C6orf15 (chromosome 6 open reading frame 15)

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Gene Gene information from NCBI Gene database.
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Entrez ID 29113
Gene name Chromosome 6 open reading frame 15
Gene symbol C6orf15
Synonyms (NCBI Gene)
STG
Chromosome 6
Chromosome location 6p21.33
miRNA miRNA information provided by mirtarbase database.
2
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miRTarBase ID miRNA Experiments Reference
MIRT028802 hsa-miR-26b-5p Microarray 19088304
MIRT028802 hsa-miR-26b-5p Microarray 19088304
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
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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 identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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MIM HGNC e!Ensembl
611401 13927 ENSG00000204542
Protein Protein information from UniProt database.
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UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
30
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Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Show/Hide Unknown Diseases (30)
Phenotype Name Clinical Significance Source Reference Evidence Score
ANTI-GAD65 AUTOIMMUNE NEUROLOGICAL SYNDROMES — GWAS catalog 35348614
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTISM SPECTRUM DISORDER — GWAS catalog 28540026
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BEHCET'S SYNDROME — GWAS catalog 23001997
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CELIAC DISEASE — GWAS catalog 39789286
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Inflammatory Bowel Diseases Inflammatory bowel disease Pubtator 32709981 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Lupus Nephritis Lupus nephritis Pubtator 24925725 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Psoriasis Psoriasis Pubtator 19620980 Associate
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Sarcoidosis Sarcoidosis GWASCAT_DG 26651848
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
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UBASH3A 4 shared diseasesCeliac disease, Graves disease, Immune system disease, Sarcoidosis 4 shared evidence sourcesGWAS catalog (Celiac disease), GWAS catalog (Graves disease), GWAS catalog (Immune system disease), GWAS catalog (Sarcoidosis) Related via 4 shared diseases including Celiac disease, Graves disease — evidence mostly GWAS catalog. TSBP1 4 shared diseasesCeliac disease, Graves disease, Membranous glomerulonephritis, Sarcoidosis 4 shared evidence sourcesGWAS catalog (Celiac disease), GWAS catalog (Graves disease), GWAS catalog (Membranous glomerulonephritis), GWAS catalog (Sarcoidosis) Related via 4 shared diseases including Celiac disease, Graves disease — evidence mostly GWAS catalog. AAMDC 2 shared diseasesGraves disease, Thyrotoxic periodic paralysis 2 shared evidence sourcesGWAS catalog (Graves disease), GWAS catalog (Thyrotoxic periodic paralysis) Related via 2 shared diseases including Graves disease, Thyrotoxic periodic paralysis — evidence mostly GWAS catalog. ITPR3 3 shared diseasesCeliac disease, Graves disease, Sarcoidosis 3 shared evidence sourcesGWAS catalog (Celiac disease), GWAS catalog (Graves disease), GWAS catalog (Sarcoidosis) Related via 3 shared diseases including Celiac disease, Graves disease — evidence mostly GWAS catalog. BTNL2 4 shared diseasesCeliac disease, Graves disease, Membranous glomerulonephritis, Sarcoidosis 3 shared evidence sourcesGWAS catalog (Celiac disease), GWAS catalog (Membranous glomerulonephritis), GWAS catalog (Sarcoidosis) Related via 4 shared diseases including Celiac disease, Graves disease — evidence mostly GWAS catalog.
Asthma Linked via 4 of 5 related genesUBASH3A, TSBP1, ITPR3, BTNL2 Hypothyroidism Linked via 3 of 5 related genesUBASH3A, TSBP1, BTNL2 Diabetes mellitus type 2 Linked via 3 of 5 related genesUBASH3A, ITPR3, BTNL2 Vitiligo Linked via 3 of 5 related genesUBASH3A, ITPR3, BTNL2 Multiple sclerosis Linked via 3 of 5 related genesTSBP1, ITPR3, BTNL2