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Syt13 Gene Detail
Summary
  • Symbol
    Syt13
  • Name
    synaptotagmin XIII
  • Synonyms
    5730409J20Rik
  • Feature Type
    protein coding gene
  • IDs
    MGI:1933945
    NCBI Gene: 80976
  • Alliance
  • Transcription Start Sites
    9 TSS
Location &
Maps
more
  • Sequence Map
    Chr2:92745446-92786403 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 2, 51.37 cM, cytoband E1
  • Mapping Data
    3 experiments
Strain
Comparison
more
  • SNPs within 2kb
    1269 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1933945
protein coding gene Chr2:92745443-92786403 (+)
129S1/SvImJ ENSMUSG00200052843
protein coding gene Chr2:89662319-89703282 (+)
A/J ENSMUSG00195052061
protein coding gene Chr2:89798775-89839878 (+)
AKR/J ENSMUSG00220052298
protein coding gene Chr2:89594533-89636052 (+)
BALB/cJ ENSMUSG00180054721
protein coding gene Chr2:89696994-89737964 (+)
C3H/HeJ ENSMUSG00175053327
protein coding gene Chr2:89959129-90000647 (+)
C57BL/6NJ ENSMUSG00215053197
protein coding gene Chr2:89789547-89830506 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0023983
protein coding gene Chr2:87047718-87088948 (+)
CAST/EiJ ENSTCUG00005050001
protein coding gene Chr2:89207945-89248624 (+)
CBA/J ENSMUSG00210034384
protein coding gene Chr2:89969481-90010449 (+)
DBA/2J ENSMUSG00185056305
protein coding gene Chr2:89693367-89734328 (+)
FVB/NJ ENSMUSG00205047589
protein coding gene Chr2:88981038-89022555 (+)
JF1/MsJ ENSUMUG00000030810
protein coding gene Chr2:89515495-89556029 (+)
LP/J ENSMUSG00230040195
protein coding gene Chr2:91443857-91484818 (+)
NOD/ShiLtJ ENSMUSG00190032719
protein coding gene Chr2:89771986-89812948 (+)
NZO/HlLtJ ENSMUSG00225051577
protein coding gene Chr2:99357764-99398776 (+)
PWK/PhJ ENSLUMG00010043955
protein coding gene Chr2:89491312-89531901 (+)
SPRET/EiJ ENSMSPG00010052024
protein coding gene Chr2:91457237-91495678 (+)
WSB/EiJ ENSIUOG00005053343
protein coding gene Chr2:89496546-89537742 (+)



Homology
more
  • Human Ortholog
    SYT13, synaptotagmin 13
  • Vertebrate Orthologs
    3
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    SYT13, synaptotagmin 13
  • Links
    NCBI Gene ID: 57586
    UniProt: Q7L8C5

  • Chr Location
    11p11.2; chr11:45240302-45286341 (-)  GRCh38

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    3 phenotypes from 2 alleles in 1 genetic background
    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.
Homozygous null mice exhibit postnatal lethality with altered epithelial organization of the pancreas, impaired pancreas endocrine cell egression and increased alpha-to-beta-cell ratio.
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
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 80976 NCBI Gene Model | MGI Sequence Detail 40958 C57BL/6J ±  kb
transcript NM_030725 RefSeq | MGI Sequence Detail 3758 C57BL/6  
polypeptide Q9EQT6 UniProt | EBI | MGI Sequence Detail 426 Not Applicable  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 59
    cDNA 54
    Primer pair 3
    Other 2

    Microarray probesets 5
Other
Accession IDs
less
MGI:1917750, MGI:2139000
References
more
  • Summaries
    All 54
    Developmental Gene Expression 14
    Gene Ontology 6
    Phenotypes 15
  • Earliest
    J:109968 Roderick TH, et al., Nineteen paracentric chromosomal inversions in mice. Genetics. 1974 Jan;76(1):109-17
  • Latest
    J:354049 Pulcrano S, et al., miR-218 Promotes Dopaminergic Differentiation and Controls Neuron Excitability and Neurotransmitter Release through the Regulation of a Synaptic-Related Genes Network. J Neurosci. 2023 Nov 29;43(48):8104-8125

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