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Gm8971 Pseudogene Detail
Summary
  • Symbol
    Gm8971
  • Name
    predicted gene 8971
Location &
Maps
more
  • Sequence Map
    Chr14:57600842-57601190 bp, + strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 14, 30.10 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    129 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3648536
 pseudogene Chr14:57600838-57601235 (+)
129S1/SvImJ ENSMUSG00200042565
 pseudogene Chr14:46186084-46186432 (+)
A/J ENSMUSG00195038063
 pseudogene Chr14:46401344-46401692 (+)
AKR/J ENSMUSG00220032167
 pseudogene Chr14:45728290-45728638 (+)
BALB/cJ ENSMUSG00180053723
 pseudogene Chr14:46023367-46023715 (+)
C3H/HeJ ENSMUSG00175052664
 pseudogene Chr14:47729900-47730248 (+)
C57BL/6NJ ENSMUSG00215051073
 pseudogene Chr14:45924024-45924372 (+)
CAROLI/EiJ no annotation
CAST/EiJ ENSTCUG00005050333
 pseudogene Chr14:47707126-47707481 (+)
CBA/J ENSMUSG00210046864
 pseudogene Chr14:46391713-46392061 (+)
DBA/2J ENSMUSG00185033091
 pseudogene Chr14:51524716-51525064 (+)
FVB/NJ ENSMUSG00205048297
 pseudogene Chr14:45793709-45794057 (+)
JF1/MsJ ENSUMUG00000050011
 pseudogene Chr14:62701124-62701473 (+)
LP/J ENSMUSG00230037442
 pseudogene Chr14:63555088-63555436 (+)
NOD/ShiLtJ ENSMUSG00190051635
 pseudogene Chr14:46158051-46158399 (+)
NZO/HlLtJ ENSMUSG00225046887
 pseudogene Chr14:53848400-53848748 (+)
PWK/PhJ ENSLUMG00010049999
 pseudogene Chr14:45617623-45617971 (+)
SPRET/EiJ ENSMSPG00010047786
 pseudogene Chr14:49143090-49143436 (+)
WSB/EiJ ENSIUOG00005044318
 pseudogene Chr14:45585714-45586062 (+)



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    4 phenotype references
  • All Mutations and Alleles
    2
  • Chemically induced (other)
    1
  • Endonuclease-mediated
    1
  • Genomic Mutations
    2 involving Gm8971
  • Find Mice (IMSR)
    0 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
    597
Sequences &
Gene Models
less
  • All Sequences
    21
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000114321 Ensembl Gene Model | MGI Sequence Detail 349 C57BL/6J ±  kb
transcript ENSMUST00000223673 Ensembl | MGI Sequence Detail 349 Not Applicable  
For the selected sequence
References
more
  • Summaries
    All 8
    Diseases 1
    Phenotypes 4
  • Earliest
    J:372803 Dominguez-Ruiz M, et al., A murine model for the del(GJB6-D13S1830) deletion recapitulating the phenotype of human DFNB1 hearing impairment: generation and functional and histopathological study. BMC Genomics. 2024 Apr 11;25(1):359
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
09/01/2026
MGI 6.24 		The Jackson Laboratory