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Gm38356 Pseudogene Detail
Summary
  • Symbol
    Gm38356
  • Name
    predicted gene, 38356
Location &
Maps
more
  • Sequence Map
    Chr3:66814692-66815099 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 3, Syntenic
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    2 from dbSNP Build 142
  • Strain Annotations
    49
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_5611584
pseudogene Chr3:66814692-66815099 (-)
129S1/SvImJ ENSMUSG00200001615
pseudogene Chr3:63567830-63568237 (-)
A/J ENSMUSG00195026929
pseudogene Chr3:63683731-63684138 (-)
AKR/J ENSMUSG00220025582
pseudogene Chr3:63708894-63709301 (-)
BALB/cJ ENSMUSG00180008517
pseudogene Chr3:63735085-63735492 (-)
C3H/HeJ ENSMUSG00175003857
pseudogene Chr3:63586045-63586452 (-)
C57BL/6NJ ENSMUSG00215007684
pseudogene Chr3:64029438-64029845 (-)
CAROLI/EiJ no annotation
CAST/EiJ ENSTCUG00005034643
pseudogene Chr9:70599861-70600235 (-)
CAST/EiJ ENSTCUG00005002558
pseudogene Chr3:60420903-60421310 (-)
CAST/EiJ ENSTCUG00005027157
pseudogene Chr13:108392810-108393217 (+)
CAST/EiJ ENSTCUG00005042730
pseudogene Chr13:50892894-50893301 (-)
CAST/EiJ ENSTCUG00005034177
pseudogene Chr2:79948042-79948449 (-)
CAST/EiJ ENSTCUG00005040282
pseudogene ChrX:114929646-114930053 (-)
CAST/EiJ ENSTCUG00005025891
pseudogene Chr14:27455724-27456131 (-)
CAST/EiJ ENSTCUG00005002554
pseudogene Chr3:55678897-55679304 (-)
CAST/EiJ ENSTCUG00005052495
pseudogene Chr17:37552582-37552989 (-)
CAST/EiJ ENSTCUG00005034093
pseudogene Chr2:76711750-76712157 (-)
CAST/EiJ ENSTCUG00005023285
pseudogene Chr1:18066976-18067383 (+)
CAST/EiJ ENSTCUG00005014391
pseudogene Chr15:41744932-41745339 (+)
CBA/J ENSMUSG00210002464
pseudogene Chr3:63670154-63670561 (-)
DBA/2J ENSMUSG00185015889
pseudogene Chr3:63831820-63832227 (-)
FVB/NJ no annotation
JF1/MsJ ENSUMUG00000014640
pseudogene Chr15:14234840-14235247 (+)
JF1/MsJ ENSUMUG00000050930
pseudogene Chr8:96924512-96924919 (+)
JF1/MsJ ENSUMUG00000055772
pseudogene Chr7:8604391-8604798 (+)
JF1/MsJ ENSUMUG00000017866
pseudogene Chr8:107510589-107510996 (+)
JF1/MsJ ENSUMUG00000031676
pseudogene ChrX:37311338-37311745 (-)
JF1/MsJ ENSUMUG00000022298
pseudogene Chr14:82444306-82444713 (+)
JF1/MsJ ENSUMUG00000016261
pseudogene Chr16:71561088-71561495 (-)
JF1/MsJ ENSUMUG00000058034
pseudogene Chr17:37477809-37478216 (-)
JF1/MsJ ENSUMUG00000022380
pseudogene Chr8:119565985-119566392 (+)
JF1/MsJ ENSUMUG00000058028
pseudogene Chr17:35839258-35839665 (+)
JF1/MsJ ENSUMUG00000012265
pseudogene Chr12:16583379-16583786 (-)
JF1/MsJ ENSUMUG00000041878
pseudogene Chr13:58526720-58527127 (-)
LP/J ENSMUSG00230002693
pseudogene Chr3:65852338-65852745 (-)
NOD/ShiLtJ ENSMUSG00190003190
pseudogene Chr3:64135426-64135833 (-)
NZO/HlLtJ ENSMUSG00225002721
pseudogene Chr3:68574854-68575261 (-)
PWK/PhJ ENSLUMG00010036912
pseudogene Chr15:91325843-91326250 (+)
PWK/PhJ ENSLUMG00010011520
pseudogene Chr14:71297459-71297866 (+)
PWK/PhJ ENSLUMG00010052539
pseudogene Chr14:50375260-50375667 (+)
PWK/PhJ ENSLUMG00010052505
pseudogene Chr14:44452171-44452578 (-)
PWK/PhJ ENSLUMG00010025590
pseudogene Chr13:57189750-57190157 (-)
PWK/PhJ ENSLUMG00010007037
pseudogene Chr1:184702730-184703137 (-)
PWK/PhJ ENSLUMG00010007049
pseudogene Chr4:30990495-30990902 (+)
PWK/PhJ ENSLUMG00010000071
pseudogene Chr3:156116623-156117030 (-)
PWK/PhJ ENSLUMG00010000073
pseudogene Chr3:155669083-155669490 (-)
PWK/PhJ ENSLUMG00010037023
pseudogene Chr11:43274071-43274478 (+)
PWK/PhJ ENSLUMG00010002067
pseudogene Chr3:145382314-145382721 (+)
PWK/PhJ ENSLUMG00010012314
pseudogene Chr16:51585107-51585514 (+)
SPRET/EiJ ENSMSPG00010023221
pseudogene Chr12:111061164-111061571 (-)
WSB/EiJ no annotation



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    4 phenotype references
  • All Mutations and Alleles
    2
  • Chemically induced (other)
    1
  • Radiation induced
    1
  • Genomic Mutations
    2 involving Gm38356
  • Find Mice (IMSR)
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
Sequences &
Gene Models
less
  • All Sequences
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000103318 Ensembl Gene Model | MGI Sequence Detail 408 C57BL/6J ±  kb
transcript ENSMUST00000194313 Ensembl | MGI Sequence Detail 408 Not Applicable  
For the selected sequence
References
more
  • Summaries
    All 5
    Diseases 1
    Phenotypes 4
  • Earliest
    J:70677 Cook SA, et al., Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene. Cytogenet Cell Genet. 2001;93(1-2):77-82
  • Latest
    J:302829 Lu J, et al., Mouse models for human hyperuricaemia: a critical review. Nat Rev Rheumatol. 2019 Jul;15(7):413-426

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)
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last database update
09/15/2026
MGI 6.29
The Jackson Laboratory