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TTC32 - tetratricopeptide repeat domain 32 Gene

Species: Homo sapiens

Gene Type: protein coding

Gene ID: 130502

About TTC32

This gene has 4 transcripts (splice variants), 193 orthologues and 18 paralogues. Ubiquitous expression in bone marrow (RPKM 8.8), prostate (RPKM 5.9) and 25 other tissues.

TTC32 Products (1)

mRNA	Protein	Name
NM_001008237.3	NP_001008238.1	tetratricopeptide repeat protein 32

Gene Ontology

Molecular Function

Molecular Function GO Annotation	Evidence	Verweise	Source
enables protein binding	IPI IPI: Inferred from physical interaction	25416956	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

TTC32 Protein Structure

TPR_4

TPR_11

0
100
151 a.a.

Protein Preferred Names	Protein Names
tetratricopeptide repeat protein 32	TPR repeat protein 32

TTC32 Protein-protein interaction Information

Type	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	Verweise
Intra	TTC32	Q5I0X7	FBF1	Homo sapiens	Q8TES7-6	Validated Y2H	25416956
Intra	TTC32	Q5I0X7	FBF1	Homo sapiens	Q8TES7-6	Y2H Prey Pooling	25416956
Intra	TTC32	Q5I0X7	FBF1	Homo sapiens	Q8TES7-6	Y2H Array	25416956
Intra	TTC32	Q5I0X7	TXN2	Homo sapiens	Q99757	Validated Y2H	32296183
Intra	TTC32	Q5I0X7	ZNF219	Homo sapiens	Q9P2Y4	Y2H Prey Pooling	25416956
Intra	TTC32	Q5I0X7	ZNF219	Homo sapiens	Q9P2Y4	Validated Y2H	25416956
Intra	TTC32	Q5I0X7	ZNF219	Homo sapiens	Q9P2Y4	Y2H Array	25416956
Intra	TTC32	Q5I0X7	ARID3A	Homo sapiens	Q99856	Validated Y2H	25416956
Intra	TTC32	Q5I0X7	ARID3A	Homo sapiens	Q99856	Y2H Array	25416956
Intra	TTC32	Q5I0X7	ARID3A	Homo sapiens	Q99856	Y2H Prey Pooling	25416956
Intra	TTC32	Q5I0X7	TRIM39	Homo sapiens	Q9HCM9	Validated Y2H	25416956
Intra	TTC32	Q5I0X7	TRIM39	Homo sapiens	Q9HCM9	Y2H Array	25416956
Intra	TTC32	Q5I0X7	ZNF18	Homo sapiens	P17022	Y2H Prey Pooling	25416956

Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases	Alias
Pyruvate Dehydrogenase E1-Alpha Deficiency	Pyruvate Dehydrogenase Deficiency Pyruvate Dehydrogenase Complex Deficiency Pyruvate Decarboxylase Deficiency Pdh Deficiency PDHAD Pyruvate Dehydrogenase Complex Deficiency Disease Ataxia With Lactic Acidosis I Ataxia With Lactic Acidosis 1 Pdh Pdhc Ataxia With Lactic Acidosis Ataxia, Intermittent, With Abnormal Pyruvate Metabolism Ataxia, Intermittent, With Pyruvate Dehydrogenase Deficiency Deficiency Of Pyruvic Dehydrogenase Ataxia, Intermittent, With Pyruvate Dehydrogenase, Or Decarboxylase, Deficiency Pdc Deficiency Intermittent Ataxia With Pyruvate Dehydrogenase Deficiency Pdhc Deficiency Pyruvate Dehydrogenase Complex E1 Component Subunit Alpha Deficiency Ataxia Intermittent With Abnormal Pyruvate Metabolism Ataxia Intermittent With Pyruvate Dehydrogenase Or Decarboxylase Deficiency Pyruvate Dehydrogenase E1 Alpha Deficiency Pdc - [Pyruvate Dehydrogenase Complex] Deficiency Ataxia With Lactic Acidosis 2

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

Pre-clinical Phase

Bioactive Molecules (1)

Art. -Nr.	Produktname	Wirkung	Reinheit	Rare Diseases
HY-RS15209	TTC32 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Bos taurus	TTC32	VGNC	VGNC:36470
Felis catus	TTC32	VGNC	VGNC:81256
Macaca mulatta	TTC32	VGNC	VGNC:82093
Rattus norvegicus	TTC32	RGD	RGD:1585566
Mus musculus	TTC32	MGD	MGI:1922766
Canis familiaris	TTC32	VGNC	VGNC:47952
Others	TTC32	NCBI