C6orf15 (chromosome 6 open reading frame 15)

Gene
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
29113
Gene name Gene Name - the full gene name approved by the HGNC.
Chromosome 6 open reading frame 15
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
C6orf15
Synonyms (NCBI Gene) Gene synonyms aliases
STG
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p21.33
miRNA miRNA information provided by mirtarbase database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(2)
miRTarBase ID miRNA Experiments Reference
MIRT028802 hsa-miR-26b-5p Microarray 19088304
MIRT028802 hsa-miR-26b-5p Microarray 19088304
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(4)
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005576 Component Extracellular region IEA
GO:0030198 Process Extracellular matrix organization IBA
GO:0031012 Component Extracellular matrix IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
611401 13927 ENSG00000204542
Protein
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Q6UXA7
Protein name Uncharacterized protein C6orf15 (Protein STG)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15809 STG 40 → 275 Simian taste bud-specific gene product family Family
PF15809 STG 268 → 310 Simian taste bud-specific gene product family Family
Tissue specificity TISSUE SPECIFICITY: Expressed in skin and tonsils. {ECO:0000269|PubMed:15217361}.
Sequence
Sequence length 325
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)
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide Unknown Diseases (11)
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
Allergic Sensitization Allergic sensitization N/A N/A GWAS
Colorectal Cancer Colorectal cancer N/A N/A GWAS
Crohn Disease Crohn's disease N/A N/A GWAS
Follicular lymphoma Follicular lymphoma N/A N/A GWAS
Show/Hide Text Mining Associations (4)
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Non Small Cell Lung Associate 33144423
Inflammatory Bowel Diseases Associate 32709981
Lupus Nephritis Associate 24925725
Psoriasis Associate 19620980