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Protein Ontology report - ferritin light chain (human)
PR:P02792 - http://purl.obolibrary.org/obo/PR_P02792
 
  Protein Forms  Complex      
Ontology Information Show OBO stanza / GPI
  PRO ID
PR:P02792   
  PRO nameferritin light chain (human) 
  Synonyms
PRO-Short-label: EXACT:hFTL
Gene-based: RELATED:FTL
Other: EXACT:ferritin L subunit (human)
  Definition"A ferritin light chain that is encoded in the genome of human." [PRO:DNx, UniProtKB:P02792] 
  PRO Categoryorganism-gene 
  ParentPR:000007692
PR:000029067
  Gene TemplateHGNC:3999 FTL (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 0                                        
         Modification0                                                  Organism-Modification 6                                        
  Term Hierarchy
  Visualization
DAG: OLS:
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Related Cross References

  Db identifiers
UniProtKB:P02792
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Protein Forms  Switch to Extended View   

Category  
PRO Form Name
Ann. Has Annotation?

Comp. In Complex?
organism-gene


PR:P02792 ferritin light chain (human), hFTL

Yes
organism-modification


PR:000047457 ferritin light chain, initiator methionine removed form (human), hFTL/InitMet-

organism-modification


PR:000070351 ferritin light chain glutathionylated 1 (human), hFTL/SGlt:1

organism-modification


PR:000070691 ferritin light chain deaminated 1 (human), hFTL/Deam:1

organism-modification


PR:000077339 ferritin light chain deaminated 2 (human), hFTL/Deam:2

organism-modification


PR:000083838 ferritin light chain cysteinylated 1 (human), hFTL/Cyst:1

organism-modification


PR:000084288 ferritin light chain deaminated 3 (human), hFTL/Deam:3

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hFTL forms found in complexes   

hFTL Component
 Complexes
PR:P02792 hFTL PR:000050342