|
ID |
Name |
Source |
pValue |
FDR B&H |
FDR B&Y |
Bonferroni |
Genes from Input
|
Genes in Annotation
|
1
|
21198641
|
SynArfGEF is a guanine nucleotide exchange factor for Arf6 and localizes preferentially at post-synaptic specializations of inhibitory synapses.
|
Pubmed
|
4.318E-7
|
2.012E-4
|
1.492E-3
|
4.024E-4
|
2
|
7
|
2
|
9647693
|
Atrophin-1, the DRPLA gene product, interacts with two families of WW domain-containing proteins.
|
Pubmed
|
4.318E-7
|
2.012E-4
|
1.492E-3
|
4.024E-4
|
2
|
7
|
3
|
24907641
|
Abnormal splicing of NEDD4 in myotonic dystrophy type 2: possible link to statin adverse reactions.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
4
|
20078934
|
[Distribution of genetic variation of neural precursor cell expressed developmentally down-regulated 4 gene in Kazak Chinese and its association with hypertension].
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
5
|
21749564
|
Differential clinical features in a pair of monozygotic twins with dentatorubropallidoluysian atrophy.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
6
|
18804462
|
Nedd4, a human ubiquitin ligase, affects actin cytoskeleton in yeast cells.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
7
|
25527121
|
NEDD4: The founding member of a family of ubiquitin-protein ligases.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
8
|
20944102
|
Evidence for a tumour suppressor function of SETD2 in human breast cancer: a new hypothesis.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
9
|
12619170
|
Relationship between utrophin and regenerating muscle fibers in duchenne muscular dystrophy.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
10
|
16595608
|
Naturally occurring utrophin correlates with disease severity in Duchenne muscular dystrophy.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
11
|
20101691
|
Deletion of 7q11.21-q11.23 and infantile spasms without deletion of MAGI2.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
12
|
7738095
|
Interaction of chromosome-6-encoded dystrophin related protein with the extracellular matrix.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
13
|
26084711
|
Brief Report: SETD2 Mutation in a Child with Autism, Intellectual Disabilities and Epilepsy.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
14
|
23065515
|
The role of a newly identified SET domain-containing protein, SETD3, in oncogenesis.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
15
|
18565486
|
Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
16
|
26015394
|
Inhibition of muscle fibrosis results in increases in both utrophin levels and the number of revertant myofibers in Duchenne muscular dystrophy.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
17
|
24931610
|
SETD2-dependent histone H3K36 trimethylation is required for homologous recombination repair and genome stability.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
18
|
11606623
|
Demonstration by fluorescence resonance energy transfer of two sites of interaction between the low-density lipoprotein receptor-related protein and the amyloid precursor protein: role of the intracellular adapter protein Fe65.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
19
|
1426262
|
Utrophin, the autosomal homologue of dystrophin, is widely-expressed and membrane-associated in cultured cell lines.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
20
|
24496234
|
Associations between keloid severity and single-nucleotide polymorphisms: importance of rs8032158 as a biomarker of keloid severity.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
21
|
25653350
|
S-SCAM, a rare copy number variation gene, induces schizophrenia-related endophenotypes in transgenic mouse model.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
22
|
10085113
|
Cleavage of atrophin-1 at caspase site aspartic acid 109 modulates cytotoxicity.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
23
|
2541343
|
An autosomal transcript in skeletal muscle with homology to dystrophin.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
24
|
27577205
|
[Clinical and genetic characteristics of patients with dentatorubro-pallidoluysian atrophy].
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
25
|
11551978
|
Distinct regions in the 3' untranslated region are responsible for targeting and stabilizing utrophin transcripts in skeletal muscle cells.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
26
|
18945675
|
Targeting artificial transcription factors to the utrophin A promoter: effects on dystrophic pathology and muscle function.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
27
|
27542250
|
Drp1-mediated mitochondrial fission promotes cell proliferation through crosstalk of p53 and NF-κB pathways in hepatocellular carcinoma.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
28
|
24509477
|
Identification of functional cooperative mutations of SETD2 in human acute leukemia.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
29
|
8649981
|
Molecular and functional analysis of the utrophin promoter.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
30
|
11095528
|
Fe65 and X11beta co-localize with and compete for binding to the amyloid precursor protein.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
31
|
18401706
|
A differential proteomic approach reveals an evolutionary conserved regulation of Nme proteins by Fe65 in C. elegans and mouse.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
32
|
9405440
|
The C2 domain of the ubiquitin protein ligase Nedd4 mediates Ca2+-dependent plasma membrane localization.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
33
|
14689444
|
Isoform-specific knockout of FE65 leads to impaired learning and memory.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
34
|
22992774
|
Pentanucleotide repeat-primed PCR for genetic diagnosis of spinocerebellar ataxia type 31.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
35
|
8965642
|
DRPLA gene (atrophin-1) sequence and mRNA expression in human brain.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
36
|
16198105
|
A and B utrophin in human muscle and sarcolemmal A-utrophin associated with tumours.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
37
|
11065130
|
A FE65 polymorphism associated with risk of developing sporadic late-onset alzheimer's disease but not with Abeta loading in brains.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
38
|
19835589
|
Herpes simplex virus type 2 tegument protein UL56 relocalizes ubiquitin ligase Nedd4 and has a role in transport and/or release of virions.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
39
|
17692845
|
Heregulin-induced epigenetic regulation of the utrophin-A promoter.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
40
|
22849377
|
Localisation and role of activin receptor-interacting protein 1 in mouse brain.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
41
|
16407196
|
Sodium butyrate ameliorates histone hypoacetylation and neurodegenerative phenotypes in a mouse model for DRPLA.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
42
|
11726694
|
The role of basal and myogenic factors in the transcriptional activation of utrophin promoter A: implications for therapeutic up-regulation in Duchenne muscular dystrophy.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
43
|
10652301
|
Utrophin transcription is activated by an intronic enhancer.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
44
|
22216264
|
Translational regulation of utrophin by miRNAs.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
45
|
7485154
|
Molecular cloning of a full-length cDNA for dentatorubral-pallidoluysian atrophy and regional expressions of the expanded alleles in the CNS.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
46
|
9738440
|
Fe65 and the protein network centered around the cytosolic domain of the Alzheimer's beta-amyloid precursor protein.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
47
|
16457992
|
Pathological pattern of Mdx mice diaphragm correlates with gradual expression of the short utrophin isoform Up71.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
48
|
26230628
|
Cis-Acting Sequence Elements and Upstream Open Reading Frame in Mouse Utrophin-A 5'-UTR Repress Cap-Dependent Translation.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
49
|
24706662
|
SETD2 mutations cooperate with chromosomal aberrations in leukemia.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|
50
|
20501857
|
Histone methyltransferase gene SETD2 is a novel tumor suppressor gene in clear cell renal cell carcinoma.
|
Pubmed
|
1.571E-4
|
6.685E-4
|
4.957E-3
|
1.464E-1
|
1
|
1
|