Phenotype Help

MLC1 / YGL106W Phenotype

Phenotype annotations for a gene are curated single mutant phenotypes that require an observable (e.g., "cell shape"), a qualifier (e.g., "abnormal"), a mutant type (e.g., null), strain background, and a reference. In addition, annotations are classified as classical genetics or high-throughput (e.g., large scale survey, systematic mutation set). Whenever possible, allele information and additional details are provided.



Annotations

A phenotype is defined as an observable (e.g., apoptosis) and a qualifier (e.g., increased). There may be more than one row with the same phenotype if that phenotype was observed in separate studies or in different conditions, strains, alleles, etc.

10 entries for 9 phenotypes


Increase the total number of rows showing on this page using the pull-down located below the table, or use the page scroll at the table's top right to browse through the table's pages; use the arrows to the right of a column header to sort by that column; filter the table using the "Filter" box at the top of the table; click on the small "i" buttons located within a cell for an annotation to view further details.

PhenotypeExperiment TypeMutant InformationStrain BackgroundChemicalDetailsReference
cytokinesis: abnormal
classical geneticsnull
Allele: mlc1-Δ
OtherStevens RC and Davis TN (1998) PMID:9700160
cytokinesis: absent
classical geneticsdominant negativeW303Treatment: synchronized
Details: cytokinesis is not completed in cells expressing GST-Mlc1p; chains of multinucleate cells accumulate; chains cannot be separated by sonication or cell wall removal
Boyne JR, et al. (2000) PMID:11082046
cytokinesis: decreased
classical geneticsconditional
Allele: mlc1-11

G114D

OtherTemperature: permissive temperature, 24 °C
Details: severe defect in cytokinesis
Luo J, et al. (2004) PMID:15210731
haploinsufficient
classical geneticsnull
Allele: mlc1-Δ
OtherStevens RC and Davis TN (1998) PMID:9700160
inviable
classical geneticsnull
Allele: mlc1-Δ
OtherStevens RC and Davis TN (1998) PMID:9700160
mitochondrial morphology: abnormal
systematic mutation setrepressibleS288C10 ug/ml doxycyclineDetails: Tet-regulated essential ORF strain collection; doxycycline represses expression
Altmann K and Westermann B (2005) PMID:16135527
protein/peptide accumulation: abnormal
Reporter: Iqg1p
classical geneticsnull
Allele: mlc1-Δ
W303Boyne JR, et al. (2000) PMID:11082046
protein/peptide distribution: abnormal
Reporter: Iqg1-3HAp
classical geneticsrepressibleW303Treatment: synchronized
Details: localization of Iqg1p to the bud neck is reduced from 18% in control cells to 1.4% of mutant cells
Boyne JR, et al. (2000) PMID:11082046
protein/peptide distribution: abnormal
Reporter: Myo1-GFP
classical geneticsconditional
Allele: mlc1-11
OtherTemperature: permissive temperature, 23 °C
Details: Myo1p targeting to the bud neck division site during cytokinesis is lost at the time of septin hourglass splitting
Fang X, et al. (2010) PMID:21173112
resistance to chemicals: increased
systematic mutation set repressibleS288C4 µg/ml miltefosineDetails: reproducible increase in miltefosine resistance relative to wt
Garcia JM, et al. (2021) PMID:34568930
Showing 1 to 10 of 10 entries

Shared Phenotypes

This diagram displays phenotype observables (purple squares) that are shared between the given gene (yellow circle) and other genes (gray circles) based on the number of phenotype observables shared (adjustable using the slider at the bottom).


Reset

Click on a gene or phenotype observable name to go to its specific page within SGD; drag any of the gene or observable objects around within the visualization for easier viewing; click “Reset” to automatically redraw the diagram; filter the genes that share observable terms with the given gene by the number of terms they share by clicking anywhere on the slider bar or dragging the tab to the desired filter number.


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