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Gm7931 Pseudogene Detail
Summary
  • Symbol
    Gm7931
  • Name
    predicted pseudogene 7931
  • Feature Type
    pseudogene
  • IDs
    MGI:3643448
    NCBI Gene: 100503799
  • Alliance
  • Transcription Start Sites
    1 TSS
Location &
Maps
more
  • Sequence Map
    Chr5:46571686-46571956 bp, + strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 5, 25.86 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    18 from dbSNP Build 142
  • Strain Annotations
    17
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3643448
pseudogene Chr5:46505013-46572780 (+)
129S1/SvImJ MGP_129S1SvImJ_G0014876
pseudogene ChrX:139362020-139362290 (-)
A/J MGP_AJ_G0014869
pseudogene ChrX:138759147-138759417 (-)
AKR/J MGP_AKRJ_G0014811
pseudogene ChrX:143172676-143174558 (-)
BALB/cJ MGP_BALBcJ_G0014825
pseudogene ChrX:137003288-137003558 (-)
C3H/HeJ MGP_C3HHeJ_G0014661
pseudogene ChrX:139481260-139481530 (-)
C57BL/6NJ MGP_C57BL6NJ_G0011695
pseudogene Chr18:34482013-34482238 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0012953
pseudogene ChrX:130372912-130373177 (-)
CAST/EiJ MGP_CASTEiJ_G0014274
pseudogene ChrX:120197647-120197917 (-)
CBA/J MGP_CBAJ_G0014650
pseudogene ChrX:147843046-147843316 (-)
DBA/2J MGP_DBA2J_G0014733
pseudogene ChrX:137827924-137828194 (-)
FVB/NJ MGP_FVBNJ_G0014716
pseudogene ChrX:137058332-137058602 (-)
LP/J no annotation
NOD/ShiLtJ MGP_NODShiLtJ_G0014760
pseudogene ChrX:155439845-155440115 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0015294
pseudogene ChrX:138675850-138676120 (-)
PWK/PhJ MGP_PWKPhJ_G0014075
pseudogene ChrX:117033545-117033815 (-)
SPRET/EiJ MGP_SPRETEiJ_G0009724
pseudogene Chr1:106418159-106418429 (+)
WSB/EiJ MGP_WSBEiJ_G0014354
pseudogene ChrX:137085770-137086040 (-)



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    6 phenotype references
  • All Mutations and Alleles
    4
  • Chemically induced (other)
    2
  • Radiation induced
    1
  • Spontaneous
    1
  • Genomic Mutations
    4 involving Gm7931
  • 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
less
  • All Sequences
  • RefSeq
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000067321 Ensembl Gene Model | MGI Sequence Detail 271 C57BL/6J ±  kb
transcript ENSMUST00000121537 Ensembl | MGI Sequence Detail 271 Not Applicable  
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)
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Funding Information
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory