All terms in DOID
| Label | Id | Description |
|---|---|---|
| PIP_box | SO_0001810 | [A polypeptide region that mediates binding to PCNA. The consensus sequence is QXX(hh)XX(aa), where (h) denotes residues with moderately hydrophobic side chains and (a) denotes residues with highly hydrophobic aromatic side chains.] |
| obsolete chronic depressive disorder | DOID_844 | |
| phosphorylation_site | SO_0001811 | [A post-translationally modified region in which residues of the protein are modified by phosphorylation.] |
| respiratory system blood vessel | UBERON_0003504 | |
| transmembrane_helix | SO_0001812 | [A region that traverses the lipid bilayer and adopts a helical secondary structure.] |
| vacuolar_sorting_signal | SO_0001813 | [A polypeptide region that targets a polypeptide to the vacuole.] |
| peptide_localization_signal | SO_0001527 | [A region of peptide sequence used to target the polypeptide molecule to a specific organelle.] |
| coding_variant_quality | SO_0001814 | |
| variant_quality | SO_0001761 | [A dependent entity that inheres in a bearer, a sequence variant.] |
| synonymous | SO_0001815 | |
| non_synonymous | SO_0001816 | |
| inframe | SO_0001817 | [An attribute describing a sequence that contains a mutation involving the deletion or insertion of one or more bases, where this number is divisible by 3.] |
| mRNA_attribute | SO_0000863 | [An attribute describing an mRNA feature.] |
| protein_altering_variant | SO_0001818 | [A sequence_variant which is predicted to change the protein encoded in the coding sequence.] |
| coding_sequence_variant | SO_0001580 | [A sequence variant that changes the coding sequence.] |
| membranoproliferative glomerulonephritis | DOID_2920 | |
| hindlimb blood vessel | UBERON_0003516 | |
| tasiRNA | SO_0001800 | [The sequence of a 21 nucleotide double stranded, polyadenylated non coding RNA, transcribed from the TAS gene.] |
| tasiRNA_primary_transcript | SO_0001801 | [A primary transcript encoding a tasiRNA.] |
| increased_polyadenylation_variant | SO_0001802 | [A transcript processing variant whereby polyadenylation of the encoded transcript is increased with respect to the reference.] |