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Ccdc22 Gene Detail
Summary
  • Symbol
    Ccdc22
  • Name
    coiled-coil domain containing 22
  • Synonyms
    DXImx40e, Sfc22
  • Feature Type
    protein coding gene
  • IDs
    MGI:1859608
    NCBI Gene: 54638
  • Gene Overview
    MyGene.info: CCDC22
Location & Maps
more
  • Genetic Map
    Chromosome X, 3.42 cM
  • Mapping Data
    4 experiments
Homology
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  • Human Ortholog
    CCDC22, coiled-coil domain containing 22
  • Vertebrate Orthologs
    9
  • Human Ortholog
    CCDC22, coiled-coil domain containing 22
    Orthology source: HGNC, HomoloGene
  • Synonyms
    CXorf37, JM1, RTSC2
  • Links
    NCBI Gene ID: 28952
    neXtProt AC: NX_O60826

  • Chr Location
    Xp11.23; chrX:49235467-49250526 (+)  GRCh38.p2

Human Diseases
more
  • Diseases
    1 with human CCDC22 associations

Human Disease Mouse Models
       Ritscher-Schinzel Syndrome 2; RTSC2   OMIM: 300963
Click on a disease name to see all genes associated with that disease.

Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    2 phenotype references
  • All Mutations and Alleles
    3
  • Targeted
    3
Gene Ontology
(GO)
Classifications
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  • All GO Annotations
  • GO References
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
receptor
receptor binding
RNA binding
transcription
transferase
transporter
Biological Process

nucleic acid-templated transcription
carbohydrate derivative metabolism
cell death
cell differentiation
cell proliferation
cellular component organization
establishment of localization
homeostatic process
immune system process
lipid metabolic process
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
non-membrane-bounded organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
synapse
vacuole
Click cells to view annotations.
Expression
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  • cDNA Data
Interactions
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Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic OTTMUSG00000016629 VEGA Gene Model | MGI Sequence Detail 11709 C57BL/6J ±  kb
transcript OTTMUST00000042494 VEGA | MGI Sequence Detail 2353 Not Applicable  
polypeptide OTTMUSP00000019092 VEGA | MGI Sequence Detail 627 Not Applicable  
For the selected sequence
Polymorphisms
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  • SNPs within 2kb
    52 from dbSNP Build 142
Protein
Information
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  • UniProt
    1 Sequence
  • Protein Ontology
    PR:000031905 coiled-coil domain-containing protein 22
  • InterPro Domains
    IPR008530 Coiled-coil domain-containing protein 22
Molecular
Reagents
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  • All nucleic 10
    Genomic 4
    cDNA 6

    Microarray probesets 3
Other
Accession IDs
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MGI:2147896
References
more
  • Summaries
    All 26
    Gene Ontology 4
    Phenotypes 2
  • Earliest
    J:62168 Means GD, et al., A transcript map of a 2-Mb BAC contig in the proximal portion of the mouse X chromosome and regional mapping of the scurfy mutation. Genomics. 2000 May 1;65(3):213-23
  • Latest
    J:153498 Diez-Roux G, et al., A high-resolution anatomical atlas of the transcriptome in the mouse embryo. PLoS Biol. 2011;9(1):e1000582

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
08/17/2016
MGI 6.05
The Jackson Laboratory