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Gm7882 Pseudogene Detail
Summary
  • Symbol
    Gm7882
  • Name
    predicted gene 7882
  • Feature Type
    pseudogene
  • IDs
    MGI:3647603
    NCBI Gene: 665994
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    Chr5:44074034-44075565 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 5, 23.85 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    239 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3647603
 pseudogene Chr5:44074034-44075856 (+)
129S1/SvImJ MGP_129S1SvImJ_G0013069
 pseudogene Chr5:42550167-42551928 (+)
A/J MGP_AJ_G0013054
 pseudogene Chr5:41081010-41082771 (+)
AKR/J MGP_AKRJ_G0013020
 pseudogene Chr5:42544385-42546146 (+)
BALB/cJ MGP_BALBcJ_G0013033
 pseudogene Chr5:41560498-41562255 (+)
C3H/HeJ MGP_C3HHeJ_G0012884
 pseudogene Chr5:42521145-42522906 (+)
C57BL/6NJ MGP_C57BL6NJ_G0013392
 pseudogene Chr5:44601465-44603226 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0011587
 pseudogene Chr5:38313594-38315328 (+)
CAST/EiJ MGP_CASTEiJ_G0012616
 pseudogene Chr5:41631668-41633923 (+)
CBA/J MGP_CBAJ_G0012851
 pseudogene Chr5:45780798-45782559 (+)
DBA/2J MGP_DBA2J_G0012929
 pseudogene Chr5:41178585-41180341 (+)
FVB/NJ MGP_FVBNJ_G0012936
 pseudogene Chr5:40604693-40606449 (+)
LP/J MGP_LPJ_G0013003
 pseudogene Chr5:43019293-43020795 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0012953
 pseudogene Chr5:46594870-46597353 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0013394
 pseudogene Chr5:42033809-42035563 (+)
PWK/PhJ MGP_PWKPhJ_G0012434
 pseudogene Chr5:40308428-40310284 (+)
SPRET/EiJ MGP_SPRETEiJ_G0012235
 pseudogene Chr5:41466329-41468140 (+)
WSB/EiJ MGP_WSBEiJ_G0012652
 pseudogene Chr5:42118889-42120645 (+)



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    6 phenotype references
  • All Mutations and Alleles
    5
  • Chemically induced (ENU)
    1
  • Chemically induced (other)
    2
  • Radiation induced
    1
  • Spontaneous
    1
  • Genomic Mutations
    5 involving Gm7882
  • Find Mice (IMSR)
    1 strains or lines available
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
    706
Sequences &
Gene Models
less
  • All Sequences
    23
  • RefSeq
    2
Representative SequencesLengthStrain/SpeciesFlank
genomic 665994 NCBI Gene Model | MGI Sequence Detail 1532 C57BL/6J ±  kb
For the selected sequence
References
more
  • Summaries
    All 10
    Diseases 1
    Phenotypes 6
  • Earliest
    J:109968 Roderick TH, et al., Nineteen paracentric chromosomal inversions in mice. Genetics. 1974 Jan;76(1):109-17
  • Latest
    J:100332 Wilson L, et al., Random mutagenesis of proximal mouse chromosome 5 uncovers predominantly embryonic lethal mutations. Genome Res. 2005 Aug;15(8):1095-105
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
12/10/2024
MGI 6.24 		The Jackson Laboratory