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Protein Coding Gene : Timd2 T cell immunoglobulin and mucin domain containing 2

Primary Identifier  MGI:2159681 Organism  mouse, laboratory
Chromosome  11 NCBI Gene Number  171284
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Enables ferritin receptor activity. Acts upstream of or within iron ion transport. Located in cell surface. Is expressed in 4-cell stage embryo; liver; liver left lobe; liver right lobe; and metanephros. Human ortholog(s) of this gene implicated in atopic dermatitis. Orthologous to human HAVCR1 (hepatitis A virus cellular receptor 1).
PHENOTYPE: Mice homozygous for a null allele exhibit an exacerbated inflammatory response. [provided by MGI curators]
  • synonyms:
  • expressed sequence AA816106,
  • expressed sequence AU019358,
  • MGI:2144396,
  • expressed sequence AU019662,
  • MGI:3034262,
  • C78111,
  • MGI:2144635,
  • T cell immunoglobulin and mucin domain containing 2,
  • AU019358,
  • TIM-2,
  • expressed sequence C78111,
  • Tim2,
  • MGI:2144392,
  • AU019662,
  • AA816106,
  • Timd2

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

1 Involved In Mutations

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

0 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For