SNX22 - sorting nexin 22 Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 79856

About SNX22

This gene has 7 transcripts (splice variants), 188 orthologues and 1 paralogue. Ubiquitous expression in thyroid (RPKM 48.1), placenta (RPKM 36.5) and 25 other tissues.

Summary

The protein encoded by this gene is a sorting nexin that is found in the cytoplasm, where it interacts with membrane-bound phosphatidylinositol 3-phosphate. The encoded protein may play a role in intracellular trafficking. Two transcript variants, one protein-coding and the Other not protein-coding, have been found for this gene. [provided by RefSeq, Dec 2012]

SNX22 Products (1)

mRNA Protein Name
NM_024798.3 NP_079074.2 sorting nexin-22

SNX22 Protein Structure

PX

PX: PX domain (18 - 105)

  • 0
  • 100
  • 193 a.a.
Protein Preferred Names Protein Names

sorting nexin-22

Related Diseases

Diseases Alias
Osteogenesis Imperfecta, Type Ix

  • Osteogenesis Imperfecta Type 9

  • Osteogenesis Imperfecta Type Ix

  • OI9

  • Oi Type Ix

  • Osteogenesis Imperfecta Sillence Type Ii/Iii Without Abnormality Of Type I Collagen

  • Oi, Type Ix

  • Oi 9

  • Osteogenesis Imperfecta 9

  • Oi-Ix
Brittle Bone Disorder

  • Osteogenesis Imperfecta

  • Brittle Bone Disease

  • Fragilitas Ossium

  • Osteopsathyrosis

  • Lobstein Disease

  • Oi

  • Vrolik Disease

  • Lobstein'S Disease

  • Lobstein'S Syndrome

  • Vrolik'S Disease

  • Porak And Durante Disease

  • Glass Bone Disease

  • Osteogenesis Imperfecta, Dominant Perinatal Lethal

  • Osteogenesis Imperfecta, Recessive Perinatal Lethal

  • Brittle Bone Syndrome

  • Oi - [Osteogenesis Imperfecta]

  • Ossium Fragility

  • Osteitis Fragilitans

  • Bony Fragility

  • Blue Sclera With Fragility Of Bone And Deafness

  • White Blue Sclera - Fragility Of Bone - Deafness
Fibrillary Astrocytoma

  • Fibrillary Astrocytic Tumors

  • Diffuse Astrocytoma

  • Gemistocytic Astrocytoma

  • Protoplasmic Astrocytoma
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 (3)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS13535 SNX22 Human Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS22814 Snx22 Mouse Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS29329 Snx22 Rat Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Rattus norvegicus SNX22 RGD RGD:1305042
Bos taurus SNX22 VGNC VGNC:35102
Mus musculus SNX22 MGD MGI:2685966
Macaca mulatta SNX22 VGNC VGNC:77720
Canis familiaris SNX22 VGNC VGNC:46632
Others SNX22 NCBI