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Pramex2 Pseudogene Detail
Summary
  • Symbol
    Pramex2
  • Name
    PRAME like, X-linked 2
  • Synonyms
    EG621322, Pramel
Location &
Maps
more
  • Sequence Map
    ChrX:134171602-134174963 bp, + strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome X, 56.79 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    163 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3643636
 pseudogene ChrX:134171599-134175117 (+)
129S1/SvImJ ENSMUSG00200048079
 pseudogene ChrX:113246872-113250233 (+)
A/J ENSMUSG00195049088
 pseudogene ChrX:117086084-117089445 (+)
AKR/J ENSMUSG00220013313
 pseudogene ChrX:110640399-110643760 (+)
BALB/cJ ENSMUSG00180039865
 pseudogene ChrX:113490788-113494149 (+)
C3H/HeJ ENSMUSG00175035714
 pseudogene ChrX:117399039-117402400 (+)
C57BL/6NJ ENSMUSG00215045152
 pseudogene ChrX:113874201-113877562 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0037522
 pseudogene ChrX:124054202-124057555 (+)
CAST/EiJ ENSTCUG00005041361
 pseudogene ChrX:114695550-114698912 (+)
CBA/J ENSMUSG00210043576
 pseudogene ChrX:114411558-114414919 (+)
DBA/2J ENSMUSG00185030206
 pseudogene ChrX:128224476-128227837 (+)
FVB/NJ ENSMUSG00205036144
 pseudogene ChrX:112885197-112888558 (+)
JF1/MsJ ENSUMUG00000030623
 pseudogene ChrX:147504476-147507825 (+)
LP/J ENSMUSG00230040799
 pseudogene ChrX:134913014-134916375 (+)
NOD/ShiLtJ ENSMUSG00190041749
 pseudogene ChrX:113723930-113727291 (+)
NZO/HlLtJ ENSMUSG00225037068
 pseudogene ChrX:139572071-139575439 (-)
PWK/PhJ ENSLUMG00010044382
 pseudogene ChrX:112190649-112194000 (+)
SPRET/EiJ ENSMSPG00010040007
 pseudogene ChrX:116799669-116803026 (-)
WSB/EiJ ENSIUOG00005037952
 pseudogene ChrX:114427482-114430843 (+)



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    2 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
    597
  • Literature Summary
    1
Sequences &
Gene Models
less
  • All Sequences
    24
  • RefSeq
    2
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000082071 Ensembl Gene Model | MGI Sequence Detail 3362 C57BL/6J ±  kb
transcript ENSMUST00000118979 Ensembl | MGI Sequence Detail 1383 Not Applicable  
polypeptide XP_017174154 RefSeq | MGI Sequence Detail 460 C57BL/6J  
For the selected sequence
Other
Accession IDs
less
MGI:6437227
References
more
  • Summaries
    All 7
    Developmental Gene Expression 1
    Diseases 1
    Phenotypes 2
  • Earliest
    J:199138 Zhou J, et al., A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male mice. Biol Reprod. 2013 Jun;88(6):159
  • Latest
    J:210663 Zhou J, et al., Respiratory failure, cleft palate and epilepsy in the mouse model of human Xq22.1 deletion syndrome. Hum Mol Genet. 2014 Jul 15;23(14):3823-9
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
09/08/2026
MGI 6.24 		The Jackson Laboratory