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Protein Ontology report - smad2 sequence variant 5 (human) PR:000000474 - http://purl.obolibrary.org/obo/PR_000000474        Annotations       Ontology Information Show OBO stanza / PAF / GPI   PRO ID PR:000000474      PRO name smad2 sequence variant 5 (human)    Synonyms PRO-Short-label: EXACT: hSMAD2/var:5 PRO-proteoform-std: EXACT: UniProtKB:Q15796, 2-343, 359-467 NARROW: UniProtKB:Q15796-1, 2-343, 359-467   Definition "A mothers against decapentaplegic homolog 2 (human) that has a fifteen-residue deletion at the position equivalent to region 344-358 of the amino acid sequence represented by UniProtKB:Q15796-1. Example: UniProtKB:Q15796-1, 2-343, 359-467." [PMID:8673135, PRO:CNA, PRO:DAN]    PRO Category organism-sequence    Parent PR:Q15796   Taxon NCBITaxon:9606 Homo sapiens   Term Hierarchy   Visualization DAG: OLS: Back to top Related Cross References   Db identifiers UniProtKB_VAR:VAR_011376 Back to top Functional Annotation (PRO-centric view) Switch to GO Centric View    PRO Term GO Annotation Evidence PR:000000474 hSMAD2/var:5 UniProtKB:Q15796, 2-343, 359-467 | UniProtKB:Q15796-1, 2-343, 359-467 associated_with_disease_progression DO:5672 large intestine cancer PMID:8673135 enables NOT GO:0003713 transcription coactivator activity PMID:8673135