Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
8464
Gene name Gene Name - the full gene name approved by the HGNC.
SPT3 homolog, SAGA and STAGA complex component
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SUPT3H
Synonyms (NCBI Gene) Gene synonyms aliases
SPT3, SPT3L
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p21.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT029827 hsa-miR-26b-5p Microarray 19088304
MIRT046510 hsa-miR-15b-5p CLASH 23622248
MIRT1403516 hsa-miR-3160-3p CLIP-seq
MIRT1403517 hsa-miR-3173-3p CLIP-seq
MIRT1403518 hsa-miR-3616-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000124 Component SAGA complex IDA 11564863
GO:0000124 Component SAGA complex IEA
GO:0000124 Component SAGA complex NAS 9674425, 19114550
GO:0003713 Function Transcription coactivator activity IBA
GO:0003713 Function Transcription coactivator activity IDA 11564863
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602947 11466 ENSG00000196284
Protein
UniProt ID O75486
Protein name Transcription initiation protein SPT3 homolog (SPT3-like protein)
Protein function Probable transcriptional activator.
PDB 7KTR , 7KTS , 8H7G
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02269 TFIID-18kDa 24 116 Transcription initiation factor IID, 18kD subunit Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in all tissues tested including pancreas, kidney, skeletal muscle, liver, lung, placenta, brain and heart.
Sequence
MNNTAASPMSTATSSSGRSTGKSISFATELQSMMYSLGDARRPLHETAVLVEDVVHTQLI
NLLQQAAEVSQLRGARVITPEDLLFLMRKDKKKLRRLLKYMFIRDYKSKIVKGIDE
DDLL
EDKLSGSNNANKRQKIAQDFLNSIDQTGELLAMFEDDEIDEVKQERMERAERQTRIMDSA
QYAEFCESRQLSFSKKASKFRDWLDCSSMEIKPNVVAMEILAYLAYETVAQLVDLALLVR
QDMVTKAGDPFSHAISATFIQYHNSAESTAACGVEAHSDAIQPCHIREAIRRYSHRIGPL
SPFTNAYRRNGMAFLAC
Sequence length 317
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Transcriptional misregulation in cancer  
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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
Asthma Asthma (childhood onset) N/A N/A GWAS
Attention Deficit Hyperactivity Disorder Attention deficit hyperactivity disorder N/A N/A GWAS
Diabetes Type 2 diabetes N/A N/A GWAS
Glaucoma Glaucoma N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 35589867
Cartilage Diseases Associate 27701424
Disorders of Sex Development Associate 24055526
Glioblastoma Associate 35550147
Gonadal Dysgenesis 46 XY Associate 24055526
Osteoarthritis Associate 30010910
Osteoarthritis Knee Associate 36089590