About   Help   FAQ
1700001O22Rik Gene Detail
Summary
  • Symbol
    1700001O22Rik
  • Name
    RIKEN cDNA 1700001O22 gene
  • Synonyms
    1700113K14Rik, 4930549G18Rik
  • Feature Type
    protein coding gene
  • IDs
    MGI:1923631
    NCBI Gene: 73598
  • Alliance
Location & Maps
more
  • Sequence Map
    Chr2:30794769-30803661 bp, - strand
  • From VEGA annotation of GRCm38

    Mouse Genome Browser

  • Download
    Sequence
      8893 bp   ±  kb flank

  • Genome Browsers
  • Genetic Map
    Chromosome 2, 21.74 cM
  • Mapping Data
    1 experiment
Homology
more
  • Human Ortholog
    C9orf50, chromosome 9 open reading frame 50
  • Vertebrate Orthologs
    6
  • Human Ortholog
    C9orf50, chromosome 9 open reading frame 50
    Orthology source: HomoloGene, HGNC
  • Links
    NCBI Gene ID: 375759
    neXtProt AC: NX_Q5SZB4
    UniProt: Q5SZB4

  • Chr Location
    9q34.11; chr9:129612225-129622275 (-)  GRCh38.p7

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    3 phenotype references
Gene Ontology
(GO)
Classifications
less
Expression
less
  • cDNA Data
Interactions
less
Sequences &
Gene Models
less
Representative SequencesLengthStrain/SpeciesFlank
genomic OTTMUSG00000011876 VEGA Gene Model | MGI Sequence Detail 8893 C57BL/6J ±  kb
transcript OTTMUST00000027982 VEGA | MGI Sequence Detail 1672 Not Applicable  
polypeptide OTTMUSP00000012697 VEGA | MGI Sequence Detail 375 Not Applicable  
For the selected sequence
Polymorphisms
less
  • SNPs within 2kb
    13 from dbSNP Build 142
Protein
Information
less
  • UniProt
    2 Sequences
  • InterPro Domains
    IPR032756 Domain of unknown function DUF4685
Molecular
Reagents
less
  • All nucleic 40
    cDNA 40

    Microarray probesets 4
Other
Accession IDs
less
MGI:1920848, MGI:1925455
References
more
  • Summaries
    All 22
    Phenotypes 3
  • 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:237827 Gineste C, et al., In vivo and in vitro investigations of heterozygous nebulin knock-out mice disclose a mild skeletal muscle phenotype. Neuromuscul Disord. 2013 Apr;23(4):357-69

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
12/05/2017
MGI 6.11
The Jackson Laboratory