Gm6207 Pseudogene Detail

Summary

• Symbol
  Gm6207
• Name
  predicted gene 6207

• Feature Type
  pseudogene
• IDs
  MGI:3645256
  NCBI Gene: 621246
• Alliance
  genome feature page

Location &
Maps

• Sequence Map
  ChrX:134020709-134023732 bp, - strand

  From NCBI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome X, 56.57 cM
• Mapping Data
  1 experiment

Strain
Comparison

• SNPs within 2kb
  7 from dbSNP Build 142
• Strain Annotations
  13

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_3645256	pseudogene	ChrX:134020709-134023733 (-)
129S1/SvImJ	no annotation
A/J	no annotation
AKR/J	ENSMUSG00220013347	pseudogene	ChrX:110728973-110731995 (+)
BALB/cJ	ENSMUSG00180039152	pseudogene	ChrX:113740444-113743456 (+)
C3H/HeJ	ENSMUSG00175033606	pseudogene	ChrX:117675589-117678600 (+)
C57BL/6NJ	ENSMUSG00215045348	pseudogene	ChrX:113723731-113726756 (-)
CAROLI/EiJ	no annotation
CAST/EiJ	ENSTCUG00005040661	pseudogene	ChrX:114544690-114547648 (-)
CBA/J	no annotation
DBA/2J	ENSMUSG00185030402	pseudogene	ChrX:128073600-128076627 (-)
FVB/NJ	ENSMUSG00205034688	pseudogene	ChrX:112734302-112737324 (-)
JF1/MsJ	ENSUMUG00000030871	pseudogene	ChrX:147191922-147194908 (-)
LP/J	ENSMUSG00230040834	pseudogene	ChrX:134762165-134765192 (-)
NOD/ShiLtJ	ENSMUSG00190041449	pseudogene	ChrX:113573327-113576350 (-)
NZO/HlLtJ	no annotation
PWK/PhJ	ENSLUMG00010044894	pseudogene	ChrX:111844987-111847976 (-)
SPRET/EiJ	no annotation
WSB/EiJ	ENSIUOG00005038609	pseudogene	ChrX:114276356-114279399 (-)

Homology

• Gene Tree
  Gm6207
  

Human Diseases

• References
  1 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  2 phenotype references
  

• All Mutations and Alleles
  1
• Targeted
  1
• Genomic Mutations
  1 involving Gm6207
• Find Mice (IMSR)
  0 strains or lines available

Expression

• Assay Results
  597

Tissue x Stage Matrix

• Other Mouse Links
  Expression Atlas

Sequences &
Gene Models

• All Sequences
  17
• RefSeq
  1

• Ensembl
  ENSMUSG00000081146 (Evidence)
• NCBI Gene
  621246

Representative Sequences			Length	Strain/Species
genomic	621246	NCBI Gene Model | MGI Sequence Detail	3024	C57BL/6J

References

• Summaries
  All 7

  Diseases 1

  Phenotypes 2
• Earliest
  J:199138 Zhou J, et al., A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male mice. Biol Reprod. 2013 Jun;88(6):159
• Latest
  J:210663 Zhou J, et al., Respiratory failure, cleft palate and epilepsy in the mouse model of human Xq22.1 deletion syndrome. Hum Mol Genet. 2014 Jul 15;23(14):3823-9