HTT

E1841267 UNEXPLORED

HTT is the human gene that encodes the huntingtin protein, whose mutation is responsible for causing Huntington's disease.

Try in SPARQL Jump to: Surface forms Referenced by

All labels observed (2)

Label Occurrences
HTT canonical 1
Htt 1

Referenced by (2)

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

Huntington's disease → affectsGene → HTT ⓘ
subject linked to: HD
HTT → hasMouseOrtholog → Htt ⓘ
subject linked to: HTT gene
linked to: HTT