Gm11507 Pseudogene Detail

Summary

• Symbol
  Gm11507
• Name
  predicted gene 11507

• Feature Type
  pseudogene
• IDs
  MGI:3650927
  NCBI Gene: 574528
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Chr11:87835229-87835640 bp, + strand

  From Ensembl annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 11, 52.32 cM

Strain
Comparison

• SNPs within 2kb
  88 from dbSNP Build 142
• Strain Annotations
  18

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_3650927	pseudogene	Chr11:87835049-87835640 (+)
129S1/SvImJ	MGP_129S1SvImJ_G0010811	pseudogene	Chr11:89605524-89605935 (+)
A/J	MGP_AJ_G0010809	pseudogene	Chr11:86146270-86146681 (+)
AKR/J	MGP_AKRJ_G0010768	pseudogene	Chr11:88755963-88756374 (+)
BALB/cJ	MGP_BALBcJ_G0010785	pseudogene	Chr11:86548508-86548919 (+)
C3H/HeJ	MGP_C3HHeJ_G0010691	pseudogene	Chr11:88781771-88782182 (+)
C57BL/6NJ	MGP_C57BL6NJ_G0011058	pseudogene	Chr11:92334011-92334422 (+)
CAROLI/EiJ	MGP_CAROLIEiJ_G0009675	pseudogene	Chr11:83164772-83165183 (+)
CAST/EiJ	MGP_CASTEiJ_G0010514	pseudogene	Chr11:89467092-89467503 (+)
CBA/J	MGP_CBAJ_G0010664	pseudogene	Chr11:96221185-96221596 (+)
DBA/2J	MGP_DBA2J_G0010705	pseudogene	Chr11:85706880-85707291 (+)
FVB/NJ	MGP_FVBNJ_G0010722	pseudogene	Chr11:85200352-85200763 (+)
LP/J	MGP_LPJ_G0010794	pseudogene	Chr11:90121796-90122207 (+)
NOD/ShiLtJ	MGP_NODShiLtJ_G0010696	pseudogene	Chr11:96262156-96262567 (+)
NZO/HlLtJ	MGP_NZOHlLtJ_G0011036	pseudogene	Chr11:88973889-88974300 (+)
PWK/PhJ	MGP_PWKPhJ_G0010403	pseudogene	Chr11:86550567-86550978 (+)
SPRET/EiJ	MGP_SPRETEiJ_G0010219	pseudogene	Chr11:88534117-88534526 (+)
WSB/EiJ	MGP_WSBEiJ_G0010567	pseudogene	Chr11:88863280-88863691 (+)

Homology

• Gene Tree
  Gm11507
  

Human Diseases

• References
  1 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  4 phenotype references
  

• All Mutations and Alleles
  3
• Chemically induced (other)
  1
• Targeted
  2
• Genomic Mutations
  3 involving Gm11507
• Find Mice (IMSR)
  0 strains or lines available

Expression

• Assay Results
  706

Tissue x Stage Matrix

• Other Mouse Links
  GEO
  Expression Atlas

Sequences &
Gene Models

• All Sequences
  22
• RefSeq
  1

• Ensembl
  ENSMUSG00000044639 (Evidence)
• NCBI Gene
  574528

Representative Sequences			Length	Strain/Species
genomic	ENSMUSG00000044639	Ensembl Gene Model | MGI Sequence Detail	412	C57BL/6J
transcript	ENSMUST00000156462	Ensembl | MGI Sequence Detail	412	Not Applicable

References

• Summaries
  All 9

  Diseases 1

  Phenotypes 4
• Earliest
  J:137335 Roderick TH, Chromosomal inversions in studies of mammalian mutagenesis. Genetics. 1979 May;92(1 Pt 1 Suppl):s121-6
• Latest
  J:109163 Yu YE, et al., A deficiency in the region homologous to human 17q21.33-q23.2 causes heart defects in mice. Genetics. 2006 May;173(1):297-307