TBC1D22A - TBC1 domain family member 22A Gene

Also Known as C22orf4; HSC79E021

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 25771

About TBC1D22A

Cytogenetic location: 22q13.31 Genomic coordinates (GRCh38): 22:46,762,650-47,175,699 (from NCBI)

This gene has 11 transcripts (splice variants), 202 orthologues and 45 paralogues. Ubiquitous expression in spleen (RPKM 2.7), lymph node (RPKM 2.5) and 25 other tissues.

Summary

Enables 14-3-3 protein binding activity and protein homodimerization activity. Predicted to be involved in activation of GTPase activity and intracellular protein transport. [provided by Alliance of Genome Resources, Apr 2022]

TBC1D22A Products (5)

mRNA Protein Name
NM_001284303.2 NP_001271232.1 TBC1 domain family member 22A isoform b
NM_001284304.2 NP_001271233.1 TBC1 domain family member 22A isoform c
NM_001284305.2 NP_001271234.1 TBC1 domain family member 22A isoform d
NM_001410803.1 NP_001397732.1 TBC1 domain family member 22A isoform e
NM_014346.5 NP_055161.1 TBC1 domain family member 22A isoform a
Molecular Function GO Annotation Evidence References Source
enables 14-3-3 protein binding IDA
IDA: Inferred from direct assay
23572552 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
23572552 GOA
enables protein homodimerization activity IDA
IDA: Inferred from direct assay
18186464 GOA
Biological Process GO Annotation Evidence References Source
NOT involved in regulation of cilium assembly IMP
IMP: Inferred from mutant phenotype
17646400 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

TBC1D22A Protein Structure

RabGAP-TBC

RabGAP-TBC: Rab-GTPase-TBC domain (227 - 469)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 517 a.a.
Protein Preferred Names Protein Names

TBC1 domain family member 22A

  • putative GTPase activator

TBC1D22A Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
TBC1D22A Q8WUA7 ACBD3 Homo sapiens Q9H3P7 23572552
Intra
TBC1D22A Q8WUA7 ACBD3 Homo sapiens Q9H3P7 33961781
Intra
TBC1D22A Q8WUA7 ACBD3 Homo sapiens Q9H3P7 23572552
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Epilepsy, Familial Temporal Lobe, 5
  • Familial Temporal Lobe Epilepsy 5

  • ETL5

  • Epilepsy, Temporal Lobe, Familial, Type 5

Febrile Seizures, Familial, 8
  • FEB8

  • Epilepsy, Childhood Absence 2

  • Generalized Epilepsy With Febrile Seizures Plus 3

  • Generalized Epilepsy With Febrile Seizures Plus, Type 3

  • Familial Febrile Seizures 8

  • Familial Febrile Convulsions 8

  • Epilepsy, Childhood Absence, Susceptibility To, 2

  • ECA2

  • GEFS+3

  • Gefs+ Type 3

  • Gefsp3

  • Epilepsy, Generalized, With Febrile Seizures Plus, Type 3

Generalized Epilepsy With Febrile Seizures Plus, Type 7
  • Febrile Seizures, Familial, 3b

  • GEFSP7

  • GEFS+7

  • Generalized Epilepsy With Febrile Seizures Plus 7

  • Gefs+, Type 7

  • Generalised Epilepsy With Febrile Seizures Plus 7

  • Generalised Epilepsy With Febrile Seizures Plus Type 7

  • Generalized Epilepsy With Febrile Seizures Plus Type 7

  • FEB3B

  • Familial Febrile Convulsions 3

  • Gefs+ Type 7

  • Epilepsy, Generalized, With Febrile Seizures Plus, Type 7

  • Generalized Epilepsy With Febrile Seizures Plus, 7

Generalized Epilepsy With Febrile Seizures Plus, Type 2
  • Febrile Seizures, Familial, 3a

  • GEFSP2

  • GEFS+2

  • Generalized Epilepsy With Febrile Seizures Plus 2

  • Gefs+, Type 2

  • Generalised Epilepsy With Febrile Seizures Plus 2

  • Generalised Epilepsy With Febrile Seizures Plus Type 2

  • Generalized Epilepsy With Febrile Seizures Plus Type 2

  • FEB3A

  • Familial Febrile Convulsions 3

  • Gefs+ Type 2

  • Epilepsy, Generalized, With Febrile Seizures Plus, Type 2

  • Febrile Convulsions, Familial, 3a

Febrile Seizures, Familial, 4
  • FEB4

  • Convulsions, Familial Febrile, 4

  • Familial Febrile Seizures 4

  • Familial Febrile Convulsions 4

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
Canis familiaris TBC1D22A VGNC VGNC:47141
Rattus norvegicus TBC1D22A RGD RGD:1306588
Bos taurus TBC1D22A VGNC VGNC:35636
Felis catus TBC1D22A VGNC VGNC:65981
Macaca mulatta TBC1D22A VGNC VGNC:82077
Mus musculus TBC1D22A MGD MGI:1289265
Others TBC1D22A NCBI