Client | Data |
---|---|
Gene | Clinical data, protein-protein interactions, biotype, TFBSs, expression, transcripts, protein, variants |
Transcript | Sequence, function prediction, XREFs, biotype, genes, proteins, exons |
Protein | Amino acid sequence, substitution scores, organism, genes, protein features, evidence, bibliography |
Variation | Variants, biological impact, consequence types |
Xref | Associated IDs from multiple databases (ENSEMBL, UCSC, UniProt, RefSeq, GO, Reactome, PDB, OMIM, RNAcentral, miRBase...) |
Genomic region | Sequence, clinical variants, conservation scores, regulatory elements, repeat sequences, genes, transcripts, variants |
Variant | Consequence types, genes, transcripts, proteins, population frequencies, HGVS, clinical significance, functional score |
Genome sequence | Cytobands |
Clinical | ClinVar, COSMIC, inheritance, evidence, pathogenicity, diseases |
TFBS | Histones, open chromatin, polymerases, transcription factors |