GPRIN1 - G protein regulated inducer of neurite outgrowth 1 Gene

Also Known as GRIN1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 114787

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 References 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
  • 400
  • 600
  • 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

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 Set / 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
Others GPRIN1 NCBI