Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
83699
Gene name Gene Name - the full gene name approved by the HGNC.
SH3 domain binding glutamate rich protein like 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SH3BGRL2
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6q14.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT044871 hsa-miR-195-5p CLASH 23622248
MIRT1344413 hsa-miR-128 CLIP-seq
MIRT1344414 hsa-miR-1287 CLIP-seq
MIRT1344415 hsa-miR-190 CLIP-seq
MIRT1344416 hsa-miR-190b CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005634 Component Nucleus IEA
GO:0005654 Component Nucleoplasm IDA
GO:0005737 Component Cytoplasm IBA
GO:0017124 Function SH3 domain binding IEA
GO:0031965 Component Nuclear membrane IDA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
615678 15567 ENSG00000198478
Protein
UniProt ID Q9UJC5
Protein name SH3 domain-binding glutamic acid-rich-like protein 2 (Fovea-associated SH3 domain-binding protein)
PDB 2CT6
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04908 SH3BGR 1 98 SH3-binding, glutamic acid-rich protein Family
Tissue specificity TISSUE SPECIFICITY: Highly expressed in brain, placenta, liver and kidney. Expressed in retina. {ECO:0000269|PubMed:12095696}.
Sequence
Sequence length 107
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
Oligodendroglioma Oligodendroglioma N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Cholangiocarcinoma Associate 35716043