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Protein Ontology report - alsin (human)
PR:Q96Q42 - http://purl.obolibrary.org/obo/PR_Q96Q42
 
  Protein Forms      
Ontology Information Show OBO stanza / GPI
  PRO ID
PR:Q96Q42   
  PRO namealsin (human) 
  Synonyms
PRO-Short-label: EXACT:hALS2
Gene-based: RELATED:ALS2 | ALS2CR6 | KIAA1563
Other: EXACT:amyotrophic lateral sclerosis 2 chromosomal region candidate gene 6 protein (human) | amyotrophic lateral sclerosis 2 protein (human)
  Definition"An alsin that is encoded in the genome of human." [PRO:DNx, UniProtKB:Q96Q42] 
  PRO Categoryorganism-gene 
  ParentPR:000003971 alsin
PR:000029067 Homo sapiens protein
  Gene TemplateHGNC:443 ALS2 (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 3                                        
         Modification0                                                  Organism-Modification 3                                        
  Term Hierarchy
  Visualization
DAG: OLS:
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Related Cross References

  Db identifiers
UniProtKB:Q96Q42
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Protein Forms  Switch to Extended View   

Category  
PRO Form Name
Ann. Has Annotation?

Comp. In Complex?
organism-gene


PR:Q96Q42 alsin (human), hALS2

organism-sequence


PR:Q96Q42-1 alsin isoform h1 (human), hALS2/iso:h1

organism-sequence


PR:Q96Q42-2 alsin isoform h2 (human), hALS2/iso:h2

organism-sequence


PR:Q96Q42-3 alsin isoform h3 (human), hALS2/iso:h3

organism-modification


PR:000069076 alsin phosphorylated 1 (human), hALS2/Phos:1

organism-modification


PR:000073523 alsin methylated 1 (human), hALS2/Me:1

organism-modification


PR:000075330 alsin deaminated 1 (human), hALS2/Deam:1