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Protein Ontology report - methylcrotonoyl-CoA carboxylase beta chain, mitochondrial sequence variant MCCB I437V (human)
PR:000026121 - http://purl.obolibrary.org/obo/PR_000026121
 
    Annotations      
Ontology Information Show OBO stanza / PAF / GPI
  PRO ID
PR:000026121   
  PRO namemethylcrotonoyl-CoA carboxylase beta chain, mitochondrial sequence variant MCCB I437V (human) 
  Synonyms
PRO-Short-label: EXACT:hMCCC2/var:MCCB I437V
  Definition"A methylcrotonoyl-CoA carboxylase beta chain, mitochondrial sequence variant (human) that lacks the region encoded by the last 64 bp in exon 14 due to the missense mutation I437V introducing a splice site at the position equivalent to Ile-437 of the amino acid sequence represented by UniProtKB:Q9HCC0-1." [PMID:11181649, PRO:CNA] 
  CommentCannot map to UniProtKB_VAR:VAR_012801 because the sequence shows only amino acid change, while the rest of the sequence remains the same. 
  PRO Categoryorganism-sequence 
  ParentPR:000026117 methylcrotonoyl-CoA carboxylase beta chain, mitochondrial sequence variant (human)
  TaxonNCBITaxon:9606 Homo sapiens
  Term Hierarchy
  Visualization
DAG: OLS:
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Functional Annotation (PRO-centric view) Switch to GO Centric View   
PRO Term GO Annotation Evidence
PR:000026121 hMCCC2/var:MCCB I437V associated_with_disease_progressionDO:0050710 3-methylcrotonyl-CoA carboxylase deficiency PMID:11181649
located_inSO:0001569 cryptic_splice_site_variant PMID:11181649