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AnalogYeast
One stop shop for finding analogs for your favorite yeast protein

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YDL002C NHP10 / SGDID:S000002160
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
YDL002C NHP10 SGDID:S000002160
Hmgb1 Hmg-1 Hmg1
High mobility group protein B1 (Amphoterin) (Heparin-binding protein p30) (High mobility group protein 1) (HMG-1)
Rattus norvegicus
1ckt_a P63159 98.80 5.00E-13 4.50E-17 91.90 0 0 0 0 0 0 0 0
YDL002C NHP10 SGDID:S000002160
TFAM TCF6 TCF6L2
Transcription factor A, mitochondrial (mtTFA) (Mitochondrial transcription factor 1) (MtTF1) (Transcription factor 6) (TCF-6) (Transcription factor 6-like 2)
Homo sapiens
Mitochondrial Dna Depletion Syndrome,Myopathy,Optic Nerve Disease,Diabetes Mellitus,Alzheimer Disease,Mitochondrial Myopathy,Mitochondrial Dna Depletion Syndrome 15,Chronic Progressive External Ophthalmoplegia,Dilated Cardiomyopathy,Sensorineural Hearing Loss,Autosomal Dominant Progressive External Ophthalmoplegia,Optic Atrophy 1,Mitochondrial Dna Maintenance Defects,Mitochondrial Disorders,Skin Carcinoma In Situ,Cholestasis,Cranial Nerve Disease,Extrahepatic Cholestasis,Parkinson Disease, Late-Onset,Body Mass Index Quantitative Trait Locus 11,Myasthenic Syndrome, Congenital, 12,Bacterial Gastritis,Perrault Syndrome,Huntington Disease,Leber Hereditary Optic Neuropathy, Modifier Of,Mitochondrial Dna Depletion Syndrome 3,Mitochondrial Dna Depletion Syndrome 4a,Aging,Kearns-Sayre Syndrome,Leigh Syndrome,Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes,Myoclonic Epilepsy Associated With Ragged-Red Fibers,Neuropathy, Ataxia, And Retinitis Pigmentosa,Oncocytoma
3tq6_a Q00059 ENSG00000108064 TFAM 98.80 1.20E-12 1.20E-16 105.30 1 1 0 0 0 0 0 0
YDL002C NHP10 SGDID:S000002160
KMT2C HALR KIAA1506 MLL3
Histone-lysine N-methyltransferase 2C (Lysine N-methyltransferase 2C) (EC 2.1.1.354) (Homologous to ALR protein) (Myeloid/lymphoid or mixed-lineage leukemia protein 3)
2.1.1.354 Homo sapiens
Plasma Cell Neoplasm,Kleefstra Syndrome,Leukemia,Leukemia, Acute Myeloid,Kleefstra Syndrome Due To A Point Mutation,Cystic Kidney Disease,Colorectal Cancer,Microcephaly,Alacrima, Achalasia, And Mental Retardation Syndrome,Kleefstra Syndrome 2,Disease Of Mental Health,Kleefstra Syndrome 1,Autism Spectrum Disorder,Kabuki Syndrome 1,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome,Nut Midline Carcinoma,Myeloma, Multiple,Cardiomyopathy, Infantile Histiocytoid
2yuk_a Q8NEZ4 ENSG00000055609 KMT2C 98.50 2.10E-11 1.80E-15 88.20 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab