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Protein Ontology report - noggin sequence variant G189C (human) PR:000000111 - http://purl.obolibrary.org/obo/PR_000000111        Annotations       Ontology Information Show OBO stanza / PAF / GPI   PRO ID PR:000000111      PRO name noggin sequence variant G189C (human)    Synonyms PRO-Short-label: EXACT: hNOG/var:G189C PRO-proteoform-std: EXACT: UniProtKB:Q13253, Gly-189, CHEBI:29950 Other: EXACT: noggin sequence variant 4 (human)   Definition "A noggin (human) that has a Cys residue at the position equivalent to Gly-189 of the amino acid sequence represented by UniProtKB:Q13253. UniProtKB:Q13253, Gly-189, CHEBI:29950." [PMID:99178269, 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_011362 Back to top Functional Annotation (PRO-centric view) Switch to GO Centric View    PRO Term GO Annotation Evidence PR:000000111 hNOG/var:G189C UniProtKB:Q13253, Gly-189, CHEBI:29950 | noggin sequence variant 4 (human) "A noggin (human) that has a Cys residue at the position equivalent to Gly-189 of the amino acid sequence represented by UniProtKB:Q13253. UniProtKB:Q13253, Gly-189, CHEBI:29950." [PMID:99178269, PRO:CNA, PRO:DAN] associated_with_disease_progression DO:0050788 proximal symphalangism PMID:99178269