Gm10787 Gene Detail

Summary

• Symbol
  Gm10787
• Name
  predicted gene 10787

• Feature Type
  lncRNA gene
• IDs
  MGI:3642150
  NCBI Gene: 100038479
• Alliance
  genome feature page
• Transcription Start Sites
  1 TSS

Location &
Maps

• Sequence Map
  Chr10:76847829-76858048 bp, + strand

  From NCBI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 10, 39.72 cM
• Mapping Data
  1 experiment

Strain
Comparison

• SNPs within 2kb
  428 from dbSNP Build 142
• Strain Annotations
  19

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_3642150	lncRNA gene	Chr10:76847826-76858049 (+)
129S1/SvImJ	ENSMUSG00200051447	lncRNA gene	Chr10:73525364-73535584 (+)
A/J	ENSMUSG00195049584	lncRNA gene	Chr10:73861993-73872213 (+)
AKR/J	ENSMUSG00220049167	lncRNA gene	Chr10:73521672-73531892 (+)
BALB/cJ	ENSMUSG00180053511	lncRNA gene	Chr10:73876437-73886658 (+)
C3H/HeJ	ENSMUSG00175053024	lncRNA gene	Chr10:73747665-73757884 (+)
C57BL/6NJ	ENSMUSG00215053370	lncRNA gene	Chr10:73485359-73495579 (+)
CAROLI/EiJ	MGP_CAROLIEiJ_G0015476	protein coding gene	Chr10:71044584-71054055 (+)
CAST/EiJ	ENSTCUG00005051842	lncRNA gene	Chr10:73379477-73389071 (+)
CBA/J	ENSMUSG00210049946	lncRNA gene	Chr10:73603871-73614090 (+)
DBA/2J	ENSMUSG00185054183	lncRNA gene	Chr10:73946168-73956388 (+)
FVB/NJ	ENSMUSG00205051527	lncRNA gene	Chr10:73638107-73648327 (+)
JF1/MsJ	ENSUMUG00000056310	lncRNA gene	Chr10:75097386-75106933 (+)
LP/J	ENSMUSG00230051199	lncRNA gene	Chr10:75715695-75725914 (+)
NOD/ShiLtJ	ENSMUSG00190052414	lncRNA gene	Chr10:73923639-73933858 (+)
NZO/HlLtJ	ENSMUSG00225048027	lncRNA gene	Chr10:80012335-80022555 (+)
PWK/PhJ	ENSLUMG00010052652	lncRNA gene	Chr10:73485464-73495019 (+)
SPRET/EiJ	ENSMSPG00010048558	lncRNA gene	Chr10:75294081-75303662 (+)
WSB/EiJ	ENSIUOG00005051184	lncRNA gene	Chr10:73528721-73538924 (+)

Homology

• Gene Tree
  Gm10787
  

Human Diseases

• References
  2 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  31 phenotype references
  

• All Mutations and Alleles
  6
• Endonuclease-mediated
  2
• Gene trapped
  1
• Targeted
  3
• Genomic Mutations
  4 involving Gm10787
• Incidental Mutations
  Mutagenetix , APF
• Find Mice (IMSR)
  5 strains or lines available

Expression

• Assay Results
  597
• cDNA Data
  2

Tissue x Stage Matrix

• Other Mouse Links
  GEO
  Expression Atlas

Sequences &
Gene Models

• All Sequences
  29
• RefSeq
  1
• UniProt
  1

• Ensembl
  ENSMUSG00000074919 (Evidence)
• NCBI Gene
  100038479

Representative Sequences			Length	Strain/Species
genomic	100038479	NCBI Gene Model | MGI Sequence Detail	10220	C57BL/6J
transcript	NR_045882	RefSeq | MGI Sequence Detail	1548	C57BL/6
polypeptide	Q3UP50	UniProt | EBI | MGI Sequence Detail	122	Not Applicable

Protein
Information

• UniProt
  1 Sequence

Molecular
Reagents

• All nucleic 2

  cDNA 2

References

• Summaries
  All 39

  Diseases 2

  Phenotypes 31
• 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:361105 Tateossian H, et al., DYRK1A kinase triplication is the major cause of Otitis Media in Down Syndrome. Elife. 2025;

TSS for Gm10787:

(View these features in JBrowse)

Transcription Start Site	Location	Distance from Gene 5'-end
Tssr94202	Chr10:76847818-76847839 (+)	0 bp