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Gm25936 Gene Detail
Summary
  • Symbol
    Gm25936
  • Name
    predicted gene, 25936
Location &
Maps
more
  • Sequence Map
    ChrX:134215065-134215178 bp, - strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome X, Syntenic
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    92 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_5455713
 snoRNA gene ChrX:134215065-134215178 (-)
129S1/SvImJ ENSMUSG00200048056
 snoRNA gene ChrX:113290312-113290425 (-)
A/J ENSMUSG00195049070
 snoRNA gene ChrX:117129528-117129641 (-)
AKR/J ENSMUSG00220013304
 snoRNA gene ChrX:110683853-110683966 (-)
BALB/cJ ENSMUSG00180039784
 snoRNA gene ChrX:113534334-113534447 (-)
C3H/HeJ no annotation
C57BL/6NJ ENSMUSG00215045858
 snoRNA gene ChrX:114049076-114049189 (-)
C57BL/6NJ ENSMUSG00215045138
 snoRNA gene ChrX:113917663-113917776 (-)
CAROLI/EiJ no annotation
CAST/EiJ ENSTCUG00005041343
 snoRNA gene ChrX:114732297-114732410 (-)
CBA/J ENSMUSG00210043548
 snoRNA gene ChrX:114454994-114455107 (-)
CBA/J ENSMUSG00210043791
 snoRNA gene ChrX:114556633-114556746 (-)
DBA/2J ENSMUSG00185030149
 snoRNA gene ChrX:128267916-128268029 (-)
FVB/NJ ENSMUSG00205036073
 snoRNA gene ChrX:112928666-112928779 (-)
JF1/MsJ ENSUMUG00000030572
 snoRNA gene ChrX:147543479-147543592 (-)
LP/J ENSMUSG00230040793
 snoRNA gene ChrX:134956452-134956565 (-)
NOD/ShiLtJ ENSMUSG00190041675
 snoRNA gene ChrX:113767395-113767508 (-)
NZO/HlLtJ ENSMUSG00225037059
 snoRNA gene ChrX:139536144-139536257 (+)
PWK/PhJ ENSLUMG00010044343
 snoRNA gene ChrX:112229189-112229302 (-)
SPRET/EiJ ENSMSPG00010040035
 snoRNA gene ChrX:116759979-116760092 (+)
WSB/EiJ ENSIUOG00005037896
 snoRNA gene ChrX:114466151-114466264 (-)



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
  • All GO Annotations
    2
  • GO References
    1
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
RNA binding
signaling receptor activity
signaling receptor binding
transcription
transferase
transporter
Biological Process

carbohydrate derivative metabolism
cell differentiation
cell population proliferation
cellular component organization
DNA-templated transcription
establishment of localization
homeostatic process
immune system process
lipid metabolic process
programmed cell death
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
membraneless organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
protein-containing complex
synapse
vacuole
Click cells to view annotations.
Sequences &
Gene Models
less
  • All Sequences
    22
Representative SequencesLengthStrain/SpeciesFlank
genomic 115486119 NCBI Gene Model | MGI Sequence Detail 114 C57BL/6J ±  kb
For the selected sequence
References
more
  • Summaries
    All 6
    Diseases 1
    Gene Ontology 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
09/08/2026
MGI 6.24 		The Jackson Laboratory