Gm17728 Gene Detail

Summary

• Symbol
  Gm17728
• Name
  predicted gene, 17728

• Feature Type
  protein coding gene
• IDs
  MGI:4937362
• Alliance
  genome feature page

Location &
Maps

• Sequence Map
  Chr17:9640892-9641290 bp, + strand

  From Ensembl annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 17, 7.33 cM
• Mapping Data
  1 experiment

Strain
Comparison

• SNPs within 2kb
  99 from dbSNP Build 142
• Strain Annotations
  18

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_4937362	protein coding gene	Chr17:9640892-9641290 (+)
129S1/SvImJ	ENSMUSG00200032994	protein coding gene	Chr17:5877031-5877429 (+)
A/J	ENSMUSG00195022504	protein coding gene	Chr17:6085802-6086200 (+)
AKR/J	ENSMUSG00220025896	protein coding gene	Chr17:6149386-6149784 (+)
BALB/cJ	ENSMUSG00180021938	protein coding gene	Chr17:5732424-5732822 (+)
C3H/HeJ	ENSMUSG00175030102	protein coding gene	Chr17:5876182-5876580 (+)
C57BL/6NJ	ENSMUSG00215024252	protein coding gene	Chr17:5884325-5884723 (+)
CAROLI/EiJ	MGP_CAROLIEiJ_G0020097	protein coding gene	Chr15:77365213-77365592 (+)
CAST/EiJ	ENSTCUG00005019967	protein coding gene	Chr17:6106918-6107316 (+)
CBA/J	ENSMUSG00210036520	protein coding gene	Chr17:5542944-5543342 (+)
DBA/2J	ENSMUSG00185021926	protein coding gene	Chr17:6635636-6636034 (+)
FVB/NJ	ENSMUSG00205007399	protein coding gene	Chr17:5944939-5945337 (+)
JF1/MsJ	ENSUMUG00000018169	protein coding gene	Chr17:6228404-6228802 (+)
LP/J	ENSMUSG00230030785	protein coding gene	Chr17:8067947-8068345 (+)
NOD/ShiLtJ	ENSMUSG00190025409	protein coding gene	Chr17:6076627-6077025 (+)
NZO/HlLtJ	ENSMUSG00225028949	protein coding gene	Chr17:9988227-9988625 (+)
PWK/PhJ	ENSLUMG00010018490	protein coding gene	Chr17:6047160-6047558 (+)
SPRET/EiJ	no annotation
WSB/EiJ	ENSIUOG00005013279	protein coding gene	Chr17:5937273-5937671 (+)

Homology

• Gene Tree
  Gm17728
  

Human Diseases

• References
  6 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  372 phenotype references
  

• All Mutations and Alleles
  1
• Radiation induced
  1
• Genomic Mutations
  1 involving Gm17728
• Find Mice (IMSR)
  9 strains or lines available

Expression

• Assay Results
  597

Tissue x Stage Matrix

• Other Mouse Links
  Expression Atlas

Sequences &
Gene Models

• All Sequences
  22
• UniProt
  1

• Ensembl
  ENSMUSG00000072968 (Evidence)

Representative Sequences			Length	Strain/Species
genomic	ENSMUSG00000072968	Ensembl Gene Model | MGI Sequence Detail	399	C57BL/6J
transcript	ENSMUST00000076982	Ensembl | MGI Sequence Detail	399	Not Applicable
polypeptide	ENSMUSP00000125941	Ensembl | MGI Sequence Detail	132	Not Applicable

Protein
Information

• UniProt
  1 Sequence

References

• Summaries
  All 375

  Diseases 6

  Phenotypes 372
• Earliest
  J:30229 Davisson MT, et al., Segmental trisomy as a mouse model for Down syndrome. Prog Clin Biol Res. 1993;384:117-33
• Latest
  J:391449 Thibodeau J, et al., Loss of cystathionine-beta-synthase contributes to elevated OXPHOS, a vulnerability in Ara-C-resistant Myeloid Leukemia in Down syndrome. Biochem Pharmacol. 2026 Feb 13;247:117815