Gm44718 Gene Detail

Summary

• Symbol
  Gm44718
• Name
  predicted gene 44718

• Feature Type
  lncRNA gene
• IDs
  MGI:5753294
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Chr7:63415622-63415980 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
  32 from dbSNP Build 142
• Strain Annotations
  18

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_5753294	lncRNA gene	Chr7:63415622-63415980 (+)
129S1/SvImJ	MGP_129S1SvImJ_G0002175	unclassified gene	Chr7:64867096-64867454 (+)
A/J	MGP_AJ_G0002151	unclassified gene	Chr7:63642132-63642490 (+)
AKR/J	MGP_AKRJ_G0002138	unclassified gene	Chr7:64981261-64981619 (+)
BALB/cJ	MGP_BALBcJ_G0002147	unclassified gene	Chr7:63378622-63378980 (+)
C3H/HeJ	MGP_C3HHeJ_G0002123	unclassified gene	Chr7:65623333-65623691 (+)
C57BL/6NJ	MGP_C57BL6NJ_G0002272	unclassified gene	Chr7:67659091-67659449 (+)
CAROLI/EiJ	MGP_CAROLIEiJ_G0001891	unclassified gene	Chr7:66603175-66603532 (+)
CAST/EiJ	MGP_CASTEiJ_G0002088	unclassified gene	Chr7:56284894-56285252 (+)
CBA/J	MGP_CBAJ_G0002117	unclassified gene	Chr7:69841079-69841437 (+)
DBA/2J	MGP_DBA2J_G0002119	unclassified gene	Chr7:62379310-62379671 (+)
FVB/NJ	MGP_FVBNJ_G0002130	unclassified gene	Chr7:62475492-62475850 (+)
LP/J	MGP_LPJ_G0002174	unclassified gene	Chr7:66104887-66105245 (+)
NOD/ShiLtJ	MGP_NODShiLtJ_G0002105	unclassified gene	Chr7:70157218-70157576 (+)
NZO/HlLtJ	MGP_NZOHlLtJ_G0002260	unclassified gene	Chr7:64235787-64236145 (+)
PWK/PhJ	MGP_PWKPhJ_G0002048	unclassified gene	Chr7:55388555-55388914 (+)
SPRET/EiJ	MGP_SPRETEiJ_G0002012	unclassified gene	Chr7:51385468-51385827 (+)
WSB/EiJ	MGP_WSBEiJ_G0002115	unclassified gene	Chr7:64631653-64632011 (+)

Homology

• Gene Tree
  Gm44718
  

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 Gm44718
• 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
  20

• Ensembl
  ENSMUSG00000108421 (Evidence)

Representative Sequences			Length	Strain/Species
genomic	ENSMUSG00000108421	Ensembl Gene Model | MGI Sequence Detail	359	C57BL/6J
transcript	ENSMUST00000206886	Ensembl | MGI Sequence Detail	359	Not Applicable

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