gene) Gene synonyms aliases
RIBA, RIN, ROC2
Chromosome Chromosome number
18
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
18q12.3
Summary Summary of gene provided in NCBI Entrez Gene.
RIN belongs to the RAS (HRAS; MIM 190020) superfamily of small GTPases (Shao et al., 1999 [PubMed 10545207]).[supplied by OMIM, Mar 2008]
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1307789 hsa-miR-3163 CLIP-seq
MIRT1307790 hsa-miR-3919 CLIP-seq
MIRT1307791 hsa-miR-4282 CLIP-seq
MIRT1307792 hsa-miR-4756-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000165 Process MAPK cascade ISS
GO:0000166 Function Nucleotide binding IEA
GO:0003682 Function Chromatin binding IEA
GO:0003924 Function GTPase activity IBA
GO:0003924 Function GTPase activity IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
609592 10017 ENSG00000152214
Protein
UniProt ID Q99578
Protein name GTP-binding protein Rit2 (EC 3.6.5.2) (Ras-like protein expressed in neurons) (Ras-like without CAAX protein 2)
Protein function Binds and exchanges GTP and GDP. Binds and modulates the activation of POU4F1 as gene expression regulator.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00071 Ras 22 183 Ras family Domain
Tissue specificity TISSUE SPECIFICITY: Neuron-specific.
Sequence
Sequence length 217
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
Colorectal Cancer Metastasis in stage I-III microsatellite instability low/stable colorectal cancer (time to event) N/A N/A GWAS
Diabetes Type 2 diabetes N/A N/A GWAS
Metabolic Syndrome Metabolic syndrome N/A N/A GWAS
Parkinson Disease Parkinson's disease N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Colorectal Neoplasms Associate 36849394
Parkinson Disease Associate 23071545