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Protein Ontology report - noggin sequence variant C184Y (human) PR:000000110 - http://purl.obolibrary.org/obo/PR_000000110        Annotations       Ontology Information Show OBO stanza / PAF / GPI   PRO ID PR:000000110      PRO name noggin sequence variant C184Y (human)    Synonyms PRO-Short-label: EXACT: hNOG/var:C184Y PRO-proteoform-std: EXACT: UniProtKB:Q13253, Cys-184, CHEBI:46858 Other: EXACT: noggin sequence variant 3 (human)   Definition "A noggin (human) that has a Tyr residue at the position equivalent to Cys-184 of the amino acid sequence represented by UniProtKB:Q13253. UniProtKB:Q13253, Cys-184, CHEBI:46858." [PMID:11846737, PRO:CNA, PRO:DAN]    PRO Category organism-sequence    Parent PR:Q13253 noggin (human)   Taxon NCBITaxon:9606 Homo sapiens   Term Hierarchy   Visualization DAG: OLS: Back to top Related Cross References   Db identifiers UniProtKB_VAR:VAR_018325 Back to top Functional Annotation (PRO-centric view) Switch to GO Centric View    PRO Term GO Annotation Evidence PR:000000110 hNOG/var:C184Y UniProtKB:Q13253, Cys-184, CHEBI:46858 | noggin sequence variant 3 (human) "A noggin (human) that has a Tyr residue at the position equivalent to Cys-184 of the amino acid sequence represented by UniProtKB:Q13253. UniProtKB:Q13253, Cys-184, CHEBI:46858." [PMID:11846737, PRO:CNA, PRO:DAN] associated_with_disease_progression DO:0050788 proximal symphalangism PMID:11846737