Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
51571
Gene name Gene Name - the full gene name approved by the HGNC.
CYFIP related Rac1 interactor B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CYRIB
Synonyms (NCBI Gene) Gene synonyms aliases
BM-009, CYRI, CYRI-B, FAM49B, L1
Chromosome Chromosome number
8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8q24.21
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001916 Process Positive regulation of T cell mediated cytotoxicity IEA
GO:0001916 Process Positive regulation of T cell mediated cytotoxicity ISS
GO:0005515 Function Protein binding IPI 25416956, 28514442, 32296183, 32814053, 33961781
GO:0005576 Component Extracellular region TAS
GO:0005739 Component Mitochondrion IDA 29059164
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
617978 25216 ENSG00000153310
Protein
UniProt ID Q9NUQ9
Protein name CYFIP-related Rac1 interactor B (L1)
Protein function Negatively regulates RAC1 signaling and RAC1-driven cytoskeletal remodeling (PubMed:30250061, PubMed:31285585). Regulates chemotaxis, cell migration and epithelial polarization by controlling the polarity, plasticity, duration and extent of prot
PDB 7AJK
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07159 DUF1394 18 320 Protein of unknown function (DUF1394) Family
Sequence
Sequence length 324
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Regulation of actin cytoskeleton   Platelet degranulation
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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
Alzheimer disease Alzheimer's disease or family history of Alzheimer's disease N/A N/A GWAS
Colorectal Cancer Colorectal cancer N/A N/A GWAS
Metabolic Syndrome Sour taste perception in obesity with metabolic syndrome N/A N/A GWAS
Rheumatoid arthritis Rheumatoid arthritis N/A N/A GWAS