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Mannr Gene Detail
Summary
  • Symbol
    Mannr
  • Name
    Mecom adjacent non-protein coding RNA
  • Synonyms
    Manr
  • Feature Type
    lncRNA gene
  • IDs
    MGI:5564803
    NCBI Gene: 102636083
  • Alliance
  • Transcription Start Sites
    1 TSS
Location &
Maps
more
  • Sequence Map
    Chr3:29945166-29978340 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 3, Syntenic
Strain
Comparison
more
  • SNPs within 2kb
    196 from dbSNP Build 142
  • Strain Annotations
    17
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_5564803
lncRNA gene Chr3:29945136-29978348 (+)
129S1/SvImJ MGP_129S1SvImJ_G0006144
lincRNA gene Chr3:27345803-27378559 (+)
A/J MGP_AJ_G0006135
lincRNA gene Chr3:27017888-27049177 (+)
AKR/J MGP_AKRJ_G0006111
lincRNA gene Chr3:27413749-27456052 (+)
BALB/cJ MGP_BALBcJ_G0006112
lincRNA gene Chr3:26705040-26747575 (+)
C3H/HeJ MGP_C3HHeJ_G0006061
lincRNA gene Chr3:27459452-27485989 (+)
C57BL/6NJ MGP_C57BL6NJ_G0006273
lincRNA gene Chr3:28838047-28878630 (+)
CAROLI/EiJ no annotation
CAST/EiJ MGP_CASTEiJ_G0005996
lincRNA gene Chr3:27309469-27348008 (+)
CBA/J MGP_CBAJ_G0006046
lincRNA gene Chr3:29556123-29589238 (+)
DBA/2J MGP_DBA2J_G0006066
lincRNA gene Chr3:26580662-26613781 (+)
FVB/NJ MGP_FVBNJ_G0006090
lincRNA gene Chr3:26035369-26062015 (+)
LP/J MGP_LPJ_G0006147
lincRNA gene Chr3:28025042-28069434 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0006079
lincRNA gene Chr3:32160544-32198818 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0006277
lincRNA gene Chr3:27156414-27191267 (+)
PWK/PhJ MGP_PWKPhJ_G0005941
lincRNA gene Chr3:26068476-26093712 (+)
SPRET/EiJ MGP_SPRETEiJ_G0005850
lincRNA gene Chr3:26664851-26691378 (+)
WSB/EiJ MGP_WSBEiJ_G0006044
lincRNA gene Chr3:27244903-27280015 (+)



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    1 phenotype from 1 allele in 1 genetic background
    5 phenotype references
Mice homozygous for a null allele are viable.
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
  • GO References
Molecular Function

Biological Process

Cellular Component

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
less
  • All Sequences
  • RefSeq
Representative SequencesLengthStrain/SpeciesFlank
genomic 102636083 NCBI Gene Model | MGI Sequence Detail 33175 C57BL/6J ±  kb
transcript NR_110437 RefSeq | MGI Sequence Detail 1435 ZRU/MplStud  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 1
    cDNA 1
References
more
  • Summaries
    All 10
    Developmental Gene Expression 2
    Diseases 1
    Gene Ontology 1
    Phenotypes 5
  • Earliest
    J:70677 Cook SA, et al., Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene. Cytogenet Cell Genet. 2001;93(1-2):77-82
  • Latest
    J:302829 Lu J, et al., Mouse models for human hyperuricaemia: a critical review. Nat Rev Rheumatol. 2019 Jul;15(7):413-426

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
04/30/2024
MGI 6.23
The Jackson Laboratory