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Sec22c Gene Detail
Summary
  • Symbol
    Sec22c
  • Name
    SEC22 homolog C, vesicle trafficking protein
  • Synonyms
    5930407I15Rik, Sec22l3
  • Feature Type
    protein coding gene
  • IDs
    MGI:2447871
    NCBI Gene: 215474
  • Alliance
  • Transcription Start Sites
    6 TSS
Location &
Maps
more
  • Sequence Map
    Chr9:121509111-121534556 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 9, 72.54 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    803 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_2447871
protein coding gene Chr9:121509111-121534614 (-)
129S1/SvImJ ENSMUSG00200027558
protein coding gene Chr9:118629754-118645403 (-)
A/J ENSMUSG00195027354
protein coding gene Chr9:117792823-117808424 (-)
AKR/J ENSMUSG00220018455
protein coding gene Chr9:118250819-118263513 (-)
BALB/cJ ENSMUSG00180025936
protein coding gene Chr9:118329837-118345439 (-)
C3H/HeJ ENSMUSG00175018066
protein coding gene Chr9:118573270-118588871 (-)
C57BL/6NJ ENSMUSG00215019735
protein coding gene Chr9:118462106-118477757 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0032827
protein coding gene Chr9:117047774-117074131 (-)
CAST/EiJ ENSTCUG00005016118
protein coding gene Chr9:118170795-118186344 (-)
CBA/J ENSMUSG00210037823
protein coding gene Chr9:118289612-118302306 (-)
DBA/2J ENSMUSG00185014184
protein coding gene Chr9:118623824-118636518 (-)
FVB/NJ ENSMUSG00205028256
protein coding gene Chr9:118461565-118477166 (-)
JF1/MsJ ENSUMUG00000039845
protein coding gene Chr9:118450754-118466130 (-)
LP/J ENSMUSG00230031890
protein coding gene Chr9:118768867-118784516 (-)
NOD/ShiLtJ ENSMUSG00190014702
protein coding gene Chr9:118226074-118241725 (-)
NZO/HlLtJ ENSMUSG00225022996
protein coding gene Chr9:119033137-119048786 (-)
PWK/PhJ ENSLUMG00010029927
protein coding gene Chr9:118341395-118354144 (-)
SPRET/EiJ ENSMSPG00010022552
protein coding gene Chr9:120044693-120060184 (-)
WSB/EiJ ENSIUOG00005018366
protein coding gene Chr9:117653206-117668858 (-)



Homology
more
  • Human Ortholog
    SEC22C, SEC22 homolog C, vesicle trafficking protein
  • Vertebrate Orthologs
    3
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    SEC22C, SEC22 homolog C, vesicle trafficking protein
  • Synonyms
    SEC22L3
  • Links
    NCBI Gene ID: 9117
    UniProt: Q9BRL7

  • Chr Location
    3p22.1; chr3:42547969-42601168 (-)  GRCh38

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    4 phenotype references
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
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000061536 Ensembl Gene Model | MGI Sequence Detail 25446 C57BL/6J ±  kb
transcript ENSMUST00000078547 Ensembl | MGI Sequence Detail 5713 Not Applicable  
polypeptide ENSMUSP00000077628 Ensembl | MGI Sequence Detail 303 Not Applicable  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 46
    cDNA 45
    Primer pair 1

    Microarray probesets 4
Other
Accession IDs
less
MGI:2444875
References
more
  • Summaries
    All 27
    Developmental Gene Expression 1
    Gene Ontology 3
    Phenotypes 4
  • Earliest
    J:80000 The FANTOM Consortium and The RIKEN Genome Exploration Research Group Phase I & II Team, Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Nature. 2002;420:563-573
  • Latest
    J:245876 Rohacek AM, et al., ESRP1 Mutations Cause Hearing Loss due to Defects in Alternative Splicing that Disrupt Cochlear Development. Dev Cell. 2017 Nov 06;43(3):318-331.e5

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