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Gm44722 Gene Detail
Summary
  • Symbol
    Gm44722
  • Name
    predicted gene 44722
  • Feature Type
    unclassified gene
  • IDs
    MGI:5753298
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    Chr7:63851837-63852272 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 7, Syntenic
Strain
Comparison
more
  • SNPs within 2kb
    114 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_5753298
 unclassified gene Chr7:63851837-63852272 (-)
129S1/SvImJ MGP_129S1SvImJ_G0002177
 unclassified gene Chr7:65330890-65331325 (-)
A/J MGP_AJ_G0002153
 unclassified gene Chr7:64072177-64072612 (-)
AKR/J MGP_AKRJ_G0002140
 unclassified gene Chr7:65426972-65427407 (-)
BALB/cJ MGP_BALBcJ_G0002149
 unclassified gene Chr7:63810667-63811102 (-)
C3H/HeJ MGP_C3HHeJ_G0002125
 unclassified gene Chr7:66073473-66073908 (-)
C57BL/6NJ MGP_C57BL6NJ_G0002274
 unclassified gene Chr7:68138491-68138926 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0001893
 unclassified gene Chr7:67020597-67021025 (-)
CAST/EiJ MGP_CASTEiJ_G0002090
 unclassified gene Chr7:56769235-56769670 (-)
CBA/J MGP_CBAJ_G0002119
 unclassified gene Chr7:70361216-70361651 (-)
DBA/2J MGP_DBA2J_G0002121
 unclassified gene Chr7:62821902-62822337 (-)
FVB/NJ MGP_FVBNJ_G0002132
 unclassified gene Chr7:62922176-62922611 (-)
LP/J MGP_LPJ_G0002176
 unclassified gene Chr7:66559872-66560307 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0002107
 unclassified gene Chr7:70634051-70634486 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0002262
 unclassified gene Chr7:64707615-64708050 (-)
PWK/PhJ MGP_PWKPhJ_G0002050
 unclassified gene Chr7:55830198-55830633 (-)
SPRET/EiJ MGP_SPRETEiJ_G0002014
 unclassified gene Chr7:51841364-51841799 (-)
WSB/EiJ MGP_WSBEiJ_G0002117
 unclassified gene Chr7:65087294-65087729 (-)



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    7 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
    19
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000108645 Ensembl Gene Model | MGI Sequence Detail 436 C57BL/6J ±  kb
For the selected sequence
References
more
  • Summaries
    All 9
    Diseases 1
    Phenotypes 7
  • Earliest
    J:260165 Fejgin K, et al., A mouse model that recapitulates cardinal features of the 15q13.3 microdeletion syndrome including schizophrenia- and epilepsy-related alterations. Biol Psychiatry. 2014 Jul 15;76(2):128-37
  • Latest
    J:348102 Unda BK, et al., Impaired OTUD7A-dependent Ankyrin regulation mediates neuronal dysfunction in mouse and human models of the 15q13.3 microdeletion syndrome. Mol Psychiatry. 2023 Apr;28(4):1747-1769
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
12/10/2024
MGI 6.24 		The Jackson Laboratory