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Protein Ontology report - nodal protein sequence variant R183Q (human) PR:000000292 - http://purl.obolibrary.org/obo/PR_000000292        Annotations       Ontology Information Show OBO stanza / PAF / GPI   PRO ID PR:000000292      PRO name nodal protein sequence variant R183Q (human)    Synonyms PRO-Short-label: EXACT: hNODAL/var:R183Q PRO-proteoform-std: EXACT: UniProtKB:Q96S42, Arg-183, CHEBI:30011 Other: EXACT: nodal protein sequence variant 1 (human)   Definition "A nodal homolog (human) that has a Gln residue at the position equivalent to Arg-183 of the amino acid sequence represented by UniProtKB:Q96S42. UniProtKB:Q96S42, Arg-183, CHEBI:30011." [PMID:9354794, PRO:CNA, PRO:DAN]    PRO Category organism-sequence    Parent PR:Q96S42 nodal homolog (human)   Taxon NCBITaxon:9606 Homo sapiens   Term Hierarchy   Visualization DAG: OLS: Back to top Related Cross References   Db identifiers UniProtKB_VAR:VAR_015111 Back to top Functional Annotation (PRO-centric view) Switch to GO Centric View    PRO Term GO Annotation Evidence PR:000000292 hNODAL/var:R183Q UniProtKB:Q96S42, Arg-183, CHEBI:30011 | nodal protein sequence variant 1 (human) "A nodal homolog (human) that has a Gln residue at the position equivalent to Arg-183 of the amino acid sequence represented by UniProtKB:Q96S42. UniProtKB:Q96S42, Arg-183, CHEBI:30011." [PMID:9354794, PRO:CNA, PRO:DAN] associated_with_disease_progression DO:0050545 visceral heterotaxy PMID:9354794