TSPAN2 - tetraspanin 2 Gene

Also Known as NET3; TSN2; TSPAN-2

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 10100

About TSPAN2

Cytogenetic location: 1p13.2 Genomic coordinates (GRCh38): 1:115,048,011-115,089,503 (from NCBI)

This gene has 4 transcripts (splice variants), 269 orthologues and 32 paralogues. Broad expression in endometrium (RPKM 16.8), urinary bladder (RPKM 10.7) and 19 other tissues.

Summary

The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015]

TSPAN2 Products (3)

mRNA Protein Name
NM_001308315.2 NP_001295244.1 tetraspanin-2 isoform 2
NM_001308316.2 NP_001295245.1 tetraspanin-2 isoform 3
NM_005725.6 NP_005716.2 tetraspanin-2 isoform 1
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
25814554 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

TSPAN2 Protein Structure

Tetraspannin

Tetraspannin: Tetraspanin family (10 - 214)

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

tetraspanin-2

  • new EST tetraspan 3

TSPAN2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
TSPAN2 O60636 SLC30A8 Homo sapiens Q8IWU4 32296183
Intra
TSPAN2 O60636 SLC30A8 Homo sapiens Q8IWU4 32296183
Intra
TSPAN2 O60636 SLC30A8 Homo sapiens Q8IWU4 32296183
Intra
TSPAN2 O60636 PGRMC2 Homo sapiens O15173 32296183
Intra
TSPAN2 O60636 PGRMC2 Homo sapiens O15173 32296183
Intra
TSPAN2 O60636 BSCL2 Homo sapiens J3KQ12 32296183
Intra
TSPAN2 O60636 BSCL2 Homo sapiens J3KQ12 32296183
Intra
TSPAN2 O60636 ATN1 Homo sapiens Q86V38 32814053
Intra
TSPAN2 O60636 ATN1 Homo sapiens Q86V38 32814053
Intra
TSPAN2 O60636 ATN1 Homo sapiens Q86V38 32814053
Intra
TSPAN2 O60636 MFF Homo sapiens Q9GZY8-5 32296183
Intra
TSPAN2 O60636 MFF Homo sapiens Q9GZY8-5 32296183
Intra
TSPAN2 O60636 MFF Homo sapiens Q9GZY8-5 32296183
Intra
TSPAN2 O60636 DCBLD2 Homo sapiens Q96PD2-2 32296183
Intra
TSPAN2 O60636 DCBLD2 Homo sapiens Q96PD2-2 32296183
Intra
TSPAN2 O60636 DCBLD2 Homo sapiens Q96PD2-2 32296183
Intra
TSPAN2 O60636 ATP1B4 Homo sapiens Q9UN42 32296183
Intra
TSPAN2 O60636 ATP1B4 Homo sapiens Q9UN42 32296183
Intra
TSPAN2 O60636 ATP1B4 Homo sapiens Q9UN42 32296183
Intra
TSPAN2 O60636 SCN3B Homo sapiens Q9NY72 32296183
Intra
TSPAN2 O60636 SCN3B Homo sapiens Q9NY72 32296183
Intra
TSPAN2 O60636 SCN3B Homo sapiens Q9NY72 32296183
Intra
TSPAN2 O60636 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
Intra
TSPAN2 O60636 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
Intra
TSPAN2 O60636 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
Intra
TSPAN2 O60636 TSPAN31 Homo sapiens Q12999 32296183
Intra
TSPAN2 O60636 TSPAN31 Homo sapiens Q12999 32296183
Intra
TSPAN2 O60636 TSPAN31 Homo sapiens Q12999 32296183
Intra
TSPAN2 O60636 CLEC14A Homo sapiens Q86T13 32296183
Intra
TSPAN2 O60636 CLEC14A Homo sapiens Q86T13 32296183
Intra
TSPAN2 O60636 CLEC14A Homo sapiens Q86T13 32296183
Intra
TSPAN2 O60636 KDELR3 Homo sapiens O43731-2 32296183
Intra
TSPAN2 O60636 KDELR3 Homo sapiens O43731-2 32296183
Intra
TSPAN2 O60636 SLC10A6 Homo sapiens Q3KNW5 32296183
Intra
TSPAN2 O60636 SLC10A6 Homo sapiens Q3KNW5 32296183
Intra
TSPAN2 O60636 SLC10A6 Homo sapiens Q3KNW5 32296183
Intra
TSPAN2 O60636 FAM209A Homo sapiens Q5JX71 32296183
Intra
TSPAN2 O60636 FAM209A Homo sapiens Q5JX71 32296183
Intra
TSPAN2 O60636 FAM209A Homo sapiens Q5JX71 32296183
Intra
TSPAN2 O60636 CLDN5 Homo sapiens O00501 32296183
Intra
TSPAN2 O60636 CLDN5 Homo sapiens O00501 32296183
Intra
TSPAN2 O60636 TMEM130 Homo sapiens Q8N3G9 32296183
Intra
TSPAN2 O60636 TMEM130 Homo sapiens Q8N3G9 32296183
Intra
TSPAN2 O60636 TMEM130 Homo sapiens Q8N3G9 32296183
Intra
TSPAN2 O60636 RNF19B Homo sapiens Q6ZMZ0 32296183
Intra
TSPAN2 O60636 RNF19B Homo sapiens Q6ZMZ0 32296183
Intra
TSPAN2 O60636 RNF19B Homo sapiens Q6ZMZ0 32296183
Intra
TSPAN2 O60636 F13A1 Homo sapiens P00488 32814053
Intra
TSPAN2 O60636 F13A1 Homo sapiens P00488 32814053
Intra
TSPAN2 O60636 F13A1 Homo sapiens P00488 32814053
Intra
TSPAN2 O60636 FGFR3 Homo sapiens P22607 32814053
Intra
TSPAN2 O60636 FGFR3 Homo sapiens P22607 32814053
Intra
TSPAN2 O60636 FGFR3 Homo sapiens P22607 32814053
Intra
TSPAN2 O60636 ABHD16A Homo sapiens O95870 32296183
Intra
TSPAN2 O60636 ABHD16A Homo sapiens O95870 32296183
Intra
TSPAN2 O60636 ABHD16A Homo sapiens O95870 32296183
Intra
TSPAN2 O60636 GSN Homo sapiens P06396 32814053
Intra
TSPAN2 O60636 GSN Homo sapiens P06396 32814053
Intra
TSPAN2 O60636 GSN Homo sapiens P06396 32814053
Intra
TSPAN2 O60636 ZFYVE27 Homo sapiens Q5T4F4 32296183
Intra
TSPAN2 O60636 ZFYVE27 Homo sapiens Q5T4F4 32296183
Intra
TSPAN2 O60636 ZFYVE27 Homo sapiens Q5T4F4 32296183
Intra
TSPAN2 O60636 IFNGR2 Homo sapiens P38484 32296183
Intra
TSPAN2 O60636 IFNGR2 Homo sapiens P38484 32296183
Intra
TSPAN2 O60636 IFNGR2 Homo sapiens P38484 32296183
Intra
TSPAN2 O60636 FKBP7 Homo sapiens Q9Y680 32296183
Intra
TSPAN2 O60636 FKBP7 Homo sapiens Q9Y680 32296183
Intra
TSPAN2 O60636 FKBP7 Homo sapiens Q9Y680 32296183
Intra
TSPAN2 O60636 GRB2 Homo sapiens P62993 25814554
Intra
TSPAN2 O60636 GRB2 Homo sapiens P62993 25814554
Intra
TSPAN2 O60636 TMX2 Homo sapiens Q9Y320 32296183
Intra
TSPAN2 O60636 TMX2 Homo sapiens Q9Y320 32296183
Intra
TSPAN2 O60636 TMX2 Homo sapiens Q9Y320 32296183
Intra
TSPAN2 O60636 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
TSPAN2 O60636 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
TSPAN2 O60636 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
TSPAN2 O60636 MGST3 Homo sapiens O14880 32296183
Intra
TSPAN2 O60636 MGST3 Homo sapiens O14880 32296183
Intra
TSPAN2 O60636 VSIR Homo sapiens Q9H7M9 32296183
Intra
TSPAN2 O60636 VSIR Homo sapiens Q9H7M9 32296183
Intra
TSPAN2 O60636 VSIR Homo sapiens Q9H7M9 32296183
Intra
TSPAN2 O60636 LEPROTL1 Homo sapiens O95214 32296183
Intra
TSPAN2 O60636 LEPROTL1 Homo sapiens O95214 32296183
Intra
TSPAN2 O60636 LEPROTL1 Homo sapiens O95214 32296183
Intra
TSPAN2 O60636 REEP4 Homo sapiens Q9H6H4 32296183
Intra
TSPAN2 O60636 REEP4 Homo sapiens Q9H6H4 32296183
Intra
TSPAN2 O60636 REEP4 Homo sapiens Q9H6H4 32296183
Intra
TSPAN2 O60636 CD79A Homo sapiens P11912 32296183
Intra
TSPAN2 O60636 CD79A Homo sapiens P11912 32296183
Intra
TSPAN2 O60636 CD79A Homo sapiens P11912 32296183
Intra
TSPAN2 O60636 PIK3R3 Homo sapiens Q92569 25814554
Intra
TSPAN2 O60636 PIK3R3 Homo sapiens Q92569 25814554
Intra
TSPAN2 O60636 PIK3R3 Homo sapiens Q92569 25814554
Intra
TSPAN2 O60636 TMEM14B Homo sapiens Q9NUH8 32296183
Intra
TSPAN2 O60636 TMEM14B Homo sapiens Q9NUH8 32296183
Intra
TSPAN2 O60636 TMEM14B Homo sapiens Q9NUH8 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Migraine, Familial Hemiplegic, 2
  • FHM2

  • Mhp2

  • Migraine, Familial Basilar

  • Familial Hemiplegic Migraine 2

  • Familial Hemiplegic Migraine-2

  • Familiar Basilar Migraine

  • Migraine, Hemiplegic, Familial, Type 2

Vasculopathy, Retinal, With Cerebral Leukoencephalopathy And Systemic Manifestations
  • Retinal Vasculopathy With Cerebral Leukoencephalopathy And Systemic Manifestations

  • Crv

  • Rvcl

  • Rvcl-S

  • Vasculopathy, Retinal, With Cerebral Leukodystrophy

  • Retinopathy, Vascular, With Cerebral And Renal Involvement And Raynaud And Migraine Phenomena

  • Retinal Vasculopathy With Cerebral Leukodystrophy

  • Retinal Vasculopathy And Cerebral Leukoencephalopathy

  • Hereditary Vascular Retinopathy

  • Hvr

  • RVCLS

  • Cerebroretinal Vasculopathy, Hereditary

  • Cerebroretinal Vasculopathy

  • Herns

  • Vasculopathy, Retinal, With Cerebral Leukodystrophy, Formerly

  • Hereditary Cerebroretinal Vasculopathy

  • Hereditary Endotheliopathy, Retinopathy, Nephropathy, Stroke

  • Hereditary Systemic Angiopathy

  • Hsa

  • Retinal Vasculopathy With Cerebral Leukodystrophy With Systemic Manifestations

  • Adrvcl

  • Autosomal Dominant Retinal Vasculopathy With Cerebral Leukodystrophy

  • Hereditary Endotheliopathy With Retinopathy-Nephropathy-Stroke

  • Vascular Retinopathy With Cerebral And Renal Involvement And Raynaud And Migraine Phenomena

Clonorchiasis
  • Oriental Liver Fluke Disease

  • Clonorchis Liver Infection

  • Clonorchiosis

  • Chinese Liver Fluke Disease

  • Hepatic Distomiasis Due To Clonorchis Sinensis

  • Infection Due To Clonorchis Sinensis

  • Hepatic Distomiasis

  • Hepatic Distomatosis

  • Chinese Liver Fluke Disorder

  • Oriental Liver Fluke Disorder

  • Clonorchis Infestation

  • Chinese Liver Fluke Infestation

  • Liver Fluke Disease Due To Clonorchis Sinensis

  • Oriental Liver Fluke Infestation

Migraine, Familial Hemiplegic, 3
  • FHM3

  • Familial Hemiplegic Migraine 3

  • Mhp3

  • Migraine, Hemiplegic, Familial, Type 3

Migraine With Or Without Aura 1
  • Migraine

  • Migraine With Or Without Aura, Susceptibility To, 1

  • Migraine Disorder

  • Migraine Variant

  • Migraines

  • Migraine Disorders

  • Mgr1

  • Mgau

  • Ma

  • Migraine With Or Without Aura

  • Classic Migraine

  • Common Migraine

  • Disorder, Migraine

  • Headache Migraine

  • Headache Migrainous

  • Migraine Headache

  • Migraine Syndrome

  • Headache Including Migraine

  • Migraine, Susceptibility To

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 TSPAN2 RGD RGD:620982
Bos taurus TSPAN2 VGNC VGNC:36435
Macaca mulatta TSPAN2 VGNC VGNC:79264
Felis catus TSPAN2 VGNC VGNC:66630
Mus musculus TSPAN2 MGD MGI:1917997
Canis familiaris TSPAN2 VGNC VGNC:47918
Others TSPAN2 NCBI