Cluster composition

Functions

Category	Name	IntersectionWithQuery	PValue	GenesInTerm	GenesInQuery	GenesInTermInQuery	ID
GeneOntologyMolecularFunction	cytoskeletal protein binding	ROCK2 MYH1 MYH2 MYH7 KIF3B MYH7B SBDS WASF2 GAS8 PKD2 DAAM1 TNNT3 NEXN KIF20B TTLL13 MYBPC1	3.20e-07	1099	65	16	GO:0008092
GeneOntologyMolecularFunction	cytoskeletal motor activity	MYH1 MYH2 MYH7 KIF3B MYH7B KIF20B	2.33e-06	118	65	6	GO:0003774
GeneOntologyMolecularFunction	microfilament motor activity	MYH1 MYH2 MYH7 MYH7B	6.94e-06	38	65	4	GO:0000146
GeneOntologyMolecularFunction	actin binding	MYH1 MYH2 MYH7 MYH7B WASF2 DAAM1 TNNT3 NEXN MYBPC1	2.37e-05	479	65	9	GO:0003779
GeneOntologyMolecularFunction	small GTPase binding	ROCK2 RBSN KIF3B GAS8 RILPL1 DAAM1	6.13e-04	321	65	6	GO:0031267
GeneOntologyMolecularFunction	ATP-dependent activity	MYH1 MYH2 MYH7 KIF3B MYH7B ATP10B SNRNP200 KIF20B	8.23e-04	614	65	8	GO:0140657
GeneOntologyMolecularFunction	actin filament binding	MYH1 MYH2 MYH7 MYH7B NEXN	8.62e-04	227	65	5	GO:0051015
GeneOntologyMolecularFunction	GTPase binding	ROCK2 RBSN KIF3B GAS8 RILPL1 DAAM1	1.11e-03	360	65	6	GO:0051020
GeneOntologyMolecularFunction	plus-end-directed microtubule motor activity	KIF3B KIF20B	1.37e-03	17	65	2	GO:0008574
GeneOntologyBiologicalProcess	microtubule cytoskeleton organization	ROCK2 KIF3B SBDS GAS8 PKD2 MAP7D2 CDK11A OOEP CNTLN MAP7 ODAD3 TTLL13	1.85e-06	720	64	12	GO:0000226
GeneOntologyBiologicalProcess	microtubule-based process	ROCK2 KIF3B SBDS GAS8 PKD2 TTC21B MAP7D2 CDK11A OOEP CNTLN MAP7 ODAD3 KIF20B TTLL13	3.46e-06	1058	64	14	GO:0007017
GeneOntologyBiologicalProcess	muscle system process	ROCK2 MYH1 MYH2 MYH7 GTF2IRD2B ACACB MYH7B GTF2IRD2 TNNT3 MYBPC1	6.63e-06	547	64	10	GO:0003012
GeneOntologyBiologicalProcess	transition between fast and slow fiber	MYH7 GTF2IRD2B GTF2IRD2	7.97e-06	13	64	3	GO:0014883
GeneOntologyBiologicalProcess	regulation of skeletal muscle adaptation	MYH7 GTF2IRD2B GTF2IRD2	3.13e-05	20	64	3	GO:0014733
GeneOntologyBiologicalProcess	regulation of muscle system process	ROCK2 MYH7 GTF2IRD2B ACACB MYH7B GTF2IRD2 TNNT3	5.56e-05	317	64	7	GO:0090257
GeneOntologyBiologicalProcess	regulation of muscle adaptation	ROCK2 MYH7 GTF2IRD2B ACACB GTF2IRD2	5.81e-05	133	64	5	GO:0043502
GeneOntologyBiologicalProcess	striated muscle adaptation	MYH7 GTF2IRD2B ACACB GTF2IRD2	7.81e-05	73	64	4	GO:0014888
GeneOntologyBiologicalProcess	skeletal muscle adaptation	MYH7 GTF2IRD2B GTF2IRD2	1.33e-04	32	64	3	GO:0043501
GeneOntologyBiologicalProcess	centrosome cycle	ROCK2 KIF3B PKD2 CDK11A CNTLN	1.56e-04	164	64	5	GO:0007098
GeneOntologyBiologicalProcess	muscle adaptation	ROCK2 MYH7 GTF2IRD2B ACACB GTF2IRD2	1.56e-04	164	64	5	GO:0043500
GeneOntologyBiologicalProcess	microtubule organizing center organization	ROCK2 KIF3B PKD2 CDK11A CNTLN	2.35e-04	179	64	5	GO:0031023
GeneOntologyBiologicalProcess	muscle contraction	ROCK2 MYH1 MYH2 MYH7 MYH7B TNNT3 MYBPC1	2.35e-04	400	64	7	GO:0006936
GeneOntologyCellularComponent	myosin filament	MYH1 MYH2 MYH7 MYH7B MYBPC1	1.36e-08	25	66	5	GO:0032982
GeneOntologyCellularComponent	myosin II complex	MYH1 MYH2 MYH7 MYH7B	1.75e-06	28	66	4	GO:0016460
GeneOntologyCellularComponent	microtubule organizing center	ROCK2 KIF3B CCDC124 CEP95 CAPRIN2 GAS8 PKD2 UPF3B RILPL1 DAAM1 CNTLN ODAD3 KIF20B	4.94e-06	919	66	13	GO:0005815
GeneOntologyCellularComponent	muscle myosin complex	MYH1 MYH2 MYH7	1.63e-05	16	66	3	GO:0005859
GeneOntologyCellularComponent	myofibril	MYH1 MYH2 MYH7 MYH7B TNNT3 NEXN MYBPC1	2.42e-05	273	66	7	GO:0030016
GeneOntologyCellularComponent	contractile muscle fiber	MYH1 MYH2 MYH7 MYH7B TNNT3 NEXN MYBPC1	3.56e-05	290	66	7	GO:0043292
GeneOntologyCellularComponent	myosin complex	MYH1 MYH2 MYH7 MYH7B	3.62e-05	59	66	4	GO:0016459
GeneOntologyCellularComponent	supramolecular fiber	MYH1 MYH2 MYH7 KIF3B MYH7B GAS8 CFAP210 MAP7 TNNT3 NEXN KIF20B TTLL13 MYBPC1	6.82e-05	1179	66	13	GO:0099512
GeneOntologyCellularComponent	supramolecular polymer	MYH1 MYH2 MYH7 KIF3B MYH7B GAS8 CFAP210 MAP7 TNNT3 NEXN KIF20B TTLL13 MYBPC1	7.31e-05	1187	66	13	GO:0099081
GeneOntologyCellularComponent	cilium	KIF3B CFAP36 GAS8 PKD2 TTC21B CFAP210 RILPL1 DAAM1 SEPTIN10 ODAD3 TTLL13	1.07e-04	898	66	11	GO:0005929
GeneOntologyCellularComponent	sarcomere	MYH1 MYH2 MYH7 TNNT3 NEXN MYBPC1	1.34e-04	249	66	6	GO:0030017
GeneOntologyCellularComponent	ciliary basal body	GAS8 PKD2 RILPL1 DAAM1 ODAD3	3.78e-04	195	66	5	GO:0036064
GeneOntologyCellularComponent	actin cytoskeleton	MYH1 MYH2 MYH7 MYH7B WASF2 DAAM1 TNNT3 NEXN	4.46e-04	576	66	8	GO:0015629
GeneOntologyCellularComponent	ciliary tip	KIF3B TTC21B ODAD3	4.70e-04	48	66	3	GO:0097542
GeneOntologyCellularComponent	A band	MYH1 MYH2 MYBPC1	5.95e-04	52	66	3	GO:0031672
GeneOntologyCellularComponent	centrosome	ROCK2 KIF3B CCDC124 CEP95 CAPRIN2 UPF3B RILPL1 CNTLN KIF20B	6.73e-04	770	66	9	GO:0005813
GeneOntologyCellularComponent	contractile ring	MYH2 KIF20B	8.72e-04	14	66	2	GO:0070938
GeneOntologyCellularComponent	cytoplasmic region	KIF3B CFAP36 GAS8 PKD2 CFAP210 ODAD3	9.53e-04	360	66	6	GO:0099568
GeneOntologyCellularComponent	Set1C/COMPASS complex	BOD1L1 CXXC1	1.14e-03	16	66	2	GO:0048188
GeneOntologyCellularComponent	plasma membrane bounded cell projection cytoplasm	KIF3B CFAP36 GAS8 CFAP210 ODAD3	3.26e-03	317	66	5	GO:0032838
GeneOntologyCellularComponent	spindle	ROCK2 KIF3B CEP95 SBDS PKD2 KIF20B	3.68e-03	471	66	6	GO:0005819
GeneOntologyCellularComponent	spindle pole	ROCK2 CEP95 SBDS KIF20B	4.03e-03	205	66	4	GO:0000922
GeneOntologyCellularComponent	axoneme	CFAP36 GAS8 CFAP210 ODAD3	4.17e-03	207	66	4	GO:0005930
GeneOntologyCellularComponent	ciliary plasm	CFAP36 GAS8 CFAP210 ODAD3	4.24e-03	208	66	4	GO:0097014
GeneOntologyCellularComponent	motile cilium	CFAP36 GAS8 PKD2 DAAM1 SEPTIN10	5.26e-03	355	66	5	GO:0031514
GeneOntologyCellularComponent	midbody	KIF3B CCDC124 VPS37B KIF20B	5.34e-03	222	66	4	GO:0030496
Domain	NPIP	NPIPA5 NPIPA1 NPIPA3 NPIPA7	1.66e-07	14	69	4	IPR009443
Domain	Myosin_N	MYH1 MYH2 MYH7 MYH7B	2.26e-07	15	69	4	PF02736
Domain	Myosin_N	MYH1 MYH2 MYH7 MYH7B	2.26e-07	15	69	4	IPR004009
Domain	Myosin_tail_1	MYH1 MYH2 MYH7 MYH7B	5.02e-07	18	69	4	PF01576
Domain	Myosin_tail	MYH1 MYH2 MYH7 MYH7B	5.02e-07	18	69	4	IPR002928
Domain	Myosin-like_IQ_dom	MYH1 MYH2 MYH7 MYH7B	6.34e-07	19	69	4	IPR027401
Domain	-	MYH1 MYH2 MYH7 MYH7B	6.34e-07	19	69	4	4.10.270.10
Domain	Myosin_head_motor_dom	MYH1 MYH2 MYH7 MYH7B	1.15e-05	38	69	4	IPR001609
Domain	MYOSIN_MOTOR	MYH1 MYH2 MYH7 MYH7B	1.15e-05	38	69	4	PS51456
Domain	Myosin_head	MYH1 MYH2 MYH7 MYH7B	1.15e-05	38	69	4	PF00063
Domain	MYSc	MYH1 MYH2 MYH7 MYH7B	1.15e-05	38	69	4	SM00242
Domain	-	GTF2IRD2B GTF2IRD2	8.03e-05	4	69	2	3.90.1460.10
Domain	GTF2I	GTF2IRD2B GTF2IRD2	8.03e-05	4	69	2	PS51139
Domain	GTF2I	GTF2IRD2B GTF2IRD2	8.03e-05	4	69	2	PF02946
Domain	MAP7_fam	MAP7D2 MAP7	8.03e-05	4	69	2	IPR008604
Domain	GTF2I	GTF2IRD2B GTF2IRD2	8.03e-05	4	69	2	IPR004212
Domain	MAP7	MAP7D2 MAP7	8.03e-05	4	69	2	PF05672
Domain	IQ	MYH1 MYH2 MYH7 MYH7B	2.29e-04	81	69	4	SM00015
Domain	IQ_motif_EF-hand-BS	MYH1 MYH2 MYH7 MYH7B	3.43e-04	90	69	4	IPR000048
Domain	IQ	MYH1 MYH2 MYH7 MYH7B	3.89e-04	93	69	4	PS50096
Domain	tRNA-bd_arm	CNTLN KIF20B	3.52e-03	24	69	2	IPR010978
Domain	P-loop_NTPase	MYH1 MYH2 MYH7 KIF3B MYH7B SEPTIN10 SNRNP200 KIF20B URGCP	3.87e-03	848	69	9	IPR027417
Domain	ATP_grasp_subdomain_2	ACACB TTLL13	5.84e-03	31	69	2	IPR013816
Pathway	KEGG_VIRAL_MYOCARDITIS	MYH1 MYH2 MYH7 MYH7B	5.94e-05	70	43	4	M12294
Pubmed	In-Depth In Vivo Crosslinking in Minutes by a Compact, Membrane-Permeable, and Alkynyl-Enrichable Crosslinker.	ROCK2 MYH1 MYH2 MYH7 GTF2IRD2B TCERG1L ACACB GUCY1A2 CWC27 MYH7B CAPRIN2 GTF2IRD2 MAP7D2 ATP10B BOD1L1 OTUD3 CFAP210 SEPTIN10 CXXC1 MYBPC1	5.92e-12	1442	71	20	35575683
Pubmed	A family of microRNAs encoded by myosin genes governs myosin expression and muscle performance.	MYH1 MYH2 MYH7 MYH7B TNNT3	1.32e-10	16	71	5	19922871
Pubmed	Genome-wide mapping of Sox6 binding sites in skeletal muscle reveals both direct and indirect regulation of muscle terminal differentiation by Sox6.	MYH1 MYH2 MYH7 MYH7B TNNT3	5.01e-09	31	71	5	21985497
Pubmed	Structural and developmental analysis of two linked myosin heavy chain genes.	MYH1 MYH2 MYH7	8.15e-09	3	71	3	1371481
Pubmed	The expression of myosin heavy chain (MHC) genes in human skeletal muscle is related to metabolic characteristics involved in the pathogenesis of type 2 diabetes.	MYH1 MYH2 MYH7	8.15e-09	3	71	3	21470888
Pubmed	Loss of Prox1 in striated muscle causes slow to fast skeletal muscle fiber conversion and dilated cardiomyopathy.	MYH1 MYH2 MYH7 TNNT3	1.57e-08	14	71	4	24938781
Pubmed	Defective excitation-contraction coupling is partially responsible for impaired contractility in hindlimb muscles of Stac3 knockout mice.	MYH1 MYH2 MYH7 TNNT3	1.57e-08	14	71	4	27184118
Pubmed	Six homeoproteins and a Iinc-RNA at the fast MYH locus lock fast myofiber terminal phenotype.	MYH1 MYH2 MYH7 TNNT3	2.14e-08	15	71	4	24852826
Pubmed	Novel retinal and cone photoreceptor transcripts revealed by human macular expression profiling.	NPIPA5 NPIPA1 NPIPA3	3.26e-08	4	71	3	18055785
Pubmed	Myosin heavy chain isoforms of the murine masseter muscle during pre- and post-natal development.	MYH1 MYH2 MYH7	8.13e-08	5	71	3	12919077
Pubmed	Sox6 is required for normal fiber type differentiation of fetal skeletal muscle in mice.	MYH1 MYH2 MYH7	8.13e-08	5	71	3	17584907
Pubmed	Distinct myogenic programs of embryonic and fetal mouse muscle cells: expression of the perinatal myosin heavy chain isoform in vitro.	MYH1 MYH2 MYH7	1.62e-07	6	71	3	1728586
Pubmed	Spatial and temporal changes in myosin heavy chain gene expression in skeletal muscle development.	MYH1 MYH2 MYH7	1.62e-07	6	71	3	10588881
Pubmed	A fast Myosin super enhancer dictates muscle fiber phenotype through competitive interactions with Myosin genes.	MYH1 MYH2 MYH7	2.84e-07	7	71	3	35210422
Pubmed	ANKK1 is found in myogenic precursors and muscle fibers subtypes with glycolytic metabolism.	MYH1 MYH2 MYH7	2.84e-07	7	71	3	29758057
Pubmed	The brain expressed x-linked gene 1 (Bex1) regulates myoblast fusion.	MYH1 MYH2 MYH7	2.84e-07	7	71	3	26586200
Pubmed	Diversity in transcriptional start site selection and alternative splicing affects the 5'-UTR of mouse striated muscle myosin transcripts.	MYH1 MYH2 MYH7	2.84e-07	7	71	3	16819597
Pubmed	Neuromuscular junction immaturity and muscle atrophy are hallmarks of the ColQ-deficient mouse, a model of congenital myasthenic syndrome with acetylcholinesterase deficiency.	MYH1 MYH2 MYH7	4.53e-07	8	71	3	26993635
Pubmed	GASP-2 overexpressing mice exhibit a hypermuscular phenotype with contrasting molecular effects compared to GASP-1 transgenics.	MYH1 MYH2 MYH7	6.79e-07	9	71	3	31960486
Pubmed	Deletion of the protein kinase A/protein kinase G target SMTNL1 promotes an exercise-adapted phenotype in vascular smooth muscle.	MYH1 MYH2 MYH7	1.33e-06	11	71	3	18310078
Pubmed	The histone code reader Spin1 controls skeletal muscle development.	MYH1 MYH2 MYH7	1.33e-06	11	71	3	29168801
Pubmed	Calcineurin is necessary for the maintenance but not embryonic development of slow muscle fibers.	MYH1 MYH2 MYH7	1.33e-06	11	71	3	16024798
Pubmed	Histone deacetylase 3 modulates Tbx5 activity to regulate early cardiogenesis.	MYH7 MYH7B TNNT3	2.30e-06	13	71	3	24565863
Pubmed	Contractile protein gene expression in primary myotubes of embryonic mouse hindlimb muscles.	MYH1 MYH2 MYH7	2.30e-06	13	71	3	8404542
Pubmed	Myopathy associated LDB3 mutation causes Z-disc disassembly and protein aggregation through PKCα and TSC2-mTOR downregulation.	MYH1 MYH2 MYH7	2.92e-06	14	71	3	33742095
Pubmed	Six1 homeoprotein drives myofiber type IIA specialization in soleus muscle.	MYH1 MYH2 MYH7 TNNT3	3.42e-06	50	71	4	27597886
Pubmed	Myosin heavy chain composition of the human genioglossus muscle.	MYH1 MYH2	4.11e-06	2	71	2	22337492
Pubmed	Myosin heavy chains IIa and IId are functionally distinct in the mouse.	MYH1 MYH2	4.11e-06	2	71	2	9585413
Pubmed	Endogenous slow and fast myosin dynamics in myofibers isolated from mice expressing GFP-Myh7 and Kusabira Orange-Myh1.	MYH1 MYH7	4.11e-06	2	71	2	35759444
Pubmed	Positive selection of a gene family during the emergence of humans and African apes.	NPIPA1 NPIPA8	4.11e-06	2	71	2	11586358
Pubmed	Characterization of diverse forms of myosin heavy chain expressed in adult human skeletal muscle.	MYH1 MYH7	4.11e-06	2	71	2	2421254
Pubmed	Analysis of mouse conceptuses with uniparental duplication/deficiency for distal chromosome 12: comparison with chromosome 12 uniparental disomy and implications for genomic imprinting.	MYH1 MYH2	4.11e-06	2	71	2	16575183
Pubmed	Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome.	GTF2IRD2B GTF2IRD2	4.11e-06	2	71	2	15388857
Pubmed	Different pathways regulate expression of the skeletal myosin heavy chain genes.	MYH1 MYH2	4.11e-06	2	71	2	11551968
Pubmed	Effects of bone fracture and surgery on plasma myosin heavy chain fragments of skeletal muscle.	MYH2 MYH7	4.11e-06	2	71	2	10579056
Pubmed	Type IIx myosin heavy chain transcripts are expressed in type IIb fibers of human skeletal muscle.	MYH1 MYH2	4.11e-06	2	71	2	7545970
Pubmed	MAP7D2 Localizes to the Proximal Axon and Locally Promotes Kinesin-1-Mediated Cargo Transport into the Axon.	MAP7D2 MAP7	4.11e-06	2	71	2	30784582
Pubmed	IKKα and alternative NF-κB regulate PGC-1β to promote oxidative muscle metabolism.	MYH1 MYH2 MYH7	5.43e-06	17	71	3	22351927
Pubmed	Slow and fast fiber isoform gene expression is systematically altered in skeletal muscle of the Sox6 mutant, p100H.	MYH2 MYH7 TNNT3	5.43e-06	17	71	3	16124007
Pubmed	Genesis of muscle fiber-type diversity during mouse embryogenesis relies on Six1 and Six4 gene expression.	MYH1 MYH2 MYH7 TNNT3	6.22e-06	58	71	4	21884692
Pubmed	The RNA-mediated estrogen receptor α interactome of hormone-dependent human breast cancer cell nuclei.	INTS10 NIFK ZNF800 MAN1A2 CCDC124 DNAJC8 CWC27 WASF2 CDK11A DAAM1 MAP7 SPTY2D1 KIF20B	9.35e-06	1497	71	13	31527615
Pubmed	Transition of myosin heavy chain isoforms in human laryngeal abductors following denervation.	MYH1 MYH2	1.23e-05	3	71	2	26059207
Pubmed	Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams-Beuren syndrome.	GTF2IRD2B GTF2IRD2	1.23e-05	3	71	2	15100712
Pubmed	Kinesin-2 mediates physical and functional interactions between polycystin-2 and fibrocystin.	KIF3B PKD2	1.23e-05	3	71	2	17008358
Pubmed	Molecular determinants of force production in human skeletal muscle fibers: effects of myosin isoform expression and cross-sectional area.	MYH1 MYH2	1.23e-05	3	71	2	25567808
Pubmed	Screening of MYH7, MYBPC3, and TNNT2 genes in Brazilian patients with hypertrophic cardiomyopathy.	MYH7 MYBPC1	1.23e-05	3	71	2	24093860
Pubmed	SETD1A Methyltransferase Is Physically and Functionally Linked to the DNA Damage Repair Protein RAD18.	DNAJC8 ZC3H4 RNPC3 BOD1L1 CXXC1 SPTY2D1	1.29e-05	251	71	6	31076518
Pubmed	Comparative sequence analysis of the complete human sarcomeric myosin heavy chain family: implications for functional diversity.	MYH1 MYH2	2.46e-05	4	71	2	10388558
Pubmed	Smooth muscle myosin light chain kinase expression in cardiac and skeletal muscle.	MYH1 MYH2	2.46e-05	4	71	2	11029314
Pubmed	Two novel/ancient myosins in mammalian skeletal muscles: MYH14/7b and MYH15 are expressed in extraocular muscles and muscle spindles.	MYH7 MYH7B	2.46e-05	4	71	2	19948655
Pubmed	Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions.	GTF2IRD2B GTF2IRD2	2.46e-05	4	71	2	21328569
Pubmed	Evaluation of embryonic and perinatal myosin gene mutations and the etiology of congenital idiopathic clubfoot.	MYH1 MYH2	2.46e-05	4	71	2	20357587
Pubmed	A human YAC transgene rescues craniofacial and neural tube development in PDGFRalpha knockout mice and uncovers a role for PDGFRalpha in prenatal lung growth.	MYH1 MYH2	2.46e-05	4	71	2	11023856
Pubmed	Control of muscle formation by the fusogenic micropeptide myomixer.	MYH1 MYH2	2.46e-05	4	71	2	28386024
Pubmed	TFII-I gene family during tooth development: candidate genes for tooth anomalies in Williams syndrome.	GTF2IRD2B GTF2IRD2	2.46e-05	4	71	2	17823943
Pubmed	Evolution of general transcription factors.	GTF2IRD2B GTF2IRD2	2.46e-05	4	71	2	23229069
Pubmed	Modulation of skeletal muscle fiber type by mitogen-activated protein kinase signaling.	MYH1 MYH2	2.46e-05	4	71	2	18417546
Pubmed	GTF2IRD2 from the Williams-Beuren critical region encodes a mobile-element-derived fusion protein that antagonizes the action of its related family members.	GTF2IRD2B GTF2IRD2	2.46e-05	4	71	2	22899722
Pubmed	Deficiency of Myo18B in mice results in embryonic lethality with cardiac myofibrillar aberrations.	MYH1 MYH2	2.46e-05	4	71	2	18761673
Pubmed	Autophagy controls neonatal myogenesis by regulating the GH-IGF1 system through a NFE2L2- and DDIT3-mediated mechanism.	MYH1 MYH2 MYH7	3.52e-05	31	71	3	30081710
Pubmed	The proximal proteome of 17 SARS-CoV-2 proteins links to disrupted antiviral signaling and host translation.	NIFK RBSN CCDC124 ACACB DNAJC8 CWC27 RTF2 MAP7D2 CXXC1 SPTY2D1	3.69e-05	1007	71	10	34597346
Pubmed	Myomesin 3, a novel structural component of the M-band in striated muscle.	MYH2 MYH7	4.09e-05	5	71	2	18177667
Pubmed	Detection of Gene and Protein Expression in Mouse Embryos and Tissue Sections.	MYH1 MYH2	4.09e-05	5	71	2	30737693
Pubmed	Developmental pattern of mouse skeletal myosin heavy chain gene transcripts in vivo and in vitro.	MYH1 MYH2	4.09e-05	5	71	2	3829126
Pubmed	Cullin-3-RING ubiquitin ligase activity is required for striated muscle function in mice.	MYH1 MYH2	4.09e-05	5	71	2	29653945
Pubmed	Sequential accumulation of mRNAs encoding different myosin heavy chain isoforms during skeletal muscle development in vivo detected with a recombinant plasmid identified as coding for an adult fast myosin heavy chain from mouse skeletal muscle.	MYH1 MYH2	4.09e-05	5	71	2	6196357
Pubmed	Multigene family for sarcomeric myosin heavy chain in mouse and human DNA: localization on a single chromosome.	MYH1 MYH2	4.09e-05	5	71	2	6879174
Pubmed	Myosin heavy chain-embryonic regulates skeletal muscle differentiation during mammalian development.	MYH1 MYH2 MYH7	4.26e-05	33	71	3	32094117
Pubmed	A hypoplastic model of skeletal muscle development displaying reduced foetal myoblast cell numbers, increased oxidative myofibres and improved specific tension capacity.	MYH1 MYH2	6.13e-05	6	71	2	20417199
Pubmed	Organization of human and mouse skeletal myosin heavy chain gene clusters is highly conserved.	MYH1 MYH2	6.13e-05	6	71	2	10077619
Pubmed	A role for Insulin-like growth factor 2 in specification of the fast skeletal muscle fibre.	MYH1 MYH2	6.13e-05	6	71	2	17559643
Pubmed	Loss of the neurodevelopmental Joubert syndrome causing protein, Ahi1, causes motor and muscle development delays independent of central nervous system involvement.	MYH2 MYH7	6.13e-05	6	71	2	30695685
Pubmed	Voltage-dependent conformational changes of Kv1.3 channels activate cell proliferation.	ROCK2 MYH7B CEP95 CAPRIN2 BOD1L1	6.89e-05	208	71	5	33230847
Pubmed	Hox11-expressing interstitial cells contribute to adult skeletal muscle at homeostasis.	MYH1 MYH2	8.57e-05	7	71	2	36815629
Pubmed	Myomaker is a membrane activator of myoblast fusion and muscle formation.	MYH1 MYH2	8.57e-05	7	71	2	23868259
Pubmed	Abnormal Mammary Development in 129:STAT1-Null Mice is Stroma-Dependent.	MYH1 TNNT3 MYBPC1	1.02e-04	44	71	3	26075897
Pubmed	Mammalian APE1 controls miRNA processing and its interactome is linked to cancer RNA metabolism.	ROCK2 NIFK GTF2IRD2B WDR46 CDK11A RILPL1 MAP7 CLEC16A URGCP	1.09e-04	925	71	9	28986522
Pubmed	Genes for skeletal muscle myosin heavy chains are clustered and are not located on the same mouse chromosome as a cardiac myosin heavy chain gene.	MYH1 MYH7	1.14e-04	8	71	2	3864153
Pubmed	Early Developmental Disruption of Type 2 Deiodinase Pathway in Mouse Skeletal Muscle Does Not Impair Muscle Function.	MYH2 MYH7	1.14e-04	8	71	2	27967605
Pubmed	A Hoxa13:Cre mouse strain for conditional gene manipulation in developing limb, hindgut, and urogenital system.	MYH1 MYH2	1.14e-04	8	71	2	25980463
Pubmed	Cell lineage- and expression-based inference of the roles of forkhead box transcription factor Foxc2 in craniofacial development.	MYH1 MYH2	1.14e-04	8	71	2	33667029
Pubmed	A Tcf4-positive mesodermal population provides a prepattern for vertebrate limb muscle patterning.	MYH1 MYH2	1.14e-04	8	71	2	14667415
Pubmed	HOXA5 plays tissue-specific roles in the developing respiratory system.	MYH1 MYH2 MYH7	1.16e-04	46	71	3	28827394
Pubmed	The Nse5/6-like SIMC1-SLF2 complex localizes SMC5/6 to viral replication centers.	NIFK CCDC124 DNAJC8 ZC3H4 RTF2 CDK11A BOD1L1 SNRNP200 KIF20B	1.38e-04	954	71	9	36373674
Pubmed	Expression of mRNA and protein-protein interaction of the antiviral endoribonuclease RNase L in mouse spleen.	GAS8 MYBPC1	1.47e-04	9	71	2	24780566
Pubmed	Developmental origin and morphogenesis of the diaphragm, an essential mammalian muscle.	MYH1 MYH2	1.83e-04	10	71	2	29679560
Pubmed	Acceleration of somitic myogenesis in embryos of myogenin promoter-MRF4 transgenic mice.	MYH1 MYH2	1.83e-04	10	71	2	8950513
Pubmed	Defining the proximal interaction networks of Arf GTPases reveals a mechanism for the regulation of PLD1 and PI4KB.	RBSN ACACB ZC3H4 CFAP36 WASF2 CLEC16A SNRNP200 SPTY2D1	1.84e-04	777	71	8	35844135
Pubmed	TXLNA enhances TBK1 phosphorylation by suppressing PPM1B recruitment.	CCDC124 DNAJC8 UPF3B MAP7	1.88e-04	138	71	4	37506885
Pubmed	The cell proliferation antigen Ki-67 organises heterochromatin.	NIFK WDR46 CXXC1 SNRNP200 SPTY2D1 KIF20B	1.94e-04	410	71	6	26949251
Pubmed	Nucleolar proteome dynamics.	DNAJC8 SBDS RTF2 WDR46 UPF3B SNRNP200	2.18e-04	419	71	6	15635413
Pubmed	Extracellular matrix protein composition dynamically changes during murine forelimb development.	MYH1 MYH2	2.23e-04	11	71	2	38303699
Pubmed	Jaw muscularization requires Dlx expression by cranial neural crest cells.	MYH1 MYH2	2.23e-04	11	71	2	20534536
Pubmed	CAP2 deficiency delays myofibril actin cytoskeleton differentiation and disturbs skeletal muscle architecture and function.	MYH2 MYH7	2.23e-04	11	71	2	30962377
Pubmed	Modulation of contractile protein gene expression in fetal murine crural muscles: emergence of muscle diversity.	MYH1 MYH2	2.23e-04	11	71	2	8136524
Pubmed	Ephrin-A3 promotes and maintains slow muscle fiber identity during postnatal development and reinnervation.	MYH2 MYH7	2.23e-04	11	71	2	26644518
Pubmed	Fibroblast-derived Hgf controls recruitment and expansion of muscle during morphogenesis of the mammalian diaphragm.	MYH1 MYH2	2.68e-04	12	71	2	36154712
Pubmed	Properties of branchiomeric and somite-derived muscle development in Tbx1 mutant embryos.	MYH2 MYH7	2.68e-04	12	71	2	18816853
Pubmed	CHD4 and the NuRD complex directly control cardiac sarcomere formation.	TNNT3 CDH4	2.68e-04	12	71	2	29891665
Pubmed	Mapping the Ku Interactome Using Proximity-Dependent Biotin Identification in Human Cells.	NIFK ZC3H4 CDK11A BOD1L1 SNRNP200	2.89e-04	283	71	5	30585729
Interaction	RSPH6A interactions	MYH1 MYH2 MYH7 TNNT3 MYBPC1	9.71e-08	34	68	5	int:RSPH6A
Interaction	TSPAN33 interactions	MYH1 MYH2 MYH7 TNNT3 MYBPC1	2.66e-06	65	68	5	int:TSPAN33
Interaction	CFAP141 interactions	MYH7 ZC3H4 WDR46 KIF20B	3.55e-05	55	68	4	int:CFAP141
Cytoband	16p13.11	NPIPA5 NPIPA1 NPIPA3	6.14e-06	23	71	3	16p13.11
Cytoband	Ensembl 112 genes in cytogenetic band chr16p13	NPIPA5 NPIPA1 NPIPA3 NPIPA7 CLEC16A	5.29e-04	426	71	5	chr16p13
Cytoband	4q22.1	FAM13A PKD2	7.48e-04	26	71	2	4q22.1
GeneFamily	Myosin heavy chains	MYH1 MYH2 MYH7 MYH7B	3.05e-08	15	41	4	1098
Coexpression	DESCARTES_FETAL_EYE_SKELETAL_MUSCLE_CELLS	MYH2 MYH7 SBDS TNNT3 NEXN MYBPC1	6.34e-06	170	70	6	M40176
Coexpression	RICKMAN_HEAD_AND_NECK_CANCER_F	MYH1 MYH2 NEXN MYBPC1	1.44e-05	55	70	4	M2043
Coexpression	HUMMERICH_BENIGN_SKIN_TUMOR_DN	MYH1 MYH2 TNNT3	2.01e-05	20	70	3	M1123
Coexpression	HUMMERICH_BENIGN_SKIN_TUMOR_DN	MYH1 MYH2 TNNT3	2.34e-05	21	70	3	MM1102
CoexpressionAtlas	BM Top 100 - skeletal muscle	MYH1 MYH7 TNNT3 NEXN MYBPC1	3.91e-06	75	67	5	BM Top 100 - skeletal muscle
CoexpressionAtlas	FacebaseRNAseq_e10.5_Neural Epithelium Flanking Eminence_top-relative-expression-ranked_500_k-means-cluster#3	ROCK2 ZNF800 MAP7D2 CFAP210 CDH4 KIF20B	3.19e-05	192	67	6	Facebase_RNAseq_e10.5_Neural Epithelium Flanking Eminence_500_K3
CoexpressionAtlas	FacebaseRNAseq_e10.5_Neural Epithelium Flanking Eminence_top-relative-expression-ranked_2500_k-means-cluster#5	ROCK2 ZNF800 RBSN CFAP36 SBDS MAP7D2 BOD1L1 UPF3B CFAP210 CDH4 KIF20B	5.35e-05	831	67	11	Facebase_RNAseq_e10.5_Neural Epithelium Flanking Eminence_2500_K5
CoexpressionAtlas	skeletal muscle	MYH1 MYH2 MYH7 MYH7B TNNT3 NEXN MYBPC1	6.63e-05	320	67	7	skeletal muscle
CoexpressionAtlas	FacebaseRNAseq_e10.5_Neural Epithelium Flanking Eminence_top-relative-expression-ranked_1000_k-means-cluster#4	ZNF800 MAP7D2 CFAP210 DAAM1 MAP7 CDH4	8.91e-05	231	67	6	Facebase_RNAseq_e10.5_Neural Epithelium Flanking Eminence_1000_K4
CoexpressionAtlas	BM Top 100 - tongue main corpus	MYH7 TNNT3 NEXN MYBPC1	1.20e-04	80	67	4	BM Top 100 - tongue main corpus
CoexpressionAtlas	FacebaseRNAseq_e10.5_Maxillary Arch_top-relative-expression-ranked_1000	ROCK2 ACACB GUCY1A2 RNPC3 SBDS RTF2 KNDC1 BOD1L1 CNTLN MAP7 KIF20B	2.48e-04	989	67	11	Facebase_RNAseq_e10.5_Maxillary Arch_1000
CoexpressionAtlas	FacebaseRNAseq_e10.5_Neural Epithelium Flanking Eminence_top-relative-expression-ranked_1000	ROCK2 ZNF800 SBDS MAP7D2 BOD1L1 UPF3B CFAP210 DAAM1 MAP7 CDH4 KIF20B	2.48e-04	989	67	11	Facebase_RNAseq_e10.5_Neural Epithelium Flanking Eminence_1000
ToppCell	H1299-infected-SARSCoV2\|infected / Cell line, Condition and Strain	CAPRIN2 WDR46 BOD1L1 UPF3B CNTLN NEXN	7.38e-07	197	71	6	0fa3e4cf93e77d78b1f97b906c5b13ca741ae17e
ToppCell	(00)_Basal-(2)_GFP_FOXI1\|(00)_Basal / shred by cell type by condition	ROCK2 NIFK MAN1A2 BOD1L1 DAAM1 SEPTIN10	7.83e-07	199	71	6	19674e1eaeb51e4196d847cb62aa437c852951d3
ToppCell	COVID-19-Heart-Mito_EC\|COVID-19 / Disease (COVID-19 only), tissue and cell type	MYH1 MYH2 MYH7 TNNT3 MYBPC1	1.32e-05	190	71	5	ea74e0e38bcaba125b48c88331e9ba09228d3178
ToppCell	PND03-Mesenchymal-Mesenchymal_myocytic-Myofibroblast_vascular-VSMC-VSMC_mature\|PND03 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif	MYH2 MAP7D2 DAAM1 TNNT3 NEXN	1.50e-05	195	71	5	43d372373367b71243c6ea958aedccde4478618f
ToppCell	COVID-19-Heart-Mito_CM\|COVID-19 / Disease (COVID-19 only), tissue and cell type	MYH2 MYH7 TNNT3 NEXN MYBPC1	1.58e-05	197	71	5	44e49943d62bfe622b40ad0460093d31540544df
ToppCell	Brain_organoid-organoid_Tanaka_cellReport-3m-Mesenchymal-Mesoderm\|3m / Sample Type, Dataset, Time_group, and Cell type.	MYH2 MYH7 TNNT3 NEXN MYBPC1	1.69e-05	200	71	5	538ae964db58c4acafe93f735b3e03fc08fdaac6
ToppCell	Hippocampus-Neuronal-Excitatory-eN2(Slc17a7_Slc17a6)-Slc17a6\|Hippocampus / BrainAtlas - Mouse McCarroll V32	MYH2 MYH7 MYH7B ATP10B	3.22e-05	113	71	4	6f270b7e59c18243e876311df721e948ce21e850
Computational	Neighborhood of TTN	MYH1 MYH2 TNNT3 MYBPC1	1.50e-06	26	36	4	GNF2_TTN
Computational	Genes in the cancer module 201.	ROCK2 MYH7 TNNT3 MYBPC1	2.19e-05	50	36	4	MODULE_201
Computational	Genes in the cancer module 202.	MYH7 TNNT3 MYBPC1	1.07e-04	28	36	3	MODULE_202
Computational	Genes in the cancer module 387.	MYH7 TNNT3 MYBPC1	5.72e-04	49	36	3	MODULE_387
Computational	Genes in the cancer module 329.	MYH7 TNNT3 MYBPC1	6.43e-04	51	36	3	MODULE_329
Drug	fast white	MYH1 MYH2 MYH7 MYH7B TNNT3 MYBPC1	2.73e-09	42	68	6	CID000024008
Drug	B0683	ROCK2 MYH1 MYH2 MYH7 MYH7B PKD2	1.37e-06	117	68	6	CID006398969
Drug	SM-2	MYH1 MYH2 MYH7 MYH7B MYBPC1	6.26e-06	87	68	5	CID000486033
Drug	formycin triphosphate	MYH1 MYH2 MYH7 MYH7B	1.64e-05	51	68	4	CID000122274
Drug	creatine	MYH1 MYH2 MYH7 GTF2IRD2B MYH7B GTF2IRD2	2.43e-05	193	68	6	CID000000586
Drug	blebbistatin	ROCK2 MYH1 MYH2 MYH7 MYH7B	2.54e-05	116	68	5	CID003476986
Drug	purealin	MYH1 MYH2 MYH7 MYH7B	2.73e-05	58	68	4	CID006419303
Drug	oxovanadium	MYH1 MYH2 MYH7 MYH7B MYBPC1	2.99e-05	120	68	5	CID000024411
Drug	2bq7	MYH1 MYH2 MYH7 MYH7B MYBPC1	3.37e-05	123	68	5	CID006540267
Disease	distal arthrogryposis (implicated_via_orthology)	MYH1 MYH2 MYH7 MYH7B MYBPC1	1.21e-10	15	64	5	DOID:0050646 (implicated_via_orthology)
Disease	dilated cardiomyopathy 1S (implicated_via_orthology)	MYH1 MYH2 MYH7 MYH7B	4.18e-09	10	64	4	DOID:0110454 (implicated_via_orthology)
Disease	autosomal dominant hyaline body myopathy (implicated_via_orthology)	MYH1 MYH2 MYH7 MYH7B	4.18e-09	10	64	4	DOID:0111269 (implicated_via_orthology)
Disease	congenital myopathy 6 (implicated_via_orthology)	MYH1 MYH2 MYH7 MYH7B	4.18e-09	10	64	4	DOID:0080719 (implicated_via_orthology)
Disease	distal arthrogryposis type 2B3 (implicated_via_orthology)	MYH1 MYH2 MYH7 MYH7B	4.18e-09	10	64	4	DOID:0111602 (implicated_via_orthology)
Disease	inclusion body myositis (implicated_via_orthology)	MYH1 MYH2 MYH7 MYH7B	4.18e-09	10	64	4	DOID:3429 (implicated_via_orthology)
Disease	distal arthrogryposis type 2A (implicated_via_orthology)	MYH1 MYH2 MYH7 MYH7B	4.18e-09	10	64	4	DOID:0111605 (implicated_via_orthology)
Disease	familial hypertrophic cardiomyopathy (implicated_via_orthology)	MYH1 MYH2 MYH7 MYH7B	4.18e-09	10	64	4	DOID:0080326 (implicated_via_orthology)
Disease	distal arthrogryposis type 1 (implicated_via_orthology)	MYH1 MYH2 MYH7 MYH7B	4.18e-09	10	64	4	DOID:0111596 (implicated_via_orthology)
Disease	distal myopathy (implicated_via_orthology)	MYH1 MYH2 MYH7 MYH7B	9.83e-09	12	64	4	DOID:11720 (implicated_via_orthology)
Disease	myotonia congenita (implicated_via_orthology)	MYH1 MYH2 MYH7 MYH7B	9.83e-09	12	64	4	DOID:2106 (implicated_via_orthology)
Disease	restrictive cardiomyopathy (implicated_via_orthology)	MYH1 MYH2 MYH7 MYH7B	1.42e-08	13	64	4	DOID:397 (implicated_via_orthology)
Disease	cardiomyopathy (implicated_via_orthology)	MYH1 MYH2 MYH7 MYH7B TNNT3	4.77e-07	71	64	5	DOID:0050700 (implicated_via_orthology)
Disease	myopathy (implicated_via_orthology)	MYH1 MYH2 MYH7 MYH7B	3.64e-06	48	64	4	DOID:423 (implicated_via_orthology)
Disease	dilated cardiomyopathy (implicated_via_orthology)	MYH1 MYH2 MYH7 MYH7B	2.81e-05	80	64	4	DOID:12930 (implicated_via_orthology)
Disease	ARTHROGRYPOSIS, DISTAL, TYPE 1	TNNT3 MYBPC1	6.91e-05	6	64	2	C0220662
Disease	Digitotalar Dysmorphism	TNNT3 MYBPC1	6.91e-05	6	64	2	C1852085
Disease	Distal arthrogryposis	TNNT3 MYBPC1	1.65e-04	9	64	2	cv:C0265213
Disease	Left ventricular noncompaction	MYH7 MYH7B	4.14e-04	14	64	2	C1960469
Disease	disease free survival, rectum cancer	TCERG1L BTC	4.77e-04	15	64	2	EFO_0000409, EFO_1000657
Disease	intrinsic cardiomyopathy (implicated_via_orthology)	DAAM1 TNNT3	9.47e-04	21	64	2	DOID:0060036 (implicated_via_orthology)
Disease	hypertrophic cardiomyopathy (is_implicated_in)	MYH7 MYH7B	1.04e-03	22	64	2	DOID:11984 (is_implicated_in)
Disease	Primary familial hypertrophic cardiomyopathy	MYH7 NEXN	1.04e-03	22	64	2	cv:C0949658
Disease	triglycerides:total lipids ratio, high density lipoprotein cholesterol measurement	INTS10 FAM13A ACACB RILPL1	1.06e-03	206	64	4	EFO_0004612, EFO_0020947
Disease	retinitis pigmentosa (implicated_via_orthology)	CWC27 SNRNP200	1.57e-03	27	64	2	DOID:10584 (implicated_via_orthology)
Disease	forced expiratory volume	KIF3B BTC CEP95 CNTLN NEXN CLEC16A MYBPC1	1.58e-03	789	64	7	EFO_0004314
Disease	Primary familial dilated cardiomyopathy	MYH7 NEXN	1.94e-03	30	64	2	cv:C0340427

Protein segments in the cluster

Peptide	Gene	Start	Entry
REIKEAHKRKRIMKE	TBC1D12	431	O60347
AHKRKRIMKERFKQE	TBC1D12	436	O60347
REKMADIYLKHRKDK	TTC21B	691	Q7Z4L5
RRREESKKLMREKKE	CWC27	456	Q6UX04
HVVRRQIRELKKMKK	CNTLN	1296	Q9NXG0
HEEMKILREVLRKSK	CFAP36	151	Q96G28
MEKKLRKIRARTQKH	ATP10B	811	O94823
TQKLRMEERFKKKER	NIFK	156	Q9BYG3
MEERFKKKERLLRKK	NIFK	161	Q9BYG3
KKKRKEEMERKRAVE	RBSN	386	Q9H1K0
IHKKRKLAEGREKTM	INTS10	366	Q9NVR2
EKKVRMDLERAKRKL	MYH7	1041	P12883
RRTEEERKHKLEMEK	NEXN	391	Q0ZGT2
KTAKEHLRKLSMKER	NPIPA1	141	Q9UND3
EIKFRKKDLIKSMRR	ACACB	2236	O00763
RLERKKRLEEIMKRT	MAP7	596	Q14244
ERLERKKRIDEIMKR	MAP7D2	536	Q96T17
KKRIDEIMKRTRKSD	MAP7D2	541	Q96T17
KELKTMEERKVKRRS	CCDC28A	86	Q8IWP9
KKLRMDTERAKRKLE	MYH7B	1091	A7E2Y1
QEKKLRMDLERAKRK	MYH2	1046	Q9UKX2
KMKESDHQIIKRRLR	KIF20B	1801	Q96Q89
TKKIMAHERREKVKR	MSANTD3	81	Q96H12
KKIRMDLERAKRKLE	MYH1	1046	P12882
KTAKEHLRKLSMKER	NPIPA3	141	F8WFD2
QEMREEKKRIRKKLR	FAM13A	956	O94988
WMEKKKRQEERHRHK	OTUD3	351	Q5T2D3
RARAEKMKHLEKNLK	OOEP	121	A6NGQ2
MKEEKEHRPKEKRVT	UPF3B	1	Q9BZI7
VEEEERHMPKRKRKQ	BOD1L1	2761	Q8NFC6
KEQRERERKMRKAKE	DAAM1	1011	Q9Y4D1
RKRAVKVKHVKRREK	CXXC1	321	Q9P0U4
MKESRLKDKQKHRVD	CYP3A43	256	Q9HB55
MKRREKERHTKQLLI	CDH4	756	P55283
MSRKEKVHHRKDEKR	CDK11A	91	Q9UQ88
HKVKRELRSKMEKEI	CEP95	766	Q96GE4
REHMLKLEAEKKKLR	CAPRIN2	201	Q6IMN6
DIREKREKIKEMMKH	MAN1A2	176	O60476
KRKEREAKEMHERKR	DNAJC8	176	O75937
EKHSRKIQDKLRRMK	KNDC1	1731	Q76NI1
MRDEKLHELKKGLRK	GTF2IRD2	481	Q86UP8
MRDEKLHELKKGLRK	GTF2IRD2B	481	Q6EKJ0
RKRRKRKKKEEEMET	BTC	146	P35070
LKEKMKIERAHMRLR	SBDS	161	Q9Y3A5
VMRKEQRKEEKEKRR	CCDC124	46	Q96CT7
KTAKEHLRKLSMKER	NPIPA7	141	E9PJI5
KTAKEHLRKLSMKER	NPIPA8	141	P0DM63
KKRMDKLKATLERTH	GUCY1A2	466	P33402
MEERRLRAKLEKKTK	RTF2	186	Q9BY42
KTAKEHLRKLSMKER	NPIPA5	141	E9PKD4
KKLENERMERKTHRE	ODAD3	311	A5D8V7
KKRIELKHDKKARAM	SPTY2D1	71	Q68D10
KKLEKKREEMHESRR	CFAP210	256	Q0VFZ6
LEMNKHKGKRRVQKR	CLEC16A	376	Q2KHT3
LKKRDKENRLRLRKM	TCERG1L	571	Q5VWI1
KAKDRMERITRKIKD	URGCP	471	Q8TCY9
MLKRQRIKREKKDFR	ZNF35	161	P13682
QRHVRKKRKIKDMLN	RNPC3	276	Q96LT9
RMDRIEKERKHQKEL	RILPL1	91	Q5EBL4
RLLKEKEKKMEDLRR	KIF3B	441	O15066
VRRKEKENRKLHMEL	ROCK2	1056	O75116
KLEIMERAKLKRREV	PKD2	866	Q13563
KRLHQEERMKLEEKR	SEPTIN10	396	Q9P0V9
VKRKRKVMDEEHRDK	WDR46	566	O15213
EEKSHRRLKRKRKKE	ZC3H4	96	Q9UPT8
QDTKDIMKEKRKHRK	WASF2	166	Q9Y6W5
RRKRDEDRHDINKMK	SNRNP200	71	O75643
TAREMKKKILAERRK	TNNT3	181	P45378
RRHIRKVHKKKMEEL	ZNF800	246	Q2TB10
RKLAHMRRVKIEKLQ	VPS37B	146	Q9H9H4
RKVGKIKREMTKEER	WDR87	1411	Q6ZQQ6
RKVMEEDKRRVKERL	TTLL13	426	A6NNM8
KKMKMLRDELDLRRK	GAS8	191	O95995
GMLKRLKRMRREEKK	MYBPC1	236	Q00872