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Protein Coding Gene : Sec16b SEC16 homolog B, endoplasmic reticulum export factor
Primary Identifier  MGI:2148802 Organism  mouse, laboratory
Chromosome  1 NCBI Gene Number  89867
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to be involved in Golgi organization and protein localization to endoplasmic reticulum exit site. Predicted to act upstream of or within peroxisome organization; protein transport; and vesicle-mediated transport. Predicted to be located in intracellular membrane-bounded organelle. Predicted to be active in ER to Golgi transport vesicle membrane and endoplasmic reticulum exit site. Is expressed in dorsal root ganglion; forelimb digit mesenchyme; hindlimb; jaw; and musculoskeletal system. Orthologous to several human genes including SEC16B (SEC16 homolog B, endoplasmic reticulum export factor).
  • synonyms:
  • Sec16b,
  • regucalcin gene promotor region related protein,
  • Rgpr-p117,
  • Rgpr,
  • Lztr2,
  • leucine zipper transcription regulator 2,
  • SEC16 homolog B, endoplasmic reticulum export factor
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Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

2 Involved In Mutations

Trail: ProteinCodingGene

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

8 Pathways

Trail: ProteinCodingGene

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





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