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Gene : HNRNPA1 Homo sapiens

Name  ? heterogeneous nuclear ribonucleoprotein A1 Cytological Location  12q13.13
Brief Description  heterogeneous nuclear ribonucleoprotein A1
Description  This gene encodes a member of a family of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs), which are RNA-binding proteins that associate with pre-mRNAs in the nucleus and influence pre-mRNA processing, as well as other aspects of mRNA metabolism and transport. The protein encoded by this gene is one of the most abundant core proteins of hnRNP complexes and plays a key role in the regulation of alternative splicing. Mutations in this gene have been observed in individuals with amyotrophic lateral sclerosis 20. Multiple alternatively spliced transcript variants have been found. There are numerous pseudogenes of this gene distributed throughout the genome. [provided by RefSeq, Feb 2016]
  • synonyms:
  • IBMPFD3,
  • hnRNP-A1,
  • HGNC:5031,
  • HNRNPA1,
  • BC009600,
  • hnRNP A1,
  • hnRNP-A1,
  • ALS20,
  • UP 1,
  • uc001sfm.4,
  • ALS20,
  • HNRPA1L3,
  • OTTHUMG00000169702,
  • HNRPA1,
  • ALS19,
  • NM_031157,
  • HNRPA1,
  • hnRNPA1
  • identifiers:
  • 3178,
  • ENSG00000135486,
  • HNRNPA1

Genome feature

Region: gene ? Length: 6362  
Location: 12:54280726-54287087 Cyto location: 12q13.13


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Function

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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

2 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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Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

41 SN Ps

5 Cross References

19 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results