Huntington's disease-like 1

Summary
Synonym
  • HDL1
  • HLN1
  • Huntington disease-like 1
  • Huntington-like neurodegenerative disorder 1
  • autosomal dominant Huntington-like neurodegenerative disorder
  • early-onset prion disease with prominent psychiatric features
Definition
A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13.
Super Class
prion disease
External Links
Disease Ontology
DOID:0090103
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying entries 61 - 70 of 81 in total
Gene ID Gene Symbol Description Source
10558 SPTLC1 serine palmitoyltransferase long chain base subunit 1
10715 CERS1 ceramide synthase 1
10858 CYP46A1 cytochrome P450 family 46 subfamily A member 1
11343 MGLL monoglyceride lipase
22933 SIRT2 sirtuin 2
23205 ACSBG1 acyl-CoA synthetase bubblegum family member 1
23475 QPRT quinolinate phosphoribosyltransferase
23583 SMUG1 single-strand-selective monofunctional uracil-DNA glycosylase 1
26033 ATRNL1 attractin like 1
27036 SIGLEC7 sialic acid binding Ig like lectin 7
Related Glycoprotein
Displaying entry 61 - 61 of 61 in total
UniProt ID Protein Name Source
Q9Y6A2 Cholesterol 24-hydroxylase
The Human Phenotype Ontology
Displaying entries 51 - 53 of 53 in total
HPO ID HPO Term
HP:0002317 Unsteady gait
HP:0011462 Young adult onset
HP:0002283 Global brain atrophy
Displaying 1 entry
Gene ID Gene Symbol Description
5621 PRNP prion protein (Kanno blood group)

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024