1. Gene
  2. OTOP2 - otopetrin 2 Gene

OTOP2 - otopetrin 2 Gene

Homo sapiens
Gene ID: 92736 | Gene type: protein coding

About OTOP2

Cytogenetic location: 17q25.1 Genomic coordinates (GRCh38): 17:74,924,273-74,933,912 (from NCBI)

This gene has 3 transcripts (splice variants), 247 orthologues and 2 paralogues. Biased expression in colon (RPKM 10.3), testis (RPKM 1.8) and 1 other tissue.

Summary

Predicted to enable proton channel activity. Predicted to be involved in proton transmembrane transport. Predicted to be located in plasma membrane. Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

OTOP2 Products(1)

mRNA Protein Name
NM_178160.3 NP_835454.1 proton channel OTOP2
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 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

OTOP2 Protein Structure

Otopetrin

Otopetrin: Otopetrin (102 - 218)

Otopetrin

Otopetrin: Otopetrin (229 - 437)

Otopetrin

Otopetrin: Otopetrin (485 - 548)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 562 a.a.
Protein Preferred Names Protein Names

proton channel OTOP2

OTOP2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
OTOP2 Q7RTS6 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
OTOP2 Q7RTS6 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
OTOP2 Q7RTS6 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
OTOP2 Q7RTS6 GJA8 Homo sapiens P48165 32296183
Intra
OTOP2 Q7RTS6 GJA8 Homo sapiens P48165 32296183
Intra
OTOP2 Q7RTS6 MANBAL Homo sapiens Q9NQG1 32296183
Intra
OTOP2 Q7RTS6 MANBAL Homo sapiens Q9NQG1 32296183
Intra
OTOP2 Q7RTS6 MANBAL Homo sapiens Q9NQG1 32296183
Intra
OTOP2 Q7RTS6 FATE1 Homo sapiens Q969F0 32296183
Intra
OTOP2 Q7RTS6 FATE1 Homo sapiens Q969F0 32296183
Intra
OTOP2 Q7RTS6 FATE1 Homo sapiens Q969F0 32296183
Intra
OTOP2 Q7RTS6 FATE1 Homo sapiens Q969F0 32296183
Intra
OTOP2 Q7RTS6 CD79A Homo sapiens P11912 32296183
Intra
OTOP2 Q7RTS6 CD79A Homo sapiens P11912 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Vertigo, Benign Recurrent

Benign Paroxysmal Positional Vertigo

Bppv

Vestibulopathy, Familial

BRV

Vertigo, Benign Paroxysmal Positional

Benign Paroxysmal Positional Nystagmus

Benign Recurrent Vertigo

Familial Benign Recurrent Vertigo

Familial Vestibulopathy

Benign Paroxysmal Nystagmus

Bppv - [Benign Positional Paroxysmal Vertigo]

Diversion Colitis
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
Felis catus OTOP2 VGNC VGNC:63996
Macaca mulatta OTOP2 VGNC VGNC:104639
Mus musculus OTOP2 MGD MGI:2388365
Bos taurus OTOP2 VGNC VGNC:32489
Rattus norvegicus OTOP2 RGD RGD:1304830