Gm44627 Gene Detail

Summary

• Symbol
  Gm44627
• Name
  predicted gene 44627

• Feature Type
  unclassified gene
• IDs
  MGI:5753203
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Chr7:63598426-63599956 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
  46 from dbSNP Build 142
• Strain Annotations
  18

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_5753203	unclassified gene	Chr7:63598426-63599956 (+)
129S1/SvImJ	MGP_129S1SvImJ_G0002176	unclassified gene	Chr7:65067963-65069493 (+)
A/J	MGP_AJ_G0002152	unclassified gene	Chr7:63823523-63825053 (+)
AKR/J	MGP_AKRJ_G0002139	unclassified gene	Chr7:65169922-65171452 (+)
BALB/cJ	MGP_BALBcJ_G0002148	unclassified gene	Chr7:63561299-63562827 (+)
C3H/HeJ	MGP_C3HHeJ_G0002124	unclassified gene	Chr7:65821004-65822578 (+)
C57BL/6NJ	MGP_C57BL6NJ_G0002273	unclassified gene	Chr7:67874409-67875939 (+)
CAROLI/EiJ	MGP_CAROLIEiJ_G0001892	unclassified gene	Chr7:66780793-66782325 (+)
CAST/EiJ	MGP_CASTEiJ_G0002089	unclassified gene	Chr7:56485221-56486734 (+)
CBA/J	MGP_CBAJ_G0002118	unclassified gene	Chr7:70056658-70058188 (+)
DBA/2J	MGP_DBA2J_G0002120	unclassified gene	Chr7:62559986-62561536 (+)
FVB/NJ	MGP_FVBNJ_G0002131	unclassified gene	Chr7:62661389-62662919 (+)
LP/J	MGP_LPJ_G0002175	unclassified gene	Chr7:66303300-66304827 (+)
NOD/ShiLtJ	MGP_NODShiLtJ_G0002106	unclassified gene	Chr7:70344834-70346364 (+)
NZO/HlLtJ	MGP_NZOHlLtJ_G0002261	unclassified gene	Chr7:64435384-64436925 (+)
PWK/PhJ	MGP_PWKPhJ_G0002049	unclassified gene	Chr7:55567487-55569165 (+)
SPRET/EiJ	MGP_SPRETEiJ_G0002013	unclassified gene	Chr7:51577798-51579334 (+)
WSB/EiJ	MGP_WSBEiJ_G0002116	unclassified gene	Chr7:64822896-64824425 (+)

Homology

• Gene Tree
  Gm44627
  

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 Gm44627
• 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
  ENSMUSG00000108418 (Evidence)

Representative Sequences			Length	Strain/Species
genomic	ENSMUSG00000108418	Ensembl Gene Model | MGI Sequence Detail	1531	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