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Gm11512 Pseudogene Detail
Summary
  • Symbol
    Gm11512
  • Name
    predicted gene 11512
  • Feature Type
    pseudogene
  • IDs
    MGI:3649366
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    Chr11:90429310-90429972 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 11, 55.05 cM
Strain
Comparison
more
  • SNPs within 2kb
    164 from dbSNP Build 142
  • Strain Annotations
    17
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3649366
 pseudogene Chr11:90429310-90429972 (-)
129S1/SvImJ MGP_129S1SvImJ_G0010815
 pseudogene Chr11:92376006-92376668 (-)
A/J MGP_AJ_G0010813
 pseudogene Chr11:88760670-88761332 (-)
AKR/J MGP_AKRJ_G0010772
 pseudogene Chr11:91490425-91491087 (-)
BALB/cJ MGP_BALBcJ_G0010789
 pseudogene Chr11:89205388-89206050 (-)
C3H/HeJ MGP_C3HHeJ_G0010695
 pseudogene Chr11:91514103-91514765 (-)
C57BL/6NJ MGP_C57BL6NJ_G0011062
 pseudogene Chr11:95276217-95276879 (-)
CAROLI/EiJ no annotation
CAST/EiJ MGP_CASTEiJ_G0010517
 pseudogene Chr11:92250092-92250754 (-)
CBA/J MGP_CBAJ_G0011390
 pseudogene Chr2:21684335-21684988 (-)
DBA/2J MGP_DBA2J_G0010709
 pseudogene Chr11:88305898-88307007 (-)
FVB/NJ MGP_FVBNJ_G0010726
 pseudogene Chr11:87817991-87818653 (-)
LP/J MGP_LPJ_G0010798
 pseudogene Chr11:92888320-92895669 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0010700
 pseudogene Chr11:99099916-99100578 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0011040
 pseudogene Chr11:91743545-91744207 (-)
PWK/PhJ MGP_PWKPhJ_G0010406
 pseudogene Chr11:89206459-89207121 (-)
SPRET/EiJ MGP_SPRETEiJ_G0010222
 pseudogene Chr11:91297062-91297968 (-)
WSB/EiJ MGP_WSBEiJ_G0010571
 pseudogene Chr11:91602028-91602783 (-)



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
    19
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000081043 Ensembl Gene Model | MGI Sequence Detail 663 C57BL/6J ±  kb
transcript ENSMUST00000119669 Ensembl | MGI Sequence Detail 663 Not Applicable  
For the selected sequence
References
more
  • Summaries
    All 7
    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
12/10/2024
MGI 6.24 		The Jackson Laboratory