Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
60626
Gene name Gene Name - the full gene name approved by the HGNC.
RIC8 guanine nucleotide exchange factor A
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RIC8A
Synonyms (NCBI Gene) Gene synonyms aliases
RIC8
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11p15.5
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT049571 hsa-miR-92a-3p CLASH 23622248
MIRT526127 hsa-miR-603 PAR-CLIP 22012620
MIRT526125 hsa-miR-6757-3p PAR-CLIP 22012620
MIRT526126 hsa-miR-892b PAR-CLIP 22012620
MIRT526124 hsa-miR-648 PAR-CLIP 22012620
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001701 Process In utero embryonic development IEA
GO:0001944 Process Vasculature development IEA
GO:0001965 Function G-protein alpha-subunit binding IBA
GO:0001965 Function G-protein alpha-subunit binding IEA
GO:0001965 Function G-protein alpha-subunit binding ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
609146 29550 ENSG00000177963
Protein
UniProt ID Q9NPQ8
Protein name Chaperone Ric-8A (Synembryn-A)
Protein function Chaperone that specifically binds and folds nascent G alpha proteins prior to G protein heterotrimer formation, promoting their stability and activity: folds GNAI1, GNAO1, GNA13 and GNAQ (By similarity). Does not fold G(s) G-alpha proteins GNAS
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10165 Ric8 66 506 Guanine nucleotide exchange factor synembryn Family
Sequence
Sequence length 531
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
Myocardial Infarction Myocardial infarction N/A N/A GWAS
Uterine Fibroids Uterine fibroids N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Meningioma Associate 29762745
Neoplasms Associate 39198848