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Gm11507 Pseudogene Detail
Summary
  • Symbol
    Gm11507
  • Name
    predicted gene 11507
  • Feature Type
    pseudogene
  • IDs
    MGI:3650927
    NCBI Gene: 574528
  • Alliance
    gene page
Location &
Maps
more
  • 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
more
  • SNPs within 2kb
    79 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
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
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    4 phenotype references
Expression
less
Expression Overview

early conceptus
embryo ectoderm
embryo endoderm
embryo mesoderm
embryo mesenchyme
extraembryonic component
alimentary system
auditory system
branchial arches
cardiovascular system
connective tissue
endocrine system
exocrine system
hemolymphoid system
integumental system
limbs
liver and biliary system
musculoskeletal system
nervous system
olfactory system
reproductive system
respiratory system
urinary system
visual system
Click cells to view annotations.


  • Assay Results
    706
Sequences &
Gene Models
less
  • All Sequences
    22
  • RefSeq
    1
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000044639 Ensembl Gene Model | MGI Sequence Detail 412 C57BL/6J ±  kb
transcript ENSMUST00000156462 Ensembl | MGI Sequence Detail 412 Not Applicable  
For the selected sequence
References
more
  • 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
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
05/07/2024
MGI 6.23 		The Jackson Laboratory