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1700122H20Rik Gene Detail
Summary
  • Symbol
    1700122H20Rik
  • Name
    RIKEN cDNA 1700122H20 gene
  • Synonyms
    Gm29205
  • Feature Type
    lncRNA gene
  • IDs
    MGI:1920867
    NCBI Gene: 73617
  • Alliance
  • Transcription Start Sites
    1 TSS
Location &
Maps
more
  • Sequence Map
    Chr17:7163339-7169117 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 17, 4.51 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    109 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1920867
lncRNA gene Chr17:7160763-7169284 (+)
129S1/SvImJ ENSMUSG00200034872
lncRNA gene Chr17:3628187-3634464 (+)
A/J ENSMUSG00195024247
lncRNA gene Chr17:3593091-3599067 (+)
AKR/J ENSMUSG00220028045
lncRNA gene Chr17:3762420-3768180 (+)
BALB/cJ ENSMUSG00180028165
lncRNA gene Chr17:4300785-4300871 (-)
C3H/HeJ ENSMUSG00175035317
lncRNA gene Chr17:3383734-3389705 (+)
C57BL/6NJ ENSMUSG00215032774
lncRNA gene Chr17:3662796-3668583 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0002989
antisense lncRNA gene Chr17:3417441-3423004 (+)
CAST/EiJ ENSTCUG00005022512
lncRNA gene Chr17:3601707-3607842 (+)
CBA/J ENSMUSG00210040059
lncRNA gene Chr17:4112733-4112819 (-)
DBA/2J ENSMUSG00185024456
lncRNA gene Chr17:4143313-4149284 (+)
FVB/NJ ENSMUSG00205010104
lncRNA gene Chr17:3708554-3714528 (+)
JF1/MsJ ENSUMUG00000037552
lncRNA gene Chr17:3729197-3735335 (+)
LP/J ENSMUSG00230035146
lncRNA gene Chr17:5549404-5555162 (+)
NOD/ShiLtJ ENSMUSG00190038182
lncRNA gene Chr17:4606674-4612646 (-)
NZO/HlLtJ ENSMUSG00225029141
lncRNA gene Chr17:7500255-7506017 (+)
PWK/PhJ ENSLUMG00010020030
lncRNA gene Chr17:3762046-3768020 (+)
SPRET/EiJ no annotation
WSB/EiJ ENSIUOG00005014622
lncRNA gene Chr17:3621679-3627293 (+)



Homology
less
Human Diseases
less
  • References
    6 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    372 phenotype references
Gene Ontology
(GO)
Classifications
less
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
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
  • cDNA Data
Sequences &
Gene Models
less
  • All Sequences
  • RefSeq
Representative SequencesLengthStrain/SpeciesFlank
genomic 73617 NCBI Gene Model | MGI Sequence Detail 5779 C57BL/6J ±  kb
transcript NR_152131 RefSeq | MGI Sequence Detail 421 C57BL/6  
For the selected sequence
Molecular
Reagents
less
  • All nucleic 1
    cDNA 1
Other
Accession IDs
less
MGI:5579911
References
more
  • Summaries
    All 382
    Diseases 6
    Phenotypes 372
  • Earliest
    J:30229 Davisson MT, et al., Segmental trisomy as a mouse model for Down syndrome. Prog Clin Biol Res. 1993;384:117-33
  • Latest
    J:391449 Thibodeau J, et al., Loss of cystathionine-beta-synthase contributes to elevated OXPHOS, a vulnerability in Ara-C-resistant Myeloid Leukemia in Down syndrome. Biochem Pharmacol. 2026 Feb 13;247:117815

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