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Gm10787 Gene Detail
Summary
  • Symbol
    Gm10787
  • Name
    predicted gene 10787
  • Feature Type
    lincRNA gene
  • IDs
    MGI:3642150
    NCBI Gene: 100038479
  • Alliance
  • Transcription Start Sites
    1 TSS
Location &
Maps
more
  • Sequence Map
    Chr10:77011995-77022214 bp, + strand
  • From NCBI annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 10, 39.72 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    89 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3642150
lincRNA gene Chr10:77011995-77022214 (+)
129S1/SvImJ MGP_129S1SvImJ_G0017391
protein coding gene Chr10:77284636-77295559 (+)
A/J MGP_AJ_G0017368
protein coding gene Chr10:74617521-74627534 (+)
AKR/J MGP_AKRJ_G0017329
protein coding gene Chr10:76622865-76632520 (+)
BALB/cJ MGP_BALBcJ_G0017328
protein coding gene Chr10:74811723-74821708 (+)
C3H/HeJ MGP_C3HHeJ_G0017152
protein coding gene Chr10:76696845-76706938 (+)
C57BL/6NJ MGP_C57BL6NJ_G0017786
protein coding gene Chr10:79994787-80005887 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0015476
protein coding gene Chr10:71044584-71054055 (+)
CAST/EiJ MGP_CASTEiJ_G0016722
protein coding gene Chr10:77039544-77049123 (+)
CBA/J MGP_CBAJ_G0017124
protein coding gene Chr10:83123436-83136915 (+)
DBA/2J MGP_DBA2J_G0017229
protein coding gene Chr10:73905529-73917653 (+)
FVB/NJ MGP_FVBNJ_G0017221
protein coding gene Chr10:73067033-73076624 (+)
LP/J MGP_LPJ_G0017302
protein coding gene Chr10:77763383-77773058 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0017250
protein coding gene Chr10:85168064-85179510 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0017825
protein coding gene Chr10:76684407-76694111 (+)
PWK/PhJ MGP_PWKPhJ_G0016506
protein coding gene Chr10:73763051-73772649 (+)
SPRET/EiJ MGP_SPRETEiJ_G0016289
protein coding gene Chr10:75921641-75931183 (+)
WSB/EiJ MGP_WSBEiJ_G0016785
protein coding gene Chr10:76660392-76671170 (+)



Homology
less
Human Diseases
less
  • References
    2 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    16 phenotype references
Expression
less
  • cDNA Data
Interactions
less
Sequences &
Gene Models
less
  • All Sequences
  • RefSeq
  • UniProt
  • UniGene
Representative SequencesLengthStrain/SpeciesFlank
genomic 100038479 NCBI Gene Model | MGI Sequence Detail 10220 C57BL/6J ±  kb
transcript NR_045882 RefSeq | MGI Sequence Detail 1548 C57BL/6  
polypeptide Q3UP50 UniProt | EBI | MGI Sequence Detail 122 Not Applicable  
For the selected sequence
Protein
Information
less
  • UniProt
    1 Sequence
Molecular
Reagents
less
  • All nucleic 2
    cDNA 2
References
more
  • Summaries
    All 24
    Diseases 2
    Phenotypes 16
  • Earliest
    J:86696 Zambrowicz BP, et al., Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention. Proc Natl Acad Sci U S A. 2003 Nov 25;100(24):14109-14
  • Latest
    J:262380 Watson-Scales S, et al., Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration. PLoS Genet. 2018 May;14(5):e1007383

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
07/09/2019
MGI 6.14
The Jackson Laboratory