About   Help   FAQ
Dnm1 Gene Detail
Summary
  • Symbol
    Dnm1
  • Name
    dynamin 1
  • Synonyms
    dynamin 1, Ftfl
  • Feature Type
    protein coding gene
  • IDs
    MGI:107384
    NCBI Gene: 13429
  • Alliance
  • Transcription Start Sites
    18 TSS
Location &
Maps
more
  • Sequence Map
    Chr2:32198483-32243350 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 2, 22.09 cM
  • Mapping Data
    3 experiments
Strain
Comparison
more
  • SNPs within 2kb
    60 from dbSNP Build 142
  • Strain Annotations
    18
  • RFLP
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_107384
protein coding gene Chr2:32198483-32243361 (-)
129S1/SvImJ MGP_129S1SvImJ_G0025602
protein coding gene Chr2:30753737-30798819 (-)
A/J MGP_AJ_G0025579
protein coding gene Chr2:29451005-29497816 (-)
AKR/J MGP_AKRJ_G0025549
protein coding gene Chr2:30499855-30552244 (-)
BALB/cJ MGP_BALBcJ_G0025576
protein coding gene Chr2:29577826-29623229 (-)
C3H/HeJ MGP_C3HHeJ_G0025336
protein coding gene Chr2:30394637-30441948 (-)
C57BL/6NJ MGP_C57BL6NJ_G0026020
protein coding gene Chr2:31691827-31744996 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0023429
protein coding gene Chr2:28179211-28223998 (-)
CAST/EiJ MGP_CASTEiJ_G0024798
protein coding gene Chr2:30330605-30381156 (-)
CBA/J MGP_CBAJ_G0025314
protein coding gene Chr2:32889881-32939492 (-)
DBA/2J MGP_DBA2J_G0025447
protein coding gene Chr2:29218940-29264954 (-)
FVB/NJ MGP_FVBNJ_G0025409
protein coding gene Chr2:29091808-29140820 (-)
LP/J MGP_LPJ_G0025533
protein coding gene Chr2:30628086-30678520 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0025440
protein coding gene Chr2:32545344-32602018 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0026078
protein coding gene Chr2:30381162-30433727 (-)
PWK/PhJ MGP_PWKPhJ_G0024546
protein coding gene Chr2:29123710-29169381 (-)
SPRET/EiJ MGP_SPRETEiJ_G0024346
protein coding gene Chr2:30536700-30590804 (-)
WSB/EiJ MGP_WSBEiJ_G0024867
protein coding gene Chr2:30552547-30604225 (-)



Homology
more
  • Human Ortholog
    DNM1, dynamin 1
  • Vertebrate Orthologs
    4
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    DNM1, dynamin 1
  • Synonyms
    DEE31, DEE31A, DEE31B, DNM, EIEE31
  • Links
    NCBI Gene ID: 1759
    neXtProt AC: NX_Q05193
    UniProt: Q05193

  • Chr Location
    9q34.11; chr9:128191655-128255248 (+)  GRCh38

Human Diseases
more
  • Diseases
    1 with Dnm1 mouse models; 2 with human DNM1 associations

Human Disease Mouse Models
      
IDs
View 2 models
      
IDs
IDs
Click on a disease name to see all genes associated with that disease.

  • Mutations/Alleles
    2 with disease annotations
  • References
    2 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    36 phenotypes from 6 alleles in 10 genetic backgrounds
    13 phenotypes from multigenic genotypes
    36 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 mice display reduced postnatal viability. Null mutation of this gene results in abnormal synaptic vesicle morphology, and recycling during neuronal activity. Other alleles are associated with seizures.
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
non-membrane-bounded 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
  • Comparison Matrix
  • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic ENSMUSG00000026825 Ensembl Gene Model | MGI Sequence Detail 44868 C57BL/6J ±  kb
    transcript ENSMUST00000139624 Ensembl | MGI Sequence Detail 3337 Not Applicable  
    polypeptide ENSMUSP00000122679 Ensembl | MGI Sequence Detail 867 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 19
      cDNA 15
      Primer pair 3
      Other 1

      Microarray probesets 5
    Other
    Accession IDs
    less
    MGD-MRK-35851, MGI:2139061, MGI:3027061
    References
    more
    • Summaries
      All 119
      Developmental Gene Expression 14
      Diseases 2
      Gene Ontology 25
      Phenotypes 36
    • Earliest
      J:33098 Gautam M, et al., Defective neuromuscular synaptogenesis in agrin-deficient mutant mice. Cell. 1996 May 17;85(4):525-35
    • Latest
      J:341354 Bonnycastle K, et al., Reversal of cell, circuit and seizure phenotypes in a mouse model of DNM1 epileptic encephalopathy. Nat Commun. 2023 Aug 30;14(1):5285

    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
    Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
    Send questions and comments to User Support.
    last database update
    03/19/2024
    MGI 6.23
    The Jackson Laboratory