Gene

Iglc3

Species
Mus musculus
Symbol
Iglc3
Name
immunoglobulin lambda constant 3
Synonyms
  • Igl-C3
  • immunoglobulin lambda chain, constant region 3
Biotype
gene segment
Automated Description
Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of IgG immunoglobulin complex. Orthologous to human IGLC1 (immunoglobulin lambda constant 1).
MGI Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR23266
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensIGLC15 of 10YesNo  
Danio rerioigic1s12 of 10YesYes  
Danio rerioigl3v52 of 10YesYes  
Danio reriozgc:1536592 of 10YesYes  
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
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

Genome location
Assembly version
GRCm39
Viewer Help
18.88410M18.88415M18.88420M18.88425M18.88430M18.88435M18.88440M
Variant Types and ConsequencesOnly variants associated to alleles are shown in the graphics above. See all variants in JBrowse.
Allele/Variant Symbol
Allele Synonyms
Category
Variant
Variant type
Molecular consequence
Has Disease Annotations
Has Phenotype Annotations
NC_000082.7:g.18884091T>Cvariant
SNP
  • 3 prime UTR variant
NC_000082.7:g.18884115T>Cvariant
SNP
  • stop retained variant
NC_000082.7:g.18884248T>Cvariant
SNP
  • missense variant
NC_000082.7:g.18884334A>Gvariant
SNP
  • synonymous variant
NC_000082.7:g.18884426G>Avariant
SNP
  • missense variant
NC_000082.7:g.18884209G>Tvariant
SNP
  • stop gained
NC_000082.7:g.18884402T>Cvariant
SNP
  • missense variant
NC_000082.7:g.18884375G>Tvariant
SNP
  • missense variant
NC_000082.7:g.18884222A>Gvariant
SNP
  • synonymous variant
NC_000082.7:g.18884239T>Avariant
SNP
  • missense variant
Showing 1 - 10 of 13 rows
per page

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
GRCm39
Viewer Help
18.88415M18.88420M18.88425M18.88430M18.88435M18.88440M

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