Gm37694 Gene Detail

Summary

• Symbol
  Gm37694
• Name
  predicted gene, 37694

• Feature Type
  unclassified gene
• IDs
  MGI:5610922
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Genome coordinates not available from the current reference assembly.

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

Strain
Comparison

• Strain Annotations
  17

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	no annotation
129S1/SvImJ	MGP_129S1SvImJ_G0000929	unclassified gene	Chr16:77817603-77819734 (+)
A/J	MGP_AJ_G0000905	unclassified gene	Chr16:74385373-74387505 (+)
AKR/J	MGP_AKRJ_G0000893	unclassified gene	Chr16:76622343-76624475 (+)
BALB/cJ	MGP_BALBcJ_G0000898	unclassified gene	Chr16:74782518-74784650 (+)
C3H/HeJ	MGP_C3HHeJ_G0000881	unclassified gene	Chr16:77075225-77077357 (+)
C57BL/6NJ	MGP_C57BL6NJ_G0001013	unclassified gene	Chr16:80309457-80311589 (+)
CAROLI/EiJ	MGP_CAROLIEiJ_G0000746	unclassified gene	Chr16:72847222-72849355 (+)
CAST/EiJ	MGP_CASTEiJ_G0000873	unclassified gene	Chr16:77487357-77489487 (+)
CBA/J	MGP_CBAJ_G0000873	unclassified gene	Chr16:83740466-83742598 (+)
DBA/2J	MGP_DBA2J_G0000877	unclassified gene	Chr16:74231561-74233693 (+)
FVB/NJ	MGP_FVBNJ_G0000889	unclassified gene	Chr16:73586285-73588417 (+)
LP/J	MGP_LPJ_G0000932	unclassified gene	Chr16:77561065-77563196 (+)
NOD/ShiLtJ	MGP_NODShiLtJ_G0000880	unclassified gene	Chr16:86951394-86953526 (+)
NZO/HlLtJ	MGP_NZOHlLtJ_G0001007	unclassified gene	Chr16:76955090-76957222 (+)
PWK/PhJ	MGP_PWKPhJ_G0000827	unclassified gene	Chr16:74428996-74431127 (+)
SPRET/EiJ	MGP_SPRETEiJ_G0000800	unclassified gene	Chr16:76577756-76579881 (+)
WSB/EiJ	MGP_WSBEiJ_G0000881	unclassified gene	Chr16:77175246-77177378 (+)

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  4 phenotype references
  

• All Mutations and Alleles
  1
• Targeted
  1
• Genomic Mutations
  1 involving Gm37694
• Find Mice (IMSR)
  0 strains or lines available

Expression

• Assay Results
  706

Tissue x Stage Matrix

• Other Mouse Links
  Expression Atlas

Sequences &
Gene Models

• All Sequences
  17

References

• Summaries
  All 5

  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;