2. Gene
  3. GPRIN1 - G protein regulated inducer of neurite outgrowth 1 Gene

GPRIN1 - G protein regulated inducer of neurite outgrowth 1 Gene

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

中文名称：G 蛋白调节神经突生长诱导因子 1

种属: Homo sapiens

同用名: GRIN1

基因 ID: 114787 | 基因类型: protein coding

关于 GPRIN1

Cytogenetic location: 5q35.2 Genomic coordinates (GRCh38): 5:176,595,802-176,610,156 (from NCBI)

This gene has 1 transcript (splice variant) and 130 orthologues. Biased expression in brain (RPKM 11.5), duodenum (RPKM 2.2) and 5 other tissues.

功能概要

预测启用磷蛋白结合活性。预计参与神经元投射发育。预计位于生长锥内。预计在质膜上有活性。 [由基因组资源联盟提供，2022 年 4 月]

Predicted to enable phosphoprotein binding activity. Predicted to be involved in neuron projection development. Predicted to be located in growth cone. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

GPRIN1 基因产物(1)

mRNA Protein Name
NM_052899.3 NP_443131.2 G protein-regulated inducer of neurite outgrowth 1
基因本体论
  • 分子功能
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
24350810 GOA
EXP：通过实验结果推断 IDA：通过直接分析推断 IPI：通过物理相互作用推断 IMP：通过突变表型推断 IGI：通过遗传相互作用推断 IEP：通过表达模式推断

GPRIN1 蛋白结构

GRIN_C

GRIN_C: G protein-regulated inducer of neurite outgrowth C-terminus (869 - 1008)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1008 a.a.
蛋白主名 其他名称

G protein-regulated inducer of neurite outgrowth 1

关联疾病

疾病名称 别名
Cerebral Creatine Deficiency Syndrome 2

Guanidinoacetate Methyltransferase Deficiency

Gamt Deficiency

Creatine Deficiency Syndrome Due To Gamt Deficiency

Deficiency Of Guanidinoacetate Methyltransferase

CCDS2

Guanidinoacetate Methyltransferase Deficiency

Deficiency, Cerebral Creatine, Syndrome, Type 2

Language Development Disorders
Cerebral Creatine Deficiency Syndrome

Deficiency, Cerebral Creatine, Syndrome
Rett Syndrome

Atypical Rett Syndrome

RTT

Rett Disorder

Rts

Autism, Dementia, Ataxia, And Loss Of Purposeful Hand Use

Rett Syndrome, Preserved Speech Variant

Rett Syndrome, Atypical

Rett'S Disorder

Rett Syndrome Variant

Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use Syndrome

Cerebroatrophic Hyperammonemia

Rett Like Syndrome

Rett'S Syndrome

Atypical Rtt

Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use

Rett Syndrome Preserved Speech Variant

Rett Syndrome Zappella Variant

Rett Syndrome, Zappella Variant
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-RS05754 GPRIN1 Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 ID
Bos taurus GPRIN1 VGNC VGNC:29609
Rattus norvegicus GPRIN1 RGD RGD:1308762
Canis familiaris GPRIN1 VGNC VGNC:51897
Mus musculus GPRIN1 MGD MGI:1349455
Macaca mulatta GPRIN1 VGNC VGNC:72998
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