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Protein Ontology report - presenilin-1 sequence variant G266S (human) PR:000037677 - http://purl.obolibrary.org/obo/PR_000037677        Annotations       Ontology Information Show OBO stanza / PAF / GPI   PRO ID PR:000037677      PRO name presenilin-1 sequence variant G266S (human)    Synonyms PRO-Short-label: EXACT: hPSEN1/var:G266S PRO-proteoform-std: EXACT: UniProtKB:P49768, Gly-266, CHEBI:29999 NARROW: UniProtKB:P49768-1, Gly-266, CHEBI:29999   Definition "A presenilin-1 sequence variant (human) that has a Ser residue at the position equivalent to Gly-266 of the amino acid sequence represented by UniProtKB:P49768-1. Example: UniProtKB:P49768-1, Gly-266, CHEBI:29999." [Alzforum:KD, PMID:11920851, PRO:DAN]    Comment Requested by=Alzforum.    PRO Category organism-sequence    Parent PR:000036285 presenilin-1 sequence variant (human)   Taxon NCBITaxon:9606 Homo sapiens   Term Hierarchy   Visualization DAG: OLS: Back to top Related Cross References   Db identifiers UniProtKB_VAR:VAR_016219 Back to top Functional Annotation (PRO-centric view) Switch to GO Centric View    PRO Term GO Annotation Evidence PR:000037677 hPSEN1/var:G266S Example: UniProtKB:P49768-1, Gly-266, CHEBI:29999 associated_with_disease_progression DO:10652 Alzheimer's disease Alzforum:psen1-g266s DO:9246 cerebral amyloid angiopathy Alzforum:psen1-g266s