Gene

Il4i1b

Species
Mus musculus
Symbol
Il4i1b
Name
interleukin 4 induced 1B
Synonyms
  • Gm21948
  • predicted gene, 21948
Biotype
protein coding gene
Automated Description
Predicted to enable L-amino-acid oxidase activity. Predicted to be involved in aromatic amino acid family catabolic process; negative regulation of T cell mediated immune response to tumor cell; and regulation of T cell activation. Predicted to be located in several cellular components, including acrosomal vesicle; immunological synapse; and sperm midpiece. Orthologous to human IL4I1 (interleukin 4 induced 1).
MGI Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
Not Available
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensIL4I110 of 10YesYes  
Rattus norvegicusIl4i19 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
Lao1151957405 of 9 
4930438A08Rik251459405 of 9 
Kdm1a360538253 of 9 
Kdm1b457139253 of 9 
Maob555040242 of 9 
Maoa652141262 of 9 
Smox760633203 of 9 
Paox854336233 of 9 

Function - GO Annotations

No function available for that gene

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
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
No data available

Alleles and Variants

Genome location
Assembly version
GRCm39
Viewer Help
44.466M44.468M44.470M44.472M44.474M44.476M44.478M44.480M44.482M44.484M44.486M44.488M44.490M
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_000073.7:g.44466514C>Tvariant
SNP
  • intron variant
NC_000073.7:g.44471262C>Tvariant
SNP
  • intron variant
NC_000073.7:g.44471331G>Tvariant
SNP
  • intron variant
NC_000073.7:g.44471587A>Tvariant
SNP
  • intron variant
NC_000073.7:g.44474008G>Avariant
SNP
  • intron variant
NC_000073.7:g.44482944G>Tvariant
SNP
  • intron variant
NC_000073.7:g.44482740G>Avariant
SNP
  • intron variant
NC_000073.7:g.44476801C>Tvariant
SNP
  • intron variant
NC_000073.7:g.44477208A>Gvariant
SNP
  • intron variant
NC_000073.7:g.44478565A>Tvariant
SNP
  • synonymous variant
Showing 1 - 10 of 500 rows
per page

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
GRCm39
Viewer Help
44.466M44.468M44.470M44.472M44.474M44.476M44.478M44.480M44.482M44.484M44.486M44.488M44.490MNM_001171024.1 (Il4i1b)ENSMUST00000047356 (Atf5)ENSMUST00000107893 (Atf5)ENSMUST00000209072 (Atf5)NM_030693.2 (Atf5)NR_033136.1 (Atf5)ENSMUST00000057195 (Nup62)ENSMUST00000207085 (Nup62)ENSMUST00000207103 (Nup62)ENSMUST00000208172 (Nup62)Maximum features displayed. See full view for more.Maximum features displayed. See full view for more.Maximum features displayed. See full view for more.

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