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

GPRIN1 - G protein regulated inducer of neurite outgrowth 1 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as GRIN1

Gene ID: 114787 | Gene type: protein coding

About 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.

Summary

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 Products(1)

mRNA Protein Name
NM_052899.3 NP_443131.2 G protein-regulated inducer of neurite outgrowth 1
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
24350810 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

GPRIN1 Protein Structure

GRIN_C

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

  • 0
  • 200
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  • 800
  • 1008 a.a.
Protein Preferred Names Protein Names

G protein-regulated inducer of neurite outgrowth 1

Related Diseases

Diseases Alias
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
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
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS05754 GPRIN1 Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source 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