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Protein Ontology report - solute carrier family 2, facilitated glucose transporter member 5 (human)
PR:P22732 - http://purl.obolibrary.org/obo/PR_P22732
 
  Protein Forms      
Ontology Information Show OBO stanza / GPI
  PRO ID
PR:P22732   
  PRO namesolute carrier family 2, facilitated glucose transporter member 5 (human) 
  Synonyms
PRO-Short-label: EXACT:hSLC2A5
Gene-based: RELATED:GLUT5 | SLC2A5
Other: EXACT:fructose transporter (human) | glucose transporter type 5, small intestine (human) | GLUT-5 (human)
  Definition"A solute carrier family 2, facilitated glucose transporter member 5 that is encoded in the genome of human." [PRO:DNx, UniProtKB:P22732
  PRO Categoryorganism-gene 
  ParentPR:000015068
PR:000029067
  Gene TemplateHGNC:11010 SLC2A5 (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 2                                        
         Modification0                                                  Organism-Modification 1                                        
  Term Hierarchy
  Visualization
DAG: OLS:
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Related Cross References

  Db identifiers
UniProtKB:P22732
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Protein Forms  Switch to Extended View   

Category  

PRO Form Name

Ann. Has Annotation?

Comp. In Complex?
organism-gene



PR:P22732 solute carrier family 2, facilitated glucose transporter member 5 (human), hSLC2A5


organism-sequence



PR:P22732-1 solute carrier family 2, facilitated glucose transporter member 5 isoform h1 (human), hSLC2A5/iso:h1


organism-sequence



PR:P22732-2 solute carrier family 2, facilitated glucose transporter member 5 isoform h2 (human), hSLC2A5/iso:h2


organism-modification



PR:000064897 solute carrier family 2, facilitated glucose transporter member 5 deaminated 1 (human), hSLC2A5/Deam:1