2. Gene
  3. NPTXR - neuronal pentraxin receptor Gene

NPTXR - neuronal pentraxin receptor Gene

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

中文名称：神经元五聚蛋白受体

种属: Homo sapiens

同用名: NPR

基因 ID: 23467 | 基因类型: protein coding

关于 NPTXR

Cytogenetic location: 22q13.1 Genomic coordinates (GRCh38): 22:38,818,452-38,844,028 (from NCBI)

This gene has 1 transcript (splice variant), 195 orthologues and 8 paralogues. Biased expression in brain (RPKM 73.3), heart (RPKM 6.6) and 3 other tissues.

功能概要

该基因编码一种类似于大鼠神经元五聚蛋白受体的蛋白质。大鼠 pentraxin 受体是一种完整的膜蛋白，被认为可以介导神经元对蛇毒毒素 taipoxin 的摄取，并将其转运到突触中。对大鼠的研究表明，该 mRNA 的翻译起始于非 AUG (CUG) 密码子。这可能也适用于小鼠和人类，基于这些物种之间的强序列保守性。[RefSeq 提供，2008 年 7 月]

This gene encodes a protein similar to the rat neuronal pentraxin receptor. The rat pentraxin receptor is an integral membrane protein that is thought to mediate neuronal uptake of the snake venom toxin, taipoxin, and its transport into the synapses. Studies in rat indicate that translation of this mRNA initiates at a non-AUG (CUG) codon. This may also be true for mouse and human, based on strong sequence conservation amongst these species. [provided by RefSeq, Jul 2008]

NPTXR 基因产物(1)

mRNA Protein Name
NM_014293.4 NP_055108.2 neuronal pentraxin receptor

NPTXR 蛋白结构

Pentaxin

Pentaxin: Pentaxin family (302 - 483)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500 a.a.
蛋白主名 其他名称

neuronal pentraxin receptor

重组 NPTXR 蛋白

目录号 产品名 蛋白编号 纯度
HY-P76522 NPTXR Protein, Human (HEK293, His) O95502 (A24-A500) ≥95%

关联疾病

疾病名称 别名
Febrile Seizures, Familial, 6

FEB6

Familial Febrile Seizures 6

Convulsions, Familial Febrile, 6

Familial Febrile Convulsions 6

Febrile Convulsions, Familial, 6
Spinocerebellar Ataxia 23

Spinocerebellar Ataxia Type 23

SCA23

Ataxia, Spinocerebellar, Type 23
Mirror Movements 1

Congenital Mirror Movement Disorder

Bimanual Synergia

Congenital Mirror Movements

Familial Congenital Controlateral Synkinesia

Familial Congenital Mirror Movements

Hereditary Congenital Controlateral Synkinesia

Hereditary Congenital Mirror Movements

Isolated Congenital Controlateral Synkinesia

Isolated Congenital Mirror Movements

Mirror Movements

MRMV1

Mirror Movements 1 And/Or Agenesis Of The Corpus Callosum

Mirror Movements, Congenital

Bimanual Synkinesis

Cmm

Mirror Movements, Type 1
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-RS09507 NPTXR Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 ID
Mus musculus NPTXR MGD MGI:1920590
Rattus norvegicus NPTXR RGD RGD:628898
Macaca mulatta NPTXR VGNC VGNC:97108
Bos taurus NPTXR VGNC VGNC:32220
Others NPTXR NCBI
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