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Snap29 Gene Detail
Summary
  • Symbol
    Snap29
  • Name
    synaptosomal-associated protein 29
  • Synonyms
    1300018G05Rik
  • Feature Type
    protein coding gene
  • IDs
    MGI:1914724
    NCBI Gene: 67474
  • Alliance
  • Transcription Start Sites
    5 TSS
Location &
Maps
more
  • Sequence Map
    Chr16:17223864-17248690 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 16, 10.79 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    498 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1914724
protein coding gene Chr16:17223850-17248691 (+)
129S1/SvImJ ENSMUSG00200041567
protein coding gene Chr16:14220398-14245242 (+)
A/J ENSMUSG00195033523
protein coding gene Chr16:13777660-13802500 (+)
AKR/J ENSMUSG00220035980
protein coding gene Chr16:14093949-14118791 (+)
BALB/cJ ENSMUSG00180032308
protein coding gene Chr16:14018901-14043747 (+)
C3H/HeJ ENSMUSG00175048784
protein coding gene Chr16:14163912-14188752 (+)
C57BL/6NJ ENSMUSG00215040484
protein coding gene Chr16:13885055-13909897 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0020514
protein coding gene Chr16:13905261-13931475 (+)
CAST/EiJ ENSTCUG00005044963
protein coding gene Chr16:14078103-14102742 (+)
CBA/J ENSMUSG00210045644
protein coding gene Chr16:14180221-14205062 (+)
DBA/2J ENSMUSG00185032704
protein coding gene Chr16:14126387-14151229 (+)
FVB/NJ ENSMUSG00205044551
protein coding gene Chr16:14133979-14158831 (+)
JF1/MsJ ENSUMUG00000049757
protein coding gene Chr16:14208178-14232932 (+)
LP/J ENSMUSG00230043502
protein coding gene Chr16:16704293-16729124 (+)
NOD/ShiLtJ ENSMUSG00190046221
protein coding gene Chr16:14266315-14291155 (+)
NZO/HlLtJ ENSMUSG00225030645
protein coding gene Chr16:19950101-19974946 (+)
PWK/PhJ ENSLUMG00010040372
protein coding gene Chr16:14090420-14115041 (+)
SPRET/EiJ ENSMSPG00010041915
protein coding gene Chr16:14117609-14139719 (+)
WSB/EiJ ENSIUOG00005033369
protein coding gene Chr16:14259279-14284339 (+)



Homology
more
  • Human Ortholog
    SNAP29, synaptosome associated protein 29
  • Vertebrate Orthologs
    3
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    SNAP29, synaptosome associated protein 29
  • Synonyms
    CEDNIK, SNAP-29
  • Links
    NCBI Gene ID: 9342
    UniProt: O95721

  • Chr Location
    22q11.21; chr22:20858537-20891214 (+)  GRCh38

Human Diseases
more
  • Diseases
    1 with Snap29 mouse models; 1 with human SNAP29 associations

Human Disease Mouse Models
      
IDs
View 2 models
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
    25 phenotypes from 3 alleles in 3 genetic backgrounds
    18 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.
Mice homozygous for a knock-out allele exhibit slightly reduced birth body size and a congenital ichtyotic phenotype associated with scaly and tight skin, hyperkeratosis, acanthosis, abnormalities in epidermal differentiation and autophagy, and increased endoplasmic reticulum stress.
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
  • Comparison Matrix
  • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic 67474 NCBI Gene Model | MGI Sequence Detail 24827 C57BL/6J ±  kb
    transcript NM_023348 RefSeq | MGI Sequence Detail 3432 C57BL/6  
    polypeptide Q9ERB0 UniProt | EBI | MGI Sequence Detail 260 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 54
      cDNA 53
      Primer pair 1
      Antibodies 2

      Microarray probesets 6
    Other
    Accession IDs
    less
    MGI:2146517, MGI:2146557, MGI:2146684
    References
    more
    • Summaries
      All 61
      Developmental Gene Expression 8
      Diseases 2
      Gene Ontology 9
      Phenotypes 18
    • Earliest
      J:60984 Ko MS, et al., Large-scale cDNA analysis reveals phased gene expression patterns during preimplantation mouse development. Development. 2000 Apr;127(8):1737-49
    • Latest
      J:359574 Eom TY, et al., Tbx1 haploinsufficiency leads to local skull deformity, paraflocculus and flocculus dysplasia, and motor-learning deficit in 22q11.2 deletion syndrome. Nat Commun. 2024 Dec 5;15(1):10510

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