Skip to main content

Table 4 Association between proteins bearing PrD predictions and diseases in human

From: Discovering putative prion sequences in complete proteomes using probabilistic representations of Q/N-rich domains

Gene

Disease

ATXN1

Spinocerebellar ataxia

Huntington’s disease

ATXN3

Machado-joseph disease

Spinocerebellar ataxias

ATXN8

Spinocerebellar Ataxia Type 8

BMP2K

Internuclear ophthalmoplegia

Ulnar neuropathy

FOXP2

Speech-language disorders

Blepharophimosis

Premature ovarian failure

Autism

Dyslexia

HTT

Huntington’s disease

Spinocerebellar ataxia

MAML

Mucoepidermoid carcinoma

Hidradenoma

Lipoadenoma

Epithelial-myoepithelial carcinoma

MED12

FG syndrome

Intellectual disability

Schizophrenia

MED15

Epicondylitis

NCOA3

Breast cancer

Ovarian carcinoma

PAXIP1

Spinocerebellar ataxia

TAF15

Chondrosarcoma

Peripheral primitive neuroectodermal tumor

Amyotrophic lateral sclerosis

Sarcoma

Liposarcoma

TOX3

Breast cancer

TPB

Spinocerebellar ataxia

Tuberculosis

 

Huntington’s disease

  1. We compiled the different diseases associated with the genes in humans for which we found PrD predictions.