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 |
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YKR090W | PXL1 | SGDID:S000001798 | Tb927.6.1700 |
Tb927.6.1700 |
Trypanosoma brucei | 6hix_bx | Q585P1 | 97.90 | 3.50E-09 | 3.40E-13 | 98.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKR090W | PXL1 | SGDID:S000001798 | LIMK2 |
LIM domain kinase 2 (LIMK-2) (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Williams-Beuren Syndrome |
1x6a_a | P53671 | ENSG00000182541 | LIMK2 | 95.30 | 0.00015 | 2.20E-08 | 48.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKR090W | PXL1 | SGDID:S000001798 | FHL2 DRAL SLIM3 |
Four and a half LIM domains protein 2 (FHL-2) (LIM domain protein DRAL) (Skeletal muscle LIM-protein 3) (SLIM-3) |
Homo sapiens | Cardiac Rupture,Hypertensive Nephropathy,Hemophagocytic Lymphohistiocytosis, Familial, 1,Hypertrophic Cardiomyopathy,Familial Isolated Dilated Cardiomyopathy,Tibial Muscular Dystrophy,Dilated Cardiomyopathy,Benign Struma Ovarii,Rhabdomyosarcoma,Hemophagocytic Lymphohistiocytosis, Familial, 4,Hemophagocytic Lymphohistiocytosis, Familial, 2,Prostate Cancer,Deafness, Autosomal Recessive 65,Hermansky-Pudlak Syndrome,Hemophagocytic Lymphohistiocytosis,Lymphoproliferative Syndrome, X-Linked, 2,Myopathy, X-Linked, With Postural Muscle Atrophy,Arrhythmogenic Right Ventricular Cardiomyopathy,Lymphoproliferative Syndrome, X-Linked, 1,Griscelli Syndrome, Type 2,Scapuloperoneal Myopathy,Left Ventricular Noncompaction,Griscelli Syndrome |
2d8z_a | Q14192 | ENSG00000115641 | FHL2 | 95.30 | 0.00016 | 2.40E-08 | 46.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKR090W | PXL1 | SGDID:S000001798 | LIMS1 PINCH PINCH1 |
LIM and senescent cell antigen-like-containing domain protein 1 (Particularly interesting new Cys-His protein 1) (PINCH-1) (Renal carcinoma antigen NY-REN-48) |
Homo sapiens | Dilated Cardiomyopathy,Colorectal Cancer |
6mif_a | P48059 | ENSG00000169756 | LIMS1 | 95.40 | 0.00013 | 1.80E-08 | 50.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKR090W | PXL1 | SGDID:S000001798 | Deaf1 |
Deformed epidermal autoregulatory factor 1 homolog (Nuclear DEAF-1-related transcriptional regulator) (NUDR) |
Mus musculus | 2mbv_a | Q9Z1T5 | 95.20 | 0.0002 | 2.70E-08 | 52.00 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YKR090W | PXL1 | SGDID:S000001798 | FHL1 SLIM1 |
Four and a half LIM domains protein 1 (FHL-1) (Skeletal muscle LIM-protein 1) (SLIM) (SLIM-1) |
Homo sapiens | Hemophagocytic Lymphohistiocytosis, Familial, 1,Myopathy,Myofibrillar Myopathy,Emery-Dreifuss Muscular Dystrophy,Clubfoot,Hypertrophic Cardiomyopathy,Progressive Muscular Dystrophy,Muscular Dystrophy,Pulmonary Artery Hypoplasia,Emery-Dreifuss Muscular Dystrophy 4, Autosomal Dominant,Emery-Dreifuss Muscular Dystrophy 5, Autosomal Dominant,X-Linked Emery-Dreifuss Muscular Dystrophy,Reducing Body Myopathy,Muscular Dystrophy, Congenital, Lmna-Related,Foot Drop,Rigid Spine Muscular Dystrophy 1,Respiratory Failure,Uruguay Faciocardiomusculoskeletal Syndrome,Fragile X Syndrome,Scapuloperoneal Myopathy, X-Linked Dominant,Myopathy, X-Linked, With Postural Muscle Atrophy,Reducing Body Myopathy, X-Linked 1a, Severe, With Infantile Or Early Childhood Onset,Reducing Body Myopathy, X-Linked 1b, With Late Childhood Or Adult Onset,Muscle Hypertrophy,Cardiomyopathy, Familial Hypertrophic, 1,Scoliosis,Scapuloperoneal Myopathy |
1x63_a | Q13642 | ENSG00000022267 | FHL1 | 96.00 | 3.30E-05 | 4.80E-09 | 52.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKR090W | PXL1 | SGDID:S000001798 | ABLIM3 KIAA0843 HMFN1661 |
Actin-binding LIM protein 3 (abLIM-3) (Actin-binding LIM protein family member 3) |
Homo sapiens | Aromatic L-Amino Acid Decarboxylase Deficiency,Fetal Erythroblastosis |
2dj7_a | O94929 | ENSG00000173210 | ABLIM3 | 95.50 | 0.0001 | 1.40E-08 | 50.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKR090W | PXL1 | SGDID:S000001798 | Isl2 |
Insulin gene enhancer protein ISL-2 (Islet-2) |
Mus musculus | 6cme_a | Q9CXV0 | 98.80 | 6.50E-13 | 8.00E-17 | 113.60 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YKR090W | PXL1 | SGDID:S000001798 | Ldb1 Nli |
LIM domain-binding protein 1 (LDB-1) (Carboxyl-terminal LIM domain-binding protein 2) (CLIM-2) (LIM domain-binding factor CLIM2) (mLdb1) (Nuclear LIM interactor) |
Mus musculus | 1rut_x | P70662 | 99.20 | 8.40E-16 | 1.00E-19 | 135.30 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YKR090W | PXL1 | SGDID:S000001798 | ABLIM2 KIAA1808 |
Actin-binding LIM protein 2 (abLIM-2) (Actin-binding LIM protein family member 2) |
Homo sapiens | 1v6g_a | Q6H8Q1 | ENSG00000163995 | ABLIM2 | 96.10 | 2.10E-05 | 3.00E-09 | 54.10 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YKR090W | PXL1 | SGDID:S000001798 | LMO4 |
LIM domain transcription factor LMO4 (Breast tumor autoantigen) (LIM domain only protein 4) (LMO-4) |
Homo sapiens | Immunodeficiency 29 |
2l4z_a | P61968 | ENSG00000143013 | LMO4 | 96.70 | 3.00E-06 | 3.70E-10 | 68.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKR090W | PXL1 | SGDID:S000001798 | TRIP6 OIP1 |
Thyroid receptor-interacting protein 6 (TR-interacting protein 6) (TRIP-6) (Opa-interacting protein 1) (OIP-1) (Zyxin-related protein 1) (ZRP-1) |
Homo sapiens | Spinal Cord Astrocytoma,Lipomatosis, Multiple |
2dlo_a | Q15654 | ENSG00000087077 | TRIP6 | 95.90 | 3.60E-05 | 5.00E-09 | 52.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKR090W | PXL1 | SGDID:S000001798 | Lhx3 Lim-3 Lim3 Plim |
LIM/homeobox protein Lhx3 (LIM homeobox protein 3) (Homeobox protein LIM-3) (Homeobox protein P-LIM) |
Mus musculus | 2jtn_a | P50481 | 99.20 | 1.30E-15 | 1.60E-19 | 131.90 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YKR090W | PXL1 | SGDID:S000001798 | FHL3 SLIM2 |
Four and a half LIM domains protein 3 (FHL-3) (Skeletal muscle LIM-protein 2) (SLIM-2) |
Homo sapiens | Glycogen Storage Disease Vii,Retinitis Pigmentosa 37 |
2cuq_a | Q13643 | ENSG00000183386 | FHL3 | 96.80 | 1.80E-06 | 2.60E-10 | 59.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKR090W | PXL1 | SGDID:S000001798 | LMO2 RBTN2 RBTNL1 RHOM2 TTG2 |
Rhombotin-2 (Cysteine-rich protein TTG-2) (LIM domain only protein 2) (LMO-2) (T-cell translocation protein 2) |
Homo sapiens | X-Linked Recessive Disease,Severe Combined Immunodeficiency,Lymphoblastic Lymphoma,T-Cell Lymphoblastic Leukemia/Lymphoma,Leukemia,Leukemia, Acute Myeloid,Leukemia, Acute Lymphoblastic,Combined Immunodeficiency,T-Cell Acute Lymphoblastic Leukemia,Adenosine Deaminase Deficiency,Phagocyte Bactericidal Dysfunction,Chronic Granulomatous Disease,Ureteral Lymphoma,Thrombocytopenia,Severe Combined Immunodeficiency, X-Linked,X-Linked Monogenic Disease,Diffuse Large B-Cell Lymphoma,Granulomatous Disease, Chronic, X-Linked,Norrie Disease |
4kfz_b | P25791 | ENSG00000135363 | LMO2 | 99.00 | 2.30E-14 | 3.00E-18 | 117.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKR090W | PXL1 | SGDID:S000001798 | TES |
Testin (TESS) |
Homo sapiens | Flying Phobia,Gnathomiasis,Retinitis Pigmentosa,Pica Disease,Anisakiasis,Vitreous Abscess,Enterobiasis,Toxocariasis,Ancylostomiasis,Hemopneumothorax,Hymenolepiasis,Sparganosis,Parasitic Helminthiasis Infectious Disease,Paramyotonia Congenita Of Von Eulenburg,Paragonimiasis,Strongyloidiasis,Taeniasis,Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema |
2xqn_t | Q9UGI8 | ENSG00000135269 | TES | 98.80 | 5.40E-13 | 7.20E-17 | 105.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKR090W | PXL1 | SGDID:S000001798 | CSRP2 |
Cysteine and glycine-rich protein 2 (Cysteine-rich protein 2) (CRP2) |
Coturnix japonica | 1a7i_a | Q05158 | 96.20 | 1.90E-05 | 2.70E-09 | 53.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKR090W | PXL1 | SGDID:S000001798 | LPXN LDLP |
Leupaxin |
Homo sapiens | Familial Hyperlipidemia,Diabetes Mellitus,Cholelithiasis,Familial Hypercholesterolemia,Chronic Pyelonephritis,Lipid Metabolism Disorder,Prostate Cancer,Type 2 Diabetes Mellitus |
1x3h_a | O60711 | ENSG00000110031 | LPXN | 95.70 | 7.10E-05 | 9.90E-09 | 51.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKR090W | PXL1 | SGDID:S000001798 | LIMD2 SB143 |
LIM domain-containing protein 2 |
Homo sapiens | Fraser Syndrome 1 |
2lzu_a | Q9BT23 | ENSG00000136490 | LIMD2 | 95.40 | 0.00012 | 1.80E-08 | 46.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKR090W | PXL1 | SGDID:S000001798 | Crip1 Crip |
Cysteine-rich protein 1 (CRP-1) (Cysteine-rich intestinal protein) (CRIP) |
Rattus norvegicus | 1iml_a | P63255 | 96.10 | 2.10E-05 | 3.00E-09 | 52.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |