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Gm17130 Gene Detail
Summary
  • Symbol
    Gm17130
  • Name
    predicted gene 17130
  • Feature Type
    lncRNA gene
  • IDs
    MGI:4937957
  • Alliance
Location &
Maps
more
  • Sequence Map
    Chr5:32163321-32168207 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 5, 17.33 cM
Strain
Comparison
more
  • SNPs within 2kb
    178 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_4937957
lncRNA gene Chr5:32163321-32168207 (-)
129S1/SvImJ MGP_129S1SvImJ_G0004053
antisense lncRNA gene Chr5:30064051-30068938 (-)
A/J MGP_AJ_G0004033
antisense lncRNA gene Chr5:29077374-29082261 (-)
AKR/J MGP_AKRJ_G0004012
antisense lncRNA gene Chr5:30239232-30244119 (-)
BALB/cJ MGP_BALBcJ_G0004020
antisense lncRNA gene Chr5:29605827-29610714 (-)
C3H/HeJ MGP_C3HHeJ_G0003966
antisense lncRNA gene Chr5:30255418-30260305 (-)
C57BL/6NJ MGP_C57BL6NJ_G0004168
antisense lncRNA gene Chr5:31872514-31877400 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0003648
antisense lncRNA gene Chr5:26745937-26750799 (-)
CAST/EiJ MGP_CASTEiJ_G0003929
antisense lncRNA gene Chr5:29335191-29340071 (-)
CBA/J MGP_CBAJ_G0003960
antisense lncRNA gene Chr5:32534774-32539661 (-)
DBA/2J MGP_DBA2J_G0003974
antisense lncRNA gene Chr5:29248848-29253734 (-)
FVB/NJ MGP_FVBNJ_G0003994
antisense lncRNA gene Chr5:28655179-28660147 (-)
LP/J MGP_LPJ_G0004055
antisense lncRNA gene Chr5:30507392-30512279 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0003982
antisense lncRNA gene Chr5:33344460-33349346 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0004163
antisense lncRNA gene Chr5:29739017-29743904 (-)
PWK/PhJ MGP_PWKPhJ_G0003883
antisense lncRNA gene Chr5:28403350-28408236 (-)
SPRET/EiJ MGP_SPRETEiJ_G0003828
antisense lncRNA gene Chr5:29214271-29219118 (-)
WSB/EiJ MGP_WSBEiJ_G0003965
antisense lncRNA gene Chr5:29821536-29826422 (-)



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    21 phenotype references
  • All Mutations and Alleles
    6
  • Chemically induced (ENU)
    1
  • Chemically induced (other)
    2
  • Radiation induced
    2
  • Spontaneous
    1
  • Genomic Mutations
    6 involving Gm17130
  • Find Mice (IMSR)
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
Sequences &
Gene Models
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  • All Sequences
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000106894 Ensembl Gene Model | MGI Sequence Detail 4887 C57BL/6J ±  kb
transcript ENSMUST00000201542 Ensembl | MGI Sequence Detail 2683 Not Applicable  
For the selected sequence
References
more
  • Summaries
    All 23
    Diseases 1
    Phenotypes 21
  • Earliest
    J:5021 Batchelor AL, et al., A comparison of the mutagenic effectiveness of chronic neutron- and gamma-irradiation of mouse spermatogonia. Mutat Res. 1966 Jun;3(3):218-29
  • Latest
    J:125425 Howell GR, et al., Mutation of a ubiquitously expressed mouse transmembrane protein (Tapt1) causes specific skeletal homeotic transformations. Genetics. 2007 Feb;175(2):699-707

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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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory