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Gene : NSUN5P1 Homo sapiens

Name  ? NSUN5 pseudogene 1 Cytological Location  7q11.23
Description  This locus represents a transcribed pseudogene of a nearby locus on chromosome 7, which encodes a putative methyltransferase. There is also a third closely related pseudogene locus in this region. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]
  • synonyms:
  • NOL1/NOP2/Sun domain family, member 5B,
  • HGNC:19146,
  • WBSCR20B,
  • OTTHUMG00000156108,
  • NOP2/Sun domain family, member 5 pseudogene 1,
  • AF416610,
  • WBSCR20B,
  • NR_033322,
  • Williams Beuren syndrome chromosome region 20B,
  • NSUN5B,
  • NSUN5B
  • identifiers:
  • 155400,
  • ENSG00000223705,
  • NSUN5P1

Genome feature

Region: gene ?
Location: No location information in HumanMine Cyto location: 7q11.23


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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

4 Cross References

9 Data Sets

6 Homologues

0 Located Features

54 Rna Seq Results