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BC065397 Gene Detail
Summary
  • Symbol
    BC065397
  • Name
    cDNA sequence BC065397
Location &
Maps
more
  • Sequence Map
    ChrX:135643706-135704113 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome X, 59.10 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    1270 from dbSNP Build 142
  • Strain Annotations
    22
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3584520
lncRNA gene ChrX:135642525-135704113 (+)
129S1/SvImJ ENSMUSG00200047544
lncRNA gene ChrX:114637916-114699462 (+)
A/J ENSMUSG00195048271
lncRNA gene ChrX:118502273-118563822 (+)
AKR/J ENSMUSG00220034040
protein coding gene ChrX:111950647-112012085 (+)
AKR/J ENSMUSG00220040565
lncRNA gene ChrX:111950671-112012216 (+)
BALB/cJ ENSMUSG00180038072
lncRNA gene ChrX:114935451-114997002 (+)
C3H/HeJ ENSMUSG00175035016
lncRNA gene ChrX:118786536-118852486 (+)
C57BL/6NJ ENSMUSG00215045370
lncRNA gene ChrX:115345215-115406760 (+)
C57BL/6NJ ENSMUSG00215044197
protein coding gene ChrX:115345191-115406629 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0013908
unclassified non-coding RNA gene ChrX:125500851-125560673 (+)
CAST/EiJ ENSTCUG00005041565
lncRNA gene ChrX:116018297-116078300 (+)
CBA/J ENSMUSG00210041762
lncRNA gene ChrX:115721524-115787463 (+)
DBA/2J ENSMUSG00185031170
lncRNA gene ChrX:129613055-129678998 (+)
FVB/NJ ENSMUSG00205026787
protein coding gene ChrX:114107806-114169252 (+)
FVB/NJ ENSMUSG00205036976
lncRNA gene ChrX:114107830-114169383 (+)
JF1/MsJ ENSUMUG00000029665
lncRNA gene ChrX:148825932-148885771 (+)
LP/J ENSMUSG00230040569
lncRNA gene ChrX:136246543-136308088 (+)
NOD/ShiLtJ ENSMUSG00190043103
lncRNA gene ChrX:115111427-115177372 (+)
NZO/HlLtJ ENSMUSG00225036981
lncRNA gene ChrX:140927021-140992979 (+)
PWK/PhJ ENSLUMG00010044030
lncRNA gene ChrX:113575606-113635512 (+)
SPRET/EiJ ENSMSPG00010039722
lncRNA gene ChrX:118139960-118199861 (+)
WSB/EiJ ENSIUOG00005039902
lncRNA gene ChrX:115780149-115846091 (+)



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    6 phenotype references
Gene Ontology
(GO)
Classifications
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Molecular Function

No experimental evidence to support Molecular Function annotation, following literature review. See J:73796.
Biological Process

No experimental evidence to support Biological Process annotation, following literature review. See J:73796.
Cellular Component

No experimental evidence to support Cellular Component annotation, following literature review. See J:73796.
Expression
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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
  • cDNA Data
Sequences &
Gene Models
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  • All Sequences
  • RefSeq
  • UniProt
Representative SequencesLengthStrain/SpeciesFlank
genomic 436230 NCBI Gene Model | MGI Sequence Detail 60408 C57BL/6J ±  kb
transcript NR_033324 RefSeq | MGI Sequence Detail 3243 C57BL/6  
polypeptide Q8BJE4 UniProt | EBI | MGI Sequence Detail 141 Not Applicable  
For the selected sequence
Protein
Information
less
  • UniProt
    1 Sequence
Molecular
Reagents
less
  • All nucleic 4
    cDNA 4

    Microarray probesets 1
Other
Accession IDs
less
MGI:2148084
References
more
  • Summaries
    All 18
    Diseases 1
    Phenotypes 6
  • Earliest
    J:86696 Zambrowicz BP, et al., Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention. Proc Natl Acad Sci U S A. 2003 Nov 25;100(24):14109-14
  • Latest
    J:199809 Clark K, et al., Gait abnormalities and progressive myelin degeneration in a new murine model of pelizaeus-merzbacher disease with tandem genomic duplication. J Neurosci. 2013 Jul 17;33(29):11788-99

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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Funding Information
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last database update
09/08/2026
MGI 6.24
The Jackson Laboratory