2. Gene
  3. SNX22 - sorting nexin 22 Gene

SNX22 - sorting nexin 22 Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：分选 nexin 22

种属: Homo sapiens

基因 ID: 79856 | 基因类型: protein coding

关于 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.

功能概要

由该基因编码的蛋白质是一种存在于细胞质中的分选连接蛋白，它在细胞质中与膜结合的磷脂酰肌醇 3-磷酸相互作用。编码的蛋白质可能在细胞内运输中发挥作用。已发现该基因的两种转录变体，一种编码蛋白质，另一种不编码蛋白质。[RefSeq 提供，2012 年 12 月]

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 基因产物(1)

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

SNX22 蛋白结构

PX

PX: PX domain (18 - 105)

  • 0
  • 100
  • 193 a.a.
蛋白主名 其他名称

sorting nexin-22

关联疾病

疾病名称 别名
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
疾病名称 别名
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS13535 SNX22 Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 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
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