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Itga10 Gene Detail
Summary
  • Symbol
    Itga10
  • Name
    integrin, alpha 10
  • Feature Type
    protein coding gene
  • IDs
    MGI:2153482
    NCBI Gene: 213119
  • Alliance
  • Transcription Start Sites
    2 TSS
Location &
Maps
more
  • Sequence Map
    Chr3:96552900-96571835 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 3, 41.93 cM, cytoband F2.2
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    454 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_2153482
protein coding gene Chr3:96552900-96571835 (+)
129S1/SvImJ ENSMUSG00200040381
protein coding gene Chr3:93181693-93200539 (+)
A/J ENSMUSG00195041531
protein coding gene Chr3:93585180-93604025 (+)
AKR/J ENSMUSG00220039519
protein coding gene Chr3:91930708-91949651 (+)
BALB/cJ ENSMUSG00180040792
protein coding gene Chr3:93527122-93545946 (+)
C3H/HeJ ENSMUSG00175027978
protein coding gene Chr3:93143597-93162439 (+)
C57BL/6NJ ENSMUSG00215016109
protein coding gene Chr3:93908104-93927053 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0025386
protein coding gene Chr3:90689974-90709702 (+)
CAST/EiJ ENSTCUG00005019588
protein coding gene Chr3:93727837-93746653 (+)
CBA/J ENSMUSG00210051044
protein coding gene Chr3:93696625-93715468 (+)
DBA/2J ENSMUSG00185040716
protein coding gene Chr3:94149132-94168069 (+)
FVB/NJ ENSMUSG00205020119
protein coding gene Chr3:92805021-92823874 (+)
JF1/MsJ ENSUMUG00000024100
protein coding gene Chr3:92992888-93011936 (+)
LP/J ENSMUSG00230040289
protein coding gene Chr3:96113531-96132370 (+)
NOD/ShiLtJ ENSMUSG00190037965
protein coding gene Chr3:94242260-94261074 (+)
NZO/HlLtJ ENSMUSG00225009046
protein coding gene Chr3:98492356-98511173 (+)
PWK/PhJ ENSLUMG00010025750
protein coding gene Chr3:92985690-93004711 (+)
SPRET/EiJ ENSMSPG00010037111
protein coding gene Chr3:93290704-93309282 (+)
WSB/EiJ ENSIUOG00005030050
protein coding gene Chr3:93643602-93662451 (+)



Homology
more
  • Human Ortholog
    ITGA10, integrin subunit alpha 10
  • Vertebrate Orthologs
    3
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    ITGA10, integrin subunit alpha 10
  • Synonyms
    PRO827
  • Links
    NCBI Gene ID: 8515
    UniProt: O75578

  • Chr Location
    1q21.1; chr1:145891206-145910111 (-)  GRCh38

Human Diseases
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  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    5 phenotypes from 1 allele in 1 genetic background
    13 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.
Homozygous null mice display slightly shortened long bones and amild abnormalities in ephysiseal plate morphology.
Gene Ontology
(GO)
Classifications
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  • 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
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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
  • Comparison Matrix
  • Sequences &
    Gene Models
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    Representative SequencesLengthStrain/SpeciesFlank
    genomic 213119 NCBI Gene Model | MGI Sequence Detail 18936 C57BL/6J ±  kb
    transcript NM_001302471 RefSeq | MGI Sequence Detail 5041 C57BL/6  
    polypeptide NP_001289400 RefSeq | MGI Sequence Detail 1166 C57BL/6  
    For the selected sequence
    Protein
    Information
    less
    • UniProt
      4 Sequences
    • InterPro Domains
      IPR013517 FG-GAP repeat
      IPR013519 Integrin alpha beta-propellor
      IPR000413 Integrin alpha chain
      IPR018184 Integrin alpha chain, C-terminal cytoplasmic region, conserved site
      IPR013649 Integrin alpha, first immunoglubulin-like domain
      IPR028994 Integrin alpha, N-terminal
      IPR048285 Integrin alpha, second immunoglobulin-like domain
      IPR032695 Integrin domain superfamily
      IPR036465 von Willebrand factor A-like domain superfamily
      IPR002035 von Willebrand factor, type A
    • GlyGen
      E9Q6R1 2 sites, 4 N-linked glycans (2 sites)
    Molecular
    Reagents
    less
    • All nucleic 18
      cDNA 16
      Primer pair 2

      Microarray probesets 3
    References
    more
    • Summaries
      All 44
      Developmental Gene Expression 8
      Diseases 1
      Gene Ontology 6
      Phenotypes 13
    • Earliest
      J:70677 Cook SA, et al., Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene. Cytogenet Cell Genet. 2001;93(1-2):77-82
    • Latest
      J:347984 Naillat F, et al., Calcium signaling induces partial EMT and renal fibrosis in a Wnt4(mCherry) knock-in mouse model. Biochim Biophys Acta Mol Basis Dis. 2024 Apr 21;1870(5):167180

    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)
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    Funding Information
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    last database update
    09/08/2026
    MGI 6.24
    The Jackson Laboratory