| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YPL210C | SRP72 | SGDID:S000006131 | TFC4 PCF1 YGR047C |
Transcription factor tau 131 kDa subunit (TFIIIC 131 kDa subunit) (Transcription factor C subunit 4) |
Saccharomyces cerevisiae | 5aio_a | P33339 | 99.00 | 4.90E-14 | 5.20E-18 | 141.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YPL210C | SRP72 | SGDID:S000006131 | PEX5 PXR1 |
Peroxisomal targeting signal 1 receptor (PTS1 receptor) (PTS1R) (PTS1-BP) (Peroxin-5) (Peroxisomal C-terminal targeting signal import receptor) (Peroxisome receptor 1) |
Homo sapiens | Refsum Disease, Classic,Peroxisome Biogenesis Disorder 1a,Peroxisome Biogenesis Disorder 2a,Zellweger Syndrome,Peroxisomal Disease,Rhizomelic Chondrodysplasia Punctata, Type 1,Chondrodysplasia Punctata Syndrome,Peroxisomal Biogenesis Disorder,Neonatal Adrenoleukodystrophy,Peroxisome Biogenesis Disorder 1b,Cataract,Rhizomelic Chondrodysplasia Punctata,Sensorineural Hearing Loss,Zellweger Spectrum Disorder,Rhizomelic Chondrodysplasia Punctata, Type 2,Primary Hyperoxaluria,Leukodystrophy,Juvenile Glaucoma,Microcephaly,Adrenoleukodystrophy,Rhizomelic Chondrodysplasia Punctata, Type 5,Peroxisome Biogenesis Disorder 2b,Mulibrey Nanism,Rhizomelic Chondrodysplasia Punctata, Type 3 |
1fch_a | P50542 | 99.20 | 2.30E-15 | 2.30E-19 | 149.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YPL210C | SRP72 | SGDID:S000006131 | PEX5 PXR1 |
Peroxisomal targeting signal 1 receptor (PTS1 receptor) (PTS1R) (PTS1-BP) (Peroxin-5) (Peroxisomal C-terminal targeting signal import receptor) (Peroxisome receptor 1) |
Homo sapiens | Refsum Disease, Classic,Peroxisome Biogenesis Disorder 1a,Peroxisome Biogenesis Disorder 2a,Zellweger Syndrome,Peroxisomal Disease,Rhizomelic Chondrodysplasia Punctata, Type 1,Chondrodysplasia Punctata Syndrome,Peroxisomal Biogenesis Disorder,Neonatal Adrenoleukodystrophy,Peroxisome Biogenesis Disorder 1b,Cataract,Rhizomelic Chondrodysplasia Punctata,Sensorineural Hearing Loss,Zellweger Spectrum Disorder,Rhizomelic Chondrodysplasia Punctata, Type 2,Primary Hyperoxaluria,Leukodystrophy,Juvenile Glaucoma,Microcephaly,Adrenoleukodystrophy,Rhizomelic Chondrodysplasia Punctata, Type 5,Peroxisome Biogenesis Disorder 2b,Mulibrey Nanism,Rhizomelic Chondrodysplasia Punctata, Type 3 |
2c0l_a | P50542 | ENSG00000139197 | PEX5 | 99.00 | 2.90E-14 | 3.10E-18 | 133.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YPL210C | SRP72 | SGDID:S000006131 | PARMER_03812 |
PARMER_03812 |
Parabacteroides merdae | 4r7s_a | A7AK45 | 99.10 | 3.60E-15 | 4.00E-19 | 136.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |