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Protein Ontology report - noggin sequence variant W217G (human) PR:000000113 - http://purl.obolibrary.org/obo/PR_000000113        Annotations       Ontology Information Show OBO stanza / PAF / GPI   PRO ID PR:000000113      PRO name noggin sequence variant W217G (human)    Synonyms PRO-Short-label: EXACT: hNOG/var:W217G PRO-proteoform-std: EXACT: UniProtKB:Q13253, Trp-217, CHEBI:29947 Other: EXACT: noggin sequence variant 6 (human)   Definition "A noggin (human) that has a Gly residue at the position equivalent to Trp-217 of the amino acid sequence represented by UniProtKB:Q13253. UniProtKB:Q13253, Trp-217, CHEBI:29947." [PMID:10080184, 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_011363 Back to top Functional Annotation (PRO-centric view) Switch to GO Centric View    PRO Term GO Annotation Evidence PR:000000113 hNOG/var:W217G UniProtKB:Q13253, Trp-217, CHEBI:29947 | noggin sequence variant 6 (human) "A noggin (human) that has a Gly residue at the position equivalent to Trp-217 of the amino acid sequence represented by UniProtKB:Q13253. UniProtKB:Q13253, Trp-217, CHEBI:29947." [PMID:10080184, PRO:CNA, PRO:DAN] associated_with_disease_progression DO:0050788 proximal symphalangism PMID:10080184