|
ID |
Name |
Source |
pValue |
FDR B&H |
FDR B&Y |
Bonferroni |
Genes from Input
|
Genes in Annotation
|
1
|
20301682
|
Hereditary Spastic Paraplegia Overview
|
Pubmed
|
7.302E-27
|
1.850E-23
|
1.556E-22
|
1.850E-23
|
11
|
63
|
2
|
10066790
|
AP-4, a novel protein complex related to clathrin adaptors.
|
Pubmed
|
4.173E-10
|
3.524E-7
|
2.965E-6
|
1.057E-6
|
3
|
4
|
3
|
30543385
|
AP-4-Associated Hereditary Spastic Paraplegia
|
Pubmed
|
4.173E-10
|
3.524E-7
|
2.965E-6
|
1.057E-6
|
3
|
4
|
4
|
10436028
|
Characterization of a fourth adaptor-related protein complex.
|
Pubmed
|
1.043E-9
|
6.605E-7
|
5.558E-6
|
2.642E-6
|
3
|
5
|
5
|
17420921
|
The role of hereditary spastic paraplegia related genes in multiple sclerosis. A study of disease susceptibility and clinical outcome.
|
Pubmed
|
1.250E-8
|
6.331E-6
|
5.327E-5
|
3.165E-5
|
3
|
10
|
6
|
18341993
|
Accumulation of AMPA receptors in autophagosomes in neuronal axons lacking adaptor protein AP-4.
|
Pubmed
|
1.718E-8
|
7.252E-6
|
6.102E-5
|
4.351E-5
|
3
|
11
|
7
|
19184135
|
Interaction of the SPG21 protein ACP33/maspardin with the aldehyde dehydrogenase ALDH16A1.
|
Pubmed
|
2.345E-7
|
8.484E-5
|
7.139E-4
|
5.939E-4
|
2
|
2
|
8
|
9714600
|
The AP-3 complex: a coat of many colours.
|
Pubmed
|
4.201E-7
|
1.330E-4
|
1.119E-3
|
1.064E-3
|
3
|
30
|
9
|
21620353
|
Adaptor protein complex 4 deficiency causes severe autosomal-recessive intellectual disability, progressive spastic paraplegia, shy character, and short stature.
|
Pubmed
|
7.032E-7
|
1.619E-4
|
1.363E-3
|
1.781E-3
|
2
|
3
|
10
|
26542808
|
Bivalent Motif-Ear Interactions Mediate the Association of the Accessory Protein Tepsin with the AP-4 Adaptor Complex.
|
Pubmed
|
7.032E-7
|
1.619E-4
|
1.363E-3
|
1.781E-3
|
2
|
3
|
11
|
26544806
|
Association between Rare Variants in AP4E1, a Component of Intracellular Trafficking, and Persistent Stuttering.
|
Pubmed
|
7.032E-7
|
1.619E-4
|
1.363E-3
|
1.781E-3
|
2
|
3
|
12
|
11707398
|
Functional and physical interactions of the adaptor protein complex AP-4 with ADP-ribosylation factors (ARFs).
|
Pubmed
|
2.343E-6
|
4.945E-4
|
4.161E-3
|
5.934E-3
|
2
|
5
|
13
|
27501351
|
Divergence in Ubiquitin Interaction and Catalysis among the Ubiquitin-Specific Protease Family Deubiquitinating Enzymes.
|
Pubmed
|
3.513E-6
|
6.356E-4
|
5.348E-3
|
8.898E-3
|
2
|
6
|
14
|
11409905
|
Similar subunit interactions contribute to assembly of clathrin adaptor complexes and COPI complex: analysis using yeast three-hybrid system.
|
Pubmed
|
3.513E-6
|
6.356E-4
|
5.348E-3
|
8.898E-3
|
2
|
6
|
15
|
24482476
|
Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders.
|
Pubmed
|
2.452E-5
|
1.277E-3
|
1.074E-2
|
6.212E-2
|
2
|
15
|
16
|
18971422
|
Aldehyde dehydrogenase 1a1 is dispensable for stem cell function in the mouse hematopoietic and nervous systems.
|
Pubmed
|
5.384E-5
|
1.277E-3
|
1.074E-2
|
1.364E-1
|
2
|
22
|
17
|
22988430
|
A genome-wide screen to identify transcription factors expressed in pelvic Ganglia of the lower urinary tract.
|
Pubmed
|
5.895E-5
|
1.277E-3
|
1.074E-2
|
1.493E-1
|
2
|
23
|
18
|
9275178
|
Identification and classification of 16 new kinesin superfamily (KIF) proteins in mouse genome.
|
Pubmed
|
6.986E-5
|
1.277E-3
|
1.074E-2
|
1.770E-1
|
2
|
25
|
19
|
22118674
|
Activity-based chemical proteomics accelerates inhibitor development for deubiquitylating enzymes.
|
Pubmed
|
1.011E-4
|
1.277E-3
|
1.074E-2
|
2.562E-1
|
2
|
30
|
20
|
19343046
|
Association study between single-nucleotide polymorphisms in 199 drug-related genes and commonly measured quantitative traits of 752 healthy Japanese subjects.
|
Pubmed
|
1.160E-4
|
1.277E-3
|
1.074E-2
|
2.938E-1
|
3
|
193
|
21
|
22626734
|
A microarray of ubiquitylated proteins for profiling deubiquitylase activity reveals the critical roles of both chain and substrate.
|
Pubmed
|
1.462E-4
|
1.277E-3
|
1.074E-2
|
3.704E-1
|
2
|
36
|
22
|
19608861
|
Lysine acetylation targets protein complexes and co-regulates major cellular functions.
|
Pubmed
|
1.631E-4
|
1.277E-3
|
1.074E-2
|
4.131E-1
|
2
|
38
|
23
|
20381070
|
Sex-specific proteome differences in the anterior cingulate cortex of schizophrenia.
|
Pubmed
|
1.808E-4
|
1.277E-3
|
1.074E-2
|
4.580E-1
|
2
|
40
|
24
|
25681447
|
SPG7 mutations are a common cause of undiagnosed ataxia.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
25
|
16759795
|
p53 Protein accumulation, cancer multiplicity, and aldehyde dehydrogenase-2 genotype in Japanese alcoholic men with early esophageal squamous cell carcinoma.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
26
|
16987144
|
Effect of over-expression of neuropathy target esterase on mammalian cell proliferation.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
27
|
26941382
|
ALDH2 Glu504Lys Confers Susceptibility to Schizophrenia and Impacts Hippocampal-Prefrontal Functional Connectivity.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
28
|
25832430
|
Seipin mutation at glycosylation sites activates autophagy in transfected cells via abnormal large lipid droplets generation.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
29
|
25759460
|
East asian variant of aldehyde dehydrogenase 2 is associated with coronary spastic angina: possible roles of reactive aldehydes and implications of alcohol flushing syndrome.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
30
|
26459808
|
VEGFR2 Trafficking, Signaling and Proteolysis is Regulated by the Ubiquitin Isopeptidase USP8.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
31
|
26899237
|
Familial Mutations and Post-translational Modifications of UCH-L1 in Parkinson's Disease and Neurodegenerative Disorders.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
32
|
27488451
|
Mitochondrial aldehyde dehydrogenase 2 deficiency aggravates energy metabolism disturbance and diastolic dysfunction in diabetic mice.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
33
|
28847041
|
Age of Drinking Initiation as a Risk Factor for Alcohol Use Disorder Symptoms is Moderated by ALDH2*2 and Ethnicity.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
34
|
21114754
|
Alcohol ingestion and colorectal neoplasia: a meta-analysis based on a Mendelian randomization approach.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
35
|
23418070
|
Association of sick building syndrome with neuropathy target esterase (NTE) activity in Japanese.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
36
|
11441142
|
Molecular characterization of L-CPT I deficiency in six patients: insights into function of the native enzyme.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
37
|
2558488
|
Neuropathology of gracile axonal dystrophy (GAD) mouse. An animal model of central distal axonopathy in primary sensory neurons.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
38
|
22393400
|
Inhibition of endothelial cell proliferation and tumor angiogenesis by up-regulating NDRG2 expression in breast cancer cells.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
39
|
25863102
|
[Study on the association of USP8 gene polymorphisms with male infertility in ethnic Han Chinese from Sichuan].
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
40
|
29892902
|
Wide phenotypic spectrum in axonal Charcot-Marie-Tooth neuropathy type 2 patients with KIF5A mutations.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
41
|
18500496
|
A novel KIF5A/SPG10 mutation in spastic paraplegia associated with axonal neuropathy.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
42
|
12123845
|
Mutation analysis and association studies of the ubiquitin carboxy-terminal hydrolase L1 gene in Huntington's disease.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
43
|
15094302
|
Lysophospholipase inhibition by organophosphorus toxicants.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
44
|
24636131
|
N-myc downstream-regulated gene 2 expression is associated with glucose transport and correlated with prognosis in breast carcinoma.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
45
|
24998256
|
Impact of chronic low to moderate alcohol consumption on blood lipid and heart energy profile in acetaldehyde dehydrogenase 2-deficient mice.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
46
|
25041530
|
Increased levels of UCHL1 are a compensatory response to disrupted ubiquitin homeostasis in spinal muscular atrophy and do not represent a viable therapeutic target.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
47
|
27866050
|
Boucher Neuhäuser Syndrome - A rare cause of inherited hypogonadotropic hypogonadism. A case of two adult siblings with two novel mutations in PNPLA6.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
48
|
26578638
|
The USP8 mutational status may predict drug susceptibility in corticotroph adenomas of Cushing's disease.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
49
|
9765594
|
Binding and activation of the human aldehyde dehydrogenase 2 promoter by hepatocyte nuclear factor 4.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|
50
|
22533991
|
Carnitine palmitoyltransferase 1A (CPT1A): a transcriptional target of PAX3-FKHR and mediates PAX3-FKHR-dependent motility in alveolar rhabdomyosarcoma cells.
|
Pubmed
|
4.975E-4
|
1.277E-3
|
1.074E-2
|
1.000E0
|
1
|
1
|