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Protein Coding Gene : Rhbdf2 rhomboid 5 homolog 2

Primary Identifier  MGI:2442473 Organism  mouse, laboratory
Chromosome  11 NCBI Gene Number  217344
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Involved in negative regulation of protein secretion. Acts upstream of or within protein localization to plasma membrane. Located in endoplasmic reticulum membrane and plasma membrane. Used to study palmoplantar keratoderma-esophageal carcinoma syndrome. Human ortholog(s) of this gene implicated in palmoplantar keratoderma-esophageal carcinoma syndrome. Orthologous to human RHBDF2 (rhomboid 5 homolog 2).
PHENOTYPE: Mice homozygous for a null mutation display impaired TNF secretion and increased sensitivity to bacterial infection induced mortality. [provided by MGI curators]
  • synonyms:
  • uncovered,
  • Rhbdf2,
  • Uncv,
  • RIKEN cDNA 4732465I17 gene,
  • cub,
  • iRhom2,
  • curly bare,
  • MGI:1890800,
  • rhomboid 5 homolog 2,
  • 4732465I17Rik,
  • MGI:1261908,
  • rhomboid, veinlet-like 6 (Drosophila),
  • Rhbdl6

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

0 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