ORAI2 - ORAI calcium release-activated calcium modulator 2 Gene

Also Known as CBCIP2; C7orf19; MEM142B; TMEM142B

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 80228

About ORAI2

Cytogenetic location: 7q22.1 Genomic coordinates (GRCh38): 7:102,433,575-102,456,825 (from NCBI)

This gene has 9 transcripts (splice variants), 204 orthologues and 2 paralogues. Broad expression in spleen (RPKM 5.4), bone marrow (RPKM 5.3) and 23 other tissues.

Summary

Predicted to enable store-operated Calcium Channel activity. Predicted to be involved in store-operated calcium entry. Predicted to be located in growth cone. Predicted to be integral component of membrane. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Apr 2022]

ORAI2 Products (4)

mRNA Protein Name
NM_001126340.3 NP_001119812.1 protein orai-2 isoform a
NM_001271818.2 NP_001258747.1 protein orai-2 isoform a
NM_001271819.2 NP_001258748.1 protein orai-2 isoform b
NM_032831.4 NP_116220.1 protein orai-2 isoform a
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
17442569 GOA
enables store-operated calcium channel activity IDA
IDA: Inferred from direct assay
17442569 GOA
enables store-operated calcium channel activity IMP
IMP: Inferred from mutant phenotype
32415068 GOA
Biological Process GO Annotation Evidence References Source
involved in store-operated calcium entry IDA
IDA: Inferred from direct assay
19182790 GOA
Cellular Component GO Annotation Evidence References Source
located in plasma membrane IDA
IDA: Inferred from direct assay
32415068 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

ORAI2 Protein Structure

Orai-1

Orai-1: Mediator of CRAC channel activity (42 - 230)

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

protein orai-2

  • CAP-binding protein complex interacting protein 2

Related Diseases

Diseases Alias
Immunodeficiency 10
  • Immune Dysfunction With T-Cell Inactivation Due To Calcium Entry Defect 2

  • Combined Immunodeficiency Due To Stim1 Deficiency

  • IMD10

  • Stim1 Deficiency

  • Cid Due To Stim1 Deficiency

  • Immune Dysfunction, With T-Cell Inactivation Due To Calcium Entry Defect 2

  • Immunodeficiency, Type 10

T Cell And Nk Cell Immunodeficiency
Amelogenesis Imperfecta, Type Iiia
  • Ai3

  • Adhcai

  • Amelogenesis Imperfecta Type 3

  • AI3A

  • Amelogenesis Imperfecta, Type Iii

  • Amelogenesis Imperfecta, Hypocalcification Type, Autosomal Dominant

  • Amelogenesis Imperfecta Type 3a

  • Amelogenesis Imperfecta Hypomineralization Type

  • Amelogenesis Imperfecta Type Iii

  • Hypocalcified Amelogenesis Imperfecta

  • Amelogenesis Imperfecta, Type 3

  • Amelogenesis Imperfecta, Hypomineralization Type

  • Autosomal Dominant Amelogenesis Imperfecta Hypocalcification Type

  • Amelogenesis Imperfecta 3a

  • Amelogenesis Imperfecta Hypocalcification Type Autosomal Dominant

Stormorken Syndrome
  • Thrombocytopathy, Asplenia, And Miosis

  • Stormorken-Sjaastad-Langslet Syndrome

  • STRMK

  • York Platelet Syndrome

  • Yps

  • Thrombocytopathy, Asplenia And Miosis

  • Thrombocytopathy Asplenia Miosis

  • Thrombocytopathy-Asplenia-Miosis Syndrome

  • Miosis Disorder

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
Mus musculus ORAI2 MGD MGI:2443195
Felis catus ORAI2 VGNC VGNC:63972
Macaca mulatta ORAI2 VGNC VGNC:75665
Rattus norvegicus ORAI2 RGD RGD:1310213
Canis familiaris ORAI2 VGNC VGNC:44138
Bos taurus ORAI2 VGNC VGNC:32444
Others ORAI2 NCBI