1. Gene
  2. TTC32 - tetratricopeptide repeat domain 32 Gene

TTC32 - tetratricopeptide repeat domain 32 Gene

Homo sapiens
Gene ID: 130502 | Gene type: protein coding

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 Reference 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_4: Tetratricopeptide repeat (9 - 30)

TPR_11

TPR_11: TPR repeat (57 - 123)

  • 0
  • 100
  • 151 a.a.
Protein Preferred Names Protein Names

tetratricopeptide repeat protein 32

TPR repeat protein 32

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

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