Gene

Mon1a

Species
Rattus norvegicus
Symbol
Mon1a
Name
MON1 homolog A, secretory trafficking associated
Synonyms
  • LOC315999
  • MON1 homolog A
Biotype
protein coding gene
Automated Description
Predicted to enable guanyl-nucleotide exchange factor activity. Predicted to be involved in protein secretion. Predicted to act upstream of or within establishment of localization in cell; intracellular iron ion homeostasis; and protein transport. Predicted to be part of Mon1-Ccz1 complex. Orthologous to human MON1A (MON1 homolog A, secretory trafficking associated).
RGD Description
Predicted to enable guanyl-nucleotide exchange factor activity. Predicted to be involved in protein secretion. Predicted to act upstream of or within establishment of localization in cell; intracellular iron ion homeostasis; and protein transport. Predicted to be part of Mon1-Ccz1 complex. Orthologous to human MON1A (MON1 homolog A, secretory trafficking associated); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; 2,4-dinitrotoluene; 4,4'-sulfonyldiphenol.
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR13027
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensMON1A9 of 10YesYes  
Mus musculusMon1a9 of 9YesYes   
Xenopus tropicalismon1a9 of 9YesYes   
Danio reriomon1a9 of 9YesYes   
Drosophila melanogasterMon19 of 9YesYes   
Caenorhabditis eleganssand-19 of 9YesYes   
Saccharomyces cerevisiaeMON19 of 9YesYes   
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Gene symbolRank Alignment Length (aa) Similarity %Identity %Method Count
Method
Ensembl ComparaHGNCInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidSGD
Mon1b155659437 of 9 

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
None
No data available

Disease Associations

Cases where the expected disease association was NOT found
Must provide at least one subject
Cell color indicative of annotation volume

Alleles and Variants

No mapped variant information available
Allele/Variant Symbol
Allele Synonyms
Category
Variant
Variant type
Molecular consequence
Has Disease Annotations
Has Phenotype Annotations
NC_051343.1:g.108583093A>Gvariant
SNP
  • intron variant
NC_051343.1:g.108584441G>Avariant
SNP
  • intron variant
NC_051343.1:g.108584725G>Avariant
SNP
  • intron variant
NC_051343.1:g.108585696C>Tvariant
SNP
  • intron variant
NC_051343.1:g.108585734T>Cvariant
NC_051343.1:g.108585742T>Cvariant
NC_051343.1:g.108586266C>Gvariant
NC_051343.1:g.108587299C>Gvariant
SNP
  • intron variant
NC_051343.1:g.108589894A>Gvariant
NC_051343.1:g.108577950G>Tvariant
SNP
  • intron variant
Showing 1 - 10 of 101 rows
per page

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
mRatBN7.2
Viewer Help
108.576M108.578M108.580M108.582M108.584M108.586M108.588M108.590M108.592M

Sequence Details

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Expression

Primary Sources
None
Other Sources
Must provide at least one subject
Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

Molecular Interactions

No data available

Genetic Interactions

No data available