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Gene : COIL Homo sapiens

Name  ? coilin Cytological Location  17q22
Brief Description  coilin
Description  The protein encoded by this gene is an integral component of Cajal bodies (also called coiled bodies). Cajal bodies are nuclear suborganelles of varying number and composition that are involved in the post-transcriptional modification of small nuclear and small nucleolar RNAs. The N-terminus of the coilin protein directs its self-oligomerization while the C-terminus influences the number of nuclear bodies assembled per cell. Differential methylation and phosphorylation of coilin likely influences its localization among nuclear bodies and the composition and assembly of Cajal bodies. This gene has pseudogenes on chromosome 4 and chromosome 14. [provided by RefSeq, Jul 2008]
  • synonyms:
  • CLN80,
  • U06632,
  • p80-coilin,
  • COIL,
  • HGNC:2184,
  • p80-coilin,
  • uc002iuu.4,
  • OTTHUMG00000178126,
  • NM_004645,
  • CLN80
  • identifiers:
  • 8161,
  • ENSG00000121058,
  • COIL

Genome feature

Region: gene ? Length: 22852  
Location: 17:56938199-56961050 reverse strand Cyto location: 17q22


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Function

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0 Pathways

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Genomics

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Proteins

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SNPs

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Disease

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

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Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

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Expression

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Other

0 Pathways

13 SN Ps

5 Cross References

15 Data Sets

3 Homologues

0 Located Features

97 Rna Seq Results