Cluster composition

Functions

Category	Name	IntersectionWithQuery	PValue	GenesInTerm	GenesInQuery	GenesInTermInQuery	ID
GeneOntologyMolecularFunction	microfilament motor activity	MYH1 MYH2 MYH3 MYH4 MYH13	3.78e-08	38	50	5	GO:0000146
GeneOntologyMolecularFunction	cytoskeletal motor activity	MYH1 MYH2 MYH3 MYH4 MYH13	1.13e-05	118	50	5	GO:0003774
GeneOntologyMolecularFunction	heparan sulfate N-deacetylase activity	NDST3 NDST1	1.84e-05	3	50	2	GO:0102140
GeneOntologyMolecularFunction	[heparan sulfate]-glucosamine N-sulfotransferase activity	NDST3 NDST1	3.68e-05	4	50	2	GO:0015016
GeneOntologyMolecularFunction	N-acetylglucosamine deacetylase activity	NDST3 NDST1	3.68e-05	4	50	2	GO:0050119
GeneOntologyMolecularFunction	actin filament binding	MYH1 MYH2 MYH3 MYH4 MYH13	2.54e-04	227	50	5	GO:0051015
GeneOntologyMolecularFunction	calmodulin binding	MYH1 MYH2 MYH3 MYH4 MYH13	2.70e-04	230	50	5	GO:0005516
GeneOntologyMolecularFunction	channel activity	ANO2 KCNH8 TRPC5 SLC24A1 RHCE KCNH4 RHD	3.13e-04	525	50	7	GO:0015267
GeneOntologyMolecularFunction	passive transmembrane transporter activity	ANO2 KCNH8 TRPC5 SLC24A1 RHCE KCNH4 RHD	3.17e-04	526	50	7	GO:0022803
GeneOntologyMolecularFunction	sulfotransferase activity	NDST3 NDST1 CHST4	3.54e-04	55	50	3	GO:0008146
GeneOntologyMolecularFunction	ammonium channel activity	RHCE RHD	3.99e-04	12	50	2	GO:0008519
GeneOntologyMolecularFunction	inorganic molecular entity transmembrane transporter activity	ANO2 KCNH8 SLC37A3 TRPC5 SLC24A1 RHCE KCNH4 RHD	5.43e-04	758	50	8	GO:0015318
GeneOntologyMolecularFunction	transmembrane transporter activity	ANO2 KCNH8 SLC37A3 SLC16A14 TRPC5 SLC24A1 ABCA7 RHCE KCNH4 RHD	5.88e-04	1180	50	10	GO:0022857
GeneOntologyMolecularFunction	heparan sulfate sulfotransferase activity	NDST3 NDST1	6.32e-04	15	50	2	GO:0034483
GeneOntologyMolecularFunction	ATP-dependent activity	MYH1 MYH2 MYH3 MYH4 MYH13 ZNFX1 ABCA7	7.96e-04	614	50	7	GO:0140657
GeneOntologyMolecularFunction	transferase activity, transferring sulphur-containing groups	NDST3 NDST1 CHST4	8.45e-04	74	50	3	GO:0016782
GeneOntologyMolecularFunction	transporter activity	ANO2 KCNH8 SLC37A3 SLC16A14 TRPC5 SLC24A1 ABCA7 RHCE KCNH4 RHD	1.16e-03	1289	50	10	GO:0005215
GeneOntologyMolecularFunction	actin binding	MYH1 MYH2 MYH3 MYH4 MYH13 TRPC5	1.20e-03	479	50	6	GO:0003779
GeneOntologyMolecularFunction	amyloid-beta binding	ADRB2 TLR2 CD74	2.13e-03	102	50	3	GO:0001540
GeneOntologyMolecularFunction	glucuronosyltransferase activity	UGT2B28 UGT2B11	3.47e-03	35	50	2	GO:0015020
GeneOntologyMolecularFunction	deacetylase activity	NDST3 NDST1	4.51e-03	40	50	2	GO:0019213
GeneOntologyMolecularFunction	inorganic cation transmembrane transporter activity	KCNH8 TRPC5 SLC24A1 RHCE KCNH4 RHD	4.60e-03	627	50	6	GO:0022890
GeneOntologyMolecularFunction	monoatomic ion channel activity	ANO2 KCNH8 TRPC5 SLC24A1 KCNH4	5.69e-03	459	50	5	GO:0005216
GeneOntologyBiologicalProcess	muscle filament sliding	MYH2 MYH3 MYH4	5.97e-06	15	50	3	GO:0030049
GeneOntologyBiologicalProcess	actin-myosin filament sliding	MYH2 MYH3 MYH4	1.07e-05	18	50	3	GO:0033275
GeneOntologyBiologicalProcess	muscle system process	MYH1 MYH2 MYH3 MYH4 ADRB2 MYH13 P2RY1 NR3C1	4.68e-05	547	50	8	GO:0003012
GeneOntologyBiologicalProcess	ammonium homeostasis	RHCE RHD	8.59e-05	6	50	2	GO:0097272
GeneOntologyBiologicalProcess	androgen metabolic process	SRD5A3 UGT2B28 UGT2B11	1.07e-04	38	50	3	GO:0008209
GeneOntologyBiologicalProcess	inorganic ion transmembrane transport	ANO2 ADRB2 KCNH8 SLC37A3 TRPC5 SLC24A1 RHCE KCNH4 RHD NEDD4	1.38e-04	1017	50	10	GO:0098660
GeneOntologyBiologicalProcess	protein sulfation	NDST1 CHST4	1.60e-04	8	50	2	GO:0006477
GeneOntologyBiologicalProcess	biphenyl catabolic process	UGT2B28 UGT2B11	1.60e-04	8	50	2	GO:0070980
GeneOntologyBiologicalProcess	heparan sulfate proteoglycan biosynthetic process, polysaccharide chain biosynthetic process	NDST3 NDST1	1.60e-04	8	50	2	GO:0015014
GeneOntologyBiologicalProcess	cellular catabolic process	ADRB2 SRD5A3 TLR2 BCAT2 RENBP UGT2B28 UGT2B11 ABCA7 MOAP1 HDC NEDD4	1.65e-04	1253	50	11	GO:0044248
GeneOntologyBiologicalProcess	glycoprotein biosynthetic process	NDST3 NDST1 SRD5A3 GALNT8 CHST4 ABCA7	2.16e-04	357	50	6	GO:0009101
GeneOntologyBiologicalProcess	biphenyl metabolic process	UGT2B28 UGT2B11	2.56e-04	10	50	2	GO:0018879
GeneOntologyBiologicalProcess	heparin biosynthetic process	NDST3 NDST1	3.12e-04	11	50	2	GO:0030210
GeneOntologyBiologicalProcess	regulation of ERK1 and ERK2 cascade	PRAMEF5 P2RY1 TLR2 CD74 ZDHHC17 ABCA7	3.23e-04	385	50	6	GO:0070372
GeneOntologyBiologicalProcess	xenobiotic glucuronidation	UGT2B28 UGT2B11	3.74e-04	12	50	2	GO:0052697
GeneOntologyBiologicalProcess	muscle contraction	MYH1 MYH2 MYH3 MYH4 ADRB2 MYH13	3.96e-04	400	50	6	GO:0006936
GeneOntologyBiologicalProcess	ammonium transmembrane transport	RHCE RHD	4.42e-04	13	50	2	GO:0072488
GeneOntologyBiologicalProcess	ERK1 and ERK2 cascade	PRAMEF5 P2RY1 TLR2 CD74 ZDHHC17 ABCA7	5.00e-04	418	50	6	GO:0070371
GeneOntologyBiologicalProcess	potassium ion transport	ADRB2 KCNH8 SLC24A1 KCNH4 NEDD4	5.02e-04	272	50	5	GO:0006813
GeneOntologyCellularComponent	muscle myosin complex	MYH1 MYH2 MYH3 MYH4 MYH13	3.02e-10	16	51	5	GO:0005859
GeneOntologyCellularComponent	myosin filament	MYH1 MYH2 MYH3 MYH4 MYH13	3.62e-09	25	51	5	GO:0032982
GeneOntologyCellularComponent	myosin II complex	MYH1 MYH2 MYH3 MYH4 MYH13	6.66e-09	28	51	5	GO:0016460
GeneOntologyCellularComponent	myosin complex	MYH1 MYH2 MYH3 MYH4 MYH13	3.20e-07	59	51	5	GO:0016459
GeneOntologyCellularComponent	ankyrin-1 complex	RHCE RHD	2.59e-04	10	51	2	GO:0170014
GeneOntologyCellularComponent	Golgi membrane	NDST3 PCSK5 NDST1 GALNT8 CHST4 CD74 ZDHHC17 ABCA7	3.30e-04	721	51	8	GO:0000139
GeneOntologyCellularComponent	myofibril	MYH1 MYH2 MYH3 MYH4 MYH13	5.27e-04	273	51	5	GO:0030016
GeneOntologyCellularComponent	outer membrane	ZNFX1 UGT2B28 UGT2B11 SLC24A1 MOAP1	6.00e-04	281	51	5	GO:0019867
GeneOntologyCellularComponent	contractile muscle fiber	MYH1 MYH2 MYH3 MYH4 MYH13	6.92e-04	290	51	5	GO:0043292
HumanPheno	Anti-erythrocyte autoantibody positivity	RHCE RHD	3.14e-05	3	17	2	HP:6000388
HumanPheno	Positive direct antiglobulin test	RHCE RHD	3.14e-05	3	17	2	HP:0032366
Domain	Myosin_N	MYH1 MYH2 MYH3 MYH4 MYH13	3.29e-10	15	50	5	IPR004009
Domain	Myosin_N	MYH1 MYH2 MYH3 MYH4 MYH13	3.29e-10	15	50	5	PF02736
Domain	Myosin_tail_1	MYH1 MYH2 MYH3 MYH4 MYH13	9.34e-10	18	50	5	PF01576
Domain	Myosin_tail	MYH1 MYH2 MYH3 MYH4 MYH13	9.34e-10	18	50	5	IPR002928
Domain	Myosin-like_IQ_dom	MYH1 MYH2 MYH3 MYH4 MYH13	1.27e-09	19	50	5	IPR027401
Domain	-	MYH1 MYH2 MYH3 MYH4 MYH13	1.27e-09	19	50	5	4.10.270.10
Domain	MYOSIN_MOTOR	MYH1 MYH2 MYH3 MYH4 MYH13	5.26e-08	38	50	5	PS51456
Domain	Myosin_head	MYH1 MYH2 MYH3 MYH4 MYH13	5.26e-08	38	50	5	PF00063
Domain	Myosin_head_motor_dom	MYH1 MYH2 MYH3 MYH4 MYH13	5.26e-08	38	50	5	IPR001609
Domain	MYSc	MYH1 MYH2 MYH3 MYH4 MYH13	5.26e-08	38	50	5	SM00242
Domain	IQ	MYH1 MYH2 MYH3 MYH4 MYH13	1.28e-06	71	50	5	PF00612
Domain	IQ	MYH1 MYH2 MYH3 MYH4 MYH13	2.46e-06	81	50	5	SM00015
Domain	IQ_motif_EF-hand-BS	MYH1 MYH2 MYH3 MYH4 MYH13	4.15e-06	90	50	5	IPR000048
Domain	IQ	MYH1 MYH2 MYH3 MYH4 MYH13	4.87e-06	93	50	5	PS50096
Domain	P-loop_NTPase	NDST3 MYH1 NDST1 MYH2 MYH3 MYH4 MYH13 SBNO1 CHST4 ZNFX1 ABCA7	1.16e-05	848	50	11	IPR027417
Domain	K_chnl_volt-dep_ELK	KCNH8 KCNH4	2.10e-05	3	50	2	IPR003950
Domain	HSNSD	NDST3 NDST1	4.20e-05	4	50	2	PF12062
Domain	Heparan_SO4_deacetylase	NDST3 NDST1	4.20e-05	4	50	2	IPR021930
Domain	Ammonium_transpt	RHCE RHD	6.99e-05	5	50	2	IPR001905
Domain	Ammonium_transp	RHCE RHD	6.99e-05	5	50	2	PF00909
Domain	NH4_transpt_AmtB-like_dom	RHCE RHD	6.99e-05	5	50	2	IPR024041
Domain	RhesusRHD	RHCE RHD	6.99e-05	5	50	2	IPR002229
Domain	Sulfotransferase_dom	NDST3 NDST1 CHST4	1.21e-04	36	50	3	IPR000863
Domain	Sulfotransfer_1	NDST3 NDST1 CHST4	1.21e-04	36	50	3	PF00685
Domain	-	RHCE RHD	1.46e-04	7	50	2	1.10.3430.10
Domain	Ammonium/urea_transptr	RHCE RHD	1.46e-04	7	50	2	IPR029020
Domain	PAS_9	KCNH8 KCNH4	3.12e-04	10	50	2	PF13426
Domain	K_chnl_volt-dep_EAG/ELK/ERG	KCNH8 KCNH4	6.26e-04	14	50	2	IPR003938
Domain	UDPGT	UGT2B28 UGT2B11	1.43e-03	21	50	2	PS00375
Domain	UDPGT	UGT2B28 UGT2B11	1.43e-03	21	50	2	PF00201
Domain	UDP_glucos_trans	UGT2B28 UGT2B11	1.43e-03	21	50	2	IPR002213
Domain	PAS_fold_3	KCNH8 KCNH4	1.71e-03	23	50	2	IPR013655
Domain	PAS_3	KCNH8 KCNH4	1.71e-03	23	50	2	PF08447
Domain	PAS-assoc_C	KCNH8 KCNH4	1.87e-03	24	50	2	IPR000700
Domain	PAC	KCNH8 KCNH4	2.19e-03	26	50	2	SM00086
Domain	PAC	KCNH8 KCNH4	2.19e-03	26	50	2	PS50113
Domain	PAC	KCNH8 KCNH4	2.19e-03	26	50	2	IPR001610
Domain	CNMP_BINDING_1	KCNH8 KCNH4	3.31e-03	32	50	2	PS00888
Domain	CNMP_BINDING_2	KCNH8 KCNH4	3.31e-03	32	50	2	PS00889
Domain	Ion_trans_dom	KCNH8 TRPC5 KCNH4	3.52e-03	114	50	3	IPR005821
Domain	Ion_trans	KCNH8 TRPC5 KCNH4	3.52e-03	114	50	3	PF00520
Domain	cNMP	KCNH8 KCNH4	3.73e-03	34	50	2	SM00100
Domain	PAS	KCNH8 KCNH4	3.73e-03	34	50	2	IPR000014
Domain	PAS	KCNH8 KCNH4	3.73e-03	34	50	2	PS50112
Domain	cNMP_binding	KCNH8 KCNH4	3.73e-03	34	50	2	PF00027
Domain	cNMP-bd_dom	KCNH8 KCNH4	3.95e-03	35	50	2	IPR000595
Domain	CNMP_BINDING_3	KCNH8 KCNH4	3.95e-03	35	50	2	PS50042
Domain	cNMP-bd-like	KCNH8 KCNH4	4.64e-03	38	50	2	IPR018490
Domain	-	KCNH8 KCNH4	7.32e-03	48	50	2	2.60.120.10
Domain	RmlC-like_jellyroll	KCNH8 KCNH4	8.24e-03	51	50	2	IPR014710
Pathway	KEGG_VIRAL_MYOCARDITIS	MYH1 MYH2 MYH3 MYH4 MYH13	1.50e-06	70	40	5	M12294
Pathway	KEGG_TIGHT_JUNCTION	MYH1 MYH2 MYH3 MYH4 MYH13	3.37e-05	132	40	5	M11355
Pathway	WP_METAPATHWAY_BIOTRANSFORMATION_PHASE_I_AND_II	NDST3 NDST1 CHST4 UGT2B28 UGT2B11	1.59e-04	183	40	5	M39588
Pathway	KEGG_MEDICUS_REFERENCE_HEPARAN_SULFATE_BIOSYNTHESIS	NDST3 NDST1	4.25e-04	11	40	2	M47921
Pathway	KEGG_STEROID_HORMONE_BIOSYNTHESIS	SRD5A3 UGT2B28 UGT2B11	5.01e-04	55	40	3	M14933
Pubmed	Organization of human and mouse skeletal myosin heavy chain gene clusters is highly conserved.	MYH1 MYH2 MYH3 MYH4 MYH13	3.32e-14	6	51	5	10077619
Pubmed	A fast Myosin super enhancer dictates muscle fiber phenotype through competitive interactions with Myosin genes.	MYH1 MYH2 MYH3 MYH4 MYH13	1.16e-13	7	51	5	35210422
Pubmed	Comparative sequence analysis of the complete human sarcomeric myosin heavy chain family: implications for functional diversity.	MYH1 MYH2 MYH4 MYH13	4.10e-12	4	51	4	10388558
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 MYH3 MYH4	2.05e-11	5	51	4	6196357
Pubmed	Developmental pattern of mouse skeletal myosin heavy chain gene transcripts in vivo and in vitro.	MYH1 MYH2 MYH3 MYH4	2.05e-11	5	51	4	3829126
Pubmed	Distinct myogenic programs of embryonic and fetal mouse muscle cells: expression of the perinatal myosin heavy chain isoform in vitro.	MYH1 MYH2 MYH3 MYH4	6.14e-11	6	51	4	1728586
Pubmed	Spatial and temporal changes in myosin heavy chain gene expression in skeletal muscle development.	MYH1 MYH2 MYH3 MYH4	6.14e-11	6	51	4	10588881
Pubmed	ANKK1 is found in myogenic precursors and muscle fibers subtypes with glycolytic metabolism.	MYH1 MYH2 MYH3 MYH4	1.43e-10	7	51	4	29758057
Pubmed	Diversity in transcriptional start site selection and alternative splicing affects the 5'-UTR of mouse striated muscle myosin transcripts.	MYH1 MYH2 MYH3 MYH4	1.43e-10	7	51	4	16819597
Pubmed	Calcineurin is necessary for the maintenance but not embryonic development of slow muscle fibers.	MYH1 MYH2 MYH3 MYH4	1.34e-09	11	51	4	16024798
Pubmed	Contractile protein gene expression in primary myotubes of embryonic mouse hindlimb muscles.	MYH1 MYH2 MYH3 MYH4	2.90e-09	13	51	4	8404542
Pubmed	Transition of myosin heavy chain isoforms in human laryngeal abductors following denervation.	MYH1 MYH2 MYH4	2.97e-09	3	51	3	26059207
Pubmed	Defective excitation-contraction coupling is partially responsible for impaired contractility in hindlimb muscles of Stac3 knockout mice.	MYH1 MYH2 MYH3 MYH4	4.06e-09	14	51	4	27184118
Pubmed	Six homeoproteins and a Iinc-RNA at the fast MYH locus lock fast myofiber terminal phenotype.	MYH1 MYH2 MYH3 MYH4	5.53e-09	15	51	4	24852826
Pubmed	Evaluation of embryonic and perinatal myosin gene mutations and the etiology of congenital idiopathic clubfoot.	MYH1 MYH2 MYH3	1.19e-08	4	51	3	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 MYH4	1.19e-08	4	51	3	11023856
Pubmed	Three linked myosin heavy chain genes clustered within 370 kb of each other show independent transcriptional and post-transcriptional regulation during differentiation of a mouse muscle cell line.	MYH1 MYH3 MYH4	1.19e-08	4	51	3	1985022
Pubmed	Smooth muscle myosin light chain kinase expression in cardiac and skeletal muscle.	MYH1 MYH2 MYH4	1.19e-08	4	51	3	11029314
Pubmed	Modulation of skeletal muscle fiber type by mitogen-activated protein kinase signaling.	MYH1 MYH2 MYH4	1.19e-08	4	51	3	18417546
Pubmed	A new role for the calcineurin/NFAT pathway in neonatal myosin heavy chain expression via the NFATc2/MyoD complex during mouse myogenesis.	MYH1 MYH2 MYH3 MYH4	2.94e-08	22	51	4	24301466
Pubmed	Detection of Gene and Protein Expression in Mouse Embryos and Tissue Sections.	MYH1 MYH2 MYH4	2.96e-08	5	51	3	30737693
Pubmed	Chronic multifocal osteomyelitis, a new recessive mutation on chromosome 18 of the mouse.	ADRB2 CD74 NR3C1	2.96e-08	5	51	3	1686018
Pubmed	Multigene family for sarcomeric myosin heavy chain in mouse and human DNA: localization on a single chromosome.	MYH1 MYH2 MYH3	2.96e-08	5	51	3	6879174
Pubmed	Myosin heavy chain isoforms of the murine masseter muscle during pre- and post-natal development.	MYH1 MYH2 MYH4	2.96e-08	5	51	3	12919077
Pubmed	A hypoplastic model of skeletal muscle development displaying reduced foetal myoblast cell numbers, increased oxidative myofibres and improved specific tension capacity.	MYH1 MYH2 MYH4	5.92e-08	6	51	3	20417199
Pubmed	A role for Insulin-like growth factor 2 in specification of the fast skeletal muscle fibre.	MYH1 MYH2 MYH4	5.92e-08	6	51	3	17559643
Pubmed	Myosin heavy chain-embryonic regulates skeletal muscle differentiation during mammalian development.	MYH1 MYH2 MYH3 MYH4	1.63e-07	33	51	4	32094117
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 MYH4	1.65e-07	8	51	3	26993635
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 MYH3 MYH4	1.65e-07	8	51	3	3864153
Pubmed	Long noncoding RNA lncMREF promotes myogenic differentiation and muscle regeneration by interacting with the Smarca5/p300 complex.	MYH1 MYH3 MYH4	1.65e-07	8	51	3	36200826
Pubmed	Cell lineage- and expression-based inference of the roles of forkhead box transcription factor Foxc2 in craniofacial development.	MYH1 MYH2 MYH4	1.65e-07	8	51	3	33667029
Pubmed	A Tcf4-positive mesodermal population provides a prepattern for vertebrate limb muscle patterning.	MYH1 MYH2 MYH4	1.65e-07	8	51	3	14667415
Pubmed	GASP-2 overexpressing mice exhibit a hypermuscular phenotype with contrasting molecular effects compared to GASP-1 transgenics.	MYH1 MYH2 MYH4	2.48e-07	9	51	3	31960486
Pubmed	Temporal regulation of the Mediator complex during muscle proliferation, differentiation, regeneration, aging, and disease.	MYH1 MYH2 MYH3 MYH4	3.25e-07	39	51	4	38690566
Pubmed	Acceleration of somitic myogenesis in embryos of myogenin promoter-MRF4 transgenic mice.	MYH1 MYH2 MYH3	3.54e-07	10	51	3	8950513
Pubmed	Extracellular matrix protein composition dynamically changes during murine forelimb development.	MYH1 MYH2 MYH4	4.86e-07	11	51	3	38303699
Pubmed	Deletion of the protein kinase A/protein kinase G target SMTNL1 promotes an exercise-adapted phenotype in vascular smooth muscle.	MYH1 MYH2 MYH4	4.86e-07	11	51	3	18310078
Pubmed	The histone code reader Spin1 controls skeletal muscle development.	MYH1 MYH2 MYH4	4.86e-07	11	51	3	29168801
Pubmed	Modulation of contractile protein gene expression in fetal murine crural muscles: emergence of muscle diversity.	MYH1 MYH2 MYH4	4.86e-07	11	51	3	8136524
Pubmed	HOXA5 plays tissue-specific roles in the developing respiratory system.	MYH1 MYH2 MYH3 MYH4	6.39e-07	46	51	4	28827394
Pubmed	Failure of Myf5 to support myogenic differentiation without myogenin, MyoD, and MRF4.	MYH1 MYH2 MYH3	8.41e-07	13	51	3	10694423
Pubmed	The inhibition of differentiation caused by TGFbeta in fetal myoblasts is dependent upon selective expression of PKCtheta: a possible molecular basis for myoblast diversification during limb histogenesis.	MYH1 MYH2 MYH3	8.41e-07	13	51	3	8948582
Pubmed	Inactivation of the myogenic bHLH gene MRF4 results in up-regulation of myogenin and rib anomalies.	MYH2 MYH3 MYH4	8.41e-07	13	51	3	7797078
Pubmed	Loss of Prox1 in striated muscle causes slow to fast skeletal muscle fiber conversion and dilated cardiomyopathy.	MYH1 MYH2 MYH4	1.07e-06	14	51	3	24938781
Pubmed	Myopathy associated LDB3 mutation causes Z-disc disassembly and protein aggregation through PKCα and TSC2-mTOR downregulation.	MYH1 MYH2 MYH4	1.07e-06	14	51	3	33742095
Pubmed	Genesis of muscle fiber-type diversity during mouse embryogenesis relies on Six1 and Six4 gene expression.	MYH1 MYH2 MYH3 MYH4	1.64e-06	58	51	4	21884692
Pubmed	MusTRD can regulate postnatal fiber-specific expression.	MYH1 MYH2 MYH4	1.64e-06	16	51	3	16494860
Pubmed	A family of microRNAs encoded by myosin genes governs myosin expression and muscle performance.	MYH1 MYH2 MYH4	1.64e-06	16	51	3	19922871
Pubmed	Slow and fast fiber isoform gene expression is systematically altered in skeletal muscle of the Sox6 mutant, p100H.	MYH2 MYH3 MYH4	1.99e-06	17	51	3	16124007
Pubmed	IKKα and alternative NF-κB regulate PGC-1β to promote oxidative muscle metabolism.	MYH1 MYH2 MYH4	1.99e-06	17	51	3	22351927
Pubmed	Organization of the gene (RHCE) encoding the human blood group RhCcEe antigens and characterization of the promoter region.	RHCE RHD	2.11e-06	2	51	2	8188244
Pubmed	E variants found in Japanese and c antigenicity alteration without substitution in the second extracellular loop.	RHCE RHD	2.11e-06	2	51	2	11724987
Pubmed	DCS-1, DCS-2, and DFV share amino acid substitutions at the extracellular RhD protein vestibule.	RHCE RHD	2.11e-06	2	51	2	17900276
Pubmed	Myosin heavy chains IIa and IId are functionally distinct in the mouse.	MYH1 MYH2	2.11e-06	2	51	2	9585413
Pubmed	RHD and RHCE molecular analysis in weak D blood donors and in patients with Rh antibodies against their own corresponding Rh antigen.	RHCE RHD	2.11e-06	2	51	2	32697929
Pubmed	The Rh blood group system: a review.	RHCE RHD	2.11e-06	2	51	2	10627438
Pubmed	Polymorphisms in the promoter regions of RHD and RHCE genes in the Chinese Han population.	RHCE RHD	2.11e-06	2	51	2	37823181
Pubmed	Sequence diversity of the Rh blood group system in Basques.	RHCE RHD	2.11e-06	2	51	2	30089826
Pubmed	Review: the molecular basis of the Rh blood group phenotypes.	RHCE RHD	2.11e-06	2	51	2	15373666
Pubmed	Intron 4 of the RH Gene in Han Chinese, Tibetan, and Mongol Populations.	RHCE RHD	2.11e-06	2	51	2	26579938
Pubmed	Accurate long-read sequencing allows assembly of the duplicated RHD and RHCE genes harboring variants relevant to blood transfusion.	RHCE RHD	2.11e-06	2	51	2	34968422
Pubmed	Transfusion strategy for weak D Type 4.0 based on RHD alleles and RH haplotypes in Tunisia.	RHCE RHD	2.11e-06	2	51	2	29193104
Pubmed	Regarding the size of Rh proteins.	RHCE RHD	2.11e-06	2	51	2	1898705
Pubmed	PCR screening for common weak D types shows different distributions in three Central European populations.	RHCE RHD	2.11e-06	2	51	2	11161244
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	2.11e-06	2	51	2	16575183
Pubmed	RH diversity in Mali: characterization of a new haplotype RHDDIVa/RHCEceTI(D2).	RHCE RHD	2.11e-06	2	51	2	25857637
Pubmed	The low-prevalence Rh antigen STEM (RH49) is encoded by two different RHCEce818T alleles that are often in cis to RHDDOL.	RHCE RHD	2.11e-06	2	51	2	22738288
Pubmed	Crosstalk between adrenergic and toll-like receptors in human mesenchymal stem cells and keratinocytes: a recipe for impaired wound healing.	ADRB2 TLR2	2.11e-06	2	51	2	24760207
Pubmed	Multiple Rh messenger RNA isoforms are produced by alternative splicing.	RHCE RHD	2.11e-06	2	51	2	1379850
Pubmed	Type IIx myosin heavy chain transcripts are expressed in type IIb fibers of human skeletal muscle.	MYH1 MYH2	2.11e-06	2	51	2	7545970
Pubmed	RHCE variants inherited with altered RHD alleles in Brazilian blood donors.	RHCE RHD	2.11e-06	2	51	2	27111588
Pubmed	Characterization of the mouse Rh blood group gene.	RHCE RHD	2.11e-06	2	51	2	10329015
Pubmed	Alteration of RH gene structure and expression in human dCCee and DCW-red blood cells: phenotypic homozygosity versus genotypic heterozygosity.	RHCE RHD	2.11e-06	2	51	2	8822955
Pubmed	Genetic recombination at the human RH locus: a family study of the red-cell Evans phenotype reveals a transfer of exons 2-6 from the RHD to the RHCE gene.	RHCE RHD	2.11e-06	2	51	2	8808597
Pubmed	Molecular background of Rh D-positive, D-negative, D(el) and weak D phenotypes in Chinese.	RHCE RHD	2.11e-06	2	51	2	12201845
Pubmed	Growth and muscle defects in mice lacking adult myosin heavy chain genes.	MYH1 MYH4	2.11e-06	2	51	2	9382868
Pubmed	Postnatal myosin heavy chain isoform expression in normal mice and mice null for IIb or IId myosin heavy chains.	MYH1 MYH4	2.11e-06	2	51	2	11150240
Pubmed	Myosin heavy chain composition of the human genioglossus muscle.	MYH1 MYH2	2.11e-06	2	51	2	22337492
Pubmed	Variant RH alleles and Rh immunisation in patients with sickle cell disease.	RHCE RHD	2.11e-06	2	51	2	24960646
Pubmed	Variability in laboratory immune parameters is associated with stress hormone receptor polymorphisms.	ADRB2 NR3C1	2.11e-06	2	51	2	22441538
Pubmed	Quantitative analysis of UGT2B28 mRNA expression by real-time RT-PCR and application to human tissue distribution study.	UGT2B28 UGT2B11	2.11e-06	2	51	2	21679149
Pubmed	RHCEceMO is frequently in cis to RHDDAU0 and encodes a hr(S) -, hr(B) -, RH:-61 phenotype in black persons: clinical significance.	RHCE RHD	2.11e-06	2	51	2	23772606
Pubmed	Comprehensive phenotypic and molecular investigation of RhD and RhCE variants in Moroccan blood donors.	RHCE RHD	2.11e-06	2	51	2	30418133
Pubmed	A convenient qualitative and quantitative method to investigate RHD-RHCE hybrid genes.	RHCE RHD	2.11e-06	2	51	2	23550903
Pubmed	Molecular cloning and primary structure of the human blood group RhD polypeptide.	RHCE RHD	2.11e-06	2	51	2	1438298
Pubmed	Determination of the N-terminal sequence of human red cell Rh(D) polypeptide and demonstration that the Rh(D), (c), and (E) antigens are carried by distinct polypeptide chains.	RHCE RHD	2.11e-06	2	51	2	3135863
Pubmed	Molecular background of D(C)(e) haplotypes within the white population.	RHCE RHD	2.11e-06	2	51	2	12084172
Pubmed	Temporal spatial expression and function of non-muscle myosin II isoforms IIA and IIB in scar remodeling.	MYH2 MYH4	2.11e-06	2	51	2	21102503
Pubmed	The analysis of nucleotide substitutions, gaps, and recombination events between RHD and RHCE genes through complete sequencing.	RHCE RHD	2.11e-06	2	51	2	10924335
Pubmed	Sequences and evolution of mammalian RH gene transcripts and proteins.	RHCE RHD	2.11e-06	2	51	2	9811965
Pubmed	A two-locus gene conversion model with selection and its application to the human RHCE and RHD genes.	RHCE RHD	2.11e-06	2	51	2	12857961
Pubmed	Specific amino acid substitutions cause distinct expression of JAL (RH48) and JAHK (RH53) antigens in RhCE and not in RhD.	RHCE RHD	2.11e-06	2	51	2	20233350
Pubmed	Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety.	RHCE RHD	2.11e-06	2	51	2	12393640
Pubmed	Molecular genetic basis of the human Rhesus blood group system.	RHCE RHD	2.11e-06	2	51	2	8220426
Pubmed	A recombination hot spot in the Rh genes revealed by analysis of unrelated donors with the rare D-- phenotype.	RHCE RHD	2.11e-06	2	51	2	8900235
Pubmed	Different pathways regulate expression of the skeletal myosin heavy chain genes.	MYH1 MYH2	2.11e-06	2	51	2	11551968
Pubmed	RHDweak partial 4.0 is associated with an altered RHCEce(48C, 105T, 733G, 744C, 1025T) allele in the Tunisian population.	RHCE RHD	2.11e-06	2	51	2	23742316
Pubmed	Isolation of a new cDNA clone encoding an Rh polypeptide associated with the Rh blood group system.	RHCE RHD	2.11e-06	2	51	2	7916743
Pubmed	A comprehensive survey of both RHD and RHCE allele frequencies in sub-Saharan Africa.	RHCE RHD	2.11e-06	2	51	2	24033223
Pubmed	RHDDOL1 and RHDDOL2 encode a partial D antigen and are in cis with the rare RHCE*ceBI allele in people of African descent.	RHCE RHD	2.11e-06	2	51	2	22690701
Interaction	ASAH2 interactions	MYH1 MYH3 MYH4	2.69e-07	6	49	3	int:ASAH2
Interaction	TSPAN33 interactions	MYH1 MYH2 MYH4 MYH13 TMEM45B	5.10e-07	65	49	5	int:TSPAN33
Interaction	RSPH6A interactions	MYH1 MYH2 MYH4 MYH13	1.36e-06	34	49	4	int:RSPH6A
Interaction	STK4 interactions	MYH1 MYH2 MYH3 MYH13 ITPRIPL1 NEDD4	2.32e-06	159	49	6	int:STK4
Interaction	TMEM260 interactions	MYH1 MYH3 MYH4	3.80e-06	13	49	3	int:TMEM260
Interaction	PRKAG2 interactions	MYH1 MYH2 MYH3 MYH4	2.24e-05	68	49	4	int:PRKAG2
Interaction	KCNH8 interactions	KCNH8 KCNH4	3.46e-05	4	49	2	int:KCNH8
Interaction	UGT2B28 interactions	UGT2B28 UGT2B11	8.63e-05	6	49	2	int:UGT2B28
Interaction	LATS1 interactions	MYH1 MYH2 MYH3 MYH4 MYH13 MOAP1 NEDD4	8.77e-05	440	49	7	int:LATS1
Interaction	ABTB2 interactions	MYH1 MYH2 MYH3 MYH4	1.06e-04	101	49	4	int:ABTB2
Interaction	MAP3K19 interactions	ZDHHC17 TRRAP	1.21e-04	7	49	2	int:MAP3K19
Interaction	UGT2B11 interactions	UGT2B28 UGT2B11	1.21e-04	7	49	2	int:UGT2B11
Interaction	AURKC interactions	MYH1 MYH4 NEDD4	1.56e-04	43	49	3	int:AURKC
Interaction	NDST4 interactions	NDST3 NDST1	1.61e-04	8	49	2	int:NDST4
Interaction	CDK3 interactions	MYH1 MYH2 MYH3 MYH13	1.69e-04	114	49	4	int:CDK3
Interaction	ABCG4 interactions	ZDHHC17 NEDD4	2.06e-04	9	49	2	int:ABCG4
Cytoband	17p13.1	MYH1 MYH2 MYH3 MYH4	9.44e-06	118	51	4	17p13.1
Cytoband	Ensembl 112 genes in cytogenetic band chr17p13	MYH1 MYH2 MYH3 MYH4 MYH13	4.18e-05	346	51	5	chr17p13
Cytoband	12p13.3	ANO2 GALNT8	5.16e-04	30	51	2	12p13.3
Cytoband	4q13.2	UGT2B28 UGT2B11	5.51e-04	31	51	2	4q13.2
Cytoband	1p36.11	RHCE RHD	2.63e-03	68	51	2	1p36.11
Cytoband	2q11.2	CREG2 ITPRIPL1	2.94e-03	72	51	2	2q11.2
Cytoband	Ensembl 112 genes in cytogenetic band chr5q33	NDST1 CD74	7.69e-03	118	51	2	chr5q33
GeneFamily	Myosin heavy chains	MYH1 MYH2 MYH3 MYH4 MYH13	8.02e-11	15	37	5	1098
GeneFamily	Sulfotransferases, membrane bound	NDST3 NDST1 CHST4	5.84e-05	37	37	3	763
GeneFamily	UDP glucuronosyltransferases	UGT2B28 UGT2B11	1.94e-03	32	37	2	363
GeneFamily	Glycosyltransferase family 6\|Blood group antigens	RHCE RHD	2.59e-03	37	37	2	454
GeneFamily	Potassium voltage-gated channels	KCNH8 KCNH4	3.03e-03	40	37	2	274
GeneFamily	ADAM metallopeptidase domain containing\|CD molecules	TLR2 CD74 RHCE RHD	8.32e-03	394	37	4	471
Coexpression	HUMMERICH_BENIGN_SKIN_TUMOR_DN	MYH1 MYH2 MYH4	7.73e-06	20	51	3	M1123
Coexpression	HUMMERICH_BENIGN_SKIN_TUMOR_DN	MYH1 MYH2 MYH4	9.00e-06	21	51	3	MM1102
Coexpression	GSE34156_UNTREATED_VS_6H_NOD2_LIGAND_TREATED_MONOCYTE_DN	SLC37A3 ELMOD2 ZNFX1 NR3C1 HDC	2.42e-05	177	51	5	M8666
Coexpression	GSE22886_TCELL_VS_BCELL_NAIVE_DN	FADS3 SBNO1 CHST4 SLC24A1 RHD	4.14e-05	198	51	5	M4426
ToppCell	renal_papilla_nuclei-Adult_normal_reference-Epithelial-Intermediate_tubule_epithelial_cell-kidney_loop_of_Henle_thin_descending_limb_epithelial_cell-Descending_Thin_Limb_Cell_Type_2\|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group	MYH1 MYH2 MYH4 ADRB2 UGT2B11	1.24e-06	164	51	5	382e42701779d12a7948690b3be72d06dd75c8b4
ToppCell	Thalamus-Neuronal-Excitatory-eN2(Slc17a7_Slc17a6)-Slc17a7-Tac2-Excitatory_Neuron.Slc17a7.Tac2.Syt15_(Medial_habenula)\|Thalamus / BrainAtlas - Mouse McCarroll V32	MYH1 MYH2 MYH4 MYH13	1.86e-06	77	51	4	7f624e9262bd0dc2ac4176f43c91a4bc0f521fe5
ToppCell	5'-Parenchyma_lung-Epithelial-Alveolar_epithelium-type_I_pneumocyte-AT1-AT1_L.0.5.2.0\|5' / 5'-vs-3', Tissue groups, Lineages, Lineage subclass, Cell_type2, Cell_subtype2_L4.5	NDST1 P4HA2 ADRB2 FADS3 ABCA7	2.18e-06	184	51	5	ca940a4f4970285ed284d5517d142abab0682044
ToppCell	facs-Trachea-18m-Mesenchymal-fibroblast-fibroblast_of_trachea-\|18m / method, tissue, age, lineage, sublineage, cell ontologies, cell type and subtype	MYH1 MYH2 MYH3 MYH4 MYH13	2.30e-06	186	51	5	bdc87e4631a8ea73e262e541aa84a28f24c94b00
ToppCell	AT1_cells-Donor_02\|World / lung cells shred on cell class, cell subclass, sample id	NDST1 ADRB2 FADS3 BCAT2 ABCA7	2.69e-06	192	51	5	0444f9e9cef7403e220e862b5a787443d3f5c9ac
ToppCell	Parenchymal-NucSeq-Stromal-Schwann\|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations	KCNH8 GALNT8 ZNFX1 RENBP	1.64e-05	133	51	4	8819fd897b97812355e1709fcc42754522d5fb27
ToppCell	Parenchymal-NucSeq-Stromal-Schwann-Schwann_nonmyelinating\|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations	KCNH8 GALNT8 ZNFX1 RENBP	1.64e-05	133	51	4	b4e68a9a223e5188f1a00c7dc9bb2d675cde1d40
ToppCell	Frontal_cortex-Neuronal-Excitatory-eN1(Slc17a7)-eN1_2-Nptxr\|Frontal_cortex / BrainAtlas - Mouse McCarroll V32	ANO2 SBNO1 SLC24A1 KCNH4	2.49e-05	148	51	4	223d6a640f3c34e73646a615593b9c0b4a4cbd6f
ToppCell	Thalamus-Neuronal-Excitatory-eN2(Slc17a7_Slc17a6)-Slc17a7-Tac2\|Thalamus / BrainAtlas - Mouse McCarroll V32	MYH1 MYH4 KCNH8 MYH13	3.38e-05	160	51	4	fe5fb0e7a79862f63529721f0a82f4f6d231d3ca
ToppCell	Thalamus-Neuronal-Excitatory-eN2(Slc17a7_Slc17a6)-Slc17a7\|Thalamus / BrainAtlas - Mouse McCarroll V32	MYH1 MYH4 KCNH8 MYH13	3.38e-05	160	51	4	7d34159363d274019e14549d1186c629ce990691
ToppCell	primary_visual_cortex-Neuronal-glutamatergic_neuron-L6_CT-L6_CT_VISp_Ctxn3_Sla\|primary_visual_cortex / Per Region, Lineage, Cell class, Cell type, Cell subtype	NDST3 NDST1 MYH2 MYH3	3.55e-05	162	51	4	4d13c271b4f63cf32980e5643b5d5951165fe8b5
ToppCell	facs-Marrow-Granulocytes-24m-Lymphocytic-naive_B_cell\|Marrow / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation	TMEM45B CHST4 CD74 RENBP	3.63e-05	163	51	4	8509b87748ec460992ae6cedbb155e1c6f6e2e48
ToppCell	facs-Marrow-Granulocytes-24m-Lymphocytic-naive_B_cell\|Marrow / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation	TMEM45B CHST4 CD74 RENBP	3.63e-05	163	51	4	e04de78a52cc886623689a913f7852200a77605b
ToppCell	3'-Parenchyma_lung-Epithelial-Alveolar_epithelium-type_I_pneumocyte-AT1-AT1_L.0.5.1.0\|3' / 5'-vs-3', Tissue groups, Lineages, Lineage subclass, Cell_type2, Cell_subtype2_L4.5	ADRB2 FADS3 GALNT8 ABCA7	4.18e-05	169	51	4	cd16e8462ee09877be962fbd9a3badcb825820b0
ToppCell	18-Distal-RBC\|Distal / Age, Tissue, Lineage and Cell class	ABCA7 RHCE RHD HDC	4.79e-05	175	51	4	cc476b4244442418b8f21721a82a36209b556b36
ToppCell	18-Distal-RBC-RBC\|Distal / Age, Tissue, Lineage and Cell class	ABCA7 RHCE RHD HDC	4.79e-05	175	51	4	7130b816e0c02309c161d8e9ad7cb4bc2469e251
ToppCell	Frontal_cortex-Neuronal-Inhibitory-iN1(Gad1Gad2_Th)-Sst-Inhibitory_Neuron.Gad1Gad2.Sst-Nr2f2_(MGE-derived_cortical_interneurons--Martinotti_cells)\|Frontal_cortex / BrainAtlas - Mouse McCarroll V32	MYH1 MYH4 MYH13	4.95e-05	62	51	3	a20620a8869721ea62984c2022ee1b484b455824
ToppCell	Frontal_cortex-Neuronal-Inhibitory-iN1(Gad1Gad2_Th)-Sst-Inhibitory_Neuron.Gad1Gad2.Sst-Nr2f2_(MGE-derived_cortical_interneurons--Martinotti_cells)-\|Frontal_cortex / BrainAtlas - Mouse McCarroll V32	MYH1 MYH4 MYH13	4.95e-05	62	51	3	ee694c06bcd924b4ddf744178ba3a99e04eed51b
ToppCell	wk_20-22-Hematologic_Lymphocytic-B-Late_pro-B\|wk_20-22 / Celltypes from embryonic and fetal-stage human lung	P4HA2 FADS3 CD74 CREG2	5.12e-05	178	51	4	4e28a8bd5a603518bfe993712ab785308691b5ff
ToppCell	PBMC-Convalescent-Lymphocyte-B-B_cell-B_naive-B_naive-1\|Convalescent / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.01)	KCNH8 FADS3 CD74 METTL8	5.46e-05	181	51	4	6df40f86c569b6ecfc3137a68d1355b012dbf6bf
ToppCell	5'-GW_trimst-1-SmallIntestine-Mesenchymal-myocytic\|GW_trimst-1 / Celltypes from developing, pediatric, Crohn's, & adult GI tract	PCSK5 P2RY1 ZNFX1 ITPRIPL1	5.58e-05	182	51	4	52274af3136d4fd4a495f5882618444661421f0f
ToppCell	5'-GW_trimst-1-SmallIntestine-Mesenchymal-myocytic-SMC_(PLPP2+)\|GW_trimst-1 / Celltypes from developing, pediatric, Crohn's, & adult GI tract	PCSK5 P2RY1 ZNFX1 ITPRIPL1	5.58e-05	182	51	4	dfde2d9950f445c6c936ac828f7210de87bb45ec
ToppCell	Hippocampus-Neuronal-Excitatory-eN2(Slc17a7_Slc17a6)-Slc17a6-Excitatory_Neuron.Slc17a6.Grp_(Neuron.Slc17a6.Grp)-\|Hippocampus / BrainAtlas - Mouse McCarroll V32	MYH1 MYH2 MOAP1	5.70e-05	65	51	3	b7bc23af54d6d2f7afd584f4df42c24d7c49e344
ToppCell	Hippocampus-Neuronal-Excitatory-eN2(Slc17a7_Slc17a6)-Slc17a6-Excitatory_Neuron.Slc17a6.Grp_(Neuron.Slc17a6.Grp)\|Hippocampus / BrainAtlas - Mouse McCarroll V32	MYH1 MYH2 MOAP1	5.70e-05	65	51	3	3b3630253f5713c4a688c74c4ea0f98c1fe42594
ToppCell	PBMC-Convalescent-Lymphocyte-B-B_cell-B_naive\|Convalescent / Location, Disease Group, Cell group, Cell class (2021.03.09)	KCNH8 FADS3 CD74 METTL8	6.07e-05	186	51	4	f352c63666273defea3e57ba3a3bfad52c4ea65b
ToppCell	PBMC-Convalescent-Lymphocyte-B-B_cell-B_naive-\|Convalescent / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.09)	KCNH8 FADS3 CD74 METTL8	6.07e-05	186	51	4	e2d265003aaea1acaf618d3f102c9933c19102e6
ToppCell	10x_3'_v3-bone_marrow_(10x_3'_v3)-lymphocytic-B_lymphocytic-memory_B_cell\|bone_marrow_(10x_3'_v3) / Per Platform+tissue_group, by lineage_subgroup, cell_group, cell_type	KCNH8 FADS3 CD74 METTL8	6.20e-05	187	51	4	b5cb8760fa667c237902d50a78dea4cb1babd607
ToppCell	AT1_cells\|World / lung cells shred on cell class, cell subclass, sample id	NDST1 FADS3 BCAT2 ABCA7	7.29e-05	195	51	4	792d6a49b0a875a00569071183d195287a9925c5
ToppCell	Parenchymal-NucSeq-Immune_Myeloid-Myeloid\|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations	CLN8 P2RY1 RHCE RHD	7.29e-05	195	51	4	027075e9c62b5754a014a9d1393e1b0f5ae42e41
ToppCell	Parenchymal-NucSeq-Immune_Myeloid-Myeloid-Megakaryocyte\|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations	CLN8 P2RY1 RHCE RHD	7.29e-05	195	51	4	1bcc0c8b1281396b1433ce5a2ec8681de47ce9ad
ToppCell	Smart-start-Cell-Wel_seq-Non-neoplastic-Lymphoid-CD4/CD8-CD8_EM-F\|Smart-start-Cell-Wel_seq / Platform, Oncotype, Lineage, Cell_class, celltype (level4), mutation group	SLC37A3 SBNO1 METTL8 HDC	7.44e-05	196	51	4	7e98380d815fbf6254289ace2af37aac6fef51e8
ToppCell	10x_3'_v2v3-Non-neoplastic-Myeloid-Mast\|10x_3'_v2v3 / Platform, Oncotype, Lineage, Cell_class, celltype (level4), mutation group	ADRB2 RENBP RHCE HDC	7.44e-05	196	51	4	0ebf7e5a9281ec1f33dccd1f8895afd513591b91
ToppCell	10x_3'_v2v3-Non-neoplastic-Myeloid-Mast-Mast\|10x_3'_v2v3 / Platform, Oncotype, Lineage, Cell_class, celltype (level4), mutation group	ADRB2 RENBP RHCE HDC	7.44e-05	196	51	4	bd482b7df2993d87c0997a40c4cbd34ba07910cb
ToppCell	Smart-start-Cell-Wel_seq-Non-neoplastic-Myeloid-TAM-MG-TAM-MG_pro-infl_II-F\|Smart-start-Cell-Wel_seq / Platform, Oncotype, Lineage, Cell_class, celltype (level4), mutation group	MYH3 ADRB2 CD74 ZNFX1	7.58e-05	197	51	4	b597c292fc1cb381a4325fed15a32966c38def28
ToppCell	AT1_cells-Donor_06\|World / lung cells shred on cell class, cell subclass, sample id	NDST1 FADS3 BCAT2 ABCA7	7.58e-05	197	51	4	80d81be244c94c435accb643449b4ce6a3462c7f
ToppCell	Epithelial_cells-AT1-AT2_cells\|Epithelial_cells / lung cells shred on cell class, cell subclass, sample id	NDST1 FADS3 BCAT2 ABCA7	7.73e-05	198	51	4	fbc46b20bcd44f2083170aacbc6f5dd00fba685c
ToppCell	5'-Adult-LargeIntestine-Hematopoietic-Myeloid\|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract	TLR2 CD74 RENBP HDC	7.89e-05	199	51	4	a4785c1921a3de18a9190e4d674ede6a90f80004
ToppCell	tumor_Lung-Endothelial_cells-Tip-like_ECs\|Endothelial_cells / Location, Cell class and cell subclass	ADRB2 P2RY1 CD74 NR3C1	7.89e-05	199	51	4	80c8641cfd84436eadf2234f1313749e2f73331f
ToppCell	Tracheal-NucSeq-Immune_Myeloid\|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations	TLR2 CD74 RENBP HDC	8.04e-05	200	51	4	ad7ae5106141669b353800fece833b3cd5bdccee
ToppCell	Caecum-(7)_Mast_cell\|Caecum / shred on region, Cell_type, and subtype	ADRB2 P2RY1 RENBP HDC	8.04e-05	200	51	4	d23fe8644ce42ace51fcde43cb4cd22a99300c02
ToppCell	Caecum-Mast_cell\|Caecum / Region, Cell class and subclass	ADRB2 P2RY1 RENBP HDC	8.04e-05	200	51	4	8791d0b3d883e7a747a23d21118817f5be4013b6
ToppCell	Caecum-(7)_Mast_cell-(70)_Mast\|Caecum / shred on region, Cell_type, and subtype	ADRB2 P2RY1 RENBP HDC	8.04e-05	200	51	4	9974285c28a633a010c4f24d035ad3685705e881
ToppCell	Caecum-Mast_cell-Mast\|Caecum / Region, Cell class and subclass	ADRB2 P2RY1 RENBP HDC	8.04e-05	200	51	4	168426e8296697d05684d71989c4eb5bb2a0489f
ToppCell	Thalamus-Neuronal-Excitatory-eN2(Slc17a7_Slc17a6)-Slc17a7-Tac2-Excitatory_Neuron.Slc17a7.Tac2.Chat_(Habenular_cholinergic_cells)\|Thalamus / BrainAtlas - Mouse McCarroll V32	LYPD4 ANO2 MYH3	1.14e-04	82	51	3	51dd9ab3ddb26d3d3395d0c1a156a12a86caf89b
Drug	fast white	MYH1 MYH2 MYH3 MYH4 MYH13	3.68e-08	42	51	5	CID000024008
Drug	AC1N9ZZC	MYH1 MYH2 MYH3 MYH4 ADRB2 KCNH8 MYH13	4.06e-08	149	51	7	CID004369374
Drug	formycin triphosphate	MYH1 MYH2 MYH3 MYH4 MYH13	1.00e-07	51	51	5	CID000122274
Drug	purealin	MYH1 MYH2 MYH3 MYH4 MYH13	1.93e-07	58	51	5	CID006419303
Drug	NSC9700	MYH1 MYH2 MYH3 MYH4 SRD5A3 MYH13 UGT2B28 NR3C1 UGT2B11 HDC	5.15e-07	578	51	10	CID000005408
Drug	clenbuterol	MYH1 MYH2 MYH3 MYH4 ADRB2 MYH13	7.57e-07	142	51	6	CID000002783
Drug	SM-2	MYH1 MYH2 MYH3 MYH4 MYH13	1.48e-06	87	51	5	CID000486033
Drug	carvedilol	MYH1 MYH2 MYH3 MYH4 ADRB2 MYH13	1.58e-06	161	51	6	CID000002585
Drug	S-(-)-Etomoxir	MYH1 MYH2 MYH3 MYH4 MYH13	2.96e-06	100	51	5	CID000060765
Drug	nifedipine	MYH1 MYH2 MYH3 MYH4 ADRB2 FADS3 MYH13 TRPC5	3.65e-06	415	51	8	CID000004485
Drug	K-Cl	MYH1 MYH2 MYH3 MYH4 ADRB2 KCNH8 MYH13 P2RY1 NR3C1	4.14e-06	567	51	9	CID000004873
Drug	Haloperidol [52-86-8]; Down 200; 10.6uM; MCF7; HT_HG-U133A	CLN8 NDST1 SRD5A3 PCNX1 ZDHHC17 ABCA7	4.50e-06	193	51	6	5273_DN
Drug	blebbistatin	MYH1 MYH2 MYH3 MYH4 MYH13	6.13e-06	116	51	5	CID003476986
Drug	B0683	MYH1 MYH2 MYH3 MYH4 MYH13	6.40e-06	117	51	5	CID006398969
Drug	oxovanadium	MYH1 MYH2 MYH3 MYH4 MYH13	7.24e-06	120	51	5	CID000024411
Drug	2bq7	MYH1 MYH2 MYH3 MYH4 MYH13	8.16e-06	123	51	5	CID006540267
Drug	wartmannin	PCSK5 MYH1 MYH2 MYH3 MYH4 MYH13 P2RY1 TRPC5 TLR2 KCNH4	1.06e-05	811	51	10	CID000005691
Drug	AC1LADJ6	MYH1 MYH2 MYH3 MYH4 MYH13	1.07e-05	130	51	5	CID000486032
Drug	Spermine	MYH1 MYH3 MYH4 ADRB2	1.21e-05	63	51	4	ctd:D013096
Drug	AC1NRBPQ	MYH1 MYH2 MYH3 MYH4 MYH13	1.38e-05	137	51	5	CID005288569
Drug	candesartan cilexetil	MYH1 MYH2 MYH3 MYH4 MYH13	1.81e-05	145	51	5	CID000002540
Drug	carbachol	MYH1 MYH2 MYH3 MYH4 ADRB2 MYH13 P2RY1 TRPC5 HDC	1.95e-05	688	51	9	CID000002551
Drug	D-triiodothyronine	MYH1 MYH2 MYH3 MYH4 ADRB2 MYH13 NR3C1	3.36e-05	409	51	7	CID000000861
Drug	LY294002	MYH1 MYH2 MYH3 MYH4 MYH13 P2RY1 TLR2 NR3C1 KCNH4	3.75e-05	748	51	9	CID000003973
Drug	oxyfedrine	PCSK5 ADRB2	4.90e-05	5	51	2	CID000027454
Drug	NSC226080	PCSK5 MYH1 MYH2 MYH3 MYH4 MYH13 NR3C1 ZDHHC17 KCNH4	5.30e-05	782	51	9	CID000005040
Drug	SN-38	PCSK5 MYH2 MYH4 UGT2B28 UGT2B11	5.67e-05	184	51	5	CID000104842
Drug	Pertussis Toxin	MYH4 ADRB2 P2RY1 NR3C1	5.87e-05	94	51	4	ctd:D037342
Drug	Kawain [500-64-1]; Down 200; 17.4uM; MCF7; HT_HG-U133A	CLN8 NDST1 FADS3 SRD5A3 NR3C1	6.61e-05	190	51	5	2299_DN
Drug	Rapamycin; Up 200; 0.1uM; MCF7; HT_HG-U133A	FADS3 SRD5A3 P2RY1 TLR2 SLC24A1	6.94e-05	192	51	5	5567_UP
Drug	creatine	MYH1 MYH2 MYH3 MYH4 MYH13	7.11e-05	193	51	5	CID000000586
Drug	Colchicine [64-86-8]; Up 200; 10uM; MCF7; HT_HG-U133A	PCSK5 NDST1 TLR2 SLC24A1 ABCA7	7.29e-05	194	51	5	3213_UP
Drug	Diphenidol hydrochloride [3254-89-5]; Up 200; 11.6uM; MCF7; HT_HG-U133A	FADS3 CHST4 CD74 SLC24A1 ABCA7	7.47e-05	195	51	5	7406_UP
Drug	(+) -Levobunolol hydrochloride [47141-41-3]; Up 200; 12.2uM; MCF7; HT_HG-U133A	NDST1 ANO2 FADS3 SRD5A3 NR3C1	8.03e-05	198	51	5	4980_UP
Drug	4-chloroaniline	MYH1 MYH2 MYH3 MYH4 MYH13	8.82e-05	202	51	5	CID000007812
Drug	verapamil	MYH1 MYH2 MYH3 MYH4 ADRB2 MYH13 ABCA7	1.05e-04	490	51	7	CID000002520
Drug	testosterone glucuronide	UGT2B28 NR3C1 UGT2B11	1.06e-04	41	51	3	CID000108192
Drug	N-ethylmaleimide	MYH1 MYH2 MYH3 MYH4 MYH13 RENBP RHD	1.36e-04	511	51	7	CID000004362
Drug	eye gene	MYH1 MYH2 MYH3 MYH4 ADRB2 MYH13	1.69e-04	369	51	6	CID000004782
Drug	salicylamide	RENBP UGT2B28 UGT2B11	1.71e-04	48	51	3	CID000005147
Drug	UDP - Na	P2RY1 GALNT8 RENBP UGT2B28 UGT2B11	1.79e-04	235	51	5	CID000001158
Drug	4-methylumbelliferone	NDST3 CHST4 UGT2B28 UGT2B11	2.18e-04	132	51	4	CID003364573
Drug	2-aminophenol	NR3C1 UGT2B11	2.19e-04	10	51	2	ctd:C027667
Drug	nylidrin	ADRB2 RHCE	2.19e-04	10	51	2	CID000004567
Disease	dilated cardiomyopathy 1S (implicated_via_orthology)	MYH1 MYH2 MYH3 MYH4 MYH13	2.56e-12	10	49	5	DOID:0110454 (implicated_via_orthology)
Disease	autosomal dominant hyaline body myopathy (implicated_via_orthology)	MYH1 MYH2 MYH3 MYH4 MYH13	2.56e-12	10	49	5	DOID:0111269 (implicated_via_orthology)
Disease	congenital myopathy 6 (implicated_via_orthology)	MYH1 MYH2 MYH3 MYH4 MYH13	2.56e-12	10	49	5	DOID:0080719 (implicated_via_orthology)
Disease	distal arthrogryposis type 2B3 (implicated_via_orthology)	MYH1 MYH2 MYH3 MYH4 MYH13	2.56e-12	10	49	5	DOID:0111602 (implicated_via_orthology)
Disease	inclusion body myositis (implicated_via_orthology)	MYH1 MYH2 MYH3 MYH4 MYH13	2.56e-12	10	49	5	DOID:3429 (implicated_via_orthology)
Disease	distal arthrogryposis type 2A (implicated_via_orthology)	MYH1 MYH2 MYH3 MYH4 MYH13	2.56e-12	10	49	5	DOID:0111605 (implicated_via_orthology)
Disease	familial hypertrophic cardiomyopathy (implicated_via_orthology)	MYH1 MYH2 MYH3 MYH4 MYH13	2.56e-12	10	49	5	DOID:0080326 (implicated_via_orthology)
Disease	distal arthrogryposis type 1 (implicated_via_orthology)	MYH1 MYH2 MYH3 MYH4 MYH13	2.56e-12	10	49	5	DOID:0111596 (implicated_via_orthology)
Disease	distal myopathy (implicated_via_orthology)	MYH1 MYH2 MYH3 MYH4 MYH13	8.03e-12	12	49	5	DOID:11720 (implicated_via_orthology)
Disease	myotonia congenita (implicated_via_orthology)	MYH1 MYH2 MYH3 MYH4 MYH13	8.03e-12	12	49	5	DOID:2106 (implicated_via_orthology)
Disease	restrictive cardiomyopathy (implicated_via_orthology)	MYH1 MYH2 MYH3 MYH4 MYH13	1.30e-11	13	49	5	DOID:397 (implicated_via_orthology)
Disease	distal arthrogryposis (implicated_via_orthology)	MYH1 MYH2 MYH3 MYH4 MYH13	3.04e-11	15	49	5	DOID:0050646 (implicated_via_orthology)
Disease	dilated cardiomyopathy (implicated_via_orthology)	MYH1 MYH2 MYH3 MYH4 ADRB2 MYH13	4.18e-09	80	49	6	DOID:12930 (implicated_via_orthology)
Disease	myopathy (implicated_via_orthology)	MYH1 MYH2 MYH3 MYH4 MYH13	1.66e-08	48	49	5	DOID:423 (implicated_via_orthology)
Disease	cardiomyopathy (implicated_via_orthology)	MYH1 MYH2 MYH3 MYH4 MYH13	1.23e-07	71	49	5	DOID:0050700 (implicated_via_orthology)
Disease	Anemia, Hemolytic, Congenital	RHCE RHD	2.70e-06	2	49	2	C0002881
Disease	phosphatidylcholine 36:4 measurement	FADS3 UGT2B28 UGT2B11	3.45e-06	18	49	3	EFO_0010382
Disease	Rh Deficiency Syndrome	RHCE RHD	8.10e-06	3	49	2	C0272052
Disease	Rh-Null, Regulator Type	RHCE RHD	8.10e-06	3	49	2	C1849387
Disease	Hypokalemia	ADRB2 NR3C1	5.64e-05	7	49	2	C0020621
Disease	asthma (is_implicated_in)	ADRB2 TLR2 NR3C1 HDC	1.36e-04	157	49	4	DOID:2841 (is_implicated_in)
Disease	Lung diseases	PCSK5 ADRB2 ELMOD2	3.00e-04	78	49	3	C0024115
Disease	sinusitis (is_marker_for)	TLR2 NR3C1	4.06e-04	18	49	2	DOID:0050127 (is_marker_for)
Disease	polycystic ovary syndrome (biomarker_via_orthology)	ADRB2 NR3C1	5.56e-04	21	49	2	DOID:11612 (biomarker_via_orthology)
Disease	lung disease (is_implicated_in)	TLR2 NR3C1	6.11e-04	22	49	2	DOID:850 (is_implicated_in)
Disease	azoospermia (implicated_via_orthology)	NDST3 NDST1	9.23e-04	27	49	2	DOID:14227 (implicated_via_orthology)
Disease	muscular atrophy (biomarker_via_orthology)	NR3C1 NEDD4	1.07e-03	29	49	2	DOID:767 (biomarker_via_orthology)
Disease	rhinitis (is_implicated_in)	TLR2 HDC	1.14e-03	30	49	2	DOID:4483 (is_implicated_in)
Disease	Bipolar Disorder	NDST3 ADRB2 TLR2 NR3C1 NEDD4	1.15e-03	477	49	5	C0005586
Disease	pulmonary sarcoidosis (is_marker_for)	TLR2 NR3C1	1.30e-03	32	49	2	DOID:13406 (is_marker_for)
Disease	phosphatidylcholine 38:5 measurement	FADS3 UGT2B28	1.38e-03	33	49	2	EFO_0010387
Disease	lung disease (biomarker_via_orthology)	TLR2 NR3C1	1.55e-03	35	49	2	DOID:850 (biomarker_via_orthology)

Protein segments in the cluster

Peptide	Gene	Start	Entry
AAHILMKMWTFGNFW	ADRB2	91	P07550
MKMWTFGNFWCEFWT	ADRB2	96	P07550
WMMDNNFSHHWKGMF	LINC00596	16	Q86U02
GHFFRFWMKWLLRQM	ELMOD2	11	Q8IZ81
IFMALWATMFLENWK	ANO2	446	Q9NQ90
FFMKMRIEHIWLQKW	CREG2	256	Q8IUH2
MAFWTQLMLLLWKNF	ABCA7	1	Q8IZY2
SVDEFWWFPHMWSHM	NDST3	371	O95803
WMMVHFDCTGFWVKD	HDC	306	P19113
VAIWMFVFHMKPWSG	P2RY1	71	P47900
KLWWPHSEAMIAFLM	RENBP	321	P51606
HQVIQWFWKAVLMMD	NEDD4	1221	P46934
MWIAMFSYLMVWWAH	SLC24A1	946	O60721
WNFKIMFHQFEMIWA	KIAA1109	521	Q2LD37
FGRWMFHTTQMIKAW	MOAP1	181	Q96BY2
AATMMWFEKLHVWLL	PCNX1	1341	Q96RV3
MEGFKNWEFMTIHCW	PCSK5	546	Q92824
SFMNVKHWPWMKLFF	MYH2	826	Q9UKX2
VKEFWWFPHMWSHMQ	NDST1	381	P52848
MSVFALLAHWMACIW	KCNH4	366	Q9UQ05
AFHNWKWLLMRNMVC	LYPD4	41	Q6UWN0
LQYSWMFLMAFALGW	NR3C1	596	P04150
NVRAFMNVKHWPWMK	MYH1	821	P12882
MKLWVSALLMAWFGV	P4HA2	1	O15460
WFHILGMMMFIWSSA	SRD5A3	201	Q9H8P0
WFRNMMGNAWALVAH	ITPRIPL1	321	Q6GPH6
LAINAFNLSWMAAMW	CENPL	211	Q8N0S6
WMDEHKHMVYLAWNI	GALNT8	436	Q9NY28
FESWMHHWLLFEMSR	CD74	181	P04233
FTDHMLMVEWNDKGW	BCAT2	61	O15382
KFVMGQLKGFSAHWW	FADS3	201	Q9Y5Q0
KKSMWGQFWSAHQRF	SBNO1	586	A3KN83
KVFEHNMWDHMQWSK	METTL8	41	Q9H825
WFFTWVGLEMNMLAF	MT-ND2	26	P03891
GWAWMMVLSSFFVHI	SLC16A14	31	Q7RTX9
NIRAFMNVKHWPWMK	MYH4	821	Q9Y623
SFMNVKHWPWMKLFF	MYH3	821	P11055
ESLFWKLNQWLMIHM	CLN8	186	Q9UBY8
LMEPAWHVWMTFKQS	CHST4	71	Q8NCG5
WIKLMNWQHSTMYLF	TMEM45B	81	Q96B21
WMFSIHLPSKMKVWQ	SUN5	116	Q8TC36
SLSAMLGALFLWMFW	RHD	206	Q02161
SLSAMLGALFLWMFW	RHCE	206	P18577
KLGWMWVFYFFILMT	SLC37A3	451	Q8NCC5
NFWMVWSEAMAHGCF	PRAMEF5	111	Q5TYX0
NIRSFMNVKHWPWMN	MYH13	821	Q9UKX3
MNVKHWPWMNLFFKI	MYH13	826	Q9UKX3
VLVWAAEYSHWMNMK	UGT2B11	26	O75310
WICFQHWKHSMMLEW	ZNFX1	771	Q9P2E3
MFWMFLNSVFHFMWV	ZDHHC17	531	Q8IUH5
IHDWWNLMDFAMNSL	TRPC5	431	Q9UL62
VLVWTGEYSHWMNMK	UGT2B28	26	Q9BY64
RFHGLWYMKMMWAWL	TLR2	611	O60603
VQMHDVLVKAWAMWG	TRRAP	3146	Q9Y4A5
SMFALLAHWMACIWY	KCNH8	361	Q96L42
LAHWMACIWYVIGKM	KCNH8	366	Q96L42