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Mir1306 Gene Detail
Summary
  • Symbol
    Mir1306
  • Name
    microRNA 1306
  • Synonyms
    mmu-mir-1306
Location &
Maps
more
  • Sequence Map
    Chr16:18102103-18102181 bp, - strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 16, 11.33 cM
Strain
Comparison
more
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3836985
 miRNA gene Chr16:18102103-18102181 (-)
129S1/SvImJ ENSMUSG00200047617
 miRNA gene Chr16:15098868-15098946 (-)
A/J ENSMUSG00195037494
 miRNA gene Chr16:14656192-14656270 (-)
AKR/J ENSMUSG00220046002
 miRNA gene Chr16:14972459-14972537 (-)
BALB/cJ ENSMUSG00180043722
 miRNA gene Chr16:14897467-14897545 (-)
C3H/HeJ ENSMUSG00175050018
 miRNA gene Chr16:15042441-15042519 (-)
C57BL/6NJ ENSMUSG00215042766
 miRNA gene Chr16:14763539-14763617 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0007488
 miRNA gene Chr16:14777857-14777935 (-)
CAST/EiJ ENSTCUG00005045453
 miRNA gene Chr16:14969676-14969754 (-)
CBA/J ENSMUSG00210048237
 miRNA gene Chr16:15058748-15058826 (-)
DBA/2J ENSMUSG00185035790
 miRNA gene Chr16:15003363-15003441 (-)
FVB/NJ ENSMUSG00205048687
 miRNA gene Chr16:15012874-15012952 (-)
JF1/MsJ ENSUMUG00000054100
 miRNA gene Chr16:15097401-15097479 (-)
LP/J ENSMUSG00230047781
 miRNA gene Chr16:17582779-17582857 (-)
NOD/ShiLtJ ENSMUSG00190050008
 miRNA gene Chr16:15144781-15144859 (-)
NZO/HlLtJ ENSMUSG00225038730
 miRNA gene Chr16:20828605-20828683 (-)
PWK/PhJ ENSLUMG00010048781
 miRNA gene Chr16:14978189-14978267 (-)
SPRET/EiJ ENSMSPG00010046899
 miRNA gene Chr16:14989511-14989589 (-)
WSB/EiJ ENSIUOG00005045322
 miRNA gene Chr16:15138146-15138224 (-)



Homology
more
  • Human Ortholog
    MIR1306, microRNA 1306
  • Vertebrate Orthologs
    1
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    MIR1306, microRNA 1306
  • Synonyms
    hsa-mir-1306, mir-1306, MIRN1306
  • Links
    NCBI Gene ID: 100302197

  • Chr Location
    chr22:20086058-20086142 (+)  GRCh38
Human Diseases
less
  • References
    5 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    146 phenotype references
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
    2
  • GO References
    1
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
    597
Sequences &
Gene Models
less
  • All Sequences
    23
  • RefSeq
    1
Representative SequencesLengthStrain/SpeciesFlank
genomic 100316814 NCBI Gene Model | MGI Sequence Detail 79 C57BL/6J ±  kb
transcript NR_035467 RefSeq | MGI Sequence Detail 79 ZRU/MplStud  
For the selected sequence
Other Database
Links
less
miRBase MI0009935
References
more
  • Summaries
    All 153
    Diseases 5
    Gene Ontology 1
    Phenotypes 146
  • Earliest
    J:57757 Lindsay EA, et al., Congenital heart disease in mice deficient for the DiGeorge syndrome region [see comments]. Nature. 1999 Sep 23;401(6751):379-83
  • Latest
    J:390319 Son GY, et al., Dysregulated calcium signaling underlies hyposalivation and microbial dysbiosis in Down syndrome. Cell Rep. 2026 Jul 1;:117619
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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Send questions and comments to User Support. 		last database update
09/01/2026
MGI 6.24 		The Jackson Laboratory