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Gene : CCDC162P Homo sapiens

Name  ? coiled-coil domain containing 162, pseudogene Cytological Location  6q21
Description  This gene is the ortholog of the mouse coiled-coil domain containing 162 gene. This locus is transcribed, but is represented as a unitary pseudogene because there are multiple changes in the coding sequence, including multiple changes that result in premature stop codons, relative to the mouse coding sequence. Transcripts from this locus are expected to encode truncated proteins, and may be candidates for nonsense-mediated decay (NMD). [provided by RefSeq, Sep 2018]
  • synonyms:
  • CCDC162,
  • bA425D10.3,
  • NR_028595,
  • bA425D10.7,
  • chromosome 6 open reading frame 183,
  • C6orf185,
  • HGNC:21565,
  • C6orf184,
  • C6orf183,
  • CCDC162,
  • C6orf183,
  • C6orf184,
  • OTTHUMG00000015342,
  • C6orf185,
  • chromosome 6 open reading frame 185,
  • chromosome 6 open reading frame 184,
  • bA487F23.3
  • identifiers:
  • 221262,
  • ENSG00000203799,
  • CCDC162P

Genome feature

Region: gene ?
Location: No location information in HumanMine Cyto location: 6q21


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Function

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Gene --> Physical and Genetic Interactions

Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

3753 SN Ps

3 Cross References

8 Data Sets

0 Homologues

0 Located Features

54 Rna Seq Results