Skip to main content Skip to navigation Skip to search
Open toolbar

Accessibility

Disclaimer
Accessibility arrangements
Home

Main menu

  • Home
  • Download
  • Information
  • Contact

Mobile Main Menu

  • Home
  • Download
  • Information
  • Contact
AnalogYeast
One stop shop for finding analogs for your favorite yeast protein

Breadcrumb

  1. Home
YJR138W IML1 / SGDID:S000003899
SGD CSV
Disease Associated
Homo Sapiens
Mus Musculus
Danio Rerio
Drosophila Melanogaster
Caenorhabditis Elegans
Arabidopsis Thaliana
Escherichia Coli
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
YJR138W IML1 SGDID:S000003899
IML1
Vacuolar membrane-associated protein Iml1
pfam Family
PF12257 100.00 3.40E-86 2.80E-90 751.60 0 0 0 0 0 0 0 0
YJR138W IML1 SGDID:S000003899
DEPDC5 KIAA0645
GATOR complex protein DEPDC5 (DEP domain-containing protein 5)
Homo sapiens
Seizure Disorder,Childhood Absence Epilepsy,Epilepsy,Congenital Lipomatous Overgrowth, Vascular Malformations, And Epidermal Nevi,Focal Epilepsy,Developmental And Epileptic Encephalopathy 14,Subependymal Glioma,Schizophrenia 13,Autosomal Dominant Epilepsy With Auditory Features,Depdc5-Related Epilepsy,Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, And Seizures Syndrome,Hepatocellular Carcinoma,Hepatitis C Virus,Alacrima, Achalasia, And Mental Retardation Syndrome,Partial Motor Epilepsy,Benign Epilepsy With Centrotemporal Spikes,West Syndrome,Disease Of Mental Health,Corneal Dystrophy, Fleck,Hypomelanosis Of Ito,Epilepsy, Familial Focal, With Variable Foci 1,Lennox-Gastaut Syndrome,Epilepsy, Familial Temporal Lobe, 3,Neonatal Period Electroclinical Syndrome,Childhood Electroclinical Syndrome,Early Onset Absence Epilepsy,Early Infantile Epileptic Encephalopathy,Dravet Syndrome,Benign Familial Infantile Epilepsy,Generalized Epilepsy With Febrile Seizures Plus,Stromal Dystrophy,Epilepsy, Myoclonic Juvenile,Autism,Autosomal Dominant Nocturnal Frontal Lobe Epilepsy,Band Heterotopia
6ces_d O75140 ENSG00000100150 DEPDC5 100.00 4.00E-241 3.00E-245 2382.00 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab