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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 noggin
PR:000029067 Homo sapiens protein
  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

Short 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
associated_with_disease_progressionDO:0050788 proximal symphalangism PMID:11857750
PR:000000108 hNOG/var:P223L
UniProtKB:Q13253, Pro-223, CHEBI:30006
associated_with_disease_progressionDO:0050788 proximal symphalangism PMID:10080184
PR:000000109 hNOG/var:P35R
UniProtKB:Q13253, Pro-35, CHEBI:29952
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
associated_with_disease_progressionDO:0050788 proximal symphalangism PMID:11846737
PR:000000111 hNOG/var:G189C
UniProtKB:Q13253, Gly-189, CHEBI:29950
associated_with_disease_progressionDO:0050788 proximal symphalangism PMID:99178269
PR:000000112 hNOG/var:R204L
UniProtKB:Q13253, Arg-204, CHEBI:30006
associated_with_disease_progressionDO:0050789 tarsal-carpal coalition syndrome PMID:11545688
PR:000000113 hNOG/var:W217G
UniProtKB:Q13253, Trp-217, CHEBI:29947
associated_with_disease_progressionDO:0050788 proximal symphalangism PMID:10080184
PR:000000114 hNOG/var:I220N
UniProtKB:Q13253, Ile-220, CHEBI:50347
associated_with_disease_progressionDO:0050788 proximal symphalangism PMID:10080184
PR:000000115 hNOG/var:Y222C
UniProtKB:Q13253, Tyr-222, CHEBI:29950
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
associated_with_disease_progressionDO:0050788 proximal symphalangism PMID:10080184
PR:000036421 hNOG/iso:1/SigPep-
UniProtKB:Q13253-1, 28-232
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