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Pramel3d Gene Detail
Summary
  • Symbol
    Pramel3d
  • Name
    PRAME like 3D
  • Synonyms
    Gm15023
  • Feature Type
    protein coding gene
  • IDs
    MGI:3805552
    NCBI Gene: 100040635
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    ChrX:134068373-134078381 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome X, 56.64 cM
Strain
Comparison
more
  • Strain Annotations
    8
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 MGP_129S1SvImJ_G0036081
 protein coding gene ChrX:132388791-132403723 (-)
A/J MGP_AJ_G0036061
 protein coding gene ChrX:132203390-132208999 (+)
AKR/J MGP_AKRJ_G0035987
 protein coding gene ChrX:136385658-136395317 (+)
BALB/cJ no annotation
C3H/HeJ no annotation
C57BL/6NJ no annotation
CAROLI/EiJ no annotation
CAST/EiJ no annotation
CBA/J no annotation
DBA/2J MGP_DBA2J_G0035889
 protein coding gene ChrX:131093860-131113759 (-)
FVB/NJ no annotation
LP/J no annotation
NOD/ShiLtJ MGP_NODShiLtJ_G0035860
 protein coding gene ChrX:148015424-148024947 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0036610
 protein coding gene ChrX:132105221-132116342 (+)
PWK/PhJ no annotation
SPRET/EiJ MGP_SPRETEiJ_G0034568
 protein coding gene ChrX:114146238-114161043 (+)
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
  • All GO Annotations
    1
  • GO References
    1
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

Click cells to view annotations.
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
    3
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
    1 Sequence
  • InterPro Domains
    IPR032675 Leucine-rich repeat domain superfamily
Molecular
Reagents
less
  • All nucleic 3
    cDNA 3
Other
Accession IDs
less
MGI:3804650
References
more
  • Summaries
    All 14
    Diseases 1
    Gene Ontology 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)
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory