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Tsix Gene Detail
Summary
  • Symbol
    Tsix
  • Name
    X (inactive)-specific transcript, opposite strand
Location &
Maps
more
  • Sequence Map
    ChrX:102475123-102528563 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome X, 46.13 cM
  • Mapping Data
    5 experiments
Strain
Comparison
more
  • SNPs within 2kb
    998 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1336196
antisense lncRNA gene ChrX:102475123-102533557 (+)
129S1/SvImJ ENSMUSG00200039083
lncRNA gene ChrX:84239351-84293665 (+)
A/J ENSMUSG00195040739
lncRNA gene ChrX:87994069-88048385 (+)
AKR/J ENSMUSG00220038391
lncRNA gene ChrX:82661538-82716036 (+)
BALB/cJ ENSMUSG00180042275
lncRNA gene ChrX:84671339-84725656 (+)
C3H/HeJ ENSMUSG00175046359
lncRNA gene ChrX:88244204-88298514 (+)
C57BL/6NJ ENSMUSG00215046285
lncRNA gene ChrX:84851522-84905595 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0004291
antisense lncRNA gene ChrX:97655913-97706496 (+)
CAST/EiJ ENSTCUG00005043289
lncRNA gene ChrX:85716208-85769135 (+)
CBA/J ENSMUSG00210046585
lncRNA gene ChrX:85134953-85189331 (+)
DBA/2J ENSMUSG00185045877
lncRNA gene ChrX:97574036-97628530 (+)
FVB/NJ ENSMUSG00205041962
lncRNA gene ChrX:84216478-84270790 (+)
JF1/MsJ ENSUMUG00000038197
lncRNA gene ChrX:118183004-118236461 (+)
LP/J ENSMUSG00230042471
lncRNA gene ChrX:104272535-104326846 (+)
NOD/ShiLtJ ENSMUSG00190038010
lncRNA gene ChrX:84292828-84347141 (+)
NZO/HlLtJ ENSMUSG00225045667
lncRNA gene ChrX:109393117-109447159 (+)
PWK/PhJ ENSLUMG00010037723
lncRNA gene ChrX:83498097-83551100 (+)
SPRET/EiJ ENSMSPG00010042858
lncRNA gene ChrX:87704313-87755360 (+)
WSB/EiJ ENSIUOG00005044261
lncRNA gene ChrX:84796146-84850600 (+)



Homology
more
  • Human Ortholog
    TSIX, TSIX transcript, XIST antisense RNA
  • Vertebrate Orthologs
    1
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    TSIX, TSIX transcript, XIST antisense RNA
  • Synonyms
    LINC00013, NCRNA00013, XIST-AS, XISTAS, XIST-AS1
  • Links
    NCBI Gene ID: 9383

  • Chr Location
    Xq13.2; chrX:73792205-73829231 (+)  GRCh38

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    24 phenotypes from 4 alleles in 4 genetic backgrounds
    17 phenotypes from multigenic genotypes
    22 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Maternal transmission of a null allele in this imprinted gene prevents Xist accumulation disrupting X-inactivation and causing early embryonic lethality.
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
  • Tissues
  • cDNA Data
  • Literature Summary
  • Comparison Matrix
  • Sequences &
    Gene Models
    less
    • All Sequences
    • RefSeq
    Representative SequencesLengthStrain/SpeciesFlank
    genomic 22097 NCBI Gene Model | MGI Sequence Detail 53441 C57BL/6J ±  kb
    transcript NR_002844 RefSeq | MGI Sequence Detail 4306 ZRU/MplStud  
    For the selected sequence
    Molecular
    Reagents
    less
    • All nucleic 12
      Genomic 1
      cDNA 4
      Primer pair 7

      Microarray probesets 1
    References
    more
    • Summaries
      All 68
      Developmental Gene Expression 13
      Phenotypes 22
    • Earliest
      J:10451 Fingeroth JD, Comparative structure and evolution of murine CR2. The homolog of the human C3d/EBV receptor (CD21). J Immunol. 1990 May 1;144(9):3458-67
    • Latest
      J:369802 Lou S, et al., Targeting microRNA-dependent control of X chromosome inactivation improves the Rett Syndrome phenotype. Nat Commun. 2025 Jul 4;16(1):6169

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