huntingtin

E1841269 UNEXPLORED

Huntingtin is a large, widely expressed human protein whose mutant form with expanded polyglutamine repeats causes Huntington’s disease by leading to progressive neurodegeneration.

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All labels observed (3)

Label Occurrences
huntingtin canonical 1
huntingtin (Huntington disease) gene 1
huntingtin protein 1

Referenced by (3)

Full triples — surface form annotated when it differs from this entity's canonical label.

HTT → fullName → huntingtin ⓘ
subject linked to: HTT gene
HTT → encodes → huntingtin protein ⓘ
subject linked to: HTT gene
linked to: huntingtin
HTT → alternativeName → huntingtin (Huntington disease) gene ⓘ
subject linked to: HTT gene
linked to: huntingtin