Gm44719 Gene Detail

Summary

• Symbol
  Gm44719
• Name
  predicted gene 44719

• Feature Type
  unclassified gene
• IDs
  MGI:5753295
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Chr7:63862938-63863086 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
  102 from dbSNP Build 142
• Strain Annotations
  18

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_5753295	unclassified gene	Chr7:63862938-63863086 (+)
129S1/SvImJ	MGP_129S1SvImJ_G0002178	unclassified gene	Chr7:65343326-65343478 (+)
A/J	MGP_AJ_G0002154	unclassified gene	Chr7:64083191-64083339 (+)
AKR/J	MGP_AKRJ_G0002141	unclassified gene	Chr7:65437866-65438018 (+)
BALB/cJ	MGP_BALBcJ_G0002150	unclassified gene	Chr7:63822409-63822848 (+)
C3H/HeJ	MGP_C3HHeJ_G0002126	unclassified gene	Chr7:66084564-66084716 (+)
C57BL/6NJ	MGP_C57BL6NJ_G0002275	unclassified gene	Chr7:68150084-68150232 (+)
CAROLI/EiJ	MGP_CAROLIEiJ_G0001894	unclassified gene	Chr7:67031489-67031633 (+)
CAST/EiJ	MGP_CASTEiJ_G0002091	unclassified gene	Chr7:56780028-56780177 (+)
CBA/J	MGP_CBAJ_G0002120	unclassified gene	Chr7:70376436-70376588 (+)
DBA/2J	MGP_DBA2J_G0002122	unclassified gene	Chr7:62833548-62833701 (+)
FVB/NJ	MGP_FVBNJ_G0002133	unclassified gene	Chr7:62933862-62934010 (+)
LP/J	MGP_LPJ_G0002177	unclassified gene	Chr7:66573820-66573968 (+)
NOD/ShiLtJ	MGP_NODShiLtJ_G0002108	unclassified gene	Chr7:70646205-70646357 (+)
NZO/HlLtJ	MGP_NZOHlLtJ_G0002263	unclassified gene	Chr7:64718742-64718891 (+)
PWK/PhJ	MGP_PWKPhJ_G0002051	unclassified gene	Chr7:55842193-55842346 (+)
SPRET/EiJ	MGP_SPRETEiJ_G0002015	unclassified gene	Chr7:51853360-51853512 (+)
WSB/EiJ	MGP_WSBEiJ_G0002118	unclassified gene	Chr7:65099823-65099972 (+)

Homology

• Gene Tree
  Gm44719
  

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 Gm44719
• 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
  ENSMUSG00000108770 (Evidence)

Representative Sequences			Length	Strain/Species
genomic	ENSMUSG00000108770	Ensembl Gene Model | MGI Sequence Detail	149	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