About   Help   FAQ
Pramel3b Gene Detail
Summary
  • Symbol
    Pramel3b
  • Name
    PRAME like 3B
  • Synonyms
    Gm7903
  • Feature Type
    protein coding gene
  • IDs
    MGI:3648697
    NCBI Gene: 666040
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    ChrX:134334584-134344579 bp, + strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome X, 57.03 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    10 from dbSNP Build 142
  • Strain Annotations
    10
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3648697
 protein coding gene ChrX:134334557-134344753 (+)
129S1/SvImJ MGP_129S1SvImJ_G0036082
 protein coding gene ChrX:132388807-132403718 (-)
A/J MGP_AJ_G0036062
 protein coding gene ChrX:132203465-132208834 (+)
AKR/J MGP_AKRJ_G0035985
 protein coding gene ChrX:136324989-136334414 (+)
BALB/cJ no annotation
C3H/HeJ MGP_C3HHeJ_G0035762
 protein coding gene ChrX:132803812-132814911 (+)
C57BL/6NJ no annotation
CAROLI/EiJ no annotation
CAST/EiJ MGP_CASTEiJ_G0035047
 protein coding gene ChrX:113488310-113494047 (+)
CBA/J MGP_CBAJ_G0035734
 protein coding gene ChrX:140433082-140446665 (-)
DBA/2J MGP_DBA2J_G0035890
 protein coding gene ChrX:131094025-131113754 (-)
FVB/NJ no annotation
LP/J MGP_LPJ_G0035983
 protein coding gene ChrX:133578164-133734082 (+)
NOD/ShiLtJ no annotation
NZO/HlLtJ no annotation
PWK/PhJ no annotation
SPRET/EiJ MGP_SPRETEiJ_G0034572
 protein coding gene ChrX:114292383-114306357 (+)
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

No experimental evidence to support Cellular Component annotation, following literature review. See J:73796.
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
Sequences &
Gene Models
less
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000096508 Ensembl Gene Model | MGI Sequence Detail 9996 C57BL/6J ±  kb
transcript ENSMUST00000113172 Ensembl | MGI Sequence Detail 3677 Not Applicable  
polypeptide ENSMUSP00000108797 Ensembl | MGI Sequence Detail 463 Not Applicable  
For the selected sequence
Other
Accession IDs
less
MGI:7466570
References
more
  • Summaries
    All 8
    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
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory