







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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YKL124W | SSH4 | SGDID:S000001607 | Trim25 Efp Zfp147 Znf147 |
E3 ubiquitin/ISG15 ligase TRIM25 (EC 6.3.2.n3) (Estrogen-responsive finger protein) (RING-type E3 ubiquitin transferase) (EC 2.3.2.27) (RING-type E3 ubiquitin transferase TRIM25) (Tripartite motif-containing protein 25) (Ubiquitin/ISG15-conjugating enzyme TRIM25) (Zinc finger protein 147) |
2.3.2.27,6.3.2.n3, | Mus musculus | 4b8e_b | Q61510 | 98.10 | 7.50E-10 | 9.20E-14 | 94.50 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YKL124W | SSH4 | SGDID:S000001607 | SPSB4 SSB4 |
SPRY domain-containing SOCS box protein 4 (SSB-4) |
Homo sapiens | 2v24_a | Q96A44 | ENSG00000175093 | SPSB4 | 98.40 | 7.40E-11 | 9.10E-15 | 101.30 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YKL124W | SSH4 | SGDID:S000001607 | TRIM25 EFP RNF147 ZNF147 |
E3 ubiquitin/ISG15 ligase TRIM25 (EC 6.3.2.n3) (Estrogen-responsive finger protein) (RING finger protein 147) (RING-type E3 ubiquitin transferase) (EC 2.3.2.27) (RING-type E3 ubiquitin transferase TRIM25) (Tripartite motif-containing protein 25) (Ubiquitin/ISG15-conjugating enzyme TRIM25) (Zinc finger protein 147) |
2.3.2.27,6.3.2.n3, | Homo sapiens | Middle East Respiratory Syndrome,Noonan Syndrome 1,Influenza,Breast Cancer,Glycogen Storage Disease Iv,Swine Influenza,Retinitis Pigmentosa 37,Aicardi-Goutieres Syndrome,Microphthalmia With Limb Anomalies |
6flm_c | Q14258 | ENSG00000121060 | TRIM25 | 98.10 | 6.30E-10 | 7.70E-14 | 95.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL124W | SSH4 | SGDID:S000001607 | SPRYD3 |
SPRY domain-containing protein 3 |
Homo sapiens | 2yyo_a | Q8NCJ5 | ENSG00000167778 | SPRYD3 | 98.50 | 1.20E-11 | 1.50E-15 | 104.20 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YKL124W | SSH4 | SGDID:S000001607 | TRIM21 RNF81 RO52 SSA1 |
E3 ubiquitin-protein ligase TRIM21 (EC 2.3.2.27) (52 kDa Ro protein) (52 kDa ribonucleoprotein autoantigen Ro/SS-A) (RING finger protein 81) (RING-type E3 ubiquitin transferase TRIM21) (Ro(SS-A)) (Sjoegren syndrome type A antigen) (SS-A) (Tripartite motif-containing protein 21) |
2.3.2.27 | Homo sapiens | Chromosomal Disease,Systemic Scleroderma,Myopathy,Mononeuritis Multiplex,Dyskinesia Of Esophagus,Subacute Cutaneous Lupus Erythematosus,Adie Pupil,Potocki-Shaffer Syndrome,Keratoconjunctivitis,Diffuse Infiltrative Lymphocytosis Syndrome,Mononeuropathy,Phototoxic Dermatitis,Antisynthetase Syndrome,Neonatal Lupus Erythematosus,Amyotrophic Lateral Sclerosis 1,Myositis,Hemorrhagic Disease,Sjogren Syndrome,Transient Neonatal Thrombocytopenia,Polyclonal Hypergammaglobulinemia,Lymph Node Disease,Telangiectasis,Autoimmune Disease,Keratoconjunctivitis Sicca,Xerophthalmia,Dry Eye Syndrome,Acute Interstitial Pneumonia,Pulmonary Embolism And Infarction,Nonspecific Interstitial Pneumonia,Collagen Disease,Heart Conduction Disease,Parotitis,Parotid Disease,Sialadenitis,Hypersensitivity Reaction Type Iv Disease,Orbital Granuloma,Neuroaspergillosis,Lupus Erythematosus,Malignant Secondary Hypertension,Mononeuritis Of Upper Limb And Mononeuritis Multiplex,Interstitial Lung Disease,Trochlear Nerve Disease,Lacrimal Apparatus Disease,Salivary Gland Disease,Endocardial Fibroelastosis,Adult Dermatomyositis,Childhood Type Dermatomyositis,Conjunctival Vascular Disease,Granulomatous Myositis,Transient Neonatal Neutropenia,Limited Scleroderma,Diffuse Scleroderma,Thrombocytopenia,Raynaud Disease,Heart Block, Congenital,Cutaneous Lupus Erythematosus,Photoparoxysmal Response 1,Exanthem,Amyotrophic Lateral Sclerosis 3,Atrioventricular Block,First-Degree Atrioventricular Block,Second-Degree Atrioventricular Block,Third-Degree Atrioventricular Block,Pericardium Disease,Lymphoid Interstitial Pneumonia,Hyperlipoproteinemia, Type V,Autoimmune Disease Of Exocrine System,Autoimmune Disease Of Musculoskeletal System,Systemic Lupus Erythematosus,Chromosomal Deletion Syndrome |
2iwg_b | P19474 | ENSG00000132109 | TRIM21 | 98.20 | 2.60E-10 | 3.30E-14 | 95.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL124W | SSH4 | SGDID:S000001607 | Ranbp10 Kiaa1464 |
Ran-binding protein 10 (RanBP10) |
Mus musculus | 5jia_d | Q6VN19 | 98.50 | 1.30E-11 | 1.60E-15 | 105.00 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YKL124W | SSH4 | SGDID:S000001607 | Ryr2 |
Ryanodine receptor 2 (RYR-2) (RyR2) (Cardiac muscle ryanodine receptor) (Cardiac muscle ryanodine receptor-calcium release channel) (Type 2 ryanodine receptor) |
Mus musculus | 4p9i_a | E9Q401 | 98.60 | 1.00E-11 | 1.20E-15 | 105.20 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YKL124W | SSH4 | SGDID:S000001607 | ASH2L ASH2L1 |
Set1/Ash2 histone methyltransferase complex subunit ASH2 (ASH2-like protein) |
Homo sapiens | Kleefstra Syndrome,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Kabuki Syndrome 1 |
5f6l_b | Q9UBL3 | ENSG00000129691 | ASH2L | 98.10 | 7.60E-10 | 9.50E-14 | 92.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKL124W | SSH4 | SGDID:S000001607 | Trim21 Ro52 Ssa1 |
E3 ubiquitin-protein ligase TRIM21 (EC 2.3.2.27) (52 kDa Ro protein) (52 kDa ribonucleoprotein autoantigen Ro/SS-A) (RING-type E3 ubiquitin transferase TRIM21) (Ro(SS-A)) (Sjoegren syndrome type A antigen) (SS-A) (Tripartite motif-containing protein 21) |
2.3.2.27 | Mus musculus | 2vok_b | Q62191 | 98.10 | 1.00E-09 | 1.20E-13 | 94.80 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YKL124W | SSH4 | SGDID:S000001607 | RANBP9 RANBPM |
Ran-binding protein 9 (RanBP9) (BPM-L) (BPM90) (Ran-binding protein M) (RanBPM) (RanBP7) |
Homo sapiens | Lissencephaly,Pulmonary Adenocarcinoma In Situ |
5ji7_a | Q96S59 | ENSG00000010017 | RANBP9 | 98.70 | 2.10E-12 | 2.60E-16 | 114.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKL124W | SSH4 | SGDID:S000001607 | HERC1 |
Probable E3 ubiquitin-protein ligase HERC1 (EC 2.3.2.26) (HECT domain and RCC1-like domain-containing protein 1) (HECT-type E3 ubiquitin transferase HERC1) (p532) (p619) |
2.3.2.26 | Homo sapiens | Autoimmune Lymphoproliferative Syndrome, Type Iii,Syndromic Intellectual Disability,Macrocephaly, Dysmorphic Facies, And Psychomotor Retardation |
4qt6_a | Q15751 | ENSG00000103657 | HERC1 | 98.20 | 2.60E-10 | 3.40E-14 | 91.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL124W | SSH4 | SGDID:S000001607 | DDX1 |
ATP-dependent RNA helicase DDX1 (EC 3.6.4.13) (DEAD box protein 1) (DEAD box protein retinoblastoma) (DBP-RB) |
3.6.4.13 | Homo sapiens | Bronchitis,Venezuelan Equine Encephalitis,Encephalitis,Neuroblastoma,Feingold Syndrome 1,Lacrimal Duct Obstruction,Retinoblastoma,Heavy Chain Disease |
4xw3_b | Q92499 | ENSG00000079785 | DDX1 | 98.60 | 9.90E-12 | 1.20E-15 | 110.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL124W | SSH4 | SGDID:S000001607 | BRE2 CPS60 YLR015W |
COMPASS component BRE2 (Brefeldin-A sensitivity protein 2) (Complex proteins associated with SET1 protein BRE2) (Set1C component BRE2) |
Saccharomyces cerevisiae | 6bx3_k | P43132 | 98.30 | 1.30E-10 | 1.20E-14 | 118.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKL124W | SSH4 | SGDID:S000001607 | TRIM72 MG53 |
Tripartite motif-containing protein 72 (Mitsugumin-53) (Mg53) |
Homo sapiens | Autosomal Recessive Limb-Girdle Muscular Dystrophy,Muscular Dystrophy,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2b,Miyoshi Muscular Dystrophy |
3kb5_a | Q6ZMU5 | ENSG00000177238 | TRIM72 | 98.10 | 9.50E-10 | 1.10E-13 | 94.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKL124W | SSH4 | SGDID:S000001607 | RYR1 |
Ryanodine receptor 1 (RYR-1) (RyR1) (Skeletal muscle calcium release channel) (Skeletal muscle ryanodine receptor) (Skeletal muscle-type ryanodine receptor) (Type 1 ryanodine receptor) |
Oryctolagus cuniculus | 4p9j_a | P11716 | 98.50 | 1.30E-11 | 1.60E-15 | 106.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKL124W | SSH4 | SGDID:S000001607 | KLLA0_C10945g |
KLLA0_C10945g |
Kluyveromyces lactis | 6chg_b | Q6CTQ1 | 98.50 | 2.20E-11 | 2.20E-15 | 122.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKL124W | SSH4 | SGDID:S000001607 | SPSB2 GRCC9 SSB2 |
SPRY domain-containing SOCS box protein 2 (SSB-2) (Gene-rich cluster protein C9) |
Homo sapiens | Congenital Muscular Dystrophy-Dystroglycanopathy A7,Acute Conjunctivitis,Acute Contagious Conjunctivitis |
5xn3_a | Q99619 | ENSG00000111671 | SPSB2 | 98.10 | 1.10E-09 | 1.30E-13 | 93.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |