| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YOR176W | HEM15 | SGDID:S000005702 | HEM15 YOR176W |
Ferrochelatase, mitochondrial (EC 4.99.1.1) (Heme synthase) (Protoheme ferro-lyase) |
4.99.1.1 | Saccharomyces cerevisiae | 1lbq_b | P16622 | 100.00 | 2.10E-61 | 1.50E-65 | 461.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YOR176W | HEM15 | SGDID:S000005702 | FECH |
Ferrochelatase, mitochondrial (EC 4.99.1.1) (Heme synthase) (Protoheme ferro-lyase) |
4.99.1.1 | Homo sapiens | Liver Disease,Sideroblastic Anemia,Inherited Metabolic Disorder,Borst-Jadassohn Intraepidermal Carcinoma,Macrocytic Anemia,Erythropoietic Protoporphyria, Autosomal Recessive,Porphyria,Cutaneous Porphyria,X-Linked Protoporphyria,Acute Porphyria,Proliferative Vasculopathy And Hydranencephaly-Hydrocephaly Syndrome,Jejunal Neoplasm,Autosomal Erythropoietic Protoporphyria,Deficiency Anemia,Porphyria, Acute Intermittent,Porphyria Cutanea Tarda,Variegate Porphyria,Skin Carcinoma,Cone-Rod Dystrophy 2,Friedreich Ataxia,Coproporphyria, Hereditary,Osteogenesis Imperfecta, Type Xviii,Protoporphyria, Erythropoietic, 1,Hemochromatosis, Type 1,Anemia, Sideroblastic, 1,Photoparoxysmal Response 1,Anemia, Sideroblastic, And Spinocerebellar Ataxia,Spastic Paraplegia 38, Autosomal Dominant,Dyschromatosis Universalis Hereditaria,Bardet-Biedl Syndrome 1 |
2hre_d | P22830 | ENSG00000066926 | FECH | 100.00 | 2.00E-56 | 1.40E-60 | 426.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |