TADA3 - transcriptional adaptor 3 Gene

Homo sapiens

Also known as ADA3; NGG1; hADA3; STAF54; TADA3L

Gene ID: 10474 | Gene type: protein coding

About TADA3

Cytogenetic location: 3p25.3 Genomic coordinates (GRCh38): 3:9,779,967-9,793,011 (from NCBI)

This gene has 6 transcripts (splice variants) and 218 orthologues. Ubiquitous expression in testis (RPKM 21.9), ovary (RPKM 20.9) and 25 other tissues.

Summary

DNA-binding transcriptional activator proteins increase the rate of transcription by interacting with the transcriptional machinery bound to the basal promoter in conjunction with adaptor proteins, possibly by acetylation and destabilization of nucleosomes. The protein encoded by this gene is a transcriptional activator adaptor and a component of the histone acetyl transferase (HAT) coactivator complex which plays a crucial role in chromatin modulation and cell cycle progression. Along with the other components of the complex, this protein links transcriptional activators bound to specific promoters, to histone acetylation and the transcriptional machinery. The protein is also involved in the stabilization and activation of the p53 tumor suppressor protein that plays a role in the cellular response to DNA damage. Alternate splicing results in multiple transcript variants of this gene. [provided by RefSeq, May 2013]

TADA3 Products(3)

mRNA	Protein	Name
NM_001278270.2	NP_001265199.1	transcriptional adapter 3 isoform a
NM_006354.5	NP_006345.1	transcriptional adapter 3 isoform a
NM_133480.4	NP_597814.1	transcriptional adapter 3 isoform b

TADA3 Protein Structure

Ada3

0
100
200
300
400
432 a.a.

Protein Preferred Names

Protein Names

transcriptional adapter 3

ADA3 homolog

Related Diseases

Diseases

Alias

Spinocerebellar Ataxia 7

Spinocerebellar Ataxia Type 7	SCA7
Opca3	Opca Iii
Olivopontocerebellar Atrophy Iii	Opca With Retinal Degeneration
Opca With Macular Degeneration And External Ophthalmoplegia	Adca, Type Ii
Autosomal Dominant Cerebellar Ataxia Type 2	Olivopontocerebellar Atrophy 3
Autosomal Dominant Cerebellar Ataxia, Type Ii	Autosomal Dominant Cerebellar Ataxia Type Ii
Adca2	Adcaii
Ataxia With Pigmentary Retinopathy	Cerebellar Syndrome-Pigmentary Maculopathy Syndrome
Olivopontocerebellar Atrophy With Retinal Degeneration	Spinocerebellar Ataxia-7
Ataxia, Spinocerebellar, Type 7

Epidermodysplasia Verruciformis 1

Epidermodysplasia Verruciformis	Epidermodysplasia Verruciformis, Susceptibility To, 1
Lutz-Lewandowsky Epidermodysplasia Verruciformis	EV1
Lewandowsky-Lutz Syndrome	Ev

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-RS14156	TADA3 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Bos taurus	TADA3	VGNC	VGNC:35566
Macaca mulatta	TADA3	VGNC	VGNC:78171
Canis familiaris	TADA3	VGNC	VGNC:47072
Mus musculus	TADA3	MGD	MGI:1915724
Rattus norvegicus	TADA3	RGD	RGD:1564009
Felis catus	TADA3	VGNC	VGNC:65924

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