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2610028H24Rik Gene Detail
Summary
  • Symbol
    2610028H24Rik
  • Name
    RIKEN cDNA 2610028H24 gene
  • Synonyms
    ORF67
  • Feature Type
    protein coding gene
  • IDs
    MGI:1924214
    NCBI Gene: 76964
  • Alliance
    genome feature page
  • Transcription Start Sites
    6 TSS
Location &
Maps
more
  • Sequence Map
    Chr10:76284915-76296944 bp, + strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 10, 38.84 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    487 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1924214
 protein coding gene Chr10:76284883-76297052 (+)
129S1/SvImJ ENSMUSG00200041311
 protein coding gene Chr10:72962044-72974076 (+)
A/J ENSMUSG00195046901
 protein coding gene Chr10:73298669-73310697 (+)
AKR/J ENSMUSG00220038449
 protein coding gene Chr10:72958383-72970413 (+)
BALB/cJ ENSMUSG00180047577
 protein coding gene Chr10:73313119-73325142 (+)
C3H/HeJ ENSMUSG00175050160
 protein coding gene Chr10:73184399-73196431 (+)
C57BL/6NJ ENSMUSG00215051491
 protein coding gene Chr10:72922034-72934061 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0015467
 protein coding gene Chr10:70484334-70502758 (+)
CAST/EiJ ENSTCUG00005049855
 protein coding gene Chr10:72804632-72816683 (+)
CBA/J ENSMUSG00210049654
 protein coding gene Chr10:73040599-73052629 (+)
DBA/2J ENSMUSG00185051951
 protein coding gene Chr10:73382864-73394895 (+)
FVB/NJ ENSMUSG00205049419
 protein coding gene Chr10:73075534-73087564 (+)
JF1/MsJ ENSUMUG00000041060
 protein coding gene Chr10:74531470-74545230 (+)
LP/J ENSMUSG00230050091
 protein coding gene Chr10:75152416-75164445 (+)
NOD/ShiLtJ ENSMUSG00190042245
 protein coding gene Chr10:73360367-73372394 (+)
NZO/HlLtJ ENSMUSG00225046172
 protein coding gene Chr10:79449114-79461143 (+)
PWK/PhJ ENSLUMG00010048886
 protein coding gene Chr10:72921826-72935548 (+)
SPRET/EiJ ENSMSPG00010035008
 protein coding gene Chr10:74715104-74723925 (+)
WSB/EiJ ENSIUOG00005047125
 protein coding gene Chr10:72964993-72977048 (+)



Homology
more
  • Human Ortholog
    C21orf58, chromosome 21 open reading frame 58
  • Vertebrate Orthologs
    3
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    C21orf58, chromosome 21 open reading frame 58
  • Links
    NCBI Gene ID: 54058
    UniProt: P58505

  • Chr Location
    21q22.3; chr21:46300181-46324460 (-)  GRCh38
Human Diseases
less
  • References
    2 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    2 phenotypes from 1 allele in 1 genetic background
    43 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
    613
  • Tissues
    16
  • cDNA Data
    7
  • Literature Summary
    2
  • Comparison Matrix
    Gene Expression + Phenotype
    • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic ENSMUSG00000009114 Ensembl Gene Model | MGI Sequence Detail 12030 C57BL/6J ±  kb
    transcript ENSMUST00000092406 Ensembl | MGI Sequence Detail 1640 Not Applicable  
    polypeptide ENSMUSP00000090061 Ensembl | MGI Sequence Detail 270 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    • UniProt
      5 Sequences
    • InterPro Domains
      IPR027904 Domain of unknown function DUF4587
      IPR038915 Proline-rich protein 29-like
    Molecular
    Reagents
    less
    • All nucleic 9
      Genomic 1
      cDNA 7
      Primer pair 1

      Microarray probesets 2
    Other
    Accession IDs
    less
    MGI:2652703
    References
    more
    • Summaries
      All 62
      Developmental Gene Expression 2
      Diseases 2
      Phenotypes 43
    • Earliest
      J:137335 Roderick TH, Chromosomal inversions in studies of mammalian mutagenesis. Genetics. 1979 May;92(1 Pt 1 Suppl):s121-6
    • Latest
      J:361105 Tateossian H, et al., DYRK1A kinase triplication is the major cause of Otitis Media in Down Syndrome. Elife. 2025;
    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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    Send questions and comments to User Support.     		last database update
    09/08/2026
    MGI 6.24     		The Jackson Laboratory