Gene Details



MYH7 and homologs in 1 species are found in 373 GeneSets:


- Entrez   - GeneNetwork   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Human CTD 10 Genes GS121575: SK-7041 interacting genes (MeSH:C497103) in CTD
Expand Tier I Human GO 475 Genes GS205825: GO:1901292 nucleoside phosphate catabolic process
Expand Tier I Human 32 Genes GS172731: HP:0011463 Childhood onset
Expand Tier I Human 112 Genes GS174327: HP:0003198 Myopathy
Expand Tier I Human 1 Genes GS176649: HP:0009077 Weakness of long finger extensor muscles
Expand Tier I Human GO 18 Genes GS208901: GO:0005859 muscle myosin complex
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human GO 133 Genes GS204692: GO:0060047 heart contraction
Expand Tier I Human GO 1510 Genes GS201792: GO:0032559 adenyl ribonucleotide binding
Expand Tier I Human 15 Genes GS172578: HP:0003691 Scapular winging
Expand Tier I Human GO 1684 Genes GS204629: GO:1901564 organonitrogen compound metabolic process
Expand Tier I Human GO 452 Genes GS205123: GO:0030029 actin filament-based process
Expand Tier I Human GO 1439 Genes GS205623: GO:0009888 tissue development
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human CTD 2 Genes GS124591: N(6)-phenyl-cAMP interacting genes (MeSH:C483758) in CTD
Expand Tier I Human GO 1839 Genes GS205510: GO:0001883 purine nucleoside binding
Expand Tier I Human GO 5216 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human CTD 4423 Genes GS123718: Ethinyl Estradiol interacting genes (MeSH:D004997) in CTD
Expand Tier I Human GO 129 Genes GS207431: GO:0005925 focal adhesion
Expand Tier I Human 96 Genes GS176759: HP:0000982 Palmoplantar keratoderma
Expand Tier I Human GO 97 Genes GS194322: GO:0003206 cardiac chamber morphogenesis
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 164 Genes GS201430: GO:0005516 calmodulin binding
Expand Tier I Human GO 354 Genes GS208384: GO:0016887 ATPase activity
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human GO 453 Genes GS196896: GO:0009205 purine ribonucleoside triphosphate metabolic process
Expand Tier I Human 23 Genes GS174442: HP:0001436 Abnormality of the foot musculature
Expand Tier I Human GO 735 Genes GS196511: GO:0030054 cell junction
Expand Tier I Human 49 Genes GS174071: HP:0009125 Lipodystrophy
Expand Tier I Human GO 113 Genes GS195905: GO:0008016 regulation of heart contraction
Expand Tier I Human CTD 434 Genes GS123811: Zinc interacting genes (MeSH:D015032) in CTD
Expand Tier I Human GO 790 Genes GS208912: GO:0046700 heterocycle catabolic process
Expand Tier I Human CTD 917 Genes GS121965: Amiodarone interacting genes (MeSH:D000638) in CTD
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 2940 Genes GS210507: GO:0006950 response to stress
Expand Tier I Human GO 449 Genes GS197054: GO:0006195 purine nucleotide catabolic process
Expand Tier I Human GO 1850 Genes GS205511: GO:0001882 nucleoside binding
Expand Tier I Human 156 Genes GS174002: HP:0000189 Narrow palate
Expand Tier I Human GO 3861 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human GO 50 Genes GS194028: GO:0032432 actin filament bundle
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human CTD 7 Genes GS125903: HS 142-1 interacting genes (MeSH:C072551) in CTD
Expand Tier III Human 3178 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human 489 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human GO 420 Genes GS194304: GO:0009164 nucleoside catabolic process
Expand Tier I Human CTD 377 Genes GS121976: Zidovudine interacting genes (MeSH:D015215) in CTD
Expand Tier I Human 107 Genes GS173786: HP:0003457 EMG abnormality
Expand Tier I Human GO 5400 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human 160 Genes GS174814: HP:0001639 Hypertrophic cardiomyopathy
Expand Tier I Human 378 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human GO 2507 Genes GS196934: GO:0065008 regulation of biological quality
Expand Tier I Human GO 521 Genes GS196912: GO:0046128 purine ribonucleoside metabolic process
Expand Tier I Human GO 394 Genes GS203085: GO:0009146 purine nucleoside triphosphate catabolic process
Expand Tier I Human GO 566 Genes GS194646: GO:0042803 protein homodimerization activity
Expand Tier I Human 24 Genes GS171839: HP:0003458 EMG: myopathic abnormalities
Expand Tier I Human GO 49 Genes GS199322: GO:0002027 regulation of heart rate
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 86 Genes GS174810: HP:0001635 Congestive heart failure
Expand Tier I Human 374 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology
Expand Tier I Human GO 1178 Genes GS207161: GO:0006928 cellular component movement
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 146 Genes GS170968: HP:0000156 High-arched palate
Expand Tier I Human 86 Genes GS172908: HP:0002450 Abnormality of the motor neurons
Expand Tier I Human GO 2719 Genes GS199273: GO:0043233 organelle lumen
Expand Tier I Human CTD 1697 Genes GS122142: Dietary Fats interacting genes (MeSH:D004041) in CTD
Expand Tier I Human CTD 162 Genes GS123134: Forskolin interacting genes (MeSH:D005576) in CTD
Expand Tier I Human 285 Genes GS171902: HP:0010987 Abnormality of cellular immune system
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human GO 136 Genes GS205437: GO:0000302 response to reactive oxygen species
Expand Tier I Human GO 216 Genes GS205761: GO:0070161 anchoring junction
Expand Tier I Human GO 423 Genes GS208185: GO:0010035 response to inorganic substance
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human GO 1840 Genes GS197443: GO:0032549 ribonucleoside binding
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 1668 Genes GS202188: GO:0044248 cellular catabolic process
Expand Tier I Human GO 128 Genes GS208922: GO:0030017 sarcomere
Expand Tier I Human 533 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human GO 1287 Genes GS205610: GO:0044430 cytoskeletal part
Expand Tier I Human CTD 9 Genes GS126191: candesartan cilexetil interacting genes (MeSH:C077793) in CTD
Expand Tier I Human GO 64 Genes GS195876: GO:0030048 actin filament-based movement
Expand Tier I Human 120 Genes GS170783: HP:0010974 Abnormality of myeloid leukocytes
Expand Tier I Human GO 44 Genes GS203110: GO:0003229 ventricular cardiac muscle tissue development
Expand Tier I Human CTD 85 Genes GS125731: nitrofen interacting genes (MeSH:C007350) in CTD
Expand Tier I Human 1 Genes GS174796: HP:0009054 Scapuloperoneal myopathy
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human GO 792 Genes GS205616: GO:0009887 organ morphogenesis
Expand Tier I Human GO 713 Genes GS204630: GO:1901565 organonitrogen compound catabolic process
Expand Tier I Human 4 Genes GS172581: HP:0003697 Scapuloperoneal amyotrophy
Expand Tier I Human GO 169 Genes GS209954: GO:0003007 heart morphogenesis
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human GO 15 Genes GS199704: GO:0007512 adult heart development
Expand Tier I Human GO 444 Genes GS200490: GO:0061061 muscle structure development
Expand Tier I Human 3 Genes GS171639: HP:0003704 Scapuloperoneal weakness
Expand Tier I Human 215 Genes GS176973: HP:0001072 Thickened skin
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 1514 Genes GS203649: GO:0030554 adenyl nucleotide binding
Expand Tier I Human 6 Genes GS171897: HP:0011103 Abnormality of the left ventricular outflow tract
Expand Tier I Human GO 39 Genes GS195875: GO:0030049 muscle filament sliding
Expand Tier I Human 74 Genes GS174070: HP:0009124 Abnormality of adipose tissue
Expand Tier I Human GO 2625 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 26 Genes GS174445: HP:0001435 Abnormality of the shoulder girdle musculature
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 739 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human GO 790 Genes GS210137: GO:0016462 pyrophosphatase activity
Expand Tier I Human GO 364 Genes GS205224: GO:0015629 actin cytoskeleton
Expand Tier I Human GO 3275 Genes GS199267: GO:0043234 protein complex
Expand Tier I Human GO 1789 Genes GS208893: GO:0005856 cytoskeleton
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human CTD 2047 Genes GS127205: Tamoxifen interacting genes (MeSH:D013629) in CTD
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human GO 401 Genes GS209401: GO:0046130 purine ribonucleoside catabolic process
Expand Tier I Human GO 401 Genes GS198972: GO:0006152 purine nucleoside catabolic process
Expand Tier I Human CTD 40 Genes GS127039: Propranolol interacting genes (MeSH:D011433) in CTD
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human GO 535 Genes GS194504: GO:1901136 carbohydrate derivative catabolic process
Expand Tier I Human 42 Genes GS174226: HP:0001446 Abnormality of the musculature of the upper limbs
Expand Tier I Human GO 621 Genes GS199651: GO:0005198 structural molecule activity
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 84 Genes GS199969: GO:0031674 I band
Expand Tier I Human 104 Genes GS173535: HP:0001874 Abnormality of neutrophils
Expand Tier I Human 1 Genes GS173749: HP:0001465 Amyotrophy involving the shoulder musculature
Expand Tier I Human 114 Genes GS176840: HP:0001911 Abnormality of granulocytes
Expand Tier I Human GO 754 Genes GS204107: GO:0072359 circulatory system development
Expand Tier I Human GO 5558 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human GO 392 Genes GS196894: GO:0009207 purine ribonucleoside triphosphate catabolic process
Expand Tier I Human GO 352 Genes GS207523: GO:0003779 actin binding
Expand Tier I Human GO 46 Genes GS200955: GO:0008307 structural constituent of muscle
Expand Tier I Human GO 140 Genes GS208346: GO:0030055 cell-substrate junction
Expand Tier I Human GO 667 Genes GS198511: GO:0006163 purine nucleotide metabolic process
Expand Tier I Human 19 Genes GS171721: HP:0003445 EMG: neuropathic changes
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human GO 1180 Genes GS195151: GO:0019637 organophosphate metabolic process
Expand Tier I Human 16 Genes GS174448: HP:0001430 Abnormality of the calf musculature
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human GO 304 Genes GS206182: GO:0060537 muscle tissue development
Expand Tier I Human CTD 453 Genes GS125669: Phenylephrine interacting genes (MeSH:D010656) in CTD
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human CTD 1468 Genes GS125062: palm oil interacting genes (MeSH:C041786) in CTD
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Human GO 3125 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human GO 392 Genes GS196898: GO:0009203 ribonucleoside triphosphate catabolic process
Expand Tier I Human GO 2353 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human GO 2098 Genes GS209551: GO:0031981 nuclear lumen
Expand Tier I Human GO 408 Genes GS206215: GO:0042454 ribonucleoside catabolic process
Expand Tier I Human GO 278 Genes GS207263: GO:0042623 ATPase activity, coupled
Expand Tier I Human GO 2494 Genes GS209235: GO:0006793 phosphorus metabolic process
Expand Tier I Human 6 Genes GS172766: HP:0001682 Subvalvular aortic stenosis
Expand Tier I Human 33 Genes GS175389: HP:0011006 Abnormality of the musculature of the neck
Expand Tier I Human CTD 1398 Genes GS124312: sodium arsenite interacting genes (MeSH:C017947) in CTD
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 51 Genes GS176228: HP:0000782 Abnormality of the scapula
Expand Tier I Human GO 524 Genes GS199459: GO:0042278 purine nucleoside metabolic process
Expand Tier I Human GO 2764 Genes GS194555: GO:0031974 membrane-enclosed lumen
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human GO 523 Genes GS204496: GO:0019693 ribose phosphate metabolic process
Expand Tier I Human GO 398 Genes GS207385: GO:0009154 purine ribonucleotide catabolic process
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human GO 375 Genes GS207935: GO:0007507 heart development
Expand Tier I Human CTD 11 Genes GS123368: Ramipril interacting genes (MeSH:D017257) in CTD
Expand Tier I Human CTD 162 Genes GS126498: Dextroamphetamine interacting genes (MeSH:D003913) in CTD
Expand Tier I Human CTD 6 Genes GS126328: Angiotensin-Converting Enzyme Inhibitors interacting genes (MeSH:D000806) in CTD
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human GO 248 Genes GS202941: GO:0006936 muscle contraction
Expand Tier I Human GO 2392 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human 18 Genes GS171642: HP:0003700 Generalized amyotrophy
Expand Tier I Human GO 277 Genes GS205557: GO:0003012 muscle system process
Expand Tier I Human GO 1993 Genes GS207862: GO:0009056 catabolic process
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 2432 Genes GS209108: GO:0000166 nucleotide binding
Expand Tier I Human GO 793 Genes GS198455: GO:0019439 aromatic compound catabolic process
Expand Tier I Human GO 5962 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human GO 292 Genes GS194519: GO:0014706 striated muscle tissue development
Expand Tier I Human GO 69 Genes GS209852: GO:0006200 ATP catabolic process
Expand Tier I Human CTD 4 Genes GS123782: GC 1 compound interacting genes (MeSH:C413355) in CTD
Expand Tier I Human GO 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 38 Genes GS171754: HP:0001711 Abnormality of the left ventricle
Expand Tier I Human GO 811 Genes GS208636: GO:0006753 nucleoside phosphate metabolic process
Expand Tier I Human GO 709 Genes GS210435: GO:0072521 purine-containing compound metabolic process
Expand Tier I Human GO 969 Genes GS195570: GO:0046983 protein dimerization activity
Expand Tier I Human 9 Genes GS176601: HP:0003803 Type 1 muscle fiber predominance
Expand Tier I Human GO 120 Genes GS194966: GO:0046034 ATP metabolic process
Expand Tier I Human 17 Genes GS174660: HP:0001421 Abnormality of the musculature of the hand
Expand Tier I Human GO 453 Genes GS210437: GO:0072523 purine-containing compound catabolic process
Expand Tier I Human 9 Genes GS172822: HP:0003687 Centrally nucleated skeletal muscle fibers
Expand Tier I Human GO 9 Genes GS201644: GO:0030898 actin-dependent ATPase activity
Expand Tier I Human 196 Genes GS173872: HP:0011368 Epidermal thickening
Expand Tier I Human 159 Genes GS176900: HP:0000218 High palate
Expand Tier I Human GO 2545 Genes GS203335: GO:0048513 organ development
Expand Tier I Human CTD 1 Genes GS127257: spiruchostatin A interacting genes (MeSH:C485419) in CTD
Expand Tier I Human GO 748 Genes GS203608: GO:0034655 nucleobase-containing compound catabolic process
Expand Tier I Human 14 Genes GS175579: HP:0003200 Ragged-red muscle fibers
Expand Tier I Human GO 858 Genes GS194645: GO:0042802 identical protein binding
Expand Tier I Human GO 519 Genes GS198012: GO:0046434 organophosphate catabolic process
Expand Tier I Human 83 Genes GS175811: HP:0011021 Abnormality of circulating enzyme level
Expand Tier I Human 200 Genes GS174812: HP:0001637 Abnormality of the myocardium
Expand Tier I Human GO 330 Genes GS205972: GO:0008015 blood circulation
Expand Tier I Human CTD 1 Genes GS123299: anacardic acid interacting genes (MeSH:C088115) in CTD
Expand Tier I Human GO 475 Genes GS203080: GO:0009141 nucleoside triphosphate metabolic process
Expand Tier I Human GO 47 Genes GS210709: GO:0070252 actin-mediated cell contraction
Expand Tier I Human GO 134 Genes GS196131: GO:0005924 cell-substrate adherens junction
Expand Tier I Human GO 1480 Genes GS205179: GO:0005524 ATP binding
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human GO 331 Genes GS205558: GO:0003013 circulatory system process
Expand Tier I Human GO 1588 Genes GS196772: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Human 98 Genes GS176756: HP:0011420 Death
Expand Tier I Human GO 64 Genes GS197028: GO:0016459 myosin complex
Expand Tier I Human GO 72 Genes GS208928: GO:0030018 Z disc
Expand Tier I Human 71 Genes GS174073: HP:0009127 Abnormality of the musculature of the limbs
Expand Tier I Human 162 Genes GS175556: HP:0011675 Arrhythmia
Expand Tier I Human CTD 870 Genes GS123911: Ozone interacting genes (MeSH:D010126) in CTD
Expand Tier I Human GO 129 Genes GS193987: GO:0048738 cardiac muscle tissue development
Expand Tier I Human GO 803 Genes GS206780: GO:0009117 nucleotide metabolic process
Expand Tier I Human GO 399 Genes GS206726: GO:0009261 ribonucleotide catabolic process
Expand Tier I Human GO 54 Genes GS193858: GO:0055008 cardiac muscle tissue morphogenesis
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 334 Genes GS194775: GO:0007517 muscle organ development
Expand Tier I Human GO 821 Genes GS194041: GO:1901361 organic cyclic compound catabolic process
Expand Tier I Human GO 2431 Genes GS209232: GO:0006796 phosphate-containing compound metabolic process
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 5369 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Human 10 Genes GS173931: HP:0001670 Asymmetric septal hypertrophy
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 220 Genes GS175994: HP:0000464 Abnormality of the neck
Expand Tier I Human GO 1836 Genes GS201799: GO:0032550 purine ribonucleoside binding
Expand Tier I Human GO 1877 Genes GS201800: GO:0032553 ribonucleotide binding
Expand Tier I Human CTD 14 Genes GS123756: Y 27632 interacting genes (MeSH:C108830) in CTD
Expand Tier I Human 15 Genes GS172526: HP:0001699 Sudden death
Expand Tier I Human 62 Genes GS172355: HP:0002460 Distal muscle weakness
Expand Tier I Human GO 1770 Genes GS194455: GO:0051239 regulation of multicellular organismal process
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 72 Genes GS171643: HP:0003701 Proximal muscle weakness
Expand Tier I Human 34 Genes GS171944: HP:0003324 Generalized muscle weakness
Expand Tier I Human GO 792 Genes GS201002: GO:0044270 cellular nitrogen compound catabolic process
Expand Tier I Human CTD 97 Genes GS125119: Isoproterenol interacting genes (MeSH:D007545) in CTD
Expand Tier I Human 35 Genes GS173690: HP:0001644 Dilated cardiomyopathy
Expand Tier I Human GO 1827 Genes GS202716: GO:0035639 purine ribonucleoside triphosphate binding
Expand Tier I Human 58 Genes GS172853: HP:0004303 Abnormality of muscle fibers
Expand Tier I Human 229 Genes GS175577: HP:0003202 Amyotrophy
Expand Tier I Human GO 793 Genes GS202822: GO:0016818 hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides
Expand Tier I Human CTD 11 Genes GS124075: Metoprolol interacting genes (MeSH:D008790) in CTD
Expand Tier I Human 17 Genes GS175993: HP:0000467 Neck muscle weakness
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human GO 623 Genes GS196553: GO:0005730 nucleolus
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 39 Genes GS198624: GO:0033275 actin-myosin filament sliding
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 758 Genes GS195665: GO:0017111 nucleoside-triphosphatase activity
Expand Tier I Human GO 47 Genes GS202919: GO:0001725 stress fiber
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human GO 3125 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Human GO 1869 Genes GS200446: GO:0017076 purine nucleotide binding
Expand Tier I Human GO 399 Genes GS203082: GO:0009143 nucleoside triphosphate catabolic process
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 44 Genes GS173157: HP:0003326 Myalgia
Expand Tier I Human GO 23 Genes GS210139: GO:0016460 myosin II complex
Expand Tier I Human GO 62 Genes GS194326: GO:0003208 cardiac ventricle morphogenesis
Expand Tier I Human 1 Genes GS175362: HP:0011916 Toe extensor amyotrophy
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human GO 1693 Genes GS209960: GO:0003008 system process
Expand Tier I Human GO 145 Genes GS206312: GO:0044449 contractile fiber part
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 130 Genes GS207524: GO:0003774 motor activity
Expand Tier I Human GO 466 Genes GS204511: GO:0048729 tissue morphogenesis
Expand Tier I Human 3 Genes GS176811: HP:0002792 Reduced vital capacity
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 1205 Genes GS194505: GO:1901135 carbohydrate derivative metabolic process
Expand Tier I Human GO 162 Genes GS206183: GO:0043292 contractile fiber
Expand Tier I Human 83 Genes GS174968: HP:0003236 Elevated serum creatine phosphokinase
Expand Tier I Human GO 855 Genes GS209614: GO:0055086 nucleobase-containing small molecule metabolic process
Expand Tier I Human GO 2511 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human GO 635 Genes GS194613: GO:0008092 cytoskeletal protein binding
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human GO 18 Genes GS209518: GO:0032982 myosin filament
Expand Tier I Human GO 754 Genes GS204108: GO:0072358 cardiovascular system development
Expand Tier I Human GO 458 Genes GS207995: GO:0009199 ribonucleoside triphosphate metabolic process
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 8137 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human GO 517 Genes GS208810: GO:0009259 ribonucleotide metabolic process
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 599 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human GO 2050 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human 1 Genes GS176336: HP:0009031 Amyotrophy of ankle musculature
Expand Tier I Human CTD 1068 Genes GS121343: Flavonoids interacting genes (MeSH:D005419) in CTD
Expand Tier I Human GO 503 Genes GS207389: GO:0009150 purine ribonucleotide metabolic process
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 5452 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human GO 90 Genes GS198725: GO:0003231 cardiac ventricle development
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human CTD 64 Genes GS124534: Norepinephrine interacting genes (MeSH:D009638) in CTD
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 255 Genes GS176610: HP:0003593 Infantile onset
Expand Tier I Human GO 455 Genes GS204054: GO:0044057 regulation of system process
Expand Tier I Human GO 199 Genes GS209187: GO:0005912 adherens junction
Expand Tier I Human 285 Genes GS175119: HP:0001881 Abnormality of leukocytes
Expand Tier I Human 195 Genes GS174813: HP:0001638 Cardiomyopathy
Expand Tier I Human GO 110 Genes GS194320: GO:0003205 cardiac chamber development
Expand Tier I Human GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human 82 Genes GS172000: HP:0001761 Pes cavus
Expand Tier I Human 246 Genes GS176806: HP:0003812 Phenotypic variability
Expand Tier I Human GO 458 Genes GS203083: GO:0009144 purine nucleoside triphosphate metabolic process
Expand Tier I Human 169 Genes GS171752: HP:0001713 Abnormality of cardiac ventricle
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 2433 Genes GS203886: GO:1901265 nucleoside phosphate binding
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human 185 Genes GS173065: HP:0003679 Pace of progression
Expand Tier I Human GO 583 Genes GS206781: GO:0009116 nucleoside metabolic process
Expand Tier I Human GO 41 Genes GS198270: GO:0055010 ventricular cardiac muscle tissue morphogenesis
Expand Tier I Human GO 798 Genes GS202828: GO:0016817 hydrolase activity, acting on acid anhydrides
Expand Tier I Human 38 Genes GS174443: HP:0001437 Abnormality of the musculature of the lower limbs
Expand Tier I Human 111 Genes GS177023: HP:0010876 Abnormality of circulating protein level
Expand Tier I Human GO 133 Genes GS205560: GO:0003015 heart process
Expand Tier I Human 39 Genes GS175557: HP:0002515 Waddling gait
Expand Tier I Human CTD 10 Genes GS124781: Monocrotaline interacting genes (MeSH:D016686) in CTD
Expand Tier I Human 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human GO 2741 Genes GS195668: GO:0042221 response to chemical stimulus
Expand Tier I Human 44 Genes GS171924: HP:0100578 Lipoatrophy
Expand Tier I Human GO 20 Genes GS203028: GO:0000146 microfilament motor activity
Expand Tier I Human CTD 220 Genes GS122551: Zinc Sulfate interacting genes (MeSH:D019287) in CTD
Expand Tier I Human GO 1852 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human GO 378 Genes GS195571: GO:0046982 protein heterodimerization activity
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 155 Genes GS172040: HP:0000962 Hyperkeratosis
Expand Tier I Human 346 Genes GS172989: HP:0001324 Muscle weakness
Expand Tier I Human GO 467 Genes GS194302: GO:0009166 nucleotide catabolic process
Expand Tier I Human GO 65 Genes GS194584: GO:0048644 muscle organ morphogenesis
Expand Tier I Human GO 2673 Genes GS205543: GO:0070013 intracellular organelle lumen
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human CTD 68 Genes GS124891: N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide interacting genes (MeSH:C063509) in CTD
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human CTD 41 Genes GS125345: Prazosin interacting genes (MeSH:D011224) in CTD
Expand Tier I Human GO 152 Genes GS208921: GO:0030016 myofibril
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 540 Genes GS206784: GO:0009119 ribonucleoside metabolic process
Expand Tier I Human 5 Genes GS171638: HP:0003707 Calf muscle pseudohypertrophy
Expand Tier I Human 72 Genes GS173062: HP:0003677 Slow progression
Expand Tier I Human 543 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human CTD 82 Genes GS122186: Dinoprostone interacting genes (MeSH:D015232) in CTD
Expand Tier I Human GO 269 Genes GS202370: GO:0006979 response to oxidative stress
Expand Tier I Human GO 1862 Genes GS201794: GO:0032555 purine ribonucleotide binding
Expand Tier I Human GO 59 Genes GS195888: GO:0060415 muscle tissue morphogenesis
Expand Tier I Human GO 56 Genes GS199374: GO:0042641 actomyosin
Expand Tier I Human GO 2486 Genes GS201249: GO:0044428 nuclear part
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human CTD 273 Genes GS125634: trichostatin A interacting genes (MeSH:C012589) in CTD
Expand Tier I Human GO 5379 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human CTD 277 Genes GS125409: Triiodothyronine interacting genes (MeSH:D014284) in CTD
Expand Tier I Human 2 Genes GS174804: HP:0009055 Generalized limb muscle atrophy
Expand Tier I Human 421 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Human 626 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Human GO 5601 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process