Yeast Systematic Name | Yeast Symbol | SGDID | Analog Name | Analog Description | EC | Organism | Disease | Structure | Uniprot | Human ID | Human Symbol | HHsearch Probability | HHsearch E_value | HHsearch P_value | HHsearch Score | Flag Disease related | Flag Homo sapiens | Flag Mus musculus | Flag Danio rerio | Flag Drosophila melanogaster | Flag Caenorhabditis elegans | Flag Arabidopsis thaliana | Flag Escherichia coli |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YKL129C | MYO3 | SGDID:S000001612 | MYSS |
Myosin heavy chain, skeletal muscle, adult |
Gallus gallus | 1o1g_a | P13538 | 100.00 | 4.00E-139 | 3.00E-143 | 1348.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKL129C | MYO3 | SGDID:S000001612 | MYO10 KIAA0799 |
Unconventional myosin-X (Unconventional myosin-10) |
Homo sapiens | Chondrocalcinosis,Usher Syndrome, Type I,Anterior Segment Dysgenesis 5,Usher Syndrome |
5i0h_b | Q9HD67 | ENSG00000145555 | MYO10 | 100.00 | 2.00E-133 | 2.00E-137 | 1276.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKL129C | MYO3 | SGDID:S000001612 | MYH11 |
Myosin-11 (Myosin heavy chain 11) (Myosin heavy chain, gizzard smooth muscle) |
Gallus gallus | 1br1_e | P10587 | 100.00 | 4.00E-136 | 3.00E-140 | 1315.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKL129C | MYO3 | SGDID:S000001612 | MYO6 |
Unconventional myosin-VI (Unconventional myosin-6) |
Sus scrofa | 6bnp_m | Q29122 | 100.00 | 3.00E-123 | 2.00E-127 | 1180.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKL129C | MYO3 | SGDID:S000001612 | Mhc CG17927 |
Myosin heavy chain, muscle |
Drosophila melanogaster | 5w1a_a | P05661 | 100.00 | 6.00E-136 | 5.00E-140 | 1312.30 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | ||||
YKL129C | MYO3 | SGDID:S000001612 | myoE dmiE DDB_G0288679 |
Myosin IE heavy chain |
Dictyostelium discoideum | 1lkx_c | Q03479 | 100.00 | 3.00E-123 | 2.00E-127 | 1182.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKL129C | MYO3 | SGDID:S000001612 | MYO1C |
Unconventional myosin-Ic (Myosin I beta) (MMI-beta) (MMIb) |
Homo sapiens | Amebiasis,Myopathy, Centronuclear, 1,Deafness, Autosomal Recessive 12,Chromosome 17p13.3, Centromeric, Duplication Syndrome,Usher Syndrome, Type I,Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna,Sclerosing Keratitis,Usher Syndrome,Miller-Dieker Lissencephaly Syndrome,Deafness, Autosomal Dominant 48 |
4byf_a | O00159 | ENSG00000197879 | MYO1C | 100.00 | 8.00E-125 | 7.00E-129 | 1202.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKL129C | MYO3 | SGDID:S000001612 | MYS |
Myosin heavy chain, striated muscle |
Argopecten irradians | 1kk8_a | P24733 | 100.00 | 2.00E-138 | 2.00E-142 | 1340.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKL129C | MYO3 | SGDID:S000001612 | MYO5C |
Unconventional myosin-Vc |
Homo sapiens | Griscelli Syndrome, Type 1,Diarrhea 2, With Microvillus Atrophy,Congenital Diarrhea,Griscelli Syndrome |
5hmp_b | Q9NQX4 | ENSG00000128833 | MYO5C | 100.00 | 1.00E-132 | 8.00E-137 | 1273.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKL129C | MYO3 | SGDID:S000001612 | Myosin 2 heavy chain striated muscle |
Myosin 2 heavy chain striated muscle |
Aphonopelma | 3jbh_g | A0A140UGH3 | 100.00 | 2.00E-130 | 2.00E-134 | 1380.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKL129C | MYO3 | SGDID:S000001612 | MYH7 MYHCB |
Myosin-7 (Myosin heavy chain 7) (Myosin heavy chain slow isoform) (MyHC-slow) (Myosin heavy chain, cardiac muscle beta isoform) (MyHC-beta) |
Homo sapiens | Ventricular Septal Defect,Muscular Disease,Heart Disease,Lymphopenia,Congenital Fiber-Type Disproportion,Mitral Valve Insufficiency,Severe Combined Immunodeficiency,Aortic Valve Disease 2,Congenital Structural Myopathy,Myopathy,Cardiomyopathy, Dilated, 1e,Myofibrillar Myopathy,Atrial Heart Septal Defect,Mitochondrial Dna Depletion Syndrome 12b,Muscle Tissue Disease,Neuromuscular Disease,Myopathy, Myosin Storage, Autosomal Dominant,Bethlem Myopathy 1,Hypertrophic Cardiomyopathy,Myosinopathies,Familial Isolated Dilated Cardiomyopathy,Rasopathy,Autosomal Dominant Distal Myopathy,Myocardial Infarction,Myopathy, Distal, 1,Muscular Dystrophy,Progressive Familial Heart Block,Tibial Muscular Dystrophy,Hyaline Body Myopathy,Atrial Standstill 1,Combined Immunodeficiency,Dilated Cardiomyopathy,Oculopharyngeal Muscular Dystrophy,Combined T And B Cell Immunodeficiency,Long Qt Syndrome,Malignant Hyperthermia,Heart Conduction Disease,Muscular Dystrophy, Congenital, Lmna-Related,Ebstein Anomaly,Cardiac Conduction Defect,Cardiomyopathy, Familial Hypertrophic, 4,Congestive Heart Failure,Endocardial Fibroelastosis,Rigid Spine Muscular Dystrophy 1,Camptocormism,Noonan Syndrome With Multiple Lentigines,Respiratory Failure,Mobitz Type Ii Atrioventricular Block,Myopathy, Myofibrillar, 9, With Early Respiratory Failure,Long Qt Syndrome 2,Danon Disease,Congenital Myasthenic Syndrome,Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/Or Dilated Cardiomyopathy,Scapuloperoneal Myopathy, Myh7-Related,Restrictive Cardiomyopathy,Arrhythmogenic Right Ventricular Cardiomyopathy,Brugada Syndrome,Stormorken Syndrome,Immune Deficiency Disease,Familial Atrial Fibrillation,Atrioventricular Block,First-Degree Atrioventricular Block,Tricuspid Valve Disease,Barth Syndrome,Holt-Oram Syndrome,Long Qt Syndrome 1,Cardiomyopathy, Familial Hypertrophic, 1,Wolff-Parkinson-White Syndrome,Intrinsic Cardiomyopathy,Peripartum Cardiomyopathy,Lipoprotein Quantitative Trait Locus,Atrial Fibrillation,Scapuloperoneal Myopathy,Cardiac Arrest,Left Ventricular Noncompaction,Myopathy, Myosin Storage, Autosomal Recessive,Catecholaminergic Polymorphic Ventricular Tachycardia,Batten-Turner Congenital Myopathy,Myopathy, Congenital, With Fiber-Type Disproportion,Miyoshi Muscular Dystrophy,Craniosynostosis 4,Cardiomyopathy, Dilated, 1b |
5tby_a | P12883 | ENSG00000092054 | MYH7 | 100.00 | 3.00E-128 | 2.00E-132 | 1358.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKL129C | MYO3 | SGDID:S000001612 | MYH7 |
Myosin-7 (Myosin heavy chain 7) (Myosin heavy chain slow isoform) (MyHC-slow) (Myosin heavy chain, cardiac muscle beta isoform) (MyHC-beta) |
Bos taurus | 5n69_b | Q9BE39 | 100.00 | 3.00E-138 | 3.00E-142 | 1338.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKL129C | MYO3 | SGDID:S000001612 | mhcA DDB_G0286355 |
Myosin-2 heavy chain (Myosin II heavy chain) |
Dictyostelium discoideum | 1w9i_a | P08799 | 100.00 | 4.00E-135 | 3.00E-139 | 1297.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKL129C | MYO3 | SGDID:S000001612 | Myo1b Myo1a Myr1 |
Unconventional myosin-Ib (Myosin I alpha) (MMI-alpha) (MMIa) (Myosin heavy chain myr 1) |
Rattus norvegicus | 4l79_a | Q05096 | 100.00 | 4.00E-128 | 3.00E-132 | 1235.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKL129C | MYO3 | SGDID:S000001612 | abpA actnA DDB_G0268632 |
Alpha-actinin A (Actin-binding protein A) (F-actin cross-linking protein) |
Dictyostelium discoideum | 5i4e_a | P05095 | ENSG00000105357 | MYH14 | 100.00 | 4.00E-129 | 3.00E-133 | 1280.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YKL129C | MYO3 | SGDID:S000001612 | MYO5A |
Unconventional myosin-Va (Dilute myosin heavy chain, non-muscle) (Myosin heavy chain p190) (Myosin-V) |
Gallus gallus | 1w7j_a | Q02440 | 100.00 | 6.00E-138 | 5.00E-142 | 1329.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKL129C | MYO3 | SGDID:S000001612 | TGGT1_235470 |
TGGT1_235470 |
Toxoplasma gondii | 6due_a | S7W634 | 100.00 | 5.00E-132 | 4.00E-136 | 1268.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKL129C | MYO3 | SGDID:S000001612 | MYO6 |
MYO6 |
Sus scrofa | 4pfo_a | F1RQI7 | 100.00 | 2.00E-132 | 2.00E-136 | 1279.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |