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Gm1947 Pseudogene Detail
Summary
  • Symbol
    Gm1947
  • Name
    predicted pseudogene 1947
  • Synonyms
    LOC384929
  • Feature Type
    pseudogene
  • IDs
    MGI:3037805
    NCBI Gene: 384929
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    ChrX:156212413-156213322 bp, + strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome X, 72.47 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    5 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3037805
 pseudogene ChrX:156212413-156213322 (+)
129S1/SvImJ MGP_129S1SvImJ_G0014957
 pseudogene ChrX:155315558-155316471 (+)
A/J MGP_AJ_G0014948
 pseudogene ChrX:154634380-154635290 (+)
AKR/J MGP_AKRJ_G0014889
 pseudogene ChrX:159495943-159496926 (+)
BALB/cJ MGP_BALBcJ_G0014902
 pseudogene ChrX:152690631-152691540 (+)
C3H/HeJ MGP_C3HHeJ_G0014740
 pseudogene ChrX:155671671-155672580 (+)
C57BL/6NJ MGP_C57BL6NJ_G0015388
 pseudogene ChrX:159896823-159897732 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0013014
 pseudogene ChrX:145994316-145995219 (+)
CAST/EiJ MGP_CASTEiJ_G0010230
 pseudogene Chr10:55703170-55704004 (-)
CBA/J MGP_CBAJ_G0014726
 pseudogene ChrX:164465491-164466400 (+)
DBA/2J MGP_DBA2J_G0014809
 pseudogene ChrX:153613455-153614364 (+)
FVB/NJ MGP_FVBNJ_G0014792
 pseudogene ChrX:152701752-152702661 (+)
LP/J MGP_LPJ_G0014910
 pseudogene ChrX:156479770-156480679 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0014836
 pseudogene ChrX:173042432-173043342 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0010726
 pseudogene Chr10:55336393-55337226 (-)
PWK/PhJ MGP_PWKPhJ_G0010132
 pseudogene Chr10:53562327-53563160 (-)
SPRET/EiJ MGP_SPRETEiJ_G0013928
 pseudogene ChrX:135244083-135244983 (+)
WSB/EiJ MGP_WSBEiJ_G0010299
 pseudogene Chr10:55553226-55554059 (-)



Homology
less
Human Diseases
less
  • References
    2 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    25 phenotype references
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
    21
  • RefSeq
    1
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000083841 Ensembl Gene Model | MGI Sequence Detail 910 C57BL/6J ±  kb
transcript ENSMUST00000122451 Ensembl | MGI Sequence Detail 910 Not Applicable  
For the selected sequence
References
more
  • Summaries
    All 29
    Diseases 2
    Phenotypes 25
  • Earliest
    J:28887 Carter TC, et al., The genetic sensitivity to X-rays of mouse foetal gonads. Genet Res. 1960;1(3):351-5
  • Latest
    J:145570 Wang X, et al., Spermine synthase deficiency leads to deafness and a profound sensitivity to alpha-difluoromethylornithine. J Biol Chem. 2009 Jan 9;284(2):930-7
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
05/07/2024
MGI 6.23 		The Jackson Laboratory