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Pramel3d Gene Detail
Summary
  • Symbol
    Pramel3d
  • Name
    PRAME like 3D
  • Synonyms
    Gm15023
Location &
Maps
more
  • Sequence Map
    ChrX:134068373-134078381 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome X, 56.64 cM
Strain
Comparison
more
  • SNPs within 2kb
    23 from dbSNP Build 142
  • Strain Annotations
    13
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3805552
protein coding gene ChrX:134068277-134078402 (-)
129S1/SvImJ ENSMUSG00200044026
protein coding gene ChrX:113467435-113477439 (+)
A/J ENSMUSG00195046142
protein coding gene ChrX:116982851-116992856 (-)
AKR/J ENSMUSG00220012821
protein coding gene ChrX:110537161-110547167 (-)
BALB/cJ ENSMUSG00180032874
protein coding gene ChrX:113387541-113397547 (-)
C3H/HeJ ENSMUSG00175031000
protein coding gene ChrX:117295801-117305809 (-)
C57BL/6NJ ENSMUSG00215044738
protein coding gene ChrX:114097263-114107268 (+)
CAROLI/EiJ no annotation
CAST/EiJ no annotation
CBA/J ENSMUSG00210038185
protein coding gene ChrX:114308345-114318353 (-)
DBA/2J ENSMUSG00185029586
protein coding gene ChrX:128121243-128131251 (-)
FVB/NJ ENSMUSG00205024065
protein coding gene ChrX:112781959-112791968 (-)
JF1/MsJ no annotation
LP/J ENSMUSG00230038077
protein coding gene ChrX:134809782-134819788 (-)
NOD/ShiLtJ ENSMUSG00190037777
protein coding gene ChrX:113947929-113957939 (+)
NZO/HlLtJ ENSMUSG00225036818
protein coding gene ChrX:139457130-139467136 (-)
PWK/PhJ no annotation
SPRET/EiJ no annotation
WSB/EiJ no annotation



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    3 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
  • cDNA Data
Sequences &
Gene Models
less
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000079432 Ensembl Gene Model | MGI Sequence Detail 10009 C57BL/6J ±  kb
transcript ENSMUST00000113183 Ensembl | MGI Sequence Detail 3698 Not Applicable  
polypeptide ENSMUSP00000108808 Ensembl | MGI Sequence Detail 462 Not Applicable  
For the selected sequence
Protein
Information
less
  • UniProt
    2 Sequences
  • InterPro Domains
    IPR032675 Leucine-rich repeat domain superfamily
    IPR050694 LRRC14/PRAME
    IPR060377 PRAME-like, C-terminal LRR domain
    IPR060378 PRAME-like, N-terminal domain
Molecular
Reagents
less
  • All nucleic 3
    cDNA 3
Other
Accession IDs
less
MGI:3804650, MGI:7466572
References
more
  • Summaries
    All 14
    Diseases 1
    Phenotypes 3
  • 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
09/15/2026
MGI 6.29
The Jackson Laboratory