heterogeneous nuclear ribonucleoprotein H2 (H') (HNRNPH2)

Description: heterogeneous nuclear ribonucleoprotein H2 (H )
Orgname: Homo sapiens
Status: 0
CurrentID: 0
Chromosome: X
GeneticSource: genomic
MapLocation: Xq22
OtherAliases: FTP3, HNRPH , HNRPH2, hnRNPH
OtherDesignations: heterogeneous nuclear ribonucleoprotein H-prime|heterogeneous nuclear ribonucleoprotein H2
NomenclatureSymbol: HNRNPH2
NomenclatureName: heterogeneous nuclear ribonucleoprotein H2 (H )
NomenclatureStatus: Official
TaxID: 9606
GeneWeight: 3747
Summary: 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 three repeats of quasi-RRM domains that binds to RNAs. It is very similar to the family member HNRPH1. This gene is thought to be involved in Fabray disease and X-linked agammaglobulinemia phenotype. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq]
ChrSort: X
ChrStart: 100663190

UniProtein db: HNRNPH2 UniProt protein knowledge database
Ensembl db: HNRNPH2 Ensembl genome database

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