[Term]
id: PR:000000116
name: noggin sequence variant Y222D (human)
def: "A noggin (human) that has an Asp residue at the position equivalent to Tyr-222 of the amino acid sequence represented by UniProtKB:Q13253. UniProtKB:Q13253, Tyr-222, CHEBI:29958." [PRO:CNA, PRO:DAN, PMID:10080184]
comment: Category=organism-sequence.
synonym: "hNOG/var:Y222D" EXACT PRO-short-label [PRO:DNx]
synonym: "noggin sequence variant 9 (human)" EXACT [PRO:DNx]
synonym: "UniProtKB:Q13253, Tyr-222, CHEBI:29958" EXACT PRO-proteoform-std [PRO:DAN]
xref: UniProtKB_VAR:VAR_011366
is_a: PR:Q13253 ! noggin (human)
relationship: only_in_taxon NCBITaxon:9606 ! Homo sapiens