Gm44765 Gene Detail

Summary

• Symbol
  Gm44765
• Name
  predicted gene 44765

• Feature Type
  unclassified gene
• IDs
  MGI:5753341
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Chr7:63933548-63934148 bp, + strand

  From Ensembl annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 7, Syntenic

Strain
Comparison

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

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_5753341	unclassified gene	Chr7:63933548-63934148 (+)
129S1/SvImJ	MGP_129S1SvImJ_G0002179	unclassified gene	Chr7:65419836-65420436 (+)
A/J	MGP_AJ_G0002155	unclassified gene	Chr7:64153850-64154450 (+)
AKR/J	MGP_AKRJ_G0002142	unclassified gene	Chr7:65508940-65509540 (+)
BALB/cJ	MGP_BALBcJ_G0002151	unclassified gene	Chr7:63894150-63894750 (+)
C3H/HeJ	MGP_C3HHeJ_G0002127	unclassified gene	Chr7:66156138-66156738 (+)
C57BL/6NJ	MGP_C57BL6NJ_G0002276	unclassified gene	Chr7:68224314-68224914 (+)
CAROLI/EiJ	MGP_CAROLIEiJ_G0001895	unclassified gene	Chr7:67099378-67099978 (+)
CAST/EiJ	MGP_CASTEiJ_G0002092	unclassified gene	Chr7:56852726-56853325 (+)
CBA/J	MGP_CBAJ_G0002121	unclassified gene	Chr7:70448829-70449429 (+)
DBA/2J	MGP_DBA2J_G0002123	unclassified gene	Chr7:62905452-62906055 (+)
FVB/NJ	MGP_FVBNJ_G0002134	unclassified gene	Chr7:63005185-63005785 (+)
LP/J	MGP_LPJ_G0002178	unclassified gene	Chr7:66652674-66653274 (+)
NOD/ShiLtJ	MGP_NODShiLtJ_G0002109	unclassified gene	Chr7:70722886-70723486 (+)
NZO/HlLtJ	MGP_NZOHlLtJ_G0002264	unclassified gene	Chr7:64791107-64791707 (+)
PWK/PhJ	MGP_PWKPhJ_G0002052	unclassified gene	Chr7:55914114-55914714 (+)
SPRET/EiJ	MGP_SPRETEiJ_G0002016	unclassified gene	Chr7:51928357-51928937 (+)
WSB/EiJ	MGP_WSBEiJ_G0002119	unclassified gene	Chr7:65174843-65175443 (+)

Homology

• Gene Tree
  Gm44765
  

Human Diseases

• References
  1 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  6 phenotype references
  

• All Mutations and Alleles
  3
• Targeted
  3
• Genomic Mutations
  3 involving Gm44765
• 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
  19

• Ensembl
  ENSMUSG00000108422 (Evidence)

Representative Sequences			Length	Strain/Species
genomic	ENSMUSG00000108422	Ensembl Gene Model | MGI Sequence Detail	601	C57BL/6J

References

• Summaries
  All 8

  Diseases 1

  Phenotypes 6
• 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