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D030056L22Rik Gene Detail
Summary
  • Symbol
    D030056L22Rik
  • Name
    RIKEN cDNA D030056L22 gene
  • Feature Type
    protein coding gene
  • IDs
    MGI:3583960
    NCBI Gene: 225995
  • Alliance
  • Transcription Start Sites
    3 TSS
Location &
Maps
more
  • Sequence Map
    Chr19:18690599-18695793 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 19, 13.20 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    230 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3583960
protein coding gene Chr19:18690557-18695793 (+)
129S1/SvImJ ENSMUSG00200019889
protein coding gene Chr19:15371705-15376931 (+)
A/J ENSMUSG00195017422
protein coding gene Chr19:15526628-15531841 (+)
AKR/J ENSMUSG00220010380
protein coding gene Chr19:15505142-15510373 (+)
BALB/cJ ENSMUSG00180018182
protein coding gene Chr19:15895661-15900881 (+)
C3H/HeJ ENSMUSG00175003718
protein coding gene Chr19:15234924-15240137 (+)
C57BL/6NJ ENSMUSG00215013722
protein coding gene Chr19:15296913-15302148 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0022806
protein coding gene Chr19:16030967-16036180 (+)
CAST/EiJ ENSTCUG00005008315
protein coding gene Chr19:15139067-15144296 (+)
CBA/J ENSMUSG00210012623
protein coding gene Chr19:15469445-15474658 (+)
DBA/2J ENSMUSG00185013548
protein coding gene Chr19:15884740-15889960 (+)
FVB/NJ ENSMUSG00205003660
protein coding gene Chr19:15295632-15300862 (+)
JF1/MsJ ENSUMUG00000017402
protein coding gene Chr19:16128093-16133304 (+)
LP/J ENSMUSG00230015760
protein coding gene Chr19:16740884-16746110 (+)
NOD/ShiLtJ ENSMUSG00190019222
protein coding gene Chr19:15250096-15255309 (+)
NZO/HlLtJ no annotation
PWK/PhJ ENSLUMG00010008426
protein coding gene Chr19:15445930-15451139 (+)
SPRET/EiJ ENSMSPG00010017880
protein coding gene Chr19:15445388-15449623 (+)
WSB/EiJ ENSIUOG00005006872
protein coding gene Chr19:14972441-14977669 (+)



Homology
more
  • Human Ortholog
    C9orf40, chromosome 9 open reading frame 40
  • Vertebrate Orthologs
    2
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    C9orf40, chromosome 9 open reading frame 40
  • Links
    NCBI Gene ID: 55071
    UniProt: Q8IXQ3

  • Chr Location
    9q21.13; chr9:74946583-74952912 (-)  GRCh38

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    3 phenotypes from 1 allele in 1 genetic background
    6 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.
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
  • Comparison Matrix
  • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic 225995 NCBI Gene Model | MGI Sequence Detail 5195 C57BL/6J ±  kb
    transcript NM_001374130 RefSeq | MGI Sequence Detail 1636 C57BL/6  
    polypeptide Q8VCE4 UniProt | EBI | MGI Sequence Detail 163 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 34
      cDNA 34

      Microarray probesets 3
    References
    more
    • Summaries
      All 24
      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:153498 Diez-Roux G, et al., A high-resolution anatomical atlas of the transcriptome in the mouse embryo. PLoS Biol. 2011;9(1):e1000582

    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