FRG2C - FSHD region gene 2 family member C Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 100288801

About FRG2C

This gene has 2 transcripts (splice variants), 57 orthologues and 2 paralogues. Low expression observed in reference dataset.

Summary

Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

FRG2C Products (2)

mRNA Protein Name
NM_001124759.5 NP_001118231.1 protein FRG2-like-2 isoform 1
NM_001410775.1 NP_001397704.1 protein FRG2-like-2 isoform 2

FRG2C Protein Structure

FRG2

FRG2: Facioscapulohumeral muscular dystrophy candidate 2 (61 - 242)

  • 0
  • 100
  • 200
  • 282 a.a.
Protein Preferred Names Protein Names

protein FRG2-like-2

  • FSHD region gene 2 family, member C-like

Related Diseases

Diseases Alias
Spondyloarthropathy 1

  • Ankylosing Spondylitis

  • Spondyloarthropathy, Susceptibility To, 1

  • SPDA1

  • Marie-Strumpell Spondylitis

  • Bechterew Syndrome

  • Spa

  • Spondylarthritis Ankylopoietica

  • Reiter Syndrome

  • Ankylosing Spondylitis, Susceptibility To

  • Bekhterev Syndrome

  • Bekhterev'S Disease

  • Marie-Strumpell Disease

  • Axial Spondylarthritis

  • Bechterew Disease

  • Marie-Struempell Disease

  • Spondylitis Ankylopoietica

  • Spondyloarthritis

  • Spondyloarthritis Ankylopoietica

  • Spas

  • Ankylosing Spondylarthritis

  • Psoriatic Arthritis

  • Reactive Arthritis

  • Rheumatoid Spondylitis

  • Spondylitis Ankylosans

  • Spondylitis Ankylosing

  • Spondylitis, Ankylosing

  • Spondylarthropathies

  • Arthritis, Psoriatic

  • Arthritis, Reactive
Tumoral Calcinosis, Hyperphosphatemic, Familial, 1

  • Hyperphosphatemic Familial Tumoral Calcinosis

  • Hftc

  • Hyperostosis-Hyperphosphatemia Syndrome

  • Familial Hyperphosphatemic Tumoral Calcinosis/Hyperphosphatemic Hyperostosis Syndrome

  • Tumoral Calcinosis, Hyperphosphatemic, Familial

  • Phptc

  • Lipocalcinogranulomatosis

  • Morbus Teutschlaender

  • Hhs

  • Hyperostosis With Hyperphosphatemia

  • Cortical Hyperostosis With Hyperphosphatemia

  • Primary Hyperphosphatemic Tumoral Calcinosis

  • Familial Tumoral Calcinosis

  • HFTC1

  • Hypercalcemic Tumoral Calcinosis

  • Hyperphosphatemia Hyperostosis

  • Hyperphosphatemia Hyperostosis Syndrome

  • Hyperphosphatemia Tumoral Calcinosis

  • Tumoral Calcinosis

  • Calcinosis, Tumoral, With Hyperphosphatemia

  • Tumoral Calcinosis, Primary Hyperphosphatemic

  • Teutschlaender Disease, Familial

  • Familial Teutschlaender Disease

  • Tumoral Calcinosis With Hyperphosphatemia

  • Familial Tumoral Calcinosis/Hyperostosis-Hyperphosphatemia Syndrome

  • Ftc/Hhs

  • Familial Tumoral Calcinosis With Hyperphosphatemia

  • Teutschlaender Disease

  • Tumoral Calcinosis Primary Hyperphosphatemic

  • Calcinosis, Tumoral, Hyperphosphatemic, Familial
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS05097 FRG2C Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Mus musculus FRG2C MGD MGI:3035485