MUM3/YOR298W Summary Help

Standard Name MUM3 1
Systematic Name YOR298W
Feature Type ORF, Verified
Description Protein of unknown function involved in outer spore wall organization; has similarity to the tafazzins superfamily of acyltransferases (1, 2)
Name Description MUddled Meiosis 1
Chromosomal Location
ChrXV:875599 to 877038 | ORF Map | GBrowse
Gbrowse
Gene Ontology Annotations All MUM3 GO evidence and references
  View Computational GO annotations for MUM3
Molecular Function
Manually curated
Biological Process
Manually curated
Cellular Component
Manually curated
Regulators 2 genes
Resources
Classical genetics
null
Large-scale survey
null
Resources
11 total interaction(s) for 9 unique genes/features.
Physical Interactions
  • Affinity Capture-MS: 1
  • Affinity Capture-RNA: 2

Genetic Interactions
  • Negative Genetic: 4
  • Synthetic Growth Defect: 4

Resources
Expression Summary
histogram
Resources
Length (a.a.) 479
Molecular Weight (Da) 57,236
Isoelectric Point (pI) 9.98
Localization
Phosphorylation PhosphoGRID | PhosphoPep Database
Structure
Homologs
sequence information
ChrXV:875599 to 877038 | ORF Map | GBrowse
SGD ORF map
Last Update Coordinates: 2011-02-03 | Sequence: 1996-07-31
Subfeature details
Relative
Coordinates
Chromosomal
Coordinates
Most Recent Updates
Coordinates Sequence
CDS 1..1440 875599..877038 2011-02-03 1996-07-31
Retrieve sequences
Analyze Sequence
S288C only
S288C vs. other species
S288C vs. other strains
Resources
External Links All Associated Seq | Entrez Gene | Entrez RefSeq Protein | MIPS | Search all NCBI (Entrez) | UniProtKB
Primary SGDIDS000005824
References cited on this page View Complete Literature Guide for MUM3
1) Engebrecht J, et al.  (1998) Yeast meiotic mutants proficient for the induction of ectopic recombination. Genetics 148(2):581-98
2) Neuwald AF  (1997) Barth syndrome may be due to an acyltransferase deficiency. Curr Biol 7(8):R465-6