Gm15318 Gene Detail

Summary

• Symbol
  Gm15318
• Name
  predicted gene 15318

• Feature Type
  lncRNA gene
• IDs
  MGI:3705106
  NCBI Gene: 102631757
• Alliance
  genome feature page
• Transcription Start Sites
  4 TSS

Location &
Maps

• Sequence Map
  Chr17:31371726-31382026 bp, + strand

  From NCBI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 17, 15.80 cM

Strain
Comparison

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

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_3705106	lncRNA gene	Chr17:31371726-31382035 (+)
129S1/SvImJ	ENSMUSG00200054063	lncRNA gene	Chr17:27059200-27069496 (+)
A/J	ENSMUSG00195054471	lncRNA gene	Chr17:27990029-28000403 (+)
AKR/J	ENSMUSG00220053825	lncRNA gene	Chr17:27018085-27028461 (+)
BALB/cJ	ENSMUSG00180050942	lncRNA gene	Chr17:27334700-27344998 (+)
C3H/HeJ	ENSMUSG00175054038	lncRNA gene	Chr17:26899286-26909660 (+)
C57BL/6NJ	ENSMUSG00215054323	lncRNA gene	Chr17:26889126-26899435 (+)
CAROLI/EiJ	MGP_CAROLIEiJ_G0003010	antisense lncRNA gene	Chr17:27024198-27034195 (+)
CAST/EiJ	ENSTCUG00005050216	lncRNA gene	Chr17:27767550-27777871 (+)
CBA/J	ENSMUSG00210050900	lncRNA gene	Chr17:26726309-26736683 (+)
DBA/2J	ENSMUSG00185053781	lncRNA gene	Chr17:29345219-29355519 (+)
FVB/NJ	ENSMUSG00205053454	lncRNA gene	Chr17:27200007-27210309 (+)
JF1/MsJ	ENSUMUG00000057953	lncRNA gene	Chr17:28519671-28529850 (+)
LP/J	ENSMUSG00230055226	lncRNA gene	Chr17:30457751-30468049 (+)
NOD/ShiLtJ	ENSMUSG00190054410	lncRNA gene	Chr17:26841353-26851667 (+)
NZO/HlLtJ	ENSMUSG00225055053	lncRNA gene	Chr17:32434241-32444538 (+)
PWK/PhJ	ENSLUMG00010053357	lncRNA gene	Chr17:26324792-26335146 (+)
SPRET/EiJ	ENSMSPG00010050283	lncRNA gene	Chr17:27597426-27607648 (+)
WSB/EiJ	ENSIUOG00005051696	lncRNA gene	Chr17:27607307-27617629 (+)

Homology

• Gene Tree
  Gm15318
  

Human Diseases

• References
  3 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  28 phenotype references
  

• All Mutations and Alleles
  4
• Targeted
  4
• Genomic Mutations
  4 involving Gm15318
• Find Mice (IMSR)
  0 strains or lines available

Expression

• Assay Results
  606
• Tissues
  8
• cDNA Data
  6
• Literature Summary
  1

Tissue x Stage Matrix

• Other Mouse Links
  GEO
  Expression Atlas

Sequences &
Gene Models

• All Sequences
  46
• RefSeq
  2

• Ensembl
  ENSMUSG00000086010 (Evidence)
• NCBI Gene
  102631757

Representative Sequences			Length	Strain/Species
genomic	102631757	NCBI Gene Model | MGI Sequence Detail	10301	C57BL/6J
transcript	NR_110502	RefSeq | MGI Sequence Detail	1661	C57BL/6

Molecular
Reagents

• All nucleic 7

  cDNA 6

  Primer pair 1

References

• Summaries
  All 37

  Developmental Gene Expression 1

  Diseases 3

  Phenotypes 28
• Earliest
  J:154298 Pereira PL, et al., A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome. Hum Mol Genet. 2009 Dec 15;18(24):4756-4769
• Latest
  J:361105 Tateossian H, et al., DYRK1A kinase triplication is the major cause of Otitis Media in Down Syndrome. Elife. 2025;

TSS for Gm15318:

(View these features in JBrowse)

Transcription Start Site	Location	Distance from Gene 5'-end
Tssr5068	Chr17:31371766-31371803 (+)	59 bp
Tssr5069	Chr17:31371838-31371849 (+)	118 bp
Tssr5070	Chr17:31380368-31380372 (+)	8,644 bp
Tssr5075	Chr17:31380510-31380541 (+)	8,800 bp