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Mir1306 Gene Detail
Summary
  • Symbol
    Mir1306
  • Name
    microRNA 1306
  • Synonyms
    mmu-mir-1306
Location &
Maps
more
  • Sequence Map
    Chr16:18284239-18284317 bp, - strand
  • From miRBase annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 16, 11.33 cM
Strain
Comparison
more
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3836985
miRNA gene Chr16:18284239-18284317 (-)
129S1/SvImJ MGP_129S1SvImJ_G0008252
miRNA gene Chr16:15499643-15499721 (-)
A/J MGP_AJ_G0008241
miRNA gene Chr16:14728306-14728384 (-)
AKR/J MGP_AKRJ_G0008224
miRNA gene Chr16:15308728-15308806 (-)
BALB/cJ MGP_BALBcJ_G0008226
miRNA gene Chr16:14877864-14877942 (-)
C3H/HeJ MGP_C3HHeJ_G0008168
miRNA gene Chr16:15471635-15471713 (-)
C57BL/6NJ MGP_C57BL6NJ_G0008420
miRNA gene Chr16:15769336-15769414 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0007488
miRNA gene Chr16:14777857-14777935 (-)
CAST/EiJ MGP_CASTEiJ_G0008039
miRNA gene Chr16:15360285-15360363 (-)
CBA/J MGP_CBAJ_G0008137
miRNA gene Chr16:16465466-16465544 (-)
DBA/2J MGP_DBA2J_G0008170
miRNA gene Chr16:14640548-14640626 (-)
FVB/NJ MGP_FVBNJ_G0008195
miRNA gene Chr16:14711616-14711694 (-)
LP/J MGP_LPJ_G0008252
miRNA gene Chr16:15277499-15277577 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0008158
miRNA gene Chr16:16105221-16105299 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0008411
miRNA gene Chr16:15247132-15247210 (-)
PWK/PhJ MGP_PWKPhJ_G0007961
miRNA gene Chr16:14912929-14913007 (-)
SPRET/EiJ MGP_SPRETEiJ_G0007852
miRNA gene Chr16:15205786-15205864 (-)
WSB/EiJ MGP_WSBEiJ_G0008116
miRNA gene Chr16:15234838-15234916 (-)



Homology
more
  • Human Ortholog
    MIR1306, microRNA 1306
  • Human Ortholog
    MIR1306, microRNA 1306
    Orthology source: HGNC
  • Synonyms
    hsa-mir-1306, mir-1306, MIRN1306
  • Links
    NCBI Gene ID: 100302197

  • Chr Location
    chr22:20086058-20086142 (+)  GRCh38.p7

Human Diseases
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  • References
    5 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    66 phenotype references
Expression
less
Interactions
less
Sequences &
Gene Models
less
  • All Sequences
  • RefSeq
Representative SequencesLengthStrain/SpeciesFlank
genomic 100316814 NCBI Gene Model | MGI Sequence Detail 79 C57BL/6J ±  kb
transcript NR_035467 RefSeq | MGI Sequence Detail 79 C57BL/6  
For the selected sequence
Other Database
Links
less
References
more
  • Summaries
    All 71
    Diseases 5
    Phenotypes 66
  • 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:279573 Fernandez A, et al., Mitochondrial Dysfunction Leads to Cortical Under-Connectivity and Cognitive Impairment. Neuron. 2019 Jun 19;102(6):1127-1142.e3

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
02/18/2020
MGI 6.14
The Jackson Laboratory