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Protein Coding Gene : Hnrnph2 heterogeneous nuclear ribonucleoprotein H2

Primary Identifier  MGI:1201779 Organism  mouse, laboratory
Chromosome  X NCBI Gene Number  56258
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable RNA binding activity. Predicted to be involved in regulation of RNA splicing. Predicted to be located in cytosol. Predicted to be part of ribonucleoprotein complex. Predicted to be active in nucleoplasm and postsynaptic density. Is expressed in brain; heart; olfactory epithelium; and spinal cord. Human ortholog(s) of this gene implicated in syndromic X-linked intellectual developmental disorder bain type. Orthologous to human HNRNPH2 (heterogeneous nuclear ribonucleoprotein H2).
  • synonyms:
  • heterogeneous nuclear ribonucleoprotein H2,
  • DXHXS1271E,
  • Ftp3,
  • Hnrph2,
  • DNA segment, Chr X, human DXS1271E,
  • Hnrnph2

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

0 Involved In Mutations

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

4 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For