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Protein Ontology report - Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene B protein (human)
PR:Q8N1D0 - http://purl.obolibrary.org/obo/PR_Q8N1D0
 
  Protein Forms      
Ontology Information Show OBO stanza / GPI
  PRO ID
PR:Q8N1D0   
  PRO nameBeckwith-Wiedemann syndrome chromosomal region 1 candidate gene B protein (human) 
  Synonyms
PRO-Short-label: EXACT:hSLC22A18AS
Gene-based: RELATED:BWR1B | BWSCR1B | ORCTL2S | SLC22A18AS | SLC22A1LS
Other: EXACT:organic cation transporter-like protein 2 antisense protein (human) | p27-Beckwith-Wiedemann region 1 B (human) | p27-BWR1B (human) | solute carrier family 22 member 1-like antisense protein (human) | solute carrier family 22 member 18 antisense protein (human)
  Definition"A Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene B protein that is encoded in the genome of human." [PRO:DNx, UniProtKB:Q8N1D0
  PRO Categoryorganism-gene 
  ParentPR:000014987
PR:000029067
  Gene TemplateHGNC:10965 SLC22A18AS (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 0                                        
  Term Hierarchy
  Visualization
DAG: OLS:
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Related Cross References

  Db identifiers
UniProtKB:Q8N1D0
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Protein Forms  Switch to Extended View   

Category  

PRO Form Name

Ann. Has Annotation?

Comp. In Complex?
organism-gene



PR:Q8N1D0 Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene B protein (human), hSLC22A18AS


organism-sequence



PR:Q8N1D0-1 Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene B protein isoform h1 (human), hSLC22A18AS/iso:h1


organism-sequence



PR:Q8N1D0-2 Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene B protein isoform h2 (human), hSLC22A18AS/iso:h2