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Camta1 Gene Detail
Summary
  • Symbol
    Camta1
  • Name
    calmodulin binding transcription activator 1
  • Synonyms
    1810059M14Rik, 2310058O09Rik
  • Feature Type
    protein coding gene
  • IDs
    MGI:2140230
    NCBI Gene: 100072
  • Alliance
    genome feature page
  • Transcription Start Sites
    16 TSS
Location &
Maps
more
  • Sequence Map
    Chr4:151143980-151946225 bp, - strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 4, 81.53 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    18726 from dbSNP Build 142
  • Strain Annotations
    27
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_2140230
 protein coding gene Chr4:151143980-151946333 (-)
129S1/SvImJ ENSMUSG00200018777
 protein coding gene Chr4:142207075-142236316 (-)
129S1/SvImJ ENSMUSGG00200054637
 protein coding gene Chr4:142941261-143010572 (-)
A/J ENSMUSGG00195054988
 protein coding gene Chr4:144577076-144646424 (-)
A/J ENSMUSG00195014640
 protein coding gene Chr4:143843464-143872632 (-)
AKR/J ENSMUSG00220023651
 protein coding gene Chr4:143429044-143458252 (-)
AKR/J ENSMUSGG00220054637
 protein coding gene Chr4:144163589-144232940 (-)
BALB/cJ ENSMUSGG00180055484
 protein coding gene Chr4:142259400-142328699 (-)
BALB/cJ ENSMUSG00180002254
 protein coding gene Chr4:141526004-141555174 (-)
C3H/HeJ ENSMUSGG00175054716
 protein coding gene Chr4:145544211-145613541 (-)
C3H/HeJ ENSMUSG00175017177
 protein coding gene Chr4:144809323-144838530 (-)
C57BL/6NJ ENSMUSGG00215055374
 protein coding gene Chr4:144387885-144457177 (-)
C57BL/6NJ ENSMUSG00215006984
 protein coding gene Chr4:143654475-143683642 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0026835
 protein coding gene Chr4:140815146-141763204 (-)
CAST/EiJ no annotation
CBA/J ENSMUSG00210004547
 protein coding gene Chr4:143460948-143490155 (-)
CBA/J ENSMUSGG00210054585
 protein coding gene Chr4:144195860-144265191 (-)
DBA/2J ENSMUSGG00185057892
 protein coding gene Chr4:147760752-147830097 (-)
DBA/2J ENSMUSG00185013976
 protein coding gene Chr4:147027074-147056318 (-)
FVB/NJ ENSMUSG00205036936
 protein coding gene Chr4:141923509-141952752 (-)
FVB/NJ ENSMUSGG00205054194
 protein coding gene Chr4:142657190-142726534 (-)
JF1/MsJ no annotation
LP/J ENSMUSG00230019446
 protein coding gene Chr4:153759115-153788363 (-)
LP/J ENSMUSGG00230055470
 protein coding gene Chr4:154493952-154563282 (-)
NOD/ShiLtJ ENSMUSGG00190054662
 protein coding gene Chr4:143859966-143929317 (-)
NOD/ShiLtJ ENSMUSG00190003855
 protein coding gene Chr4:143126694-143155901 (-)
NZO/HlLtJ ENSMUSGG00225055276
 protein coding gene Chr4:158487559-158556844 (-)
NZO/HlLtJ ENSMUSG00225023621
 protein coding gene Chr4:157754271-157783478 (-)
PWK/PhJ no annotation
SPRET/EiJ ENSMSPG00010022863
 protein coding gene Chr4:144244633-145048402 (-)
WSB/EiJ no annotation



Homology
more
  • Human Ortholog
    CAMTA1, calmodulin binding transcription activator 1
  • Vertebrate Orthologs
    4
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    CAMTA1, calmodulin binding transcription activator 1
  • Synonyms
    CANPMR, CECBA
  • Links
    NCBI Gene ID: 23261
    UniProt: Q9Y6Y1

  • Chr Location
    1p36.31-p36.23; chr1:6785454-7769706 (+)  GRCh38
Human Diseases
more
  • Diseases
    1 with human CAMTA1 associations

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

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    12 phenotypes from 2 alleles in 2 genetic backgrounds
    2 phenotypes from multigenic genotypes
    2 images
    15 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.
Global or nervous system deletion of this gene results in decreased body size, severe ataxia, progressive Purkinje cell degeneration, and cerebellar atrophy.
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
    14
  • GO References
    7
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
    796
  • Tissues
    162
  • cDNA Data
    25
  • Literature Summary
    8
  • Comparison Matrix
    Gene Expression + Phenotype
    • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic 100072 NCBI Gene Model | MGI Sequence Detail 802246 C57BL/6J ±  kb
    transcript NM_001081557 RefSeq | MGI Sequence Detail 8448 C57BL/6  
    polypeptide A2A891 UniProt | EBI | MGI Sequence Detail 1682 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 32
      Genomic 1
      cDNA 25
      Primer pair 6

      Microarray probesets 12
    Other
    Accession IDs
    less
    MGI:1922837, MGI:1922929, MGI:2140626
    References
    more
    • Summaries
      All 50
      Developmental Gene Expression 8
      Gene Ontology 7
      Phenotypes 15
    • Earliest
      J:93290 Araki K, et al., Exchangeable gene trap using the Cre/mutated lox system. Cell Mol Biol (Noisy-Le-Grand). 1999 Jul;45(5):737-50
    • Latest
      J:342617 Dali O, et al., Transgenerational epigenetic effects imposed by neonicotinoid thiacloprid exposure. Life Sci Alliance. 2024 Feb;7(2)
    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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    Send questions and comments to User Support.     		last database update
    09/15/2026
    MGI 6.29     		The Jackson Laboratory