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Pramel3c Gene Detail
Summary
  • Symbol
    Pramel3c
  • Name
    PRAME like 3C
  • Synonyms
    Gm5128
  • Feature Type
    protein coding gene
  • IDs
    MGI:3647038
    NCBI Gene: 331529
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    ChrX:134274033-134284142 bp, + strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome X, 56.94 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    22 from dbSNP Build 142
  • Strain Annotations
    8
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3647038
 protein coding gene ChrX:134274006-134284149 (+)
129S1/SvImJ MGP_129S1SvImJ_G0036083
 protein coding gene ChrX:132546888-132562249 (+)
A/J no annotation
AKR/J no annotation
BALB/cJ no annotation
C3H/HeJ MGP_C3HHeJ_G0035760
 protein coding gene ChrX:132731890-132742988 (+)
C57BL/6NJ no annotation
CAROLI/EiJ no annotation
CAST/EiJ MGP_CASTEiJ_G0035048
 protein coding gene ChrX:113488310-113494215 (+)
CBA/J no annotation
DBA/2J MGP_DBA2J_G0035891
 protein coding gene ChrX:131246213-131266339 (+)
FVB/NJ no annotation
LP/J MGP_LPJ_G0035982
 protein coding gene ChrX:133514306-133734401 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0035859
 protein coding gene ChrX:147921641-147937709 (+)
NZO/HlLtJ no annotation
PWK/PhJ no annotation
SPRET/EiJ MGP_SPRETEiJ_G0034569
 protein coding gene ChrX:114146243-114161197 (+)
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 ENSMUSG00000094004 Ensembl Gene Model | MGI Sequence Detail 10110 C57BL/6J ±  kb
transcript ENSMUST00000180198 Ensembl | MGI Sequence Detail 3836 Not Applicable  
polypeptide ENSMUSP00000137160 Ensembl | MGI Sequence Detail 463 Not Applicable  
For the selected sequence
Molecular
Reagents
less
  • All nucleic 1
    cDNA 1

    Microarray probesets 2
Other
Accession IDs
less
MGI:7466571
References
more
  • Summaries
    All 10
    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
11/12/2024
MGI 6.24 		The Jackson Laboratory