| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YDR402C | DIT2 | SGDID:S000002810 | cypC CYP152A1 BSU02100 |
Fatty-acid peroxygenase (EC 1.11.2.4) (Cytochrome P450 152A1) (Cytochrome P450BsBeta) (Fatty acid beta-hydroxylase) |
1.11.2.4 | Bacillus subtilis | 1izo_a | O31440 | 100.00 | 9.30E-53 | 5.10E-57 | 374.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YDR402C | DIT2 | SGDID:S000002810 | CYP11A1 CYP11A |
Cholesterol side-chain cleavage enzyme, mitochondrial (EC 1.14.15.6) (CYPXIA1) (Cholesterol desmolase) (Cytochrome P450 11A1) (Cytochrome P450(scc)) |
1.14.15.6 | Homo sapiens | Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital Anomalies,Steroid Inherited Metabolic Disorder,Ovarian Hyperstimulation Syndrome,Polycystic Ovary Syndrome,Hyperandrogenism,Epilepsy,Disorder Of Sexual Development,Adrenal Adenoma,Familial Glucocorticoid Deficiency,Conn'S Syndrome,Adrenal Gland Disease,Acute Adrenal Insufficiency,Amelogenesis Imperfecta,Smith-Lemli-Opitz Syndrome,Testicular Sex Cord-Stromal Neoplasm,Cryptorchidism, Unilateral Or Bilateral,Autoimmune Hepatitis Type 2,Leydig Cell Tumor,Polyendocrinopathy,Infertility,Adrenal Cortical Hypofunction,Inherited Isolated Adrenal Insufficiency Due To Partial Cyp11a1 Deficiency,Juvenile Nasopharyngeal Angiofibroma,Premature Menopause,Autoimmune Polyendocrine Syndrome,Hypospadias,Ovarian Disease,46,Xy Sex Reversal,46,Xy Sex Reversal 2,Choriocarcinoma,Body Mass Index Quantitative Trait Locus 11,Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal, Partial Or Complete,Adrenal Cortical Carcinoma,Pseudohermaphroditism,Adrenal Carcinoma,Adrenal Cortex Disease,Asperger Syndrome,Antley-Bixler Syndrome,Hypoadrenocorticism, Familial,Adrenal Cortical Adenoma,Lipoid Congenital Adrenal Hyperplasia,Amelogenesis Imperfecta, Type Ig |
3n9y_b | P05108 | ENSG00000140459 | CYP11A1 | 100.00 | 1.60E-49 | 8.40E-54 | 364.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YDR402C | DIT2 | SGDID:S000002810 | CYP11B1 S11BH |
Cytochrome P450 11B1, mitochondrial (CYPXIB1) (Cytochrome P-450c11) (Cytochrome P450C11) (Steroid 11-beta-hydroxylase, CYP11B1) (EC 1.14.15.4) |
1.14.15.4 | Homo sapiens | Steroid Inherited Metabolic Disorder,Adrenal Rest Tumor,Adrenal Adenoma,Adenoma,Familial Glucocorticoid Deficiency,Syndromic Microphthalmia,Hyperaldosteronism, Familial, Type I,Conn'S Syndrome,Adrenal Gland Disease,Hypokalemia,Apparent Mineralocorticoid Excess,Carney Complex Variant,Familial Hyperaldosteronism,46,Xy Sex Reversal,46,Xy Sex Reversal 2,Liddle Syndrome 1,Achalasia-Addisonianism-Alacrima Syndrome,Adrenal Cortical Carcinoma,Functional Colonic Disease,Adrenal Carcinoma,Adrenal Cortex Disease,Asperger Syndrome,Microphthalmia, Syndromic 10,Adrenal Cortical Adenoma,Hypertension, Essential,Endocrine Organ Benign Neoplasm,Lipoid Congenital Adrenal Hyperplasia,Adrenal Hyperplasia, Congenital, Due To Steroid 11-Beta-Hydroxylase Deficiency,Corticosterone Methyloxidase Type I Deficiency,Primary Pigmented Nodular Adrenocortical Disease,Pseudohypoaldosteronism, Type I, Autosomal Recessive |
6m7x_b | P15538 | ENSG00000160882 | CYP11B1 | 100.00 | 1.60E-49 | 8.50E-54 | 363.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YDR402C | DIT2 | SGDID:S000002810 | MaF1660_ph0012 |
MaF1660_ph0012 |
Mycobacterium phage | 6n6q_b | V5UQK0 | 100.00 | 1.30E-49 | 7.30E-54 | 363.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |