1. Gene
  2. CNIH2 - cornichon family AMPA receptor auxiliary protein 2 Gene

CNIH2 - cornichon family AMPA receptor auxiliary protein 2 Gene

Homo sapiens

Also known as Cnil; CNIH-2

Gene ID: 254263 | Gene type: protein coding

About CNIH2

Cytogenetic location: 11q13.2 Genomic coordinates (GRCh38): 11:66,278,175-66,284,206 (from NCBI)

This gene has 6 transcripts (splice variants), 185 orthologues and 4 paralogues. Biased expression in brain (RPKM 22.4), adrenal (RPKM 2.7) and 1 other tissue.

Summary

The protein encoded by this gene is an auxiliary subunit of the ionotropic glutamate receptor of the AMPA subtype. AMPA receptors mediate fast synaptic neurotransmission in the central nervous system. This protein has been reported to interact with the Type I AMPA Receptor regulatory protein isoform gamma-8 to control assembly of hippocampal AMPA Receptor complexes, thereby modulating receptor gating and pharmacology. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]

CNIH2 Products(1)

mRNA Protein Name
NM_182553.3 NP_872359.1 protein cornichon homolog 2
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
20805473 GOA
Biological Process GO Annotation Evidence Reference Source
involved in regulation of AMPA receptor activity IDA
IDA: Inferred from direct assay
20805473 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

CNIH2 Protein Structure

Cornichon

Cornichon: Cornichon protein (1 - 46)

Cornichon

Cornichon: Cornichon protein (56 - 152)

  • 0
  • 100
  • 160 a.a.
Protein Preferred Names Protein Names

protein cornichon homolog 2

cornichon homolog 2

CNIH2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
CNIH2 Q6PI25 HIBADH Homo sapiens P31937 32296183
Intra
CNIH2 Q6PI25 HIBADH Homo sapiens P31937 32296183
Intra
CNIH2 Q6PI25 TMPRSS2 Homo sapiens O15393-2 32296183
Intra
CNIH2 Q6PI25 TMPRSS2 Homo sapiens O15393-2 32296183
Intra
CNIH2 Q6PI25 GORAB Homo sapiens Q5T7V8 32296183
Intra
CNIH2 Q6PI25 GORAB Homo sapiens Q5T7V8 32296183
Intra
CNIH2 Q6PI25 CD53 Homo sapiens P19397 32296183
Intra
CNIH2 Q6PI25 CD53 Homo sapiens P19397 32296183
Intra
CNIH2 Q6PI25 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
CNIH2 Q6PI25 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
CNIH2 Q6PI25 TMEM14B Homo sapiens Q9NUH8 32296183
Intra
CNIH2 Q6PI25 TMEM14B Homo sapiens Q9NUH8 32296183
Intra
CNIH2 Q6PI25 TMEM14B Homo sapiens Q9NUH8 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Schizophrenia

SCZD

Schizophrenia With Or Without An Affective Disorder

Schizophrenia 12

Schizophrenia, Susceptibility To

Schizophrenia-1

Dementia Praecox

Schizophrenia 1

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 CNIH2 RGD RGD:1304930
Canis familiaris CNIH2 VGNC VGNC:39400
Felis catus CNIH2 VGNC VGNC:61016
Macaca mulatta CNIH2 VGNC VGNC:71366
Mus musculus CNIH2 MGD MGI:1277225
Bos taurus CNIH2 VGNC VGNC:106695