SUPT6H (SPT6 homolog, histone chaperone and transcription elongation factor)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 6830 |
| Gene name | SPT6 homolog, histone chaperone and transcription elongation factor |
| Gene symbol | SUPT6H |
| Synonyms (NCBI Gene) |
SPT6SPT6Hemb-5
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| Chromosome | 17 |
| Chromosome location | 17q11.2 |
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miRNA
miRNA information provided by mirtarbase database.
307
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
26
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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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.
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Q7KZ85 | ||||||||||||||||||||||||||||||||||||||||
| Protein name | Transcription elongation factor SPT6 (hSPT6) (Histone chaperone suppressor of Ty6) (Tat-cotransactivator 2 protein) (Tat-CT2 protein) | ||||||||||||||||||||||||||||||||||||||||
| Protein function | Histone H3-H4 chaperone that plays a key role in the regulation of transcription elongation and mRNA processing. Enhances the transcription elongation by RNA polymerase II (RNAPII) and is also required for the efficient activation of transcripti | ||||||||||||||||||||||||||||||||||||||||
| PDB | 6GME , 6GMH , 6TED , 7OOP , 7OPC , 7OPD , 7UNC , 7UND , 8A3Y , 8OEU , 8OEV , 8OF0 , 9EGX , 9EGY , 9EGZ , 9EH0 , 9EH2 | ||||||||||||||||||||||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Ubiquitously expressed. | ||||||||||||||||||||||||||||||||||||||||
| Sequence |
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| Sequence length | 1726 | ||||||||||||||||||||||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||||||||||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
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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)
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