YER168C CCA1 / SGDID:S000000970
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
YER168C CCA1 SGDID:S000000970
aq_2158
CC-adding tRNA nucleotidyltransferase (C-adding TNT) (EC 2.7.7.-) (CC-adding enzyme)
 2.7.7.- Aquifex aeolicus
3wfo_a O67911 100.00 2.60E-61 2.00E-65 520.80 0 0 0 0 0 0 0 0
YER168C CCA1 SGDID:S000000970
BBI08_05760
BBI08_05760
 Planococcus halocryophilus
6ibp_a A0A1C7DQ98 100.00 9.80E-49 7.30E-53 408.70 0 0 0 0 0 0 0 0
YER168C CCA1 SGDID:S000000970
TM_0715
TM_0715
 Thermotoga maritima
3h38_a Q9WZH4 100.00 5.00E-51 3.80E-55 430.80 0 0 0 0 0 0 0 0
YER168C CCA1 SGDID:S000000970
cca
CCA-adding enzyme (EC 2.7.7.72) (CCA tRNA nucleotidyltransferase) (tRNA CCA-pyrophosphorylase) (tRNA adenylyl-/cytidylyl- transferase) (tRNA nucleotidyltransferase) (tRNA-NT)
 2.7.7.72 Geobacillus stearothermophilus
1miv_a Q7SIB1 100.00 5.10E-52 3.90E-56 433.60 0 0 0 0 0 0 0 0
YER168C CCA1 SGDID:S000000970
aq_411
A-adding tRNA nucleotidyltransferase (A-adding TNT) (EC 2.7.7.-) (A-adding enzyme)
 2.7.7.- Aquifex aeolicus
4wby_a O66728 100.00 1.50E-52 1.10E-56 438.20 0 0 0 0 0 0 0 0
YER168C CCA1 SGDID:S000000970
TRNT1 CGI-47
CCA tRNA nucleotidyltransferase 1, mitochondrial (EC 2.7.7.72) (Mitochondrial tRNA nucleotidyl transferase, CCA-adding) (mt CCA-adding enzyme) (mt tRNA CCA-diphosphorylase) (mt tRNA CCA-pyrophosphorylase) (mt tRNA adenylyltransferase)
 2.7.7.72 Homo sapiens
Sideroblastic Anemia,Retinitis Pigmentosa,Plasma Cell Neoplasm,B Cell Deficiency,Cataract 3, Multiple Types,Nystagmus 2, Congenital, Autosomal Dominant,Cataract,Sensorineural Hearing Loss,Cataract 4, Multiple Types,Lens Disease,Contractural Arachnodactyly, Congenital,Cataract 21, Multiple Types,Sideroblastic Anemia With B-Cell Immunodeficiency, Periodic Fevers, And Developmental Delay,Distal Arthrogryposis,Autosomal Recessive Disease,Cataract 37,Mental Retardation, Autosomal Recessive 2,Autosomal Recessive Non-Syndromic Intellectual Disability,Retinitis Pigmentosa And Erythrocytic Microcytosis,Myeloma, Multiple
 4x4w_a Q96Q11 ENSG00000072756 TRNT1 100.00 7.80E-49 5.90E-53 410.80 1 1 0 0 0 0 0 0