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Gene : HNRNPU Homo sapiens

Name  ? heterogeneous nuclear ribonucleoprotein U Cytological Location  1q44
Brief Description  heterogeneous nuclear ribonucleoprotein U
Description  This gene encodes a member of a family of proteins that bind nucleic acids and function in the formation of ribonucleoprotein complexes in the nucleus with heterogeneous nuclear RNA (hnRNA). The encoded protein has affinity for both RNA and DNA, and binds scaffold-attached region (SAR) DNA. Mutations in this gene have been associated with epileptic encephalopathy, early infantile, 54. A pseudogene of this gene has been identified on chromosome 14. [provided by RefSeq, Jun 2017]
  • synonyms:
  • chromosome 1 open reading frame 199,
  • HNRNPU-AS1,
  • hnRNPU,
  • HNRNPU,
  • HNRNPU antisense RNA 1,
  • EIEE54,
  • NM_031844,
  • non-protein coding RNA 201,
  • C1orf199,
  • HNRNPU-AS1,
  • U21.1,
  • NCRNA00201,
  • HNRPU,
  • scaffold attachment factor A,
  • FLJ37978,
  • HGNC:5048,
  • heterogeneous nuclear ribonucleoprotein U (scaffold attachment factor A),
  • SAFA,
  • X65488,
  • GRIP120,
  • uc001iba.2,
  • OTTHUMG00000040396,
  • FLJ30202,
  • hnRNP U,
  • HNRPU,
  • HNRNPU antisense RNA 1 (non-protein coding),
  • pp120,
  • SAF-A,
  • SAF-A
  • identifiers:
  • 3192,
  • ENSG00000153187,
  • HNRNPU

Genome feature

Region: gene ? Length: 14247  
Location: 1:244850297-244864543 reverse strand Cyto location: 1q44


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Function

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Gene -> HPO annotation (Human Phenotype Ontology)

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Proteins

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SNPs

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Disease

1 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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Expression

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Other

1 SN Ps

5 Cross References

19 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results