TBC1D22A - TBC1 domain family member 22A Gene

Homo sapiens

Also known as C22orf4; HSC79E021

Gene ID: 25771 | Gene type: protein coding

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

TBC1D22A Protein Structure

RabGAP-TBC

0
100
200
300
400
517 a.a.

Protein Preferred Names

Protein Names

TBC1 domain family member 22A

putative GTPase activator

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

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS14236	TBC1D22A Human Pre-designed siRNA Set A		/	Unkown

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

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