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
YIL026C IRR1 / SGDID:S000001288
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
YIL026C IRR1 SGDID:S000001288
STAG
STAG domain
pfam Family
PF08514 99.70 2.40E-22 1.90E-26 193.90 0 0 0 0 0 0 0 0
YIL026C IRR1 SGDID:S000001288
ZYRO0D15994g
ZYRO0D15994g
Zygosaccharomyces rouxii
4uvk_a C5DWM3 100.00 1.00E-135 1.00E-139 1289.50 0 0 0 0 0 0 0 0
YIL026C IRR1 SGDID:S000001288
IRR1 SCC3 YIL026C
Cohesin subunit SCC3 (Irregular cell behavior protein 1)
Saccharomyces cerevisiae
4uvj_a P40541 100.00 1.20E-42 1.00E-46 406.80 0 0 0 0 0 0 0 0
YIL026C IRR1 SGDID:S000001288
STAG2 SA2
Cohesin subunit SA-2 (SCC3 homolog 2) (Stromal antigen 2)
Homo sapiens
Cornelia De Lange Syndrome,Roberts-Sc Phocomelia Syndrome,Holoprosencephaly,Semilobar Holoprosencephaly,Alobar Holoprosencephaly,Leukemia, Acute Myeloid,Microcephaly,Fanconi Anemia, Complementation Group A,Laryngotracheitis,Septooptic Dysplasia,Xq25 Duplication Syndrome,Myelodysplastic Syndrome,Mullegama-Klein-Martinez Syndrome,Ewing Sarcoma,Holoprosencephaly 13, X-Linked
4pjw_a Q8N3U4 ENSG00000101972 STAG2 100.00 2.00E-102 2.00E-106 1003.90 1 1 0 0 0 0 0 0
YIL026C IRR1 SGDID:S000001288
STAG1 SA1 SCC3
Cohesin subunit SA-1 (SCC3 homolog 1) (Stromal antigen 1)
Homo sapiens
Cornelia De Lange Syndrome,Roberts-Sc Phocomelia Syndrome,Mental Retardation, Autosomal Dominant 47,Friedreich Ataxia,Amelogenesis Imperfecta, Type If,Syndromic Intellectual Disability
6qb5_a Q8WVM7 ENSG00000118007 STAG1 100.00 5.30E-62 4.30E-66 556.70 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab