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Allele: ssc1-V189P

Allele Name
ssc1-V189P 1
SGD ID
SGD:S000314757
Affected Gene
SSC1
Allele Type
missense variant 1
Description
V189P; analogous to a mutation in N-terminal nucleotide binding domain of human ortholog HSPA9 associated with congenital sideroblastic anemia 1

References

List of references used specifically to curate the information in Overview section.

  1. Vishwanathan V and D'Silva P (2022) Loss of Function of mtHsp70 Chaperone Variants Leads to Mitochondrial Dysfunction in Congenital Sideroblastic Anemia. Front Cell Dev Biol 10:847045 PMID: 35252210

Resources

Mutant Strains

Addgene Plasmids | DNASU Plasmids | PlasmID | Thermo Scientific | YGRC

Phenotype Resources

dHITS | FitDB | HIPHOP Chemogenomics | HIP HOP Profiles | PhenoM | PROPHECY | SCMD | ScreenTroll | TheCellVision

Ontology

Yeast Phenotype Ontology

Interactions Resources

BioGRID | CYC2008 | GeneMANIA | IMP | InterologFinder | ModelArchive | TheCellMap | YeastRC Mass Spec