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Gm15798 Pseudogene Detail
Summary
  • Symbol
    Gm15798
  • Name
    predicted gene 15798
Location &
Maps
more
  • Sequence Map
    Chr16:18763008-18763415 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 16, 11.73 cM
Strain
Comparison
more
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3802099
 pseudogene Chr16:18762953-18763465 (-)
129S1/SvImJ MGP_129S1SvImJ_G0011250
 pseudogene Chr16:16212354-16212761 (-)
A/J MGP_AJ_G0011234
 pseudogene Chr16:15400753-15401160 (-)
AKR/J MGP_AKRJ_G0011197
 pseudogene Chr16:16025614-16026021 (-)
BALB/cJ MGP_BALBcJ_G0011204
 pseudogene Chr16:15563733-15564140 (-)
C3H/HeJ MGP_C3HHeJ_G0011102
 pseudogene Chr16:16180890-16181297 (-)
C57BL/6NJ MGP_C57BL6NJ_G0011498
 pseudogene Chr16:16527396-16527803 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0010082
 pseudogene Chr16:15425555-15425962 (-)
CAST/EiJ MGP_CASTEiJ_G0010926
 pseudogene Chr16:16065312-16065719 (-)
CBA/J MGP_CBAJ_G0011082
 pseudogene Chr16:17207317-17207724 (-)
DBA/2J MGP_DBA2J_G0011129
 pseudogene Chr16:15311122-15311529 (-)
FVB/NJ MGP_FVBNJ_G0011133
 pseudogene Chr16:15381461-15381868 (-)
LP/J MGP_LPJ_G0011225
 pseudogene Chr16:15964911-15965318 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0011127
 pseudogene Chr16:16853281-16853688 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0011480
 pseudogene Chr16:15941185-15941592 (-)
PWK/PhJ MGP_PWKPhJ_G0010803
 pseudogene Chr16:15601912-15602319 (-)
SPRET/EiJ MGP_SPRETEiJ_G0010628
 pseudogene Chr16:15891014-15891421 (-)
WSB/EiJ MGP_WSBEiJ_G0010974
 pseudogene Chr16:15964856-15965263 (-)



Homology
less
Human Diseases
less
  • References
    3 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    49 phenotype references
Expression
less
Expression Overview

early conceptus
embryo ectoderm
embryo endoderm
embryo mesoderm
embryo mesenchyme
extraembryonic component
alimentary system
auditory system
branchial arches
cardiovascular system
connective tissue
endocrine system
exocrine system
hemolymphoid system
integumental system
limbs
liver and biliary system
musculoskeletal system
nervous system
olfactory system
reproductive system
respiratory system
urinary system
visual system
Click cells to view annotations.


  • Assay Results
    706
Sequences &
Gene Models
less
  • All Sequences
    22
  • RefSeq
    1
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000083658 Ensembl Gene Model | MGI Sequence Detail 408 C57BL/6J ±  kb
transcript ENSMUST00000120082 Ensembl | MGI Sequence Detail 408 Not Applicable  
For the selected sequence
References
more
  • Summaries
    All 54
    Diseases 3
    Phenotypes 49
  • Earliest
    J:67796 Merscher S, et al., TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome. Cell. 2001 Feb 23;104(4):619-29
  • Latest
    J:374652 Thakur P, et al., An antisense oligonucleotide-based strategy to ameliorate cognitive dysfunction in the 22q11.2 Deletion Syndrome. Elife. 2025 May 27;13
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
09/30/2025
MGI 6.24 		The Jackson Laboratory