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Timd2 Gene Detail
Summary
  • Symbol
    Timd2
  • Name
    T cell immunoglobulin and mucin domain containing 2
  • Synonyms
    Tim2, TIM-2
  • Feature Type
    protein coding gene
  • IDs
    MGI:2159681
    NCBI Gene: 171284
  • Alliance
  • Transcription Start Sites
    7 TSS
Location &
Maps
more
  • Sequence Map
    Chr11:46559787-46597888 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 11, 28.05 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    1707 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_2159681
protein coding gene Chr11:46559787-46597934 (-)
129S1/SvImJ MGP_129S1SvImJ_G0018199
protein coding gene Chr11:45558638-45648725 (-)
A/J MGP_AJ_G0018171
protein coding gene Chr11:43799995-43871346 (-)
AKR/J MGP_AKRJ_G0018137
protein coding gene Chr11:45130068-45180117 (-)
BALB/cJ MGP_BALBcJ_G0018140
protein coding gene Chr11:43952543-44030816 (-)
C3H/HeJ MGP_C3HHeJ_G0017954
protein coding gene Chr11:45109650-45201749 (-)
C57BL/6NJ MGP_C57BL6NJ_G0018594
protein coding gene Chr11:46963527-47013446 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0016249
protein coding gene Chr11:41764618-41802140 (-)
CAST/EiJ MGP_CASTEiJ_G0017517
protein coding gene Chr11:45300203-45340505 (-)
CBA/J MGP_CBAJ_G0017926
protein coding gene Chr11:49097748-49189097 (-)
DBA/2J MGP_DBA2J_G0018036
protein coding gene Chr11:43598303-43644739 (-)
FVB/NJ MGP_FVBNJ_G0018030
protein coding gene Chr11:43262987-43307263 (-)
LP/J MGP_LPJ_G0018108
protein coding gene Chr11:45828247-45907426 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0018054
protein coding gene Chr11:50667162-50718152 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0018633
protein coding gene Chr11:45268168-45306441 (-)
PWK/PhJ MGP_PWKPhJ_G0017297
protein coding gene Chr11:43695635-43736822 (-)
SPRET/EiJ MGP_SPRETEiJ_G0017090
protein coding gene Chr11:45084671-45127694 (-)
WSB/EiJ MGP_WSBEiJ_G0017567
protein coding gene Chr11:44937283-45012200 (-)



Homology
more
  • Human Ortholog
    HAVCR1, hepatitis A virus cellular receptor 1
  • Vertebrate Orthologs
    2
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    HAVCR1, hepatitis A virus cellular receptor 1
  • Synonyms
    CD365, HAVCR, HAVCR-1, KIM-1, KIM1, TIM, TIM-1, TIM1, TIMD-1, TIMD1
  • Links
    NCBI Gene ID: 26762
    neXtProt AC: NX_Q96D42
    UniProt: Q96D42

  • Chr Location
    5q33.3; chr5:157026742-157069407 (-)  GRCh38

Human Diseases
more
  • Diseases
    1 with human HAVCR1 associations

Human Disease Mouse Models
      
IDs
Click on a disease name to see all genes associated with that disease.

Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    6 phenotypes from 1 allele in 1 genetic background
    8 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
  • All Mutations and Alleles
    5
  • Chemically induced (other)
    1
  • Endonuclease-mediated
    1
  • Targeted
    3
  • Genomic Mutations
    1 involving Timd2
  • Incidental Mutations
    APF , CvDC
  • Find Mice (IMSR)
Mice homozygous for a null allele exhibit an exacerbated inflammatory response.
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
  • GO References
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
RNA binding
signaling receptor activity
signaling receptor binding
transcription
transferase
transporter
Biological Process

carbohydrate derivative metabolism
cell differentiation
cell population proliferation
cellular component organization
DNA-templated transcription
establishment of localization
homeostatic process
immune system process
lipid metabolic process
programmed cell death
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
membraneless organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
protein-containing complex
synapse
vacuole
Click cells to view annotations.
Expression
less
Expression Overview

early conceptus
embryo ectoderm
embryo endoderm
embryo mesoderm
embryo mesenchyme
extraembryonic component
alimentary system
auditory system
branchial arches
cardiovascular system
connective tissue
endocrine system
exocrine system
hemolymphoid system
integumental system
limbs
liver and biliary system
musculoskeletal system
nervous system
olfactory system
reproductive system
respiratory system
urinary system
visual system
Click cells to view annotations.


  • Assay Results
  • Tissues
  • cDNA Data
  • Literature Summary
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000040413 Ensembl Gene Model | MGI Sequence Detail 38102 C57BL/6J ±  kb
transcript ENSMUST00000169584 Ensembl | MGI Sequence Detail 2926 Not Applicable  
polypeptide ENSMUSP00000131540 Ensembl | MGI Sequence Detail 305 Not Applicable  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 93
    cDNA 90
    Primer pair 2
    Other 1

    Microarray probesets 6
Other
Accession IDs
less
MGI:2144392, MGI:2144396, MGI:2144635, MGI:3034262
References
more
  • Summaries
    All 42
    Developmental Gene Expression 5
    Gene Ontology 5
    Phenotypes 8
  • Earliest
    J:137335 Roderick TH, Chromosomal inversions in studies of mammalian mutagenesis. Genetics. 1979 May;92(1 Pt 1 Suppl):s121-6
  • Latest
    J:344223 Zhang W, et al., NLRP14 deficiency causes female infertility with oocyte maturation defects and early embryonic arrest by impairing cytoplasmic UHRF1 abundance. Cell Rep. 2023 Dec 26;42(12):113531

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory