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Snord64 Gene Detail
Summary
  • Symbol
    Snord64
  • Name
    small nucleolar RNA, C/D box 64
  • Synonyms
    MBII-13
  • Feature Type
    snoRNA gene
  • IDs
    MGI:3819546
    NCBI Gene: 100217429
  • Alliance
  • Transcription Start Sites
    1 TSS
Location &
Maps
more
  • Sequence Map
    Chr7:59628559-59628604 bp, - strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 7, 34.04 cM
Strain
Comparison
more
  • SNPs within 2kb
    31 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3819546
snoRNA gene Chr7:59628556-59628622 (-)
129S1/SvImJ MGP_129S1SvImJ_G0039390
snoRNA gene Chr7:60777655-60777721 (-)
A/J MGP_AJ_G0039388
snoRNA gene Chr7:59690736-59690802 (-)
AKR/J MGP_AKRJ_G0039312
snoRNA gene Chr7:60999028-60999094 (-)
BALB/cJ MGP_BALBcJ_G0039367
snoRNA gene Chr7:59295171-59295237 (-)
C3H/HeJ MGP_C3HHeJ_G0039027
snoRNA gene Chr7:61318655-61318721 (-)
C57BL/6NJ MGP_C57BL6NJ_G0039917
snoRNA gene Chr7:63424852-63424918 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0036586
snoRNA gene Chr7:62125160-62125226 (-)
CAST/EiJ MGP_CASTEiJ_G0038160
snoRNA gene Chr7:52294796-52294862 (-)
CBA/J MGP_CBAJ_G0038996
snoRNA gene Chr7:65511114-65511180 (-)
DBA/2J MGP_DBA2J_G0039184
snoRNA gene Chr7:58620539-58620605 (-)
FVB/NJ MGP_FVBNJ_G0039142
snoRNA gene Chr7:58598139-58598205 (-)
LP/J MGP_LPJ_G0039231
snoRNA gene Chr7:61921252-61921318 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0039146
snoRNA gene Chr7:65253935-65254001 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0040015
snoRNA gene Chr7:60290138-60290204 (-)
PWK/PhJ MGP_PWKPhJ_G0037833
snoRNA gene Chr7:51595545-51595611 (-)
SPRET/EiJ MGP_SPRETEiJ_G0037588
snoRNA gene Chr7:47755811-47755877 (-)
WSB/EiJ MGP_WSBEiJ_G0038386
snoRNA gene Chr7:60612119-60612185 (-)



Homology
less
Human Diseases
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  • References
    4 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    28 phenotype references
Expression
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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
  • Tissues
  • Literature Summary
Sequences &
Gene Models
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  • All Sequences
  • RefSeq
Representative SequencesLengthStrain/SpeciesFlank
genomic 100217429 NCBI Gene Model | MGI Sequence Detail 46 C57BL/6J ±  kb
For the selected sequence
Molecular
Reagents
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  • All nucleic 1
    Other 1
References
more
  • Summaries
    All 36
    Developmental Gene Expression 2
    Diseases 4
    Phenotypes 28
  • 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:303877 Saitow F, et al., Upregulated 5-HT1A receptor-mediated currents in the prefrontal cortex layer 5 neurons in the 15q11-13 duplication mouse model of autism. Mol Brain. 2020 Aug 24;13(1):115

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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last database update
05/10/2022
MGI 6.19
The Jackson Laboratory