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Gene : C16orf89 Homo sapiens

Name  ? chromosome 16 open reading frame 89 Cytological Location  16p13.3
Brief Description  chromosome 16 open reading frame 89
Description  This gene is expressed predominantly in the thyroid. Based on expression patterns similar to thyroid transcription factors and proteins, this gene may function in the development and function of the thyroid. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]
  • synonyms:
  • C16orf89,
  • NM_152459,
  • MGC45438,
  • OTTHUMG00000159314,
  • uc010bud.4,
  • HGNC:28687
  • identifiers:
  • 146556,
  • ENSG00000153446,
  • C16orf89

Genome feature

Region: gene ? Length: 23374  
Location: 16:5042772-5066145 reverse strand Cyto location: 16p13.3


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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

503 SN Ps

4 Cross References

14 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results