1. Gene
  2. GLRA3 - glycine receptor alpha 3 Gene

GLRA3 - glycine receptor alpha 3 Gene

Homo sapiens
Gene ID: 8001 | Gene type: protein coding

About GLRA3

Cytogenetic location: 4q34.1 Genomic coordinates (GRCh38): 4:174,636,920-174,829,247 (from NCBI)

This gene has 4 transcripts (splice variants), 201 orthologues and 45 paralogues. Biased expression in brain (RPKM 2.6), adrenal (RPKM 0.4) and 1 other tissue.

Summary

This gene encodes a member of the ligand-gated ion channel protein family. The encoded protein is a member of the glycine receptor subfamily. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013]

GLRA3 Products(2)

mRNA Protein Name
NM_001042543.3 NP_001036008.1 glycine receptor subunit alpha-3 isoform b precursor
NM_006529.4 NP_006520.2 glycine receptor subunit alpha-3 isoform a precursor

GLRA3 Protein Structure

Neur_chan_LBD

Neur_chan_LBD: Neurotransmitter-gated ion-channel ligand binding domain (47 - 253)

Neur_chan_memb

Neur_chan_memb: Neurotransmitter-gated ion-channel transmembrane region (260 - 370)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 464 a.a.
Protein Preferred Names Protein Names

glycine receptor subunit alpha-3

glycine receptor, alpha-3 polypeptide

Related Diseases

Diseases Alias
Hyperekplexia

Hereditary Hyperekplexia

Kok Disease

Congenital Stiff Man Syndrome

Familial Startle Disease

Sthe

Stiff-Baby Syndrome

Hereditary Hyperexplexia

Startle Disease

Exaggerated Startle Reaction

Hyperexplexia Hereditary

Startle Disease, Familial

Startle Reaction, Exaggerated

Stiff-Man Syndrome, Congenital

Stiff-Person Syndrome, Congenital

Congenital Stiff-Man Syndrome

Congenital Stiff-Person Syndrome

Familial Hyperekplexia

Startle Syndrome

Stiff Baby Syndrome

Hyperekplexia, Hereditary

Stiff-Person Syndrome

Brain Stem Infarction

Brain Stem Infarctions

Brainstem Infarction

Autosomal Recessive Intellectual Developmental Disorder

Mental Retardation, Autosomal Recessive

Autosomal Recessive Mental Retardation

Autosomal Recessive Non-Syndromic Mental Retardation

Autosomal Recessive Non-Syndromic Intellectual Disability

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

Orthologs Information

Species Symbol Source ID
Rattus norvegicus GLRA3 RGD RGD:621229
Canis familiaris GLRA3 VGNC VGNC:41270
Mus musculus GLRA3 MGD MGI:95749
Felis catus GLRA3 VGNC VGNC:62590
Macaca mulatta GLRA3 VGNC VGNC:73076
Bos taurus GLRA3 VGNC VGNC:56969