Gm8996 Pseudogene Detail

Summary

• Symbol
  Gm8996
• Name
  predicted gene 8996

• Feature Type
  pseudogene
• IDs
  MGI:3647165
  NCBI Gene: 668140
• Alliance
  gene page
• Transcription Start Sites
  1 TSS

Location &
Maps

• Sequence Map
  Chr14:57454690-57455099 bp, + strand

  From NCBI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 14, 30.10 cM
• Mapping Data
  1 experiment

Strain
Comparison

• SNPs within 2kb
  116 from dbSNP Build 142
• Strain Annotations
  1

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_3647165	pseudogene	Chr14:57454690-57455099 (+)
129S1/SvImJ	no annotation
A/J	no annotation
AKR/J	no annotation
BALB/cJ	no annotation
C3H/HeJ	no annotation
C57BL/6NJ	no annotation
CAROLI/EiJ	no annotation
CAST/EiJ	no annotation
CBA/J	no annotation
DBA/2J	no annotation
FVB/NJ	no annotation
LP/J	no annotation
NOD/ShiLtJ	no annotation
NZO/HlLtJ	no annotation
PWK/PhJ	no annotation
SPRET/EiJ	no annotation
WSB/EiJ	no annotation

Homology

• Gene Tree
  Gm8996
  

Human Diseases

• References
  1 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  3 phenotype references
  

• All Mutations and Alleles
  2
• Chemically induced (other)
  1
• Endonuclease-mediated
  1
• Genomic Mutations
  2 involving Gm8996
• 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
  4

• Ensembl
  ENSMUSG00000114754 (Evidence)
• NCBI Gene
  668140

Representative Sequences			Length	Strain/Species
genomic	668140	NCBI Gene Model | MGI Sequence Detail	410	C57BL/6J

References

• Summaries
  All 7

  Diseases 1

  Phenotypes 3
• Earliest
  J:23389 Roderick TH, Using inversions to detect and study recessive lethals and detrimentals in mice, in Utilization of Mammalian Specific Locus Studies in Hazard Evaluation and Estimation of Genetic Risk. 1983:135-67.
• Latest
  J:345081 Dominguez-Ruiz M, et al., A Murine Model for the del(GJB6-D13S1830) Deletion Recapitulating the Phenotype of Human DFNB1 Hearing Impairment: Generation and Functional and Histopathological Study. 2024;

TSS for Gm8996:

(View these features in JBrowse)

Transcription Start Site	Location	Distance from Gene 5'-end
Tssr125866	Chr14:57454665-57454675 (+)	-20 bp