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Snurf Gene Detail
Summary
  • Symbol
    Snurf
  • Name
    SNRPN upstream reading frame
  • Synonyms
    MGC:18604, MGC:30325
  • Feature Type
    protein coding gene
  • IDs
    MGI:1891236
    NCBI Gene: 84704
  • Alliance
    genome feature page
  • Transcription Start Sites
    5 TSS
Location &
Maps
more
  • Sequence Map
    Chr7:59645197-59654797 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 7, 34.04 cM
  • Mapping Data
    3 experiments
Strain
Comparison
more
  • SNPs within 2kb
    334 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1891236
 protein coding gene Chr7:59632243-59654947 (-)
129S1/SvImJ ENSMUSG00200008403
 protein coding gene Chr7:46558500-46568101 (-)
A/J ENSMUSG00195010553
 protein coding gene Chr7:50798167-50807766 (-)
AKR/J no annotation
BALB/cJ ENSMUSG00180010751
 protein coding gene Chr7:47588452-47598066 (-)
C3H/HeJ ENSMUSG00175003185
 protein coding gene Chr7:48332758-48342359 (-)
C57BL/6NJ ENSMUSG00215001962
 protein coding gene Chr7:47434574-47444174 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0029816
 protein coding gene Chr7:62141971-62150874 (-)
CAST/EiJ ENSTCUG00005012046
 protein coding gene Chr7:50958278-50967923 (-)
CBA/J ENSMUSG00210017436
 protein coding gene Chr7:48435078-48444679 (-)
DBA/2J ENSMUSG00185006012
 protein coding gene Chr7:52830109-52839796 (-)
FVB/NJ ENSMUSG00205001274
 protein coding gene Chr7:48125001-48134602 (-)
JF1/MsJ ENSUMUG00000013888
 protein coding gene Chr7:57546365-57556042 (-)
LP/J ENSMUSG00230005842
 protein coding gene Chr7:58606094-58615695 (-)
NOD/ShiLtJ ENSMUSG00190003517
 protein coding gene Chr7:48472051-48481650 (-)
NZO/HlLtJ ENSMUSG00225009487
 protein coding gene Chr7:56808217-56817818 (-)
PWK/PhJ ENSLUMG00010002233
 protein coding gene Chr7:46998821-47008492 (-)
SPRET/EiJ ENSMSPG00010001294
 protein coding gene Chr7:47197271-47206367 (-)
WSB/EiJ ENSIUOG00005005072
 protein coding gene Chr7:48687557-48697179 (-)



Homology
more
  • Human Ortholog
    SNURF, SNRPN upstream open reading frame
  • Vertebrate Orthologs
    3
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    SNURF, SNRPN upstream open reading frame
  • Links
    NCBI Gene ID: 8926
    UniProt: Q9Y675

  • Chr Location
    15q11.2; chr15:24954987-24978723 (+)  GRCh38
Human Diseases
more
  • Diseases
    1 with human SNRPN associations

Human Disease Mouse Models
      
IDs
 View 4 models
Click on a disease name to see all genes associated with that disease.

  • References
    4 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    35 phenotype references
  • All Mutations and Alleles
    4
  • Endonuclease-mediated
    1
  • Radiation induced
    1
  • Targeted
    1
  • Transgenic
    1
  • Genomic Mutations
    3 involving Snurf
  • Find Mice (IMSR)
    4 strains or lines available
This marker is part of a bicistronic gene with Snrpn. All alleles are listed on the Snrpn detail page.
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
    7
  • GO References
    7
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.
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
    961
  • Tissues
    37
  • cDNA Data
    8
  • Literature Summary
    4
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000102627 Ensembl Gene Model | MGI Sequence Detail 9601 C57BL/6J ±  kb
transcript ENSMUST00000194059 Ensembl | MGI Sequence Detail 216 Not Applicable  
polypeptide ENSMUSP00000141531 Ensembl | MGI Sequence Detail 71 Not Applicable  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 10
    cDNA 10

    Microarray probesets 2
References
more
  • Summaries
    All 68
    Developmental Gene Expression 4
    Diseases 4
    Gene Ontology 7
    Phenotypes 35
  • Earliest
    J:56614 Gabriel JM, et al., A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes. Proc Natl Acad Sci U S A. 1999 Aug 3;96(16):9258-63
  • Latest
    J:390137 Otani Y, et al., Restoration of axon initial segment plasticity via chemogenetic activation rescues autism-related behaviors. Cell Death Dis. 2026 May 19;17(1)
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