Mitochondria Phenome Knowledgebase

Gene Symbol WWOX
Ensembl ID ENSG00000186153 Entrez 51741
Gene Alias D16S432E; FOR; FRA16D; HHCMA56; PRO0128; WOX1; WWOX v8 Subcellular Locations Cytoplasm Mitochondria Nucleus
Map Position 16q23.3-q24.1 Subcell PMIDs 10786676 11744990 14695174 15664696
OMIM Gene 605131 Protein Complex
Swissprot ID Q9NZC7 Swissprot Description Oxidoreductase
OMIM Disease Esophageal squamous cell carcinoma (ESCC) [133239]; Pancreatic carcinoma [260350]

Gene-Feature associations that are associated with 1 Gene

Gene OMIM Disease Phenotypic Feature Phenotype Annotation Clinical Category PMIDs
WWOX 133239 Neoplasms oncologic #11956080 #16152610
WWOX 260350 Neoplasms oncologic #15073125
WWOX 133239 Glandular-and-epithelial-neoplasms oncologic #11956080 #16152610
WWOX 133239 Squamous-cell-neoplasms squamous cell carcinoma; esophageal squamous cell carcinoma; oral squamous cell carcinoma; carcinogenesis; oral cancer oncologic 11956080 16152610
WWOX 260350 Digestive-system-neoplasms oncologic #15073125
WWOX 260350 Pancreatic-neoplasms pancreas cancer; pancreatic carcinogenesis; pancreatic adenocarcinoma oncologic 15073125

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