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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
  • Genetic Map
    Chromosome X, 56.79 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    52 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3643636
pseudogene ChrX:134171599-134175117 (+)
129S1/SvImJ MGP_129S1SvImJ_G0040706
pseudogene ChrX:132515429-132518790 (+)
A/J MGP_AJ_G0040705
pseudogene ChrX:131960455-131963891 (+)
AKR/J MGP_AKRJ_G0040630
pseudogene ChrX:136188177-136191538 (+)
BALB/cJ MGP_BALBcJ_G0040698
pseudogene ChrX:130355627-130358988 (+)
C3H/HeJ MGP_C3HHeJ_G0040330
pseudogene ChrX:132553723-132557084 (+)
C57BL/6NJ MGP_C57BL6NJ_G0041400
pseudogene ChrX:136387982-136391343 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0037522
pseudogene ChrX:124054202-124057555 (+)
CAST/EiJ MGP_CASTEiJ_G0039373
pseudogene ChrX:113446426-113449788 (+)
CBA/J MGP_CBAJ_G0040301
pseudogene ChrX:140550304-140553665 (+)
DBA/2J MGP_DBA2J_G0040516
pseudogene ChrX:131215785-131219183 (+)
FVB/NJ MGP_FVBNJ_G0040439
pseudogene ChrX:130523287-130526648 (+)
LP/J MGP_LPJ_G0040553
pseudogene ChrX:133407266-133410627 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0040442
pseudogene ChrX:147874201-147877562 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0041452
pseudogene ChrX:131918708-131922076 (+)
PWK/PhJ MGP_PWKPhJ_G0039020
pseudogene ChrX:110393519-110396887 (+)
SPRET/EiJ MGP_SPRETEiJ_G0038740
pseudogene ChrX:114104577-114107934 (+)
WSB/EiJ MGP_WSBEiJ_G0039620
pseudogene ChrX:130281377-130284738 (+)



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
  • Literature Summary
Sequences &
Gene Models
less
  • All Sequences
  • RefSeq
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
References
more
  • Summaries
    All 6
    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)
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Funding Information
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last database update
05/21/2024
MGI 6.23
The Jackson Laboratory