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XB-GENEPAGE-1009747
???displayGene.symbol???: c4h19orf12
???displayGene.name???: chromosome 4 C19orf12 homolog
???displayGene.synonyms???
c19orf12
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???displayGene.geneFunction??? Protein Function
![]() InterPro
![]() ???displayGene.geneInteractants???
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Diseases: Disease Ontology: hereditary spastic paraplegia 43
MIM:
SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE; SPG43
External Links:
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???displayGene.expression??? | Development Stages Embryonic Tissues Adult Tissues | |||||||||||
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