| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YIL143C | SSL2 | SGDID:S000001405 | CTHT_0009470 |
CTHT_0009470 |
Chaetomium thermophilum | 5m59_a | G0S0B9 | 99.60 | 1.50E-20 | 1.30E-24 | 245.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YIL143C | SSL2 | SGDID:S000001405 | SNRPB COD SNRPB1 |
Small nuclear ribonucleoprotein-associated proteins B and B' (snRNP-B) (Sm protein B/B') (Sm-B/B') (SmB/B') |
Homo sapiens | Burn-Mckeown Syndrome,Spinal Muscular Atrophy,Muscular Atrophy,Lupus Erythematosus,Isolated Pierre Robin Sequence,Cerebrocostomandibular Syndrome,Disease Of Mental Health,Mandibulofacial Dysostosis, Guion-Almeida Type,Otospondylomegaepiphyseal Dysplasia, Autosomal Dominant,Systemic Lupus Erythematosus,Acrofacial Dysostosis 1, Nager Type,Pierre Robin Syndrome |
6qdv_b | P14678 | ENSG00000125835 | SNRPB | 99.70 | 4.30E-21 | 3.70E-25 | 249.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YIL143C | SSL2 | SGDID:S000001405 | ERCC3 XPB XPBC |
General transcription and DNA repair factor IIH helicase subunit XPB (TFIIH subunit XPB) (EC 3.6.4.12) (Basic transcription factor 2 89 kDa subunit) (BTF2 p89) (DNA excision repair protein ERCC-3) (DNA repair protein complementing XP-B cells) (TFIIH basal transcription factor complex 89 kDa subunit) (TFIIH 89 kDa subunit) (TFIIH p89) (Xeroderma pigmentosum group B-complementing protein) |
3.6.4.12 | Homo sapiens | Cerebro-Oculo-Facio-Skeletal Syndrome,Ichthyosis,Retinitis Pigmentosa,Hair Disease,Robinow Syndrome, Autosomal Recessive 1,Cockayne Syndrome A,Xeroderma Pigmentosum-Cockayne Syndrome Complex,Xeroderma Pigmentosum Group E,Trichothiodystrophy 1, Photosensitive,Cockayne Syndrome,Trichothiodystrophy,Breast Cancer,Xeroderma Pigmentosum, Complementation Group C,Xeroderma Pigmentosum, Complementation Group D,Xeroderma Pigmentosum, Variant Type,Xeroderma Pigmentosum, Complementation Group F,Xeroderma Pigmentosum, Complementation Group G,Skin Carcinoma,Xeroderma Pigmentosum, Complementation Group B,Xfe Progeroid Syndrome,Autosomal Recessive Disease,Trichothiodystrophy 2, Photosensitive,Trichothiodystrophy 3, Photosensitive,Ifap Syndrome 1, With Or Without Bresheck Syndrome,Uv-Sensitive Syndrome |
4ern_a | P19447 | ENSG00000163161 | ERCC3 | 99.60 | 1.70E-20 | 1.40E-24 | 199.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YIL143C | SSL2 | SGDID:S000001405 | BRR2 RSS1 SNU246 YER172C SYGP-ORF66 |
Pre-mRNA-splicing helicase BRR2 (EC 3.6.4.13) (Protein Snu246) |
3.6.4.13 | Saccharomyces cerevisiae | 5dca_a | P32639 | 99.80 | 3.90E-25 | 3.20E-29 | 290.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YIL143C | SSL2 | SGDID:S000001405 | SSL2 LOM3 RAD25 UVS112 YIL143C |
General transcription and DNA repair factor IIH helicase subunit XPB (TFIIH subunit XPB) (EC 3.6.4.12) (DNA repair helicase RAD25) (RNA polymerase II transcription factor B subunit SSL2) (TFB subunit SSL2) (Suppressor of stem-loop mutation 2) |
3.6.4.12 | Saccharomyces cerevisiae | 5fmf_1 | Q00578 | 100.00 | 5.20E-34 | 4.40E-38 | 326.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YIL143C | SSL2 | SGDID:S000001405 | HAS1 YMR290C |
ATP-dependent RNA helicase HAS1 (EC 3.6.4.13) (Helicase associated with SET1 protein 1) |
3.6.4.13 | Saccharomyces cerevisiae | 5z3g_y | Q03532 | 99.60 | 4.00E-20 | 3.40E-24 | 210.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YIL143C | SSL2 | SGDID:S000001405 | SUB2 YDL084W |
ATP-dependent RNA helicase SUB2 (EC 3.6.4.13) (Suppressor of BRR1 protein 2) |
3.6.4.13 | Saccharomyces cerevisiae | 5suq_a | Q07478 | 99.60 | 6.10E-20 | 5.40E-24 | 204.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |