Gm37466 Gene Detail

Summary

• Symbol
  Gm37466
• Name
  predicted gene, 37466

• Feature Type
  unclassified gene
• IDs
  MGI:5610694
• Alliance
  genome feature page

Location &
Maps

• Sequence Map
  Chr16:77178838-77179489 bp, + strand

  From Ensembl annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 16, Syntenic
• Mapping Data
  1 experiment

Strain
Comparison

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

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_5610694	unclassified gene	Chr16:77178838-77179489 (+)
129S1/SvImJ	ENSMUSG00200016149	unclassified gene	Chr16:74054785-74055436 (+)
A/J	ENSMUSG00195023607	unclassified gene	Chr16:73838177-73838828 (+)
AKR/J	ENSMUSG00220018357	unclassified gene	Chr16:74022091-74022742 (+)
BALB/cJ	ENSMUSG00180002196	unclassified gene	Chr16:73913578-73914229 (+)
C3H/HeJ	ENSMUSG00175009328	unclassified gene	Chr16:74201175-74201826 (+)
C57BL/6NJ	ENSMUSG00215001694	unclassified gene	Chr16:74037468-74038119 (+)
CAROLI/EiJ	MGP_CAROLIEiJ_G0000734	unclassified gene	Chr16:72546395-72547058 (+)
CAST/EiJ	ENSTCUG00005007802	unclassified gene	Chr16:73851531-73852195 (+)
CBA/J	ENSMUSG00210019940	unclassified gene	Chr16:74146246-74146897 (+)
DBA/2J	ENSMUSG00185005415	unclassified gene	Chr16:74072862-74073513 (+)
FVB/NJ	ENSMUSG00205016137	unclassified gene	Chr16:73933702-73934353 (+)
JF1/MsJ	ENSUMUG00000012546	unclassified gene	Chr16:74226805-74227456 (+)
LP/J	ENSMUSG00230020164	unclassified gene	Chr16:76641099-76641750 (+)
NOD/ShiLtJ	ENSMUSG00190011546	unclassified gene	Chr16:74072456-74073107 (+)
NZO/HlLtJ	ENSMUSG00225029586	unclassified gene	Chr16:79846449-79847100 (+)
PWK/PhJ	ENSLUMG00010005059	unclassified gene	Chr16:73880392-73881043 (+)
SPRET/EiJ	ENSMSPG00010015771	unclassified gene	Chr16:74753780-74754443 (+)
WSB/EiJ	ENSIUOG00005017627	unclassified gene	Chr16:74063752-74064403 (+)

Homology

• Gene Tree
  Gm37466
  

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  4 phenotype references
  

• All Mutations and Alleles
  1
• Targeted
  1
• Genomic Mutations
  1 involving Gm37466
• Find Mice (IMSR)
  0 strains or lines available

Expression

• Assay Results
  597

Tissue x Stage Matrix

• Other Mouse Links
  Expression Atlas

Sequences &
Gene Models

• All Sequences
  20

• Ensembl
  ENSMUSG00000103972 (Evidence)

Representative Sequences			Length	Strain/Species
genomic	ENSMUSG00000103972	Ensembl Gene Model | MGI Sequence Detail	652	C57BL/6J

References

• Summaries
  All 6

  Phenotypes 4
• Earliest
  J:227899 Lana-Elola E, et al., Genetic dissection of Down syndrome-associated congenital heart defects using a new mouse mapping panel. Elife. 2016 Jan 14;5:e11614
• Latest
  J:361105 Tateossian H, et al., DYRK1A kinase triplication is the major cause of Otitis Media in Down Syndrome. Elife. 2025;