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XB-GENEPAGE-854549
???displayGene.symbol???: dync1h1
???displayGene.name???: dynein cytoplasmic 1 heavy chain 1
???displayGene.synonyms???
LOC108699777
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???displayGene.geneFunction??? microtubule motor component Protein Function
![]() ???displayGene.geneInteractants???
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Diseases: Disease Ontology: autosomal dominant intellectual developmental disorder
MIM:
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O; CMT2O
External Links:
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???displayGene.expression??? | Development Stages Embryonic Tissues Adult Tissues | |||||||||||
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