| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YLR149C | YLR149C | SGDID:S000004139 | SKI8 REC103 YGL213C |
Antiviral protein SKI8 (Superkiller protein 8) |
Saccharomyces cerevisiae | 1sq9_a | Q02793 | 98.80 | 4.70E-13 | 6.50E-17 | 122.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR149C | YLR149C | SGDID:S000004139 | FZR1 CDH1 FYR FZR KIAA1242 |
Fizzy-related protein homolog (Fzr) (CDC20-like protein 1) (Cdh1/Hct1 homolog) (hCDH1) |
Homo sapiens | Breast Cancer |
4ui9_r | Q9UM11 | ENSG00000105325 | FZR1 | 98.70 | 1.60E-12 | 1.90E-16 | 133.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YLR149C | YLR149C | SGDID:S000004139 | Guanine nucleotide-binding protein subunit beta-like protein |
Guanine nucleotide-binding protein subunit beta-like protein |
Leishmania donovani | 5t2a_7 | Q9BIJ5 | 98.80 | 5.30E-13 | 7.30E-17 | 118.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR149C | YLR149C | SGDID:S000004139 | SPBPJ4664.04 |
Putative coatomer subunit alpha (Alpha-coat protein) (Alpha-COP) |
Schizosaccharomyces pombe | 4j87_a | Q96WV5 | 98.70 | 1.40E-12 | 2.00E-16 | 115.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR149C | YLR149C | SGDID:S000004139 | ATG16L1 APG16L UNQ9393/PRO34307 |
Autophagy-related protein 16-1 (APG16-like 1) |
Homo sapiens | Inflammatory Bowel Disease 1,Ulcerative Colitis,Uveoparotid Fever,Crohn'S Disease,Anorectal Stricture,Inflammatory Bowel Disease 10,Inflammatory Bowel Disease,Inflammatory Bowel Disease 5,Inflammatory Bowel Disease 6,Inflammatory Bowel Disease 18,Autoimmune Disease Of Gastrointestinal Tract,Colitis,Ileitis,Ileocolitis,Crohn'S Colitis,Salmonellosis,Celiac Disease 1 |
5nuv_a | Q676U5 | ENSG00000085978 | ATG16L1 | 98.70 | 2.00E-12 | 2.80E-16 | 113.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YLR149C | YLR149C | SGDID:S000004139 | LRRK2 PARK8 |
Leucine-rich repeat serine/threonine-protein kinase 2 (EC 2.7.11.1) (EC 3.6.5.-) (Dardarin) |
2.7.11.1,3.6.5.-, | Homo sapiens | Supranuclear Palsy, Progressive, 1,Rem Sleep Behavior Disorder,Spinocerebellar Atrophy,Tremor,Prion Disease,Gaucher'S Disease,Hereditary Late-Onset Parkinson Disease,Sphingolipidosis,Klippel-Feil Syndrome 1,Alzheimer Disease,Ulnar Nerve Lesion,Radial Nerve Lesion,Amyotrophic Lateral Sclerosis 1,Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Parkinsonism,Movement Disease,Isolated Klippel-Feil Syndrome,Testicular Disease,Essential Tremor,Von Economo'S Disease,Dementia,Lrrk2 Parkinson Disease,Sleep Disorder,Dystonia,Nervous System Disease,Klippel-Feil Syndrome,Crohn'S Disease,Parkinson Disease, Late-Onset,Peripheral Nervous System Disease,Parkinson Disease 3, Autosomal Dominant,Parkinson Disease 1, Autosomal Dominant,Athetosis,Pick Disease Of Brain,Postencephalitic Parkinson Disease,Klippel-Feil Syndrome 1, Autosomal Dominant,Autosomal Dominant Cerebellar Ataxia,Disease Of Mental Health,Gaucher Disease, Type I,Toxic Encephalopathy,Failure Of Tooth Eruption, Primary,Rheumatoid Arthritis,Dementia, Lewy Body,Ophthalmomyiasis,Inflammatory Bowel Disease,Gerstmann-Straussler Disease,Parkinson Disease 21,Kufor-Rakeb Syndrome,Leprosy 3,Parkinson Disease 10,Parkinson Disease 8, Autosomal Dominant,Alzheimer Disease 8,Aphasia,Multiple System Atrophy 1,Color Agnosia,Mitochondrial Complex I Deficiency, Nuclear Type 1,Early-Onset Parkinson'S Disease,Parkinson Disease 2, Autosomal Recessive Juvenile,Frontotemporal Dementia,3-Methylglutaconic Aciduria, Type Iii,Parkinson Disease 15, Autosomal Recessive Early-Onset |
6dlo_b | Q5S007 | ENSG00000188906 | LRRK2 | 98.70 | 2.10E-12 | 2.80E-16 | 120.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YLR149C | YLR149C | SGDID:S000004139 | Tc00.1047053511211.120 Tc00.1047053511211.130 |
Tc00.1047053511211.120 Tc00.1047053511211.130 |
Trypanosoma cruzi | 5opt_p | Q4DTN2 | 98.70 | 1.30E-12 | 1.80E-16 | 115.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR149C | YLR149C | SGDID:S000004139 | CDC20 |
Cell division cycle protein 20 homolog (p55CDC) |
Homo sapiens | Polyposis Syndrome, Hereditary Mixed, 1,Mosaic Variegated Aneuploidy Syndrome,Neuronal Ceroid Lipofuscinosis,Prostate Cancer,Ceroid Lipofuscinosis, Neuronal, 2,Ceroid Lipofuscinosis, Neuronal, 1,Mosaic Variegated Aneuploidy Syndrome 1 |
4ggc_a | Q12834 | ENSG00000117399 | CDC20 | 99.10 | 3.00E-15 | 4.00E-19 | 133.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YLR149C | YLR149C | SGDID:S000004139 | CIA1 YDR267C |
Cytosolic iron-sulfur protein assembly protein 1 |
Saccharomyces cerevisiae | 2hes_x | Q05583 | 98.70 | 2.00E-12 | 2.70E-16 | 115.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR149C | YLR149C | SGDID:S000004139 | SEC13 ANU3 YLR208W L8167.4 |
Protein transport protein SEC13 |
Saccharomyces cerevisiae | 2pm7_d | Q04491 | 98.80 | 4.20E-13 | 5.70E-17 | 118.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR149C | YLR149C | SGDID:S000004139 | TUP1 AAR1 AER2 AMM1 CYC9 FLK1 SFL2 UMR7 YCR084C YCR84C |
General transcriptional corepressor TUP1 (Flocculation suppressor protein) (Glucose repression regulatory protein TUP1) (Repressor AER2) |
Saccharomyces cerevisiae | 1erj_a | P16649 | 98.70 | 1.20E-12 | 1.50E-16 | 126.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR149C | YLR149C | SGDID:S000004139 | slp1 SPAC821.08c |
WD repeat-containing protein slp1 |
Schizosaccharomyces pombe | 4aez_a | P78972 | 98.80 | 5.80E-13 | 7.60E-17 | 124.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR149C | YLR149C | SGDID:S000004139 | RAE1 MRNP41 |
mRNA export factor (Rae1 protein homolog) (mRNA-associated protein mrnp 41) |
Homo sapiens | Anterior Horn Cell Disease,Vulto-Van Silfhout-De Vries Syndrome,Autosomal Dominant Non-Syndromic Intellectual Disability,Lethal Congenital Contracture Syndrome 1,Lethal Congenital Contracture Syndrome |
3mmy_g | P78406 | ENSG00000101146 | RAE1 | 98.80 | 6.70E-13 | 9.00E-17 | 122.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YLR149C | YLR149C | SGDID:S000004139 | SEC13 D3S1231E SEC13A SEC13L1 SEC13R |
Protein SEC13 homolog (GATOR complex protein SEC13) (SEC13-like protein 1) (SEC13-related protein) |
Homo sapiens | Anemia, Congenital Dyserythropoietic, Type Ii,Chylomicron Retention Disease,Craniolenticulosutural Dysplasia |
3bg1_a | P55735 | ENSG00000157020 | SEC13 | 98.80 | 3.10E-13 | 4.30E-17 | 119.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YLR149C | YLR149C | SGDID:S000004139 | CDH1 HCT1 YGL003C |
APC/C activator protein CDH1 (CDC20 homolog 1) (Homolog of CDC twenty 1) |
Saccharomyces cerevisiae | 4bh6_f | P53197 | 99.00 | 4.00E-14 | 5.40E-18 | 125.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR149C | YLR149C | SGDID:S000004139 | RSA4 YCR072C YCR72C |
Ribosome assembly protein 4 (Notchless protein homolog 1) (Ribosome biogenesis factor RSA4) |
Saccharomyces cerevisiae | 4wjv_d | P25382 | 98.70 | 1.70E-12 | 2.40E-16 | 117.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR149C | YLR149C | SGDID:S000004139 | EED |
Polycomb protein EED (hEED) (Embryonic ectoderm development protein) (WD protein associating with integrin cytoplasmic tails 1) (WAIT-1) |
Homo sapiens | Eed-Related Overgrowth,Cohen-Gibson Syndrome,Nutmeg Liver,Weaver Syndrome,Myelodysplastic Syndrome |
5u69_a | O75530 | ENSG00000074266 | EED | 98.70 | 1.70E-12 | 2.40E-16 | 117.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YLR149C | YLR149C | SGDID:S000004139 | CNAG_05465 |
CNAG_05465 |
Cryptococcus neoformans | 4d6v_a | J9W3X8 | 98.70 | 1.70E-12 | 2.30E-16 | 115.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YLR149C | YLR149C | SGDID:S000004139 | WD_REPEATS_REGION domain-containing protein |
WD_REPEATS_REGION domain-containing protein |
Oryctolagus cuniculus | 3jah_gg | G1SJB4 | 98.70 | 1.40E-12 | 1.90E-16 | 115.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |