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Protein Ontology report - noggin (human)
PR:Q13253 - http://purl.obolibrary.org/obo/PR_Q13253
 
  Protein Forms  Annotations      
Ontology Information Show OBO stanza / GPI
  PRO ID
PR:Q13253   
  PRO namenoggin (human) 
  Synonyms
PRO-Short-label: EXACT:hNOG
Gene-based: RELATED:NOG
  Definition"A noggin that is encoded in the genome of human." [PRO:CNA, UniProtKB:Q13253
  PRO Categoryorganism-gene 
  ParentPR:000000021
PR:000029067
  Gene TemplateHGNC:7866 NOG (human)
  TaxonNCBITaxon:9606 Homo sapiens
  Terms by PRO Category
Organism-Independent Organism-Specific
         Category          Number of Terms          Category          Number of Terms
         Gene0                                                  Organism-Gene 1                                        
         Sequence0                                                  Organism-Sequence 11                                        
         Modification0                                                  Organism-Modification 2                                        
  Term Hierarchy
  Visualization
DAG: OLS:
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Related Cross References

  Db identifiers
UniProtKB:Q13253
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Protein Forms  Switch to Extended View   

Category  

PRO Form Name

Ann. Has Annotation?

Comp. In Complex?
organism-gene



PR:Q13253 noggin (human), hNOG


organism-sequence



PR:000000107 noggin sequence variant P35S (human), hNOG/var:P35S

Yes

organism-sequence



PR:000000108 noggin sequence variant P223L (human), hNOG/var:P223L

Yes

organism-sequence



PR:000000109 noggin sequence variant P35R (human), hNOG/var:P35R

Yes

organism-sequence



PR:000000110 noggin sequence variant C184Y (human), hNOG/var:C184Y

Yes

organism-sequence



PR:000000111 noggin sequence variant G189C (human), hNOG/var:G189C

Yes

organism-sequence



PR:000000112 noggin sequence variant R204L (human), hNOG/var:R204L

Yes

organism-sequence



PR:000000113 noggin sequence variant W217G (human), hNOG/var:W217G

Yes

organism-sequence



PR:000000114 noggin sequence variant I220N (human), hNOG/var:I220N

Yes

organism-sequence



PR:000000115 noggin sequence variant Y222C (human), hNOG/var:Y222C

Yes

organism-sequence



PR:000000116 noggin sequence variant Y222D (human), hNOG/var:Y222D

Yes

organism-sequence



PR:Q13253-1 noggin isoform 1 (human), hNOG/iso:1


organism-modification



PR:000036421 noggin isoform 1, signal peptide removed form (human), hNOG/iso:1/SigPep-

Yes

organism-modification



PR:000057007 noggin O-glycosylated 1 (human), hNOG/OGlyco:1


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Functional Annotation (PRO-centric view) Switch to GO Centric View   
PRO Term GO Annotation Evidence
PR:000000107
hNOG/var:P35S
UniProtKB:Q13253, Pro-35, CHEBI:29999 | noggin sequence variant 1 (human)
associated_with_disease_progressionDO:0050788 proximal symphalangism PMID:11857750
PR:000000108
hNOG/var:P223L
UniProtKB:Q13253, Pro-223, CHEBI:30006 | noggin sequence variant 10 (human)
associated_with_disease_progressionDO:0050788 proximal symphalangism PMID:10080184
PR:000000109
hNOG/var:P35R
UniProtKB:Q13253, Pro-35, CHEBI:29952 | noggin sequence variant 2 (human)
associated_with_disease_progressionDO:0050788 proximal symphalangism PMID:11545688
DO:0050789 tarsal-carpal coalition syndrome PMID:11545688
PR:000000110
hNOG/var:C184Y
UniProtKB:Q13253, Cys-184, CHEBI:46858 | noggin sequence variant 3 (human)
associated_with_disease_progressionDO:0050788 proximal symphalangism PMID:11846737
PR:000000111
hNOG/var:G189C
UniProtKB:Q13253, Gly-189, CHEBI:29950 | noggin sequence variant 4 (human)
associated_with_disease_progressionDO:0050788 proximal symphalangism PMID:99178269
PR:000000112
hNOG/var:R204L
UniProtKB:Q13253, Arg-204, CHEBI:30006 | noggin sequence variant 5 (human)
associated_with_disease_progressionDO:0050789 tarsal-carpal coalition syndrome PMID:11545688
PR:000000113
hNOG/var:W217G
UniProtKB:Q13253, Trp-217, CHEBI:29947 | noggin sequence variant 6 (human)
associated_with_disease_progressionDO:0050788 proximal symphalangism PMID:10080184
PR:000000114
hNOG/var:I220N
UniProtKB:Q13253, Ile-220, CHEBI:50347 | noggin sequence variant 7 (human)
associated_with_disease_progressionDO:0050788 proximal symphalangism PMID:10080184
PR:000000115
hNOG/var:Y222C
UniProtKB:Q13253, Tyr-222, CHEBI:29950 | noggin sequence variant 8 (human)
associated_with_disease_progressionDO:0050788 proximal symphalangism PMID:11545688
DO:0050789 tarsal-carpal coalition syndrome PMID:10080184
PR:000000116
hNOG/var:Y222D
UniProtKB:Q13253, Tyr-222, CHEBI:29958 | noggin sequence variant 9 (human)
associated_with_disease_progressionDO:0050788 proximal symphalangism PMID:10080184
PR:000036421
hNOG/iso:1/SigPep-
UniProtKB:Q13253-1, 28-232 | PRO_0000019813
acts_upstream_of_or_withinGO:0030514 negative regulation of BMP signaling pathway PMID:12478285
enablesGO:0005515 protein binding with PR:000036517 hBMP7/iso:1/mature/NGlyco:1 PMID:12478285
located_inGO:0005615 extracellular space PMID:11562478