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Syt10 Gene Detail
Summary
  • Symbol
    Syt10
  • Name
    synaptotagmin X
  • Feature Type
    protein coding gene
  • IDs
    MGI:1859546
    NCBI Gene: 54526
  • Alliance
  • Transcription Start Sites
    3 TSS
Location &
Maps
more
  • Sequence Map
    Chr15:89666596-89726063 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 15, 44.96 cM, cytoband F1
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    488 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1859546
protein coding gene Chr15:89657221-89726181 (-)
129S1/SvImJ MGP_129S1SvImJ_G0022242
protein coding gene Chr15:90997204-91066025 (-)
A/J MGP_AJ_G0022201
protein coding gene Chr15:87513160-87572594 (-)
AKR/J MGP_AKRJ_G0022176
protein coding gene Chr15:90113075-90173087 (-)
BALB/cJ MGP_BALBcJ_G0022207
protein coding gene Chr15:87633971-87693227 (-)
C3H/HeJ MGP_C3HHeJ_G0021977
protein coding gene Chr15:90112592-90189211 (-)
C57BL/6NJ MGP_C57BL6NJ_G0022652
protein coding gene Chr15:94311312-94378266 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0020177
protein coding gene Chr15:83705908-83761176 (-)
CAST/EiJ MGP_CASTEiJ_G0021499
protein coding gene Chr15:90883676-90949239 (-)
CBA/J MGP_CBAJ_G0021944
protein coding gene Chr15:97522726-97587213 (-)
DBA/2J MGP_DBA2J_G0022071
protein coding gene Chr15:86968948-87027178 (-)
FVB/NJ MGP_FVBNJ_G0022050
protein coding gene Chr15:86034907-86092656 (-)
LP/J MGP_LPJ_G0022142
protein coding gene Chr15:91155857-91222581 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0022070
protein coding gene Chr15:101899575-101967693 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0022667
protein coding gene Chr15:90171576-90234706 (-)
PWK/PhJ MGP_PWKPhJ_G0021240
protein coding gene Chr15:87022648-87084494 (-)
SPRET/EiJ MGP_SPRETEiJ_G0021074
protein coding gene Chr15:89910744-89975112 (-)
WSB/EiJ MGP_WSBEiJ_G0021548
protein coding gene Chr15:90648921-90717741 (-)



Homology
more
  • Human Ortholog
    SYT10, synaptotagmin 10
  • Vertebrate Orthologs
    3
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    SYT10, synaptotagmin 10
  • Links
    NCBI Gene ID: 341359
    neXtProt AC: NX_Q6XYQ8
    UniProt: Q6XYQ8

  • Chr Location
    12p11.1; chr12:33374238-33439819 (-)  GRCh38

Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    3 phenotypes from 1 allele in 1 genetic background
    3 phenotypes from multigenic genotypes
    30 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-in allele exhibit minor circadian rhythm impairments.
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
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000063260 Ensembl Gene Model | MGI Sequence Detail 59468 C57BL/6J ±  kb
transcript ENSMUST00000029441 Ensembl | MGI Sequence Detail 1845 Not Applicable  
polypeptide ENSMUSP00000029441 Ensembl | MGI Sequence Detail 523 Not Applicable  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 8
    cDNA 6
    Primer pair 1
    Other 1

    Microarray probesets 3
References
more
  • Summaries
    All 53
    Developmental Gene Expression 3
    Diseases 1
    Gene Ontology 7
    Phenotypes 30
  • Earliest
    J:7688 Lane PW, et al., Association of megacolon with a new dominant spotting gene (Dom) in the mouse. J Hered. 1984 Nov-Dec;75(6):435-9
  • Latest
    J:341739 Altaha B, et al., Genetic and environmental circadian disruption induce weight gain through changes in the gut microbiome. Mol Metab. 2022 Nov 2;66:101628

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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory