PR:000000021	noggin	NOG		participates_in	GO:0030509	BMP signaling pathway			PANTHER:PTHR10494:SF2|PIRSF:PIRSF008129|UniProtKB:P97466|UniProtKB:Q13253	ISS		PANTHER:PTHR10494:SF2|PIRSF:PIRSF008129|UniProtKB:P97466|UniProtKB:Q13253	PANTHER:PTHR10494:SF2|PIRSF:PIRSF008129|UniProtKB:P97466|UniProtKB:Q13253	20080301	PRO:CNA	
PR:000000021	noggin	NOG		participates_in	GO:0007275	multicellular organism development			PANTHER:PTHR10494:SF2|PIRSF:PIRSF008129|UniProtKB:P97466|UniProtKB:Q13253	ISS		PANTHER:PTHR10494:SF2|PIRSF:PIRSF008129|UniProtKB:P97466|UniProtKB:Q13253	PANTHER:PTHR10494:SF2|PIRSF:PIRSF008129|UniProtKB:P97466|UniProtKB:Q13253	20080301	PRO:CNA	
PR:000000021	noggin	NOG		has_part	Pfam:PF05806	Noggin			PANTHER:PTHR10494:SF2|PIRSF:PIRSF008129	ISS		PANTHER:PTHR10494:SF2|PIRSF:PIRSF008129	PANTHER:PTHR10494:SF2|PIRSF:PIRSF008129|UniProtKB:P97466|UniProtKB:Q13253	20080301	PRO:CNA	
PR:000000021	noggin	NOG		participates_in	GO:0030514	negative regulation of BMP signaling pathway			PANTHER:PTHR10494:SF2|PIRSF:PIRSF008129|UniProtKB:P97466|UniProtKB:Q13253	ISS		PANTHER:PTHR10494:SF2|PIRSF:PIRSF008129|UniProtKB:P97466|UniProtKB:Q13253	PANTHER:PTHR10494:SF2|PIRSF:PIRSF008129|UniProtKB:P97466|UniProtKB:Q13253	20080301	PRO:CNA	
PR:000000107	noggin sequence variant P35S (human)	hNOG/var:P35S|noggin sequence variant 1 (human)|UniProtKB:Q13253, Pro-35, CHEBI:29999		associated_with_disease_progression	DOID:0050788	proximal symphalangism			PMID:11857750	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_018324	20080301	PRO:CNA	
PR:000000108	noggin sequence variant P223L (human)	hNOG/var:P223L|noggin sequence variant 10 (human)|UniProtKB:Q13253, Pro-223, CHEBI:30006		associated_with_disease_progression	DOID:0050788	proximal symphalangism			PMID:10080184	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_011367	20080301	PRO:CNA	
PR:000000109	noggin sequence variant P35R (human)	hNOG/var:P35R|noggin sequence variant 2 (human)|UniProtKB:Q13253, Pro-35, CHEBI:29952		associated_with_disease_progression	DOID:0050789	tarsal-carpal coalition syndrome			PMID:11545688	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_011361	20080301	PRO:CNA	
PR:000000109	noggin sequence variant P35R (human)	hNOG/var:P35R|noggin sequence variant 2 (human)|UniProtKB:Q13253, Pro-35, CHEBI:29952		associated_with_disease_progression	DOID:0050788	proximal symphalangism			PMID:11545688	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_011361	20080301	PRO:CNA	
PR:000000110	noggin sequence variant C184Y (human)	hNOG/var:C184Y|noggin sequence variant 3 (human)|UniProtKB:Q13253, Cys-184, CHEBI:46858		associated_with_disease_progression	DOID:0050788	proximal symphalangism			PMID:11846737	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_018325	20080301	PRO:CNA	
PR:000000111	noggin sequence variant G189C (human)	hNOG/var:G189C|noggin sequence variant 4 (human)|UniProtKB:Q13253, Gly-189, CHEBI:29950		associated_with_disease_progression	DOID:0050788	proximal symphalangism			PMID:99178269	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_011362	20080301	PRO:CNA	
PR:000000112	noggin sequence variant R204L (human)	hNOG/var:R204L|noggin sequence variant 5 (human)|UniProtKB:Q13253, Arg-204, CHEBI:30006		associated_with_disease_progression	DOID:0050789	tarsal-carpal coalition syndrome			PMID:11545688	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_011326	20080301	PRO:CNA	
PR:000000113	noggin sequence variant W217G (human)	hNOG/var:W217G|noggin sequence variant 6 (human)|UniProtKB:Q13253, Trp-217, CHEBI:29947		associated_with_disease_progression	DOID:0050788	proximal symphalangism			PMID:10080184	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_011363	20080301	PRO:CNA	
PR:000000114	noggin sequence variant I220N (human)	hNOG/var:I220N|noggin sequence variant 7 (human)|UniProtKB:Q13253, Ile-220, CHEBI:50347		associated_with_disease_progression	DOID:0050788	proximal symphalangism			PMID:10080184	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_011364	20080301	PRO:CNA	
PR:000000115	noggin sequence variant Y222C (human)	hNOG/var:Y222C|noggin sequence variant 8 (human)|UniProtKB:Q13253, Tyr-222, CHEBI:29950		associated_with_disease_progression	DOID:0050789	tarsal-carpal coalition syndrome			PMID:10080184	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_011365	20080301	PRO:CNA	
PR:000000115	noggin sequence variant Y222C (human)	hNOG/var:Y222C|noggin sequence variant 8 (human)|UniProtKB:Q13253, Tyr-222, CHEBI:29950		associated_with_disease_progression	DOID:0050788	proximal symphalangism			PMID:11545688	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_011365	20080301	PRO:CNA	
PR:000000116	noggin sequence variant Y222D (human)	hNOG/var:Y222D|noggin sequence variant 9 (human)|UniProtKB:Q13253, Tyr-222, CHEBI:29958		associated_with_disease_progression	DOID:0050788	proximal symphalangism			PMID:10080184	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_011366	20080301	PRO:CNA	
PR:000036421	noggin isoform 1, signal peptide removed form (human)	hNOG/iso:1/SigPep-|PRO_0000019813|UniProtKB:Q13253-1, 28-232		capable_of	GO:0005515	protein binding		PR:000036517	PMID:12478285	IPI	NCBITaxon:9606		UniProtKB:Q13253-1	20080301	PRO:CNA	
PR:000036421	noggin isoform 1, signal peptide removed form (human)	hNOG/iso:1/SigPep-|PRO_0000019813|UniProtKB:Q13253-1, 28-232		located_in	GO:0005615	extracellular space			PMID:11562478	IDA	NCBITaxon:9606		UniProtKB:Q13253-1	20080301	PRO:CNA	
PR:000036421	noggin isoform 1, signal peptide removed form (human)	hNOG/iso:1/SigPep-|PRO_0000019813|UniProtKB:Q13253-1, 28-232		participates_in	GO:0030514	negative regulation of BMP signaling pathway			PMID:12478285	IDA	NCBITaxon:9606		UniProtKB:Q13253-1	20080301	PRO:CNA