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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
  • Transcription Start Sites
    4 TSS
Location &
Maps
more
  • Sequence Map
    Chr10:76449081-76461110 bp, + strand
  • From Ensembl annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 10, 38.84 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    37 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1924214
protein coding gene Chr10:76449020-76461218 (.)
129S1/SvImJ MGP_129S1SvImJ_G0017382
protein coding gene Chr10:76687600-76699981 (+)
A/J MGP_AJ_G0017359
protein coding gene Chr10:74040153-74048744 (+)
AKR/J MGP_AKRJ_G0017320
protein coding gene Chr10:76038603-76049313 (+)
BALB/cJ MGP_BALBcJ_G0017319
protein coding gene Chr10:74244570-74255574 (+)
C3H/HeJ MGP_C3HHeJ_G0017143
protein coding gene Chr10:76114506-76124856 (+)
C57BL/6NJ MGP_C57BL6NJ_G0017777
protein coding gene Chr10:79401631-79412044 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0015467
protein coding gene Chr10:70484334-70502758 (+)
CAST/EiJ MGP_CASTEiJ_G0016713
protein coding gene Chr10:76427697-76441648 (+)
CBA/J MGP_CBAJ_G0017115
protein coding gene Chr10:82505625-82514148 (+)
DBA/2J MGP_DBA2J_G0017220
protein coding gene Chr10:73349259-73358001 (+)
FVB/NJ MGP_FVBNJ_G0017212
protein coding gene Chr10:72504478-72514833 (+)
LP/J MGP_LPJ_G0017293
protein coding gene Chr10:77187223-77197310 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0017241
protein coding gene Chr10:84561725-84573422 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0017816
protein coding gene Chr10:76092310-76103873 (+)
PWK/PhJ MGP_PWKPhJ_G0016497
protein coding gene Chr10:73185650-73200556 (+)
SPRET/EiJ MGP_SPRETEiJ_G0016280
protein coding gene Chr10:75325433-75335289 (+)
WSB/EiJ MGP_WSBEiJ_G0016776
protein coding gene Chr10:76075187-76084416 (+)



Homology
more
  • Human Ortholog
    C21orf58, chromosome 21 open reading frame 58
  • Vertebrate Orthologs
    5
  • Human Ortholog
    C21orf58, chromosome 21 open reading frame 58
    Orthology source: HGNC
  • Links
    NCBI Gene ID: 54058
    neXtProt AC: NX_P58505
    UniProt: P58505

  • Chr Location
    21q22.3; chr21:46300426-46323899 (-)  GRCh38.p7

Human Diseases
less
  • References
    2 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    23 phenotype references
Gene Ontology
(GO)
Classifications
less
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
Interactions
less
Sequences &
Gene Models
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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 41
    Developmental Gene Expression 2
    Diseases 2
    Phenotypes 23
  • Earliest
    J:137335 Roderick TH, Chromosomal inversions in studies of mammalian mutagenesis. Genetics. 1979 May;92(1 Pt 1 Suppl):s121-6
  • Latest
    J:262380 Watson-Scales S, et al., Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration. PLoS Genet. 2018 May;14(5):e1007383

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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last database update
12/11/2018
MGI 6.13
The Jackson Laboratory