Gene

myl9.L

Species
Xenopus laevis
Symbol
myl9.L
Name
myosin light chain 9
Synonyms
  • myl9.L
  • myosin light chain 9
Biotype
gene
Automated Description
Predicted to enable calcium ion binding activity. Predicted to be part of myosin complex. Human ortholog(s) of this gene implicated in familial hypertrophic cardiomyopathy and megacystis-microcolon-intestinal hypoperistalsis syndrome. Orthologous to human MYL9 (myosin light chain 9).
XBXL Description
Myosin regulatory light chain, EF-Hand protein superfamily
https://www.xenbase.org/gene/showgene.do?method=display&geneId=5949812
Cross References
Additional Information
Literature

Orthology

Gene tree
Not Available
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
Other Sources
None

Disease Associations

Cases where the expected disease association was NOT found
Cell color indicative of annotation volume

Transgenic Alleles

Models

Sequence Feature Viewer

Genome location
Assembly version
XL9.2
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Sequence Details

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Expression

Primary Sources
Other Sources
None
Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

Molecular Interactions

Genetic Interactions