1. Gene
  2. CLRN3 - clarin 3 Gene

CLRN3 - clarin 3 Gene

Homo sapiens

Also known as TMEM12; USH3AL1

Gene ID: 119467 | Gene type: protein coding

About CLRN3

This gene has 1 transcript (splice variant), 198 orthologues and 2 paralogues. Biased expression in small intestine (RPKM 43.6), colon (RPKM 38.2) and 5 other tissues.

Summary

Located in extracellular exosome. [provided by Alliance of Genome Resources, Apr 2022]

CLRN3 Products(1)

mRNA Protein Name
NM_152311.5 NP_689524.1 clarin-3
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
28514442 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

CLRN3 Protein Structure

Claudin_2

Claudin_2: PMP-22/EMP/MP20/Claudin tight junction (20 - 199)

  • 0
  • 100
  • 200
  • 226 a.a.
Protein Preferred Names Protein Names

clarin-3

transmembrane protein 12

CLRN3 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra CLRN3 Q8NCR9 NME2P1 Homo sapiens O60361
Anti Tag CoIP
28514442
Intra CLRN3 Q8NCR9 NME2P1 Homo sapiens O60361
Anti Tag CoIP
33961781
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Usher Syndrome, Type Iiia

Usher Syndrome Type 3

Ush3

Usher Syndrome Type 3a

USH3A

Usher Syndrome, Type Iii

Usher Syndrome, Type 3

Usher Syndrome, Type 3a

Usher Syndrome Type Iiia

Usher Syndrome 3a

Usher'S Syndrome Type 3

Usher Syndrome Iii

Usher Syndrome Type Iii

Usher Syndrome

Deafness-Retinitis Pigmentosa Syndrome

Dystrophia Retinae Pigmentosa-Dysostosis Syndrome

Graefe-Usher Syndrome

Hallgren Syndrome

Usher'S Syndrome

Retinitis Pigmentosa-Deafness Syndrome

Retinitis Pigmentosa-Hearing Loss Syndrome

Ush

Usher Syndromes

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
Bos taurus CLRN3 VGNC VGNC:27464
Canis familiaris CLRN3 VGNC VGNC:39361
Rattus norvegicus CLRN3 RGD RGD:1305043
Mus musculus CLRN3 MGD MGI:2142022
Macaca mulatta CLRN3 VGNC VGNC:106025