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Mir185 Gene Detail
Summary
  • Symbol
    Mir185
  • Name
    microRNA 185
  • Synonyms
    Mirn185, mmu-mir-185
  • Feature Type
    miRNA gene
  • IDs
    MGI:2676849
    NCBI Gene: 387180
  • Alliance
Location &
Maps
more
  • Sequence Map
    Chr16:18327401-18327465 bp, - strand
  • From miRBase annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 16, 11.35 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_2676849
miRNA gene Chr16:18327401-18327465 (-)
129S1/SvImJ MGP_129S1SvImJ_G0008254
miRNA gene Chr16:15545475-15545539 (-)
A/J MGP_AJ_G0008243
miRNA gene Chr16:14773370-14773434 (-)
AKR/J MGP_AKRJ_G0008226
miRNA gene Chr16:15361542-15361606 (-)
BALB/cJ MGP_BALBcJ_G0008228
miRNA gene Chr16:14921925-14921989 (-)
C3H/HeJ MGP_C3HHeJ_G0008170
miRNA gene Chr16:15513454-15513518 (-)
C57BL/6NJ MGP_C57BL6NJ_G0008422
miRNA gene Chr16:15819565-15819629 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0007490
miRNA gene Chr16:14813626-14813690 (-)
CAST/EiJ MGP_CASTEiJ_G0008041
miRNA gene Chr16:15406824-15406888 (-)
CBA/J MGP_CBAJ_G0008139
miRNA gene Chr16:16516878-16516942 (-)
DBA/2J MGP_DBA2J_G0008172
miRNA gene Chr16:14691610-14691674 (-)
FVB/NJ MGP_FVBNJ_G0008197
miRNA gene Chr16:14743293-14743357 (-)
LP/J MGP_LPJ_G0008254
miRNA gene Chr16:15321342-15321406 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0008160
miRNA gene Chr16:16153031-16153095 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0008413
miRNA gene Chr16:15290920-15290984 (-)
PWK/PhJ MGP_PWKPhJ_G0007963
miRNA gene Chr16:14963532-14963596 (-)
SPRET/EiJ MGP_SPRETEiJ_G0007854
miRNA gene Chr16:15259744-15259808 (-)
WSB/EiJ MGP_WSBEiJ_G0008118
miRNA gene Chr16:15288010-15288074 (-)



Homology
more
  • Human Ortholog
    MIR185, microRNA 185
  • Human Ortholog
    MIR185, microRNA 185
    Orthology source: HGNC
  • Synonyms
    miR-185, MIRN185
  • Links
    NCBI Gene ID: 406961

  • Chr Location
    chr22:20033139-20033220 (+)  GRCh38.p7

Human Diseases
less
  • References
    5 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    66 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 death
cell differentiation
cell population proliferation
cellular component organization
establishment of localization
homeostatic process
immune system process
lipid metabolic process
nucleic acid-templated transcription
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
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
  • Literature Summary
Interactions
less
Sequences &
Gene Models
less
  • All Sequences
  • RefSeq
Representative SequencesLengthStrain/SpeciesFlank
genomic 387180 NCBI Gene Model | MGI Sequence Detail 65 C57BL/6J ±  kb
transcript NR_029571 RefSeq | MGI Sequence Detail 65 C57BL/6  
For the selected sequence
Molecular
Reagents
less
  • All nucleic 4
    Primer pair 3
    Other 1
Other Database
Links
less
References
more
  • Summaries
    All 80
    Developmental Gene Expression 6
    Diseases 5
    Gene Ontology 2
    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:278079 Murano T, et al., Transcriptomic immaturity inducible by neural hyperexcitation is shared by multiple neuropsychiatric disorders. Commun Biol. 2019;2:32

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
10/08/2019
MGI 6.14
The Jackson Laboratory