Cluster composition

Functions

Category	Name	IntersectionWithQuery	PValue	GenesInTerm	GenesInQuery	GenesInTermInQuery	ID
GeneOntologyMolecularFunction	ATP-dependent activity	ATP6V0A1 CENPE RTEL1 EIF4A3 CHD3 CHD4 SRCAP ACSL4 IFIH1 UBA7 KIF3B CLU ASCC3 DNAH8 CHD5 EIF4A2 DNAH17 ABCB11 ABCC12 MYO15A POLQ HSPA14 TOP2B	4.91e-08	614	198	23	GO:0140657
GeneOntologyMolecularFunction	helicase activity	RTEL1 EIF4A3 CHD3 CHD4 SRCAP IFIH1 ASCC3 CHD5 EIF4A2 POLQ	4.10e-06	158	198	10	GO:0004386
GeneOntologyMolecularFunction	ATP hydrolysis activity	RTEL1 EIF4A3 CHD3 CHD4 SRCAP IFIH1 KIF3B CLU ASCC3 DNAH8 CHD5 EIF4A2 ABCB11 ABCC12 POLQ HSPA14	8.89e-06	441	198	16	GO:0016887
GeneOntologyMolecularFunction	ATP-dependent activity, acting on DNA	RTEL1 CHD3 CHD4 SRCAP ASCC3 CHD5 POLQ TOP2B	3.97e-05	127	198	8	GO:0008094
GeneOntologyMolecularFunction	catalytic activity, acting on DNA	RTEL1 CHD3 CHD4 SRCAP ASCC3 POLK SETMAR CRY1 CHD5 POLQ TOP2B	6.43e-05	262	198	11	GO:0140097
GeneOntologyMolecularFunction	[heparan sulfate]-glucosamine 3-sulfotransferase 3 activity	HS3ST3B1 HS3ST3A1	9.78e-05	2	198	2	GO:0033872
GeneOntologyMolecularFunction	catalytic activity, acting on a nucleic acid	RTEL1 EIF4A3 CHD3 CHD4 SRCAP IFIH1 ASCC3 POLK EXOSC9 SETMAR DUS4L CRY1 CHD5 EIF4A2 RTCA POLQ TOP2B	2.48e-04	645	198	17	GO:0140640
GeneOntologyMolecularFunction	ATP-dependent chromatin remodeler activity	CHD3 CHD4 SRCAP CHD5	4.79e-04	37	198	4	GO:0140658
GeneOntologyBiologicalProcess	action potential initiation	SCN11A KCNQ2 KCNQ3	8.08e-06	5	194	3	GO:0099610
GeneOntologyBiologicalProcess	sensory perception	SCN11A PDE4A RPL38 OR4N4 OR4F4 RGS9 LRIT3 OR4F5 KCNQ2 KCNQ3 OR4F17 TRPM8 DIAPH3 OR4K15 OTOA OR4N2 TMC2 OR4N5 OR4K13 OR4M1 GRIN1 THRB TNF MYO15A SLC24A1 CFAP69	9.02e-06	1072	194	26	GO:0007600
GeneOntologyBiologicalProcess	excitatory chemical synaptic transmission	KCNQ2 KCNQ3 CHRDL1 GRIN1	1.26e-05	16	194	4	GO:0098976
Domain	CHD_N	CHD3 CHD4 CHD5	1.09e-06	3	193	3	IPR012958
Domain	CHD_C2	CHD3 CHD4 CHD5	1.09e-06	3	193	3	IPR012957
Domain	CHDCT2	CHD3 CHD4 CHD5	1.09e-06	3	193	3	PF08074
Domain	CHDNT	CHD3 CHD4 CHD5	1.09e-06	3	193	3	PF08073
Domain	DUF1086	CHD3 CHD4 CHD5	1.09e-06	3	193	3	IPR009462
Domain	DUF1087	CHD3 CHD4 CHD5	1.09e-06	3	193	3	IPR009463
Domain	DUF1087	CHD3 CHD4 CHD5	1.09e-06	3	193	3	PF06465
Domain	DUF1086	CHD3 CHD4 CHD5	1.09e-06	3	193	3	PF06461
Domain	DUF1087	CHD3 CHD4 CHD5	1.09e-06	3	193	3	SM01147
Domain	DUF1086	CHD3 CHD4 CHD5	1.09e-06	3	193	3	SM01146
Domain	Helicase_C	EIF4A3 CHD3 CHD4 SRCAP IFIH1 ASCC3 CHD5 EIF4A2 POLQ	1.67e-06	107	193	9	PF00271
Domain	HELICc	EIF4A3 CHD3 CHD4 SRCAP IFIH1 ASCC3 CHD5 EIF4A2 POLQ	1.67e-06	107	193	9	SM00490
Domain	Helicase_C	EIF4A3 CHD3 CHD4 SRCAP IFIH1 ASCC3 CHD5 EIF4A2 POLQ	1.81e-06	108	193	9	IPR001650
Domain	HELICASE_CTER	EIF4A3 CHD3 CHD4 SRCAP IFIH1 ASCC3 CHD5 EIF4A2 POLQ	1.95e-06	109	193	9	PS51194
Domain	HELICASE_ATP_BIND_1	EIF4A3 CHD3 CHD4 SRCAP IFIH1 ASCC3 CHD5 EIF4A2 POLQ	1.95e-06	109	193	9	PS51192
Domain	DEXDc	EIF4A3 CHD3 CHD4 SRCAP IFIH1 ASCC3 CHD5 EIF4A2 POLQ	1.95e-06	109	193	9	SM00487
Domain	Helicase_ATP-bd	EIF4A3 CHD3 CHD4 SRCAP IFIH1 ASCC3 CHD5 EIF4A2 POLQ	2.11e-06	110	193	9	IPR014001
Domain	ZF_ZZ_2	DMD UTRN CREBBP NBR1	3.02e-05	18	193	4	PS50135
Domain	ZF_ZZ_1	DMD UTRN CREBBP NBR1	3.02e-05	18	193	4	PS01357
Domain	ZZ	DMD UTRN CREBBP NBR1	3.02e-05	18	193	4	PF00569
Domain	Znf_ZZ	DMD UTRN CREBBP NBR1	3.79e-05	19	193	4	IPR000433
Domain	ZnF_ZZ	DMD UTRN CREBBP NBR1	3.79e-05	19	193	4	SM00291
Domain	KCNQC3-Ank-G_bd	KCNQ2 KCNQ3	1.06e-04	2	193	2	PF11956
Domain	Dystrophin	DMD UTRN	1.06e-04	2	193	2	IPR016344
Domain	Ankyrin-G_BS	KCNQ2 KCNQ3	1.06e-04	2	193	2	IPR020969
Domain	P-loop_NTPase	CENPE RTEL1 EIF4A3 CHD3 CHD4 SRCAP IFIH1 NWD2 KIF3B ASCC3 HS3ST3B1 HS3ST3A1 DNAH8 MRAS CHD5 EIF4A2 ABCB11 ABCC12 MYO15A POLQ NLRP4	1.91e-04	848	193	21	IPR027417
Domain	-	RTEL1 EIF4A3 CHD3 CHD4 SRCAP IFIH1 NWD2 ASCC3 HS3ST3B1 HS3ST3A1 DNAH8 MRAS CHD5 EIF4A2 ABCB11 ABCC12 MYO15A POLQ NLRP4	2.76e-04	746	193	19	3.40.50.300
Domain	Abhydrolase_1	ABHD12B ABHD2 LIPA ABHD13	2.80e-04	31	193	4	PF00561
Domain	SNF2_N	CHD3 CHD4 SRCAP CHD5	3.17e-04	32	193	4	IPR000330
Domain	SNF2_N	CHD3 CHD4 SRCAP CHD5	3.17e-04	32	193	4	PF00176
Domain	AB_hydrolase_1	ABHD12B ABHD2 LIPA ABHD13	3.58e-04	33	193	4	IPR000073
Domain	DNA/RNA_helicase_DEAH_CS	RTEL1 CHD3 CHD4 CHD5	4.50e-04	35	193	4	IPR002464
Domain	PI3/4_kinase_CS	PIK3C2A PI4KB PRKDC	4.51e-04	15	193	3	IPR018936
Domain	-	PIK3C2A PI4KB PRKDC	5.51e-04	16	193	3	1.10.1070.11
Domain	PI3Kc	PIK3C2A PI4KB PRKDC	5.51e-04	16	193	3	SM00146
Domain	DEAH_ATP_HELICASE	RTEL1 CHD3 CHD4 CHD5	6.20e-04	38	193	4	PS00690
Domain	PI3_PI4_kinase	PIK3C2A PI4KB PRKDC	7.91e-04	18	193	3	PF00454
Domain	PI3_4_KINASE_1	PIK3C2A PI4KB PRKDC	7.91e-04	18	193	3	PS00915
Domain	PI3_4_KINASE_2	PIK3C2A PI4KB PRKDC	7.91e-04	18	193	3	PS00916
Domain	PI3/4_kinase_cat_dom	PIK3C2A PI4KB PRKDC	7.91e-04	18	193	3	IPR000403
Domain	PI3_4_KINASE_3	PIK3C2A PI4KB PRKDC	7.91e-04	18	193	3	PS50290
Domain	ARM-type_fold	RALGAPA1 NBEAL1 NCBP1 PIK3C2A UTP20 DIAPH3 HEATR5B NBEA RALGAPA2 PRKDC CFAP69	8.28e-04	339	193	11	IPR016024
Domain	2Fe2S_fd_BS	NDUFS1 AOX1	1.04e-03	5	193	2	IPR006058
Domain	K_chnl_volt-dep_KCNQ_C	KCNQ2 KCNQ3	1.04e-03	5	193	2	IPR013821
Domain	Cyt_P450_E_grp-II	CYP3A7 CYP3A4	1.04e-03	5	193	2	IPR002402
Domain	K_chnl_volt-dep_KCNQ	KCNQ2 KCNQ3	1.04e-03	5	193	2	IPR003937
Domain	ThyrH_rcpt	THRA THRB	1.04e-03	5	193	2	IPR001728
Domain	DUF4704	NBEAL1 NBEA	1.04e-03	5	193	2	IPR031570
Domain	DUF4704	NBEAL1 NBEA	1.04e-03	5	193	2	PF15787
Domain	KCNQ_channel	KCNQ2 KCNQ3	1.04e-03	5	193	2	PF03520
Domain	2FE2S_FER_1	NDUFS1 AOX1	1.04e-03	5	193	2	PS00197
Domain	WW	STXBP4 DMD UTRN WWC1	1.39e-03	47	193	4	PF00397
Domain	WW	STXBP4 DMD UTRN WWC1	1.51e-03	48	193	4	SM00456
Domain	Cyt_P450_E_CYP3A	CYP3A7 CYP3A4	1.55e-03	6	193	2	IPR008072
Domain	2FE2S_FER_2	NDUFS1 AOX1	1.55e-03	6	193	2	PS51085
Domain	PH_BEACH	NBEAL1 NBEA	1.55e-03	6	193	2	PF14844
Domain	2Fe-2S_ferredoxin-type	NDUFS1 AOX1	1.55e-03	6	193	2	IPR001041
Domain	Fer2	NDUFS1 AOX1	1.55e-03	6	193	2	PF00111
Domain	EF-hand_dom_typ1	DMD UTRN	1.55e-03	6	193	2	IPR015153
Domain	EF-hand_dom_typ2	DMD UTRN	1.55e-03	6	193	2	IPR015154
Domain	EF-hand_2	DMD UTRN	1.55e-03	6	193	2	PF09068
Domain	EF-hand_3	DMD UTRN	1.55e-03	6	193	2	PF09069
Domain	ACTININ_2	DMD UTRN CLMN	1.65e-03	23	193	3	PS00020
Domain	ACTININ_1	DMD UTRN CLMN	1.65e-03	23	193	3	PS00019
Domain	Actinin_actin-bd_CS	DMD UTRN CLMN	1.65e-03	23	193	3	IPR001589
Domain	Chromo_domain	CHD3 CHD4 CHD5	1.87e-03	24	193	3	IPR023780
Domain	WW_DOMAIN_1	STXBP4 DMD UTRN WWC1	1.89e-03	51	193	4	PS01159
Domain	WW_DOMAIN_2	STXBP4 DMD UTRN WWC1	1.89e-03	51	193	4	PS50020
Domain	WW_dom	STXBP4 DMD UTRN WWC1	2.03e-03	52	193	4	IPR001202
Domain	Ephrin_rec_like	EPHB6 SCUBE1 EPHA5	2.11e-03	25	193	3	SM01411
Domain	Tyr-kin_ephrin_A/B_rcpt-like	EPHB6 SCUBE1 EPHA5	2.11e-03	25	193	3	IPR011641
Domain	Chromo	CHD3 CHD4 CHD5	2.37e-03	26	193	3	PF00385
Pubmed	The E3 ubiquitin ligase HECTD1 contributes to cell proliferation through an effect on mitosis.	CENPE RPN1 EIF4A3 NCBP1 CHD3 PRPF6 CHD4 LARP4 ZC3H11A ACAD11 UTP20 BOP1 ASCC3 MED17 SYNCRIP EXOSC9 IBTK STAU2 PRKDC HSPA14 TOP2B	3.89e-09	759	201	21	35915203
Pubmed	In-Depth In Vivo Crosslinking in Minutes by a Compact, Membrane-Permeable, and Alkynyl-Enrichable Crosslinker.	SCN11A ELOA2 ACACB RPN1 EIF4A3 DACT2 NCBP1 CHD3 PRPF6 CHD4 SRCAP NEB NDUFS1 TASOR2 ACSL4 FAM186A DIAPH3 DMD DNAH8 SYNCRIP RNF17 YY1 CHD5 EIF4A2 PRKDC POLQ CFAP69 TOP2B	2.14e-08	1442	201	28	35575683
Pubmed	Defining the membrane proteome of NK cells.	CENPE RPN1 EIF4A3 PRPF6 CHD4 LARP4 ACSL4 KIF3B PIK3C2A STAMBPL1 ASCC3 MED17 HEATR5B SYNCRIP DOCK10 LGALS8 CHD5 STAU2 APOL3 ABHD13 PRKDC NBR1 HSPA14	3.40e-07	1168	201	23	19946888
Pubmed	Adenovirus DNA binding protein interacts with the SNF2-related CBP activator protein (SrCap) and inhibits SrCap-mediated transcription.	SRCAP KAT2B CREBBP	7.57e-07	4	201	3	11581372
Pubmed	Proteomic profiling of VCP substrates links VCP to K6-linked ubiquitylation and c-Myc function.	RPL38 RPN1 EIF4A3 PRPF6 CHD4 SRCAP LARP4 NDUFS1 ACSL4 ZC3H11A PIK3C2A UTP20 BOP1 ASCC3 PPIH UTRN SYNCRIP ARHGAP23 DOCK10 CREBBP RTCA MRPS15 PRKDC TOP2B	1.18e-06	1353	201	24	29467282
Pubmed	Impaired plasma membrane localization of ubiquitin ligase complex underlies 3-M syndrome development.	EPHB6 RPN1 PRPF6 LARP4 SNX19 TASOR2 BOP1 DEUP1 EXOSC9 MTERF3 CCNB3 STAU2 MRPS15 POLQ	1.34e-06	496	201	14	31343991
Pubmed	Nuclear receptor coactivator ACTR is a novel histone acetyltransferase and forms a multimeric activation complex with P/CAF and CBP/p300.	KAT2B CREBBP THRA THRB	1.41e-06	15	201	4	9267036
Pubmed	The p300/YY1/miR-500a-5p/HDAC2 signalling axis regulates cell proliferation in human colorectal cancer.	RPN1 RPS6KA3 CHD3 CHD4 UTP20 DMD SYNCRIP EXOSC9 YY1 DENND4C PRKDC	1.48e-06	298	201	11	30737378
Pubmed	TNF-alpha regulates mouse fetal hepatic maturation induced by oncostatin M and extracellular matrices.	TAT ABCB11 TNF	1.89e-06	5	201	3	15349890
Pubmed	Identification of SUMO Binding Proteins Enriched after Covalent Photo-Cross-Linking.	RPS6KA3 CHD3 PRPF6 CHD4 SRCAP S100A10 ZC3H11A SYNCRIP EXOSC9 EIF4A2 PRKDC	4.17e-06	332	201	11	32786267
Pubmed	TNF-α inhibits glucocorticoid receptor-induced gene expression by reshaping the GR nuclear cofactor profile.	ELOA2 ACACB NEB NDUFS1 PLEKHH1 ACSL4 ACAD11 PI4KB SYPL1 MED17 NBEA CREBBP PREPL APOL3 TNF	5.23e-06	638	201	15	31182584
Pubmed	L-arginine decreases inflammation and modulates the nuclear factor-kappaB/matrix metalloproteinase cascade in mdx muscle fibers.	DMD UTRN TNF	1.04e-05	8	201	3	18458097
Pubmed	TRAM-1, A novel 160-kDa thyroid hormone receptor activator molecule, exhibits distinct properties from steroid receptor coactivator-1.	KAT2B CREBBP THRB	1.56e-05	9	201	3	9346901
Pubmed	HDLBP Promotes Hepatocellular Carcinoma Proliferation and Sorafenib Resistance by Suppressing Trim71-dependent RAF1 Degradation.	RPN1 RPS6KA3 NCBP1 CHD3 PRPF6 CHD4 LARP4 PRKD3 ACSL4 LENG8 S100A10 ACAD11 PIK3C2A BOP1 ASCC3 PPIH EXOSC9 LGALS8 IBTK C3P1 STAU2 HSPA14	1.63e-05	1371	201	22	36244648
Pubmed	New roles for the de-ubiquitylating enzyme OTUD4 in an RNA-protein network and RNA granules.	RALGAPA1 EIF4A3 NCBP1 PRKD3 LENG8 ZC3H11A KIF3B KCNQ2 ASCC3 SYNCRIP EIF4A2 STAU2	1.77e-05	462	201	12	31138677
Pubmed	Systematic analysis of the protein interaction network for the human transcription machinery reveals the identity of the 7SK capping enzyme.	RPL38 EIF4A3 NCBP1 PRPF6 SRCAP KAT2B MED17 PPIH SYNCRIP ARHGAP23 EIF4A2	1.88e-05	390	201	11	17643375
Pubmed	Chr21 protein-protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer's disease.	EPHB6 ATP6V0A1 EIF4A3 NCBP1 CHD4 KDM6B PLEKHH1 S100A10 UBA7 CLU KLHL7 KCNQ2 STAMBPL1 UTRN EXOSC9 SETMAR NBEA CREBBP PREPL EIF4A2 PRKDC	1.97e-05	1285	201	21	35914814
Pubmed	A role of DNA-PK for the metabolic gene regulation in response to insulin.	KAT2B PRKDC TOP2B	2.21e-05	10	201	3	19303849
Pubmed	mRNA export through an additional cap-binding complex consisting of NCBP1 and NCBP3.	EIF4A3 NCBP1 LENG8	2.21e-05	10	201	3	26382858
Pubmed	Systematic bromodomain protein screens identify homologous recombination and R-loop suppression pathways involved in genome integrity.	CHD3 CHD4 SRCAP ZNF518A KAT2B ACAD11 CLU ASCC3 PPIH WWC1 ARHGAP23 AOX1 ECT2L RALGAPA2 YY1 CREBBP THRA CCNB3 CHD5	2.87e-05	1116	201	19	31753913
Pubmed	Functional proteomics establishes the interaction of SIRT7 with chromatin remodeling complexes and expands its role in regulation of RNA polymerase I transcription.	RPL38 NCBP1 PRPF6 CHD4 LARP4 NDUFS1 TASOR2 ZC3H11A UTP20 BOP1 ASCC3 UTRN SYNCRIP PRKDC	3.00e-05	653	201	14	22586326
Pubmed	Interactomes of Glycogen Synthase Kinase-3 Isoforms.	KIAA0586 ASCC3 UTRN WWC1 DENND4C IBTK STAU2 NBR1	3.17e-05	209	201	8	36779422
Pubmed	Decreased myocardial nNOS, increased iNOS and abnormal ECGs in mouse models of Duchenne muscular dystrophy.	DMD UTRN	3.32e-05	2	201	2	10525423
Pubmed	Neurodevelopmental control by thyroid hormone receptors.	THRA THRB	3.32e-05	2	201	2	11861164
Pubmed	Digging Deeper into CYP3A Testosterone Metabolism: Kinetic, Regioselectivity, and Stereoselectivity Differences between CYP3A4/5 and CYP3A7.	CYP3A7 CYP3A4	3.32e-05	2	201	2	28986474
Pubmed	Fundamentally distinct roles of thyroid hormone receptor isoforms in a thyrotroph cell line are due to differential DNA binding.	THRA THRB	3.32e-05	2	201	2	22570333
Pubmed	Divergent roles for thyroid hormone receptor beta isoforms in the endocrine axis and auditory system.	THRA THRB	3.32e-05	2	201	2	10430610
Pubmed	In Vivo Genome Editing Restores Dystrophin Expression and Cardiac Function in Dystrophic Mice.	DMD UTRN	3.32e-05	2	201	2	28790199
Pubmed	Individual functions of the histone acetyl transferases CBP and p300 in regulating the inflammatory response of synovial fibroblasts.	KAT2B CREBBP	3.32e-05	2	201	2	34304080
Pubmed	COG complex-mediated recycling of Golgi glycosyltransferases is essential for normal protein glycosylation.	COG3 COG7	3.32e-05	2	201	2	16420527
Pubmed	Audiogenic seizure susceptibility in thyroid hormone receptor beta-deficient mice.	THRA THRB	3.32e-05	2	201	2	11496110
Pubmed	KCNQ channels show conserved ethanol block and function in ethanol behaviour.	KCNQ2 KCNQ3	3.32e-05	2	201	2	23209695
Pubmed	Reconstitution of muscarinic modulation of the KCNQ2/KCNQ3 K(+) channels that underlie the neuronal M current.	KCNQ2 KCNQ3	3.32e-05	2	201	2	10684873
Pubmed	Does diacylglycerol regulate KCNQ channels?	KCNQ2 KCNQ3	3.32e-05	2	201	2	16721610
Pubmed	Mutant thyroid hormone receptors (TRs) isolated from distinct cancer types display distinct target gene specificities: a unique regulatory repertoire associated with two renal clear cell carcinomas.	THRA THRB	3.32e-05	2	201	2	21622534
Pubmed	Correlation of Utrophin Levels with the Dystrophin Protein Complex and Muscle Fibre Regeneration in Duchenne and Becker Muscular Dystrophy Muscle Biopsies.	DMD UTRN	3.32e-05	2	201	2	26974331
Pubmed	Mice devoid of all known thyroid hormone receptors are viable but exhibit disorders of the pituitary-thyroid axis, growth, and bone maturation.	THRA THRB	3.32e-05	2	201	2	10346821
Pubmed	Apo-dystrophin-1 and apo-dystrophin-2, products of the Duchenne muscular dystrophy locus: expression during mouse embryogenesis and in cultured cell lines.	DMD UTRN	3.32e-05	2	201	2	7987307
Pubmed	Comparative analysis of the human dystrophin and utrophin gene structures.	DMD UTRN	3.32e-05	2	201	2	11861579
Pubmed	Distinct mechanical properties in homologous spectrin-like repeats of utrophin.	DMD UTRN	3.32e-05	2	201	2	30914715
Pubmed	Haploinsufficiency of utrophin gene worsens skeletal muscle inflammation and fibrosis in mdx mice.	DMD UTRN	3.32e-05	2	201	2	17889902
Pubmed	Ventilatory dysfunction in mdx mice: impact of tumor necrosis factor-alpha deletion.	DMD TNF	3.32e-05	2	201	2	12929194
Pubmed	Impaired hair growth and wound healing in mice lacking thyroid hormone receptors.	THRA THRB	3.32e-05	2	201	2	25254665
Pubmed	Altered pathological progression of diaphragm and quadriceps muscle in TNF-deficient, dystrophin-deficient mice.	DMD TNF	3.32e-05	2	201	2	11053690
Pubmed	Characterization of the Ang/Tie2 Signaling Pathway in the Diaphragm Muscle of DMD Mice.	DMD UTRN	3.32e-05	2	201	2	37626761
Pubmed	Naturally Occurring Amino Acids in Helix 10 of the Thyroid Hormone Receptor Mediate Isoform-Specific TH Gene Regulation.	THRA THRB	3.32e-05	2	201	2	28911178
Pubmed	Hormone selectivity in thyroid hormone receptors.	THRA THRB	3.32e-05	2	201	2	11222741
Pubmed	The N- and C-Terminal Domains Differentially Contribute to the Structure and Function of Dystrophin and Utrophin Tandem Calponin-Homology Domains.	DMD UTRN	3.32e-05	2	201	2	26516677
Pubmed	Assessment of cardiac function in three mouse dystrophinopathies by magnetic resonance imaging.	DMD UTRN	3.32e-05	2	201	2	22209498
Pubmed	Prevention of the dystrophic phenotype in dystrophin/utrophin-deficient muscle following adenovirus-mediated transfer of a utrophin minigene.	DMD UTRN	3.32e-05	2	201	2	10694796
Pubmed	The major dermatomyositis-specific Mi-2 autoantigen is a presumed helicase involved in transcriptional activation.	CHD3 CHD4	3.32e-05	2	201	2	7575689
Pubmed	Effects of thyroid hormone receptor gene disruption on myosin isoform expression in mouse skeletal muscles.	THRA THRB	3.32e-05	2	201	2	10848522
Pubmed	Increased adipogenesis in bone marrow but decreased bone mineral density in mice devoid of thyroid hormone receptors.	THRA THRB	3.32e-05	2	201	2	15780976
Pubmed	Conditional transgenic suppression of M channels in mouse brain reveals functions in neuronal excitability, resonance and behavior.	KCNQ2 KCNQ3	3.32e-05	2	201	2	15608631
Pubmed	Enhanced currents through L-type calcium channels in cardiomyocytes disturb the electrophysiology of the dystrophic heart.	DMD UTRN	3.32e-05	2	201	2	24337461
Pubmed	Activation of calcineurin and stress activated protein kinase/p38-mitogen activated protein kinase in hearts of utrophin-dystrophin knockout mice.	DMD UTRN	3.32e-05	2	201	2	11297940
Pubmed	Benign neonatal sleep myoclonus: an autosomal dominant form not allelic to KCNQ2 or KCNQ3.	KCNQ2 KCNQ3	3.32e-05	2	201	2	22447848
Pubmed	Identification by mass spectrometry and functional characterization of two phosphorylation sites of KCNQ2/KCNQ3 channels.	KCNQ2 KCNQ3	3.32e-05	2	201	2	16319223
Pubmed	TRα protects against atherosclerosis in male mice: identification of a novel anti-inflammatory property for TRα in mice.	THRA THRB	3.32e-05	2	201	2	24797634
Pubmed	Human muscle-derived cell populations isolated by differential adhesion rates: phenotype and contribution to skeletal muscle regeneration in Mdx/SCID mice.	DMD PRKDC	3.32e-05	2	201	2	21854253
Pubmed	Rescue of severely affected dystrophin/utrophin-deficient mice through scAAV-U7snRNA-mediated exon skipping.	DMD UTRN	3.32e-05	2	201	2	22388933
Pubmed	Suppression of the deafness and thyroid dysfunction in Thrb-null mice by an independent mutation in the Thra thyroid hormone receptor alpha gene.	THRA THRB	3.32e-05	2	201	2	11726557
Pubmed	Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy.	KCNQ2 KCNQ3	3.32e-05	2	201	2	9872318
Pubmed	Development and validation of a medium-throughput electrophysiological assay for KCNQ2/3 channel openers using QPatch HT.	KCNQ2 KCNQ3	3.32e-05	2	201	2	23002961
Pubmed	Utrophin Compensates dystrophin Loss during Mouse Spermatogenesis.	DMD UTRN	3.32e-05	2	201	2	28785010
Pubmed	Restoration of all dystrophin protein interactions by functional domains in trans does not rescue dystrophy.	DMD UTRN	3.32e-05	2	201	2	16307000
Pubmed	Expression of the dystrophin isoform Dp116 preserves functional muscle mass and extends lifespan without preventing dystrophy in severely dystrophic mice.	DMD UTRN	3.32e-05	2	201	2	21949353
Pubmed	Dystrophin and utrophin "double knockout" dystrophic mice exhibit a spectrum of degenerative musculoskeletal abnormalities.	DMD UTRN	3.32e-05	2	201	2	23097179
Pubmed	The role of utrophin and Dp71 for assembly of different dystrophin-associated protein complexes (DPCs) in the choroid plexus and microvasculature of the brain.	DMD UTRN	3.32e-05	2	201	2	15501597
Pubmed	Establishment of yeast reporter assay systems to detect ligands of thyroid hormone receptors alpha and beta.	THRA THRB	3.32e-05	2	201	2	19853653
Pubmed	Locomotor deficiencies and aberrant development of subtype-specific GABAergic interneurons caused by an unliganded thyroid hormone receptor alpha1.	THRA THRB	3.32e-05	2	201	2	18287507
Pubmed	Systemic human minidystrophin gene transfer improves functions and life span of dystrophin and dystrophin/utrophin-deficient mice.	DMD UTRN	3.32e-05	2	201	2	18973234
Pubmed	The two major isoforms of thyroid hormone receptor, TRα1 and TRβ1, preferentially partner with distinct panels of auxiliary proteins.	THRA THRB	3.32e-05	2	201	2	24325866
Pubmed	Serum TNF-α Level as a Possible Predictor of Inhibitor Levels in Severe Hemophilia A.	F8 TNF	3.32e-05	2	201	2	34778454
Pubmed	Retardation of post-natal development caused by a negatively acting thyroid hormone receptor alpha1.	THRA THRB	3.32e-05	2	201	2	12356724
Pubmed	The T3R alpha gene encoding a thyroid hormone receptor is essential for post-natal development and thyroid hormone production.	THRA THRB	3.32e-05	2	201	2	9250685
Pubmed	Renin-angiotensin-aldosterone system inhibitors improve membrane stability and change gene-expression profiles in dystrophic skeletal muscles.	DMD UTRN	3.32e-05	2	201	2	27881412
Pubmed	Blockade of tumor necrosis factor in collagen-induced arthritis reveals a novel immunoregulatory pathway for Th1 and Th17 cells.	TNF PRKDC	3.32e-05	2	201	2	18936235
Pubmed	Expression of CYP3A4 and CYP3A7 in Human Foetal Tissues and its Correlation with Nuclear Receptors.	CYP3A7 CYP3A4	3.32e-05	2	201	2	25689036
Pubmed	Utrophin influences mitochondrial pathology and oxidative stress in dystrophic muscle.	DMD UTRN	3.32e-05	2	201	2	29065908
Pubmed	Stabilization of the cardiac sarcolemma by sarcospan rescues DMD-associated cardiomyopathy.	DMD UTRN	3.32e-05	2	201	2	31039133
Pubmed	Dystrophin and dystrophin-related protein in the brains of normal and mdx mice.	DMD UTRN	3.32e-05	2	201	2	8159184
Pubmed	Dystrophin and utrophin: genetic analyses of their role in skeletal muscle.	DMD UTRN	3.32e-05	2	201	2	10679963
Pubmed	TAT-μUtrophin mitigates the pathophysiology of dystrophin and utrophin double-knockout mice.	DMD UTRN	3.32e-05	2	201	2	21565990
Pubmed	Immunohistochemical markers of CYP3A4 and CYP3A7: a new tool towards personalized pharmacotherapy of hepatocellular carcinoma.	CYP3A7 CYP3A4	3.32e-05	2	201	2	27349315
Pubmed	Isometric force and endurance in skeletal muscle of mice devoid of all known thyroid hormone receptors.	THRA THRB	3.32e-05	2	201	2	12562961
Pubmed	The c-erb-A gene encodes a thyroid hormone receptor.	THRA THRB	3.32e-05	2	201	2	2879243
Pubmed	Distinct behavioral phenotypes in male mice lacking the thyroid hormone receptor α1 or β isoforms.	THRA THRB	3.32e-05	2	201	2	23567476
Pubmed	Novel non-genomic signaling of thyroid hormone receptors in thyroid carcinogenesis.	THRA THRB	3.32e-05	2	201	2	19549593
Pubmed	Dystrophin and dystrophin-related protein (utrophin) distribution in normal and dystrophin-deficient skeletal muscles.	DMD UTRN	3.32e-05	2	201	2	8186702
Pubmed	Contemporary cardiac issues in Duchenne muscular dystrophy. Working Group of the National Heart, Lung, and Blood Institute in collaboration with Parent Project Muscular Dystrophy.	DMD UTRN	3.32e-05	2	201	2	25940966
Pubmed	KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes.	KCNQ2 KCNQ3	3.32e-05	2	201	2	18625963
Pubmed	Cardiac dysfunction and pathology in the dystrophin and utrophin-deficient mouse during development of dilated cardiomyopathy.	DMD UTRN	3.32e-05	2	201	2	22266080
Pubmed	Postnatal overexpression of the CT GalNAc transferase inhibits muscular dystrophy in mdx mice without altering muscle growth or neuromuscular development: evidence for a utrophin-independent mechanism.	DMD UTRN	3.32e-05	2	201	2	17300937
Pubmed	Transcriptional activity of multiple copies of a subtelomerically located olfactory receptor gene that is polymorphic in number and location.	OR4F4 OR4F17	3.32e-05	2	201	2	11689484
Pubmed	Comparative sequencing of a multicopy subtelomeric region containing olfactory receptor genes reveals multiple interactions between non-homologous chromosomes.	OR4F4 OR4F17	3.32e-05	2	201	2	11689483
Pubmed	Gestational di-(2-ethylhexyl) phthalate exposure causes fetal intrauterine growth restriction through disturbing placental thyroid hormone receptor signaling.	THRA THRB	3.32e-05	2	201	2	29753845
Pubmed	Corticostriatal plasticity is necessary for learning intentional neuroprosthetic skills.	RGS9 GRIN1	3.32e-05	2	201	2	22388818
Pubmed	Early treatment with lisinopril and spironolactone preserves cardiac and skeletal muscle in Duchenne muscular dystrophy mice.	DMD UTRN	3.32e-05	2	201	2	21768542
Pubmed	Thyroxine-thyroid hormone receptor interactions.	THRA THRB	3.32e-05	2	201	2	15466465
GeneFamily	Olfactory receptors, family 4	OR4N4 OR4F4 OR4F5 OR4F17 OR4K15 OR4N2 OR4N5 OR4K13 OR4M1	7.66e-07	129	141	9	151
GeneFamily	Zinc fingers ZZ-type\|Lysine acetyltransferases	DMD UTRN CREBBP NBR1	9.96e-06	18	141	4	91
GeneFamily	PHD finger proteins\|NuRD complex	CHD3 CHD4 CHD5	9.70e-05	12	141	3	1305
GeneFamily	Abhydrolase domain containing	ABHD12B ABHD2 ABHD13	6.41e-04	22	141	3	4
GeneFamily	Components of oligomeric golgi complex	COG3 COG7	1.64e-03	8	141	2	493
GeneFamily	Cytochrome P450 family 3	CYP3A7 CYP3A4	1.64e-03	8	141	2	1002
GeneFamily	WD repeat domain containing\|BEACH domain containing	NBEAL1 NBEA	2.10e-03	9	141	2	1230
GeneFamily	X-linked mental retardation\|RNA helicases	IFIH1 ASCC3	3.17e-03	11	141	2	1168
Coexpression	HOELZEL_NF1_TARGETS_UP	TRAF3IP2 RPS6KA3 S100A10 ACAD11 STAMBPL1 HS3ST3B1 HS3ST3A1 GSAP CCNB3	1.38e-06	141	199	9	M2142
Drug	telithromycin	CYP3A4 THRA ABCB11 TNF	1.90e-07	7	198	4	ctd:C106791
Drug	desethylamiodarone	CYP3A4 THRA THRB TNF	3.73e-06	13	198	4	ctd:C036116
Disease	Glioblastoma Multiforme	EPHB6 RPS6KA3 INSRR PRKD3 POLK DEUP1 NLK	5.99e-06	111	182	7	C1621958
Disease	intellectual disability (is_implicated_in)	EIF4A3 RPS6KA3 ACSL4 DMD	3.39e-05	30	182	4	DOID:1059 (is_implicated_in)
Disease	Stevens-Johnson syndrome (is_marker_for)	CLU TNF	3.78e-05	2	182	2	DOID:0050426 (is_marker_for)
Disease	Benign neonatal seizures	KCNQ2 KCNQ3	3.78e-05	2	182	2	cv:C0220669
Disease	benign neonatal seizures (implicated_via_orthology)	KCNQ2 KCNQ3	3.78e-05	2	182	2	DOID:14264 (implicated_via_orthology)
Disease	Intellectual Disability	RALGAPA1 EIF4A3 GON4L CHD3 KDM6B ASCC3 TAT NBEA GRIN1 YY1 PREPL	1.12e-04	447	182	11	C3714756
Disease	thyroid hormone resistance syndrome (implicated_via_orthology)	THRA THRB	1.13e-04	3	182	2	DOID:11633 (implicated_via_orthology)
Disease	benign neonatal seizures (is_implicated_in)	KCNQ2 KCNQ3	1.13e-04	3	182	2	DOID:14264 (is_implicated_in)
Disease	cicatricial pemphigoid (is_marker_for)	CLU TNF	1.13e-04	3	182	2	DOID:11656 (is_marker_for)
Disease	tacrolimus measurement	CYP3A7 CYP3A4	2.25e-04	4	182	2	EFO_0008458
Disease	Generalized Thyroid Hormone Resistance	THRA THRB	2.25e-04	4	182	2	C4722330
Disease	estrone conjugate measurement	CYP3A7 CYP3A4	2.25e-04	4	182	2	EFO_0007971
Disease	tauro-beta-muricholate measurement	CYP3A7 CYP3A4	3.74e-04	5	182	2	EFO_0800213
Disease	glyco-beta-muricholate measurement	CYP3A7 CYP3A4	3.74e-04	5	182	2	EFO_0800569
Disease	Adenoid Cystic Carcinoma	INSRR KDM6B SRCAP CREBBP PRKDC	3.96e-04	100	182	5	C0010606
Disease	dehydroisoandrosterone sulfate DHEA-S measurement	CYP3A7 CYP3A4	5.58e-04	6	182	2	EFO_0021119
Disease	Familial benign neonatal epilepsy	KCNQ2 KCNQ3	5.58e-04	6	182	2	C0220669
Disease	androstenediol (3beta,17beta) monosulfate (1) measurement	CYP3A7 CYP3A4	5.58e-04	6	182	2	EFO_0800294
Disease	X-24574 measurement	CYP3A7 CYP3A4	7.79e-04	7	182	2	EFO_0800897
Disease	Alzheimer disease	FBXO40 PRKD3 CLU SYPL1 WWC1 CASS4 ECHDC3 FAR2 CLMN MYO15A	9.09e-04	485	182	10	MONDO_0004975
Disease	Mental Retardation, X-Linked 1	RPS6KA3 ACSL4 DMD	1.00e-03	32	182	3	C2931498
Disease	Cholestasis of pregnancy	ABCB11 TNF	1.03e-03	8	182	2	C0268318
Disease	Ventricular Dysfunction	DMD TNF	1.03e-03	8	182	2	C0242973
Disease	cystic fibrosis (implicated_via_orthology)	ABCB11 ABCC12	1.32e-03	9	182	2	DOID:1485 (implicated_via_orthology)
Disease	androstenediol (3beta,17beta) disulfate (1) measurement	CYP3A7 CYP3A4	1.32e-03	9	182	2	EFO_0800278
Disease	egg allergy measurement	COG7 ABCB11	1.32e-03	9	182	2	EFO_0007018
Disease	4-androsten-3alpha,17alpha-diol monosulfate (3) measurement	CYP3A7 CYP3A4	1.65e-03	10	182	2	EFO_0022090
Disease	5alpha-androstan-3beta,17alpha-diol disulfate measurement	CYP3A7 CYP3A4	1.65e-03	10	182	2	EFO_0800289
Disease	long QT syndrome (implicated_via_orthology)	KCNQ2 KCNQ3	1.65e-03	10	182	2	DOID:2843 (implicated_via_orthology)
Disease	Adenocarcinoma of lung (disorder)	INSRR ACSL4 CREBBP PRKDC PSKH2 EPHA5	1.81e-03	206	182	6	C0152013
Disease	DNA repair protein RAD51 homolog 4 measurement	CYP3A7 CYP3A4	2.01e-03	11	182	2	EFO_0801531
Disease	Macrocephaly	CHD3 THRA	2.01e-03	11	182	2	C0221355
Disease	nucleus accumbens volume change measurement	WWC1 ECHDC3	2.01e-03	11	182	2	EFO_0021493
Disease	androstenediol (3beta,17beta) monosulfate (2) measurement	CYP3A7 CYP3A4	2.01e-03	11	182	2	EFO_0800295
Disease	Diaphragmatic Hernia	THRA THRB TNF	2.07e-03	41	182	3	C0019284
Disease	Night blindness, congenital stationary, type 1	LRIT3 SLC24A1	2.40e-03	12	182	2	C3501847
Disease	Night Blindness, Congenital Stationary, Type 1A	LRIT3 SLC24A1	2.40e-03	12	182	2	C3495587
Disease	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)	LRIT3 SLC24A1	2.40e-03	12	182	2	C1864877
Disease	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B	LRIT3 SLC24A1	2.40e-03	12	182	2	C1850362
Disease	X-Linked Csnb	LRIT3 SLC24A1	2.40e-03	12	182	2	C3711543
Disease	Trigeminal Neuralgia	GRIN1 TNF	2.40e-03	12	182	2	C0040997
Disease	fructose measurement, glucose measurement, galactose measurement	THRB FAR2	2.40e-03	12	182	2	EFO_0004468, EFO_0010477, EFO_0010481
Disease	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A	LRIT3 SLC24A1	2.40e-03	12	182	2	C1848172
Disease	Secondary Trigeminal Neuralgia	GRIN1 TNF	2.40e-03	12	182	2	C0393787
Disease	Trigeminal Neuralgia, Idiopathic	GRIN1 TNF	2.40e-03	12	182	2	C0393786
Disease	5alpha-androstan-3beta,17beta-diol monosulfate (2) measurement	CYP3A7 CYP3A4	2.40e-03	12	182	2	EFO_0800291
Disease	acute myeloid leukemia (implicated_via_orthology)	CREBBP TOP2B	2.40e-03	12	182	2	DOID:9119 (implicated_via_orthology)
Disease	fatty acid measurement, fetal genotype effect measurement, breast milk measurement	COG3 DIAPH3	2.82e-03	13	182	2	EFO_0005110, EFO_0007959, EFO_0009092
Disease	Fulminant Hepatic Failure with Cerebral Edema	TNF PRKDC	2.82e-03	13	182	2	C0751197
Disease	Hepatic Stupor	TNF PRKDC	2.82e-03	13	182	2	C0751198
Disease	Cone-rod synaptic disorder, congenital nonprogressive	LRIT3 SLC24A1	2.82e-03	13	182	2	C4041558
Disease	Hepatic Encephalopathy	TNF PRKDC	2.82e-03	13	182	2	C0019151
Disease	Hepatic Coma	TNF PRKDC	2.82e-03	13	182	2	C0019147
Disease	developmental and epileptic encephalopathy (implicated_via_orthology)	KCNQ2 KCNQ3	2.82e-03	13	182	2	DOID:0112202 (implicated_via_orthology)
Disease	androstenediol (3alpha, 17alpha) monosulfate (3) measurement	CYP3A7 CYP3A4	2.82e-03	13	182	2	EFO_0800293
Disease	5alpha-pregnan-3beta,20beta-diol monosulfate (1) measurement	CYP3A7 CYP3A4	2.82e-03	13	182	2	EFO_0800284
Disease	Endogenous depression	ACSL4 S100A10 CREBBP	2.88e-03	46	182	3	C0011573
Disease	Amyotrophic Lateral Sclerosis, Familial	CLU CREBBP TNF	3.26e-03	48	182	3	C4551993
Disease	Amyotrophic Lateral Sclerosis, Sporadic	CLU CREBBP TNF	3.26e-03	48	182	3	C1862941
Disease	Kawasaki disease (is_marker_for)	CLU TNF	3.28e-03	14	182	2	DOID:13378 (is_marker_for)
Disease	silicosis (biomarker_via_orthology)	RTEL1 TNF	3.28e-03	14	182	2	DOID:10325 (biomarker_via_orthology)
Disease	beta-hydroxyisovalerate measurement	PLEKHG5 S100A10	3.28e-03	14	182	2	EFO_0800125
Disease	X-21470 measurement	CYP3A7 CYP3A4	3.28e-03	14	182	2	EFO_0800817
Disease	fatty acid measurement, breast milk measurement, parental genotype effect measurement	COG3 DIAPH3	3.28e-03	14	182	2	EFO_0005110, EFO_0005939, EFO_0009092
Disease	Arthritis, Psoriatic	TRAF3IP2 TNF	3.28e-03	14	182	2	C0003872
Disease	5alpha-androstan-3alpha,17alpha-diol monosulfate measurement	CYP3A7 CYP3A4	3.28e-03	14	182	2	EFO_0800283
Disease	AMYOTROPHIC LATERAL SCLEROSIS 1	CLU CREBBP TNF	3.66e-03	50	182	3	C1862939
Disease	16a-hydroxy DHEA 3-sulfate measurement	CYP3A7 CYP3A4	3.77e-03	15	182	2	EFO_0800301
Disease	X-21410 measurement	CYP3A7 CYP3A4	4.29e-03	16	182	2	EFO_0800813
Disease	Seasonal Affective Disorder	PDE4A CRY1	4.29e-03	16	182	2	C0085159
Disease	Drug-induced agranulocytosis	HS3ST3A1 GSAP	4.29e-03	16	182	2	HP_0012235
Disease	andro steroid monosulfate C19H28O6S (1) measurement	CYP3A7 CYP3A4	4.29e-03	16	182	2	EFO_0800305
Disease	Vitiligo	IFIH1 TNF	4.84e-03	17	182	2	C0042900
Disease	Night blindness, congenital stationary	LRIT3 SLC24A1	4.84e-03	17	182	2	C0339535
Disease	Psoriasis	TRAF3IP2 IFIH1 TNF	5.29e-03	57	182	3	C0033860
Disease	Pustulosis of Palms and Soles	TRAF3IP2 IFIH1 TNF	5.29e-03	57	182	3	C0030246
Disease	alcoholic hepatitis (biomarker_via_orthology)	ABCB11 TNF	5.42e-03	18	182	2	DOID:12351 (biomarker_via_orthology)
Disease	5alpha-androstan-3alpha,17beta-diol monosulfate (1) measurement	CYP3A7 CYP3A4	5.42e-03	18	182	2	EFO_0800288
Disease	testosterone measurement	CYP3A7 PDE4A CENPE CYP3A4 KDM6B SRCAP LARP4 KAT2B FAM186A CHRDL1 UTRN MRAS C3P1 THRB MYO15A SLC24A1	5.73e-03	1275	182	16	EFO_0004908
Disease	metabolonic lactone sulfate measurement	CYP3A7 CYP3A4	6.04e-03	19	182	2	EFO_0800659
Disease	thrombin activatable fibrinolysis inhibitor activation peptide measurement	OTOA DOCK10	6.04e-03	19	182	2	EFO_0008582
Disease	anorectal malformation	RTEL1 CLU	6.04e-03	19	182	2	MONDO_0019938
Disease	etiocholanolone glucuronide measurement	CYP3A7 CYP3A4	6.04e-03	19	182	2	EFO_0800362

Protein segments in the cluster

Peptide	Gene	Start	Entry
VFEPLSMNLREVLKK	PRPF4B	766	Q13523
PDFSLFDVVLKMRKQ	PTPN18	256	Q99952
FDVVLKMRKQRPAAV	PTPN18	261	Q99952
VMTRPDLDKTKIFLF	ABHD13	176	Q7L211
FIPSLVEKEKVSRMV	BOP1	246	Q14137
AANAMKLERFEIPIK	ACSL4	656	O60488
MESKFREKLEPKIRE	ESYT3	136	A0FGR9
PLFDSVIKKMEAAIR	ARSH	501	Q5FYA8
TVVIEDIKKMCRVLP	ATG4A	176	Q8WYN0
MPKVLRDVEALKQEA	COG7	66	P83436
ARMLPEDIKRFASIV	CASS4	566	Q9NQ75
EDERIFPKSKVTDIM	CXorf58	161	Q96LI9
IVPLAKRVDKFRQFM	CSGALNACT1	266	Q8TDX6
VFKNMPAKTELIVRV	CHD5	936	Q8TDI0
PLETAMLKRAKELFT	BCAR3	531	O75815
PKSLSEKRENVMFVL	ABHD2	356	P08910
SEVIKAQVKDLMIPR	DYNLT5	111	Q8N7M0
SRPKFDEIVNMLDKL	EPHA5	921	P54756
IFLDRLKPMFSKQTI	FAM220A	211	Q7Z4H9
TLMDALRKDKIIFPN	ABHD12B	271	Q7Z5M8
FDIVKNPMDLSTIKR	CREBBP	1126	Q92793
KEIPMERVIAAAKQA	ABCB11	1181	O95342
LKTIEKCREMIPAFR	ECT2L	671	Q008S8
FKRELKTKEPVIMST	DMD	2851	P11532
IKEPERKIKELFSVM	DEUP1	321	Q05D60
APLREKDFSIKKEMV	DIAPH3	141	Q9NSV4
EIAMIKVAAPRAVSK	ACAD11	706	Q709F0
FFEVAKIPALDMLKL	CCNB3	1366	Q8WWL7
LTPEKIRMACEDKFT	AOX1	1306	Q06278
RKIANIERFVKIPEM	NWD2	261	Q9ULI1
VMNKSPAAKEVFKER	NBEAL1	386	Q6ZS30
LRVKDRESFPMILVA	MRAS	111	O14807
RMKIELFADVVPKTA	PPIH	26	O43447
IVAPRMLVDFLSEKK	OR4N4C	76	A0A096LPK9
RPRMAFLQKIEALVK	RGS9	11	O75916
RDFKNKMLPLLEVAE	OLFML3	56	Q9NRN5
SILKTLFEVMATKPE	ZFYVE28	751	Q9HCC9
VKDFNREKLPLMIFA	ACACB	2141	O00763
SLKRVEMKIRPEDFK	ANGPTL7	331	O43827
KFPEILLQAASKMAR	OTOA	781	Q7RTW8
LMEKLFRTSPDLKVI	FAR2	26	Q96K12
FLRAIKATPMAVADV	FAR2	261	Q96K12
AAKKVAPLMAKAIRD	ELOA2	731	Q8IYF1
VEVFPLKARKSMERE	FAM171A1	461	Q5VUB5
KKPFAIKVMETRERE	PSKH2	86	Q96QS6
AAVMAVIAKTPALRK	GPR61	61	Q9BZJ8
AMSKDTKLIVVVRDP	HS3ST3B1	216	Q9Y662
SDMAKKTFNPIRAIV	TAT	46	P17735
PKFVREVLEKCMRLS	NCBP1	446	Q09161
RRPVAKVMALEDLSK	SLC24A1	616	O60721
KKRRIMKAPAAEAVA	GPANK1	71	O95872
VFLMPSRVEISLVKA	ITGB1BP2	281	Q9UKP3
LPAKERQTIVELAKM	KAT2B	236	Q92831
EKEELLKEMRFISPR	WWC1	346	Q8IX03
PFKREKSFEIVIMVL	LGALS8	96	O00214
ELMVKFPLKEIQSTR	MYO15A	3451	Q9UKN7
PVRMLQTVAKKFDFS	IBTK	716	Q9P2D0
MEFAVKIIDKSKRDP	RPS6KA3	446	P51812
LKFARKPLCMLDIFV	KCNQ3	191	O43525
ERKVALKAMIKTFRP	LENG8	736	Q96PV6
KFMTDPIRILVKRDE	EIF4A3	231	P38919
VARTVKISDPDLFKM	KDM6B	1521	O15054
RKLKVLEMPSEVCAF	HMGN2P46	151	Q86SG4
LFPIAMRLERVCKKD	CYP3A4	366	P08684
PEVMAKVKVLFVRNL	SYNCRIP	331	O60506
ARAVPRKVALEMLFT	ECHDC3	191	Q96DC8
QRITAFKMEKAPIDT	EXOSC9	291	Q06265
LKFARKPFCVIDIMV	KCNQ2	161	O43526
APKMITDFFSQRKVI	OR4F5	71	Q8NH21
FATPKMIVDFLRERK	OR4K13	76	Q8NH42
FATPKMIADFLVERK	OR4K15	76	Q8NH41
ITAPKMLIDFFVERK	OR4M1	76	Q8NGD0
IVAPRMLVDFLSAKK	OR4N2	76	Q8NGD1
IVAPRMLVDFLSEKK	OR4N4	76	Q8N0Y3
IVVPRMLVDFLSEKK	OR4N5	76	Q8IXE1
RPVVSTDMAKLFDKI	PIK3C2A	216	O00443
ERDLLKKFRIPVDTM	PDE4A	401	P27815
FDPKILEVVRETKCM	DNAH8	601	Q96JB1
DVAIKVIDKMRFPTK	PRKD3	601	O94806
AMSKDTKLIVVVRDP	HS3ST3A1	231	Q9Y663
TEFKKVTPLIHDRML	F8	1056	P00451
MVDILAKVRFPLISK	KLHL7	226	Q8IXQ5
KDPKRAMEAFNLVRE	NLRP4	316	Q96MN2
KMIELSKVVDPAIVL	LRIT3	211	Q3SXY7
LSIVRDKKFMTLDPV	MED17	116	Q9NVC6
RMLVFDPSKRISAKD	NLK	406	Q9UBE8
APKMITDFFSQRKVI	OR4F17	71	Q8NGA8
FETSLPRKMAEILVA	RALGAPA2	1221	Q2PPJ7
PRKMAEILVATVAFL	RALGAPA2	1226	Q2PPJ7
VIDAMLERIKPEKTV	PTPRS	1601	Q13332
PESMSAREKAIIAKL	PPP1R3A	741	Q16821
KPMLRAFGDIVRALK	FADS2B	456	A8MWK0
TEDIALPLMKVLSFK	GSAP	506	A4D1B5
FKTVMGAAPELKVRL	HEATR5B	2021	Q9P2D3
PTCRETMLAVKFIAK	CPA3	396	P15088
AEKIKRSPMDKVLRF	DACT2	496	Q5SW24
SVIKPFEEKAAKRIM	DOCK10	381	Q96BY6
ELTVMKSFFVDLKLP	C3P1	61	Q6ZMU1
IEKISKRMFEELPHF	CHRDL1	391	Q9BU40
IFIKAIPVDRMETKN	DNAH17	4406	Q9UFH2
VSRMKKAVEDDVFIP	GCFC2	611	P16383
KRSKMEVDEALVFRP	EPM2AIP1	6	Q7L775
DVFKNMPAKTELIVR	CHD3	971	Q12873
KTRDAAFKILNPMTV	COG3	641	Q96JB2
MRKKALFILPFVSVA	POLQ	136	O75417
KRFQTLISKMEPLEI	CRY1	151	Q16526
REDPFKEKLLEIMTR	IFIH1	546	Q9BYX4
FEPKMTRSKLKEVVE	GON4L	321	Q3T8J9
PVLAVRVLFEMKTAR	DENND4C	836	Q5VZ89
DRLKVFKEVMRDITP	APOL3	261	O95236
AEFIKRTILKIPMNE	CENPN	6	Q96H22
VLEVTKKFMRDPIRI	EIF4A2	221	Q14240
VLFRSLKMVELFPET	FBXO40	136	Q9UH90
PIMARIKAINTFFAK	LARP4	266	Q71RC2
PRECIEFLKEASVMK	INSRR	1021	P14616
MASKPEKRVASSVFI	FBLIM1	1	Q8WUP2
SLKFSEMKIRPVRED	FIBCD1	446	Q8N539
TPMIVAADFVKSIKA	DUS4L	56	O95620
LFPVAMRLERVCKKD	CYP3A7	366	P24462
VQKPFLKLLMEEDRT	FAM186A	2261	A6NE01
DVFKNMPSKTELIVR	CHD4	961	Q14839
DVFKPMDLNRVIKLL	CFAP69	41	A5D8W1
EMFPRSFIKLLRSKV	SCUBE1	966	Q8IWY4
KPFLSEDTRKKIMVL	SEC14L2	206	O76054
MEQFKPKDSALLRIE	CENPE	1406	Q02224
AEVFRKDLISAMKLP	JADE3	41	Q92613
VNPEDVARLIFSKMK	HSPA14	111	Q0VDF9
SKADVAQMVRKAPFL	MTERF3	236	Q96E29
APKMITDFFSQRKVI	OR4F4	71	Q96R69
FMKKIVANPEDTRSL	MRPS15	111	P82914
RDLARKMEALKPLFV	RTEL1	576	Q9NZ71
SRKLPMIDFVVTLVA	SYPL1	146	Q16563
LLVPEIDEVMRKVSK	UTP20	2236	O75691
KVVKMSPIERLEHAF	UTRN	201	P46939
MTEKKESEVLLARPF	SLC6A16	91	Q9GZN6
EVRMRTNLPIFKLKE	SNX12	51	Q9UMY4
RIIPEITAMKADASK	TOP2B	1241	Q02880
RLMKIEKFFPHVLEK	GINS4	96	Q9BRT9
FKALPDSMVSVKRKA	NBR1	616	Q14596
RMCLVEIEKAPKVVA	NDUFS1	76	P28331
MPRKIEEIKDFLLTA	RPL38	1	P63173
SAPTARVFMKSVKLE	PRPF6	671	O94906
PKKAALVMQTEAARD	SAMD3	76	Q8N6K7
AKKPEDFVRINRMAL	NBEA	2471	Q8NFP9
LVAAFDKMIRKPDTL	EPHB6	911	O15197
AVVLLMFPKEKEAFL	PRSS47P	11	A8MTI9
FSITKDPAAEARMKV	RPN1	461	P04843
FPRKKMFVTATLVVI	SLC9A4	446	Q6AI14
PKVREKDIEMFLESS	STRIP1	426	Q5VSL9
RIDSMVPKLALFAAK	SETMAR	236	Q53H47
PEMREKAATVFNTLK	SPESP1	321	Q6UW49
PMTEEIVTKDRLFKA	PGBD1	256	Q96JS3
FLLRRVKVDVEKQMP	SRCAP	836	Q6ZRS2
RLAPEREFIKSLMAI	PI4KB	321	Q9UBF8
PSVRFKAEKLEMALN	STXBP4	211	Q6ZWJ1
VMKFSIAILPFSIKA	ABCC12	386	Q96J65
LTKEDLRVLMEKEFP	S100A10	26	P60903
VTPDMKSIAKADLIV	ASCC3	1411	Q8N3C0
FLAVIKAIDPSLVDM	CLMN	221	Q96JQ2
RDKTVMIIVAISPKY	TRAF3IP2	461	O43734
VEVSRKNPKFMETVA	CLU	421	P10909
LFKKTPRQIALMDVG	CNOT11	196	Q9UKZ1
PVSLRDALVFMELAK	RNF17	636	Q9BXT8
KTEEPRAKEAVVAMI	PLEKHG5	501	O94827
EKEMRKLFNIPAERE	USP4	166	Q13107
LPICEAAAMRKVVKV	RALGAPA1	421	Q6GYQ0
KFFLLEPQMKVAALR	SECTM1	181	Q8WVN6
ALKRNMPVSFEVIKE	STAU2	216	Q9NUL3
EVLKAISRKFMPLDQ	UBA7	371	P41226
IIMAVAPLFDTKIFR	SLC26A11	411	Q86WA9
IPLEEKSKIMNRAFF	KIF3B	591	O15066
LLKRMIDPVKEEASA	STX17	86	P56962
RLEPMDTIFVKNVKE	ARHGAP23	91	Q9P227
KMLKEFAKAAIRVQP	ROPN1	16	Q9HAT0
IMKKLKEIAFPRTDE	STAMBPL1	106	Q96FJ0
LAEFARMKPRKIKED	YY1	276	P25490
LAPKRKAVEMHAAVI	ZC3H11A	666	O75152
VLPFKVAKDMAAAAV	RTCA	201	O00442
AAMKLISPRDFVDLV	STARD5	106	Q9NSY2
TRVVDFAKKLPMFCE	THRB	281	P10828
AVMDFIKDLPIRKVS	POLK	341	Q9UBT6
TKTFETIAIIAMEKP	TEX11	771	Q8IYF3
LPENMDAFEKVRTKL	PREPL	86	Q4J6C6
DAPEVVSVMKTIAKF	ZNF518A	1356	Q6AHZ1
DARIAFVKKPFMVSR	SNX19	661	Q92543
EKLIFRMAAPKIAEA	PLEKHH1	1301	Q9ULM0
LTRKVKMPDVELFVN	POGLUT2	221	Q6UW63
KSMLFKRELQPSEEV	NDUFB1	41	O75438
SKVPADLLKRAFVRM	PRKDC	3876	P78527
RFVEKEIRKANIPIM	ATP6V0A1	66	Q93050
RSMPKLEIFEKIESQ	ZNF165	191	P49910
VKKVLRTVMTDPFTE	SCN11A	566	Q9UI33
ITRVVDFAKKLPMFS	THRA	226	P10827
PISKSMLERLSKFEV	TPTE2	36	Q6XPS3
SEEMLKAKKRVFPLS	TASOR2	326	Q5VWN6
PRMAATQKLVKDIID	ZFAND1	106	Q8TCF1
PMAKKLTELREAQEF	TMC2	176	Q8TDI7
VMFTALIKDRPKFVR	TRPM8	461	Q7Z2W7
VLPMKKDVDRTEVVF	XRRA1	316	Q6P2D8
MIRDVELAEEALPKK	TNF	6	P01375
MPVFKEVKVHLLEDA	KIAA0586	126	Q9BVV6
IFRMLKEKEPRVEEA	ZNF175	76	Q9Y473
QIPELAKRIKMFFAL	LIPA	186	P38571
DMRVDAIPIKAAKAS	NEB	2771	P20929
LVKKEIPRSTLDSFM	GRIN1	541	Q05586