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Gm4950 Pseudogene Detail
Summary
  • Symbol
    Gm4950
  • Name
    predicted pseudogene 4950
  • Feature Type
    pseudogene
  • IDs
    MGI:3649015
    NCBI Gene: 240289
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    Chr18:51998339-51998953 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 18, 28.10 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    24 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3649015
 pseudogene Chr18:51998253-51998990 (-)
129S1/SvImJ MGP_129S1SvImJ_G0024425
 protein coding gene Chr18:50991301-50993132 (-)
A/J MGP_AJ_G0024391
 protein coding gene Chr18:49006127-49006744 (-)
AKR/J MGP_AKRJ_G0024361
 protein coding gene Chr18:50393926-50394543 (-)
BALB/cJ MGP_BALBcJ_G0024391
 protein coding gene Chr18:49183614-49184231 (-)
C3H/HeJ MGP_C3HHeJ_G0024158
 protein coding gene Chr18:50522359-50522976 (-)
C57BL/6NJ MGP_C57BL6NJ_G0024837
 protein coding gene Chr18:52680765-52682004 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0022006
 protein coding gene Chr18:8957968-8958588 (+)
CAST/EiJ MGP_CASTEiJ_G0032942
 protein coding gene Chr8:89372696-89373413 (-)
CBA/J MGP_CBAJ_G0024128
 protein coding gene Chr18:54236714-54237814 (-)
DBA/2J MGP_DBA2J_G0024258
 protein coding gene Chr18:48696746-48697363 (-)
FVB/NJ MGP_FVBNJ_G0024225
 protein coding gene Chr18:48174173-48175973 (-)
LP/J MGP_LPJ_G0024343
 protein coding gene Chr18:51013061-51013667 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0024255
 protein coding gene Chr18:55977862-55978479 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0024884
 protein coding gene Chr18:50377567-50378184 (-)
PWK/PhJ MGP_PWKPhJ_G0023376
 protein coding gene Chr18:48751777-48752617 (-)
SPRET/EiJ MGP_SPRETEiJ_G0023182
 protein coding gene Chr18:50558872-50559489 (-)
WSB/EiJ MGP_WSBEiJ_G0033054
 protein coding gene Chr8:89783906-89784423 (-)



Homology
less
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    1 phenotype reference
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 ENSMUSG00000069379 Ensembl Gene Model | MGI Sequence Detail 615 C57BL/6J ±  kb
transcript ENSMUST00000091905 Ensembl | MGI Sequence Detail 615 Not Applicable  
For the selected sequence
References
more
  • Summaries
    All 5
    Phenotypes 1
  • Earliest
    J:327181 Lewis MA, et al., Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme. BMC Biol. 2022 Mar 17;20(1):67
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
04/23/2024
MGI 6.23 		The Jackson Laboratory