help  | about  | cite  | software

Gene : HNRNPH1 Homo sapiens

Name  ? heterogeneous nuclear ribonucleoprotein H1 Cytological Location  5q35.3
Brief Description  heterogeneous nuclear ribonucleoprotein H1
description  This gene encodes a member of a subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins that complex with heterogeneous nuclear RNA. 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 may shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has three repeats of quasi-RRM domains that bind to RNA and is very similar to the family member HNRPF. This gene may be associated with hereditary lymphedema type I. Alternatively spliced transcript variants have been described [provided by RefSeq, Mar 2012]
  • synonyms:
  • OTTHUMG00000130908,
  • HNRPH1,
  • HGNC:5041,
  • HNRPH,
  • HNRNPH1,
  • HNRPH1,
  • hnRNPH,
  • BC001348,
  • NM_005520,
  • uc003mkh.5,
  • heterogeneous nuclear ribonucleoprotein H1 (H),
  • hnRNPH
  • identifiers:
  • 3187,
  • ENSG00000169045,

Genome feature

Region: gene ? Length: 20607  
Location: 5:179614178-179634784 reverse strand Cyto location: 5q35.3

Uni Prot Comments Displayer

Protein Atlas Displayer

Gene Expression Atlas Tissues Displayer

Gene Expression Atlas Diseases Displayer

Publication Counts Displayer

Curated Proteins Displayer


Gene Ontology Displayer

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


J Browse Displayer

Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

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]


Homologue Displayer

Gene --> Orthologues


Cytoscape Network Displayer

Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



3756 SN Ps

5 Cross References

16 Data Sets

15 Homologues

0 Located Features

97 Rna Seq Results