| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YBR098W | MMS4 | SGDID:S000000302 | FANCM KIAA1596 |
Fanconi anemia group M protein (Protein FACM) (EC 3.6.4.13) (ATP-dependent RNA helicase FANCM) (Fanconi anemia-associated polypeptide of 250 kDa) (FAAP250) (Protein Hef ortholog) |
3.6.4.13 | Homo sapiens | Male Infertility With Azoospermia Or Oligozoospermia Due To Single Gene Mutation,Fanconi Anemia, Complementation Group V,Fanconi Anemia, Complementation Group R,Fanconi Anemia, Complementation Group U,Infertility,Fanconi Anemia, Complementation Group I,Fanconi Anemia, Complementation Group J,Fanconi Anemia, Complementation Group Q,Aplastic Anemia,Ovarian Cancer,Esophageal Atresia,Breast Cancer,Hereditary Breast Ovarian Cancer Syndrome,Fanconi Anemia, Complementation Group O,Deficiency Anemia,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group D2,Fanconi Anemia, Complementation Group A,Xeroderma Pigmentosum, Complementation Group F,Ovarian Germ Cell Cancer,Spermatogenic Failure 28,Premature Ovarian Failure 15,Retinoblastoma,Fanconi Anemia, Complementation Group N,Fanconi Anemia, Complementation Group P,Fanconi Anemia, Complementation Group D1,Seckel Syndrome,Fanconi Anemia, Complementation Group T,Bloom Syndrome |
4bxo_a | Q8IYD8 | ENSG00000187790 | FANCM | 99.10 | 1.20E-14 | 1.20E-18 | 142.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YBR098W | MMS4 | SGDID:S000000302 | PF2015 |
ATP-dependent RNA helicase, putative |
Pyrococcus furiosus | 1j23_a | Q8TZH8 | 98.50 | 3.00E-11 | 2.70E-15 | 109.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YBR098W | MMS4 | SGDID:S000000302 | APE_1436.1 |
APE_1436.1 |
Aeropyrum pernix | 2bgw_a | Q9YC15 | 99.30 | 1.60E-16 | 1.70E-20 | 150.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YBR098W | MMS4 | SGDID:S000000302 | MUS81 |
Crossover junction endonuclease MUS81 (EC 3.1.22.-) |
3.1.22.- | Homo sapiens | Interstitial Nephritis, Karyomegalic,Rothmund-Thomson Syndrome, Type 2,Baller-Gerold Syndrome,Cutis Laxa, Autosomal Recessive, Type Ia,Efemp2-Related Cutis Laxa,Fbln5-Related Cutis Laxa,Cutis Laxa,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Xeroderma Pigmentosum, Complementation Group F,Xeroderma Pigmentosum, Complementation Group G,Seckel Syndrome,Schimke Immunoosseous Dysplasia,Cutis Laxa, Autosomal Recessive, Type Ib,Larsen Syndrome,Autosomal Recessive Cutis Laxa Type I,Rapadilino Syndrome |
4p0p_a | Q96NY9 | ENSG00000172732 | MUS81 | 99.90 | 5.80E-27 | 6.00E-31 | 236.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YBR098W | MMS4 | SGDID:S000000302 | PF2015 |
PF2015 |
Pyrococcus furiosus | 1j24_a | Q8TZH8 | 97.80 | 8.00E-09 | 7.80E-13 | 92.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YBR098W | MMS4 | SGDID:S000000302 | mus81 |
Crossover junction endonuclease MUS81 (EC 3.1.22.-) |
3.1.22.- | Danio rerio | 2ziv_a | Q7SXA9 | 99.80 | 3.00E-24 | 3.10E-28 | 217.30 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | |||
| YBR098W | MMS4 | SGDID:S000000302 | FAAP24 C19orf40 |
Fanconi anemia core complex-associated protein 24 (Fanconi anemia-associated protein of 24 kDa) |
Homo sapiens | Fanconi Anemia, Complementation Group V,Lymphoproliferative Syndrome 2,Fanconi Anemia, Complementation Group I,Fanconi Anemia, Complementation Group J,Aplastic Anemia,Fanconi Anemia, Complementation Group O,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group D2,Fanconi Anemia, Complementation Group A,Xeroderma Pigmentosum, Complementation Group F,Fanconi Anemia, Complementation Group N,Fanconi Anemia, Complementation Group P,Fanconi Anemia, Complementation Group D1,Seckel Syndrome,Fanconi Anemia, Complementation Group T |
4bxo_b | Q9BTP7 | ENSG00000131944 | FAAP24 | 98.80 | 4.70E-13 | 4.80E-17 | 127.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YBR098W | MMS4 | SGDID:S000000302 | EME1 MMS4 |
Crossover junction endonuclease EME1 (EC 3.1.22.-) (MMS4 homolog) (hMMS4) |
3.1.22.- | Homo sapiens | Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Xeroderma Pigmentosum, Complementation Group F,Xeroderma Pigmentosum, Complementation Group G |
2ziv_b | Q96AY2 | ENSG00000154920 | EME1 | 100.00 | 9.90E-39 | 9.90E-43 | 332.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |