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Gene : NME1-NME2 Homo sapiens

Name  ? NME1-NME2 readthrough Cytological Location  17q21.33
Brief Description  NME1-NME2 readthrough
description  This locus represents naturally occurring read-through transcription between the neighboring NME1 and NME2 genes. The significance of this read-through transcription and the function of the resulting protein product have not yet been determined. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Nov 2010]
  • synonyms:
  • NME1-NME2,
  • OTTHUMG00000137475,
  • NM_001018136,
  • NMELV,
  • HGNC:33531,
  • DQ109675,
  • uc002itj.4,
  • NM23-LV,
  • NMELV,
  • NM23-LV
  • identifiers:
  • 654364,
  • ENSG00000011052,
  • NME1-NME2

Genome feature

Region: gene ? Length: 18209  
Location: 17:51153536-51171744 Cyto location: 17q21.33

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Gene Ontology Displayer

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene Structure Displayer

Overlapping Features Displayer

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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 --> Orthologues


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Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



0 SN Ps

4 Cross References

12 Data Sets

0 Homologues

0 Located Features

37 Rna Seq Results