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Pramel3e Gene Detail
Summary
  • Symbol
    Pramel3e
  • Name
    PRAME like 3E
  • Synonyms
    AV320801
  • Feature Type
    protein coding gene
  • IDs
    MGI:3035227
    NCBI Gene: 331531
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    ChrX:134395337-134405343 bp, + strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome X, 57.12 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    5 from dbSNP Build 142
  • Strain Annotations
    9
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3035227
 protein coding gene ChrX:134395314-134405504 (+)
129S1/SvImJ MGP_129S1SvImJ_G0036084
 protein coding gene ChrX:132800117-132815049 (+)
A/J no annotation
AKR/J MGP_AKRJ_G0035988
 protein coding gene ChrX:136446583-136456223 (+)
BALB/cJ no annotation
C3H/HeJ no annotation
C57BL/6NJ no annotation
CAROLI/EiJ no annotation
CAST/EiJ MGP_CASTEiJ_G0035046
 protein coding gene ChrX:113488235-113494063 (+)
CBA/J no annotation
DBA/2J no annotation
FVB/NJ no annotation
LP/J MGP_LPJ_G0035984
 protein coding gene ChrX:133642205-133734247 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0035863
 protein coding gene ChrX:148154826-148164434 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0036606
 protein coding gene ChrX:131816678-131827799 (-)
PWK/PhJ MGP_PWKPhJ_G0034739
 protein coding gene ChrX:110431143-110436699 (+)
SPRET/EiJ MGP_SPRETEiJ_G0034571
 protein coding gene ChrX:114292378-114306893 (+)
WSB/EiJ no annotation



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    2 phenotype references
Gene Ontology
(GO)
Classifications
less
Molecular Function

No experimental evidence to support Molecular Function annotation, following literature review. See J:73796.
Biological Process

No experimental evidence to support Biological Process annotation, following literature review. See J:73796.
Cellular Component
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
  • cDNA Data
    1
Sequences &
Gene Models
less
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000054994 Ensembl Gene Model | MGI Sequence Detail 10007 C57BL/6J ±  kb
transcript ENSMUST00000068340 Ensembl | MGI Sequence Detail 3698 Not Applicable  
polypeptide ENSMUSP00000068753 Ensembl | MGI Sequence Detail 462 Not Applicable  
For the selected sequence
Protein
Information
less
  • UniProt
    1 Sequence
  • InterPro Domains
    IPR032675 Leucine-rich repeat domain superfamily
    IPR050694 PRAME domain-containing protein
Molecular
Reagents
less
  • All nucleic 1
    cDNA 1

    Microarray probesets 1
Other
Accession IDs
less
MGI:7466573
References
more
  • Summaries
    All 14
    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
11/19/2024
MGI 6.24 		The Jackson Laboratory