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Gene : HNRNPDL Homo sapiens

Name  ? heterogeneous nuclear ribonucleoprotein D like Cytological Location  4q21.22
Brief Description  heterogeneous nuclear ribonucleoprotein D like
Description  This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has two RRM domains that bind to RNAs. Three alternatively spliced transcript variants have been described for this gene. One of the variants is probably not translated because the transcript is a candidate for nonsense-mediated mRNA decay. The protein isoforms encoded by this gene are similar to its family member HNRPD. [provided by RefSeq, May 2011]
  • synonyms:
  • limb girdle muscular dystrophy 1G (autosomal dominant),
  • laAUF1,
  • JKTBP,
  • NM_005463,
  • HGNC:5037,
  • D89092,
  • JKTBP,
  • LGMD1G,
  • laAUF1,
  • LGMDD3,
  • JKTBP2,
  • HNRNPDL,
  • HNRPDL,
  • HNRPDL,
  • HNRNP,
  • LGMD1G,
  • OTTHUMG00000130299
  • identifiers:
  • 9987,
  • ENSG00000152795,
  • HNRNPDL

Genome feature

Region: gene ? Length: 7662  
Location: 4:82422564-82430225 reverse strand Cyto location: 4q21.22


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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)

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Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

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Expression

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Other

24 SN Ps

5 Cross References

18 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results