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4932438H23Rik Gene Detail
Summary
  • Symbol
    4932438H23Rik
  • Name
    RIKEN cDNA 4932438H23 gene
  • Feature Type
    protein coding gene
  • IDs
    MGI:1921637
    NCBI Gene: 74387
  • Alliance
  • Transcription Start Sites
    8 TSS
Location &
Maps
more
  • Sequence Map
    Chr16:91044646-91069624 bp, - strand
  • From NCBI annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 16, 52.35 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    914 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1921637
protein coding gene Chr16:91044646-91095122 (-)
129S1/SvImJ MGP_129S1SvImJ_G0023034
protein coding gene Chr16:92035506-92078930 (-)
A/J MGP_AJ_G0023002
protein coding gene Chr16:87743985-87785141 (-)
AKR/J MGP_AKRJ_G0022972
protein coding gene Chr16:90383291-90425405 (-)
BALB/cJ MGP_BALBcJ_G0023004
protein coding gene Chr16:88264278-88304548 (-)
C3H/HeJ MGP_C3HHeJ_G0022765
protein coding gene Chr16:90950067-90991420 (-)
C57BL/6NJ MGP_C57BL6NJ_G0023451
protein coding gene Chr16:95018522-95060326 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0020953
protein coding gene Chr16:85449657-85491898 (-)
CAST/EiJ MGP_CASTEiJ_G0022284
protein coding gene Chr16:91502473-91546128 (-)
CBA/J MGP_CBAJ_G0022734
protein coding gene Chr16:99075007-99123138 (-)
DBA/2J MGP_DBA2J_G0022868
protein coding gene Chr16:87643379-87685419 (-)
FVB/NJ MGP_FVBNJ_G0022842
protein coding gene Chr16:86773326-86813309 (-)
LP/J MGP_LPJ_G0022938
protein coding gene Chr16:91731053-91794861 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0022863
protein coding gene Chr16:103639752-103695354 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0023469
protein coding gene Chr16:90895288-90939118 (-)
PWK/PhJ MGP_PWKPhJ_G0022029
protein coding gene Chr16:87816513-87859629 (-)
SPRET/EiJ MGP_SPRETEiJ_G0021859
protein coding gene Chr16:90459499-90503217 (-)
WSB/EiJ MGP_WSBEiJ_G0022336
protein coding gene Chr16:91141313-91185201 (-)



Homology
more
  • Human Ortholog
    C21orf62, chromosome 21 open reading frame 62
  • Vertebrate Orthologs
    9
  • Human Ortholog
    C21orf62, chromosome 21 open reading frame 62
    Orthology source: HGNC, HomoloGene
  • Synonyms
    B37, C21orf120, PRED81
  • Links
    NCBI Gene ID: 56245
    neXtProt AC: NX_Q9NYP8
    UniProt: Q9NYP8

  • Chr Location
    21q22.11; chr21:32790673-32813808 (-)  GRCh38.p7

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    11 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
less
Representative SequencesLengthStrain/SpeciesFlank
genomic 74387 NCBI Gene Model | MGI Sequence Detail 24979 C57BL/6J ±  kb
transcript NM_028905 RefSeq | MGI Sequence Detail 2684 C57BL/6  
polypeptide Q9D4G1 UniProt | EBI | MGI Sequence Detail 230 Not Applicable  
For the selected sequence
Protein
Information
less
  • UniProt
    2 Sequences
  • InterPro Domains
    IPR029250 Protein of unknown function DUF4571
Molecular
Reagents
less
  • All nucleic 9
    cDNA 6
    Primer pair 2
    Other 1

    Microarray probesets 3
Other
Accession IDs
less
MGI:2146457
References
more
  • Summaries
    All 30
    Developmental Gene Expression 4
    Phenotypes 11
  • Earliest
    J:65060 Kawai J, et al., Functional annotation of a full-length mouse cDNA collection. Nature. 2001 Feb 8;409(6821):685-90
  • 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
12/04/2018
MGI 6.13
The Jackson Laboratory