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A930018P22Rik Gene Detail
Summary
  • Symbol
    A930018P22Rik
  • Name
    RIKEN cDNA A930018P22 gene
  • Feature Type
    protein coding gene
  • IDs
    MGI:1915493
    NCBI Gene: 68243
  • Alliance
  • Transcription Start Sites
    4 TSS
Location &
Maps
more
  • Sequence Map
    Chr2:103953114-103955091 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 2, 54.56 cM, cytoband E3
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    118 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1915493
protein coding gene Chr2:103953114-103955094 (+)
129S1/SvImJ ENSMUSG00200002020
protein coding gene Chr2:100763141-100765124 (+)
A/J ENSMUSG00195000650
protein coding gene Chr2:100931459-100933442 (+)
AKR/J ENSMUSG00220001570
protein coding gene Chr2:100681572-100683555 (+)
BALB/cJ ENSMUSG00180020019
protein coding gene Chr2:100732528-100734511 (+)
C3H/HeJ ENSMUSG00175009605
protein coding gene Chr2:101012521-101014504 (+)
C57BL/6NJ ENSMUSG00215013041
protein coding gene Chr2:100837184-100839164 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0024023
protein coding gene Chr2:97589381-97591360 (+)
CAST/EiJ ENSTCUG00005001558
protein coding gene Chr2:100096770-100098757 (+)
CBA/J ENSMUSG00210038416
protein coding gene Chr2:101010321-101012304 (+)
DBA/2J ENSMUSG00185005534
protein coding gene Chr2:100729342-100731325 (+)
FVB/NJ ENSMUSG00205009745
protein coding gene Chr2:100063768-100065748 (+)
JF1/MsJ ENSUMUG00000021370
protein coding gene Chr2:100424635-100426610 (+)
LP/J ENSMUSG00230005952
protein coding gene Chr2:102478666-102480649 (+)
NOD/ShiLtJ ENSMUSG00190022226
protein coding gene Chr2:100843863-100845843 (+)
NZO/HlLtJ ENSMUSG00225007994
protein coding gene Chr2:110385824-110387807 (+)
PWK/PhJ ENSLUMG00010023935
protein coding gene Chr2:100433584-100435559 (+)
SPRET/EiJ ENSMSPG00010033069
protein coding gene Chr2:102461524-102463505 (+)
WSB/EiJ ENSIUOG00005001358
protein coding gene Chr2:100528542-100530522 (+)



Homology
more
  • Human Ortholog
    C11orf91, chromosome 11 open reading frame 91
  • Vertebrate Orthologs
    2
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    C11orf91, chromosome 11 open reading frame 91
  • Links
    NCBI Gene ID: 100131378
    UniProt: Q3C1V1

  • Chr Location
    11p13; chr11:33698261-33706550 (-)  GRCh38

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    7 phenotype references
  • All Mutations and Alleles
    7
  • Chemically induced (other)
    1
  • Endonuclease-mediated
    1
  • Gene trapped
    3
  • Radiation induced
    1
  • Targeted
    1
  • Genomic Mutations
    2 involving A930018P22Rik
  • Incidental Mutations
  • Find Mice (IMSR)
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

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
Representative SequencesLengthStrain/SpeciesFlank
genomic 68243 NCBI Gene Model | MGI Sequence Detail 1978 C57BL/6J ±  kb
transcript NM_026634 RefSeq | MGI Sequence Detail 819 C57BL/6  
polypeptide Q9D1Z2 UniProt | EBI | MGI Sequence Detail 194 Not Applicable  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 5
    cDNA 5

    Microarray probesets 3
References
more
  • Summaries
    All 23
    Phenotypes 7
  • Earliest
    J:109968 Roderick TH, et al., Nineteen paracentric chromosomal inversions in mice. Genetics. 1974 Jan;76(1):109-17
  • Latest
    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

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
09/08/2026
MGI 6.24
The Jackson Laboratory