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Gene : CCDC169-SOHLH2 Homo sapiens

Name  ? CCDC169-SOHLH2 readthrough Cytological Location  13q13.3
Brief Description  CCDC169-SOHLH2 readthrough
Description  This locus represents naturally occurring read-through transcription between the neighboring C13orf38 (chromosome 13 open reading frame 38) and SOHLH2 (spermatogenesis and oogenesis specific basic helix-loop-helix 2) genes. The read-through transcript encodes a fusion protein that shares sequence identity with the products of each individual gene. [provided by RefSeq, Nov 2010]
  • synonyms:
  • C13orf38-SOHLH2,
  • uc010tei.3,
  • NM_001198910.1,
  • C13orf38-SOHLH2,
  • HGNC:38866,
  • SOHLH2,
  • C13orf38-SOHLH2 readthrough,
  • TEB1,
  • OTTHUMG00000162258,
  • CCDC169-SOHLH2
  • identifiers:
  • 100526761,
  • ENSG00000250709,
  • CCDC169-SOHLH2

Genome feature

Region: gene ? Length: 129598  
Location: 13:36168217-36297814 reverse strand Cyto location: 13q13.3

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


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]


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Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



0 Pathways

0 SNPs

3 Cross References

8 Data Sets

0 Homologues

0 Located Features

43 Rna Seq Results