TACC3 - transforming acidic coiled-coil containing protein 3 Gene

Also Known as ERIC1; Tacc4; ERIC-1; maskin

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 10460

About TACC3

Cytogenetic location: 4p16.3 Genomic coordinates (GRCh38): 4:1,721,521-1,745,171 (from NCBI)

This gene has 17 transcripts (splice variants), 199 orthologues, 2 paralogues and is associated with 2 phenotypes. Broad expression in testis (RPKM 25.6), bone marrow (RPKM 24.9) and 16 other tissues.

Summary

This gene encodes a member of the transforming acidic colied-coil protein family. The encoded protein is a motor spindle protein that may play a role in stabilization of the mitotic spindle. This protein may also play a role in growth a differentiation of certain Cancer cells. [provided by RefSeq, Nov 2011]

TACC3 Products (2)

mRNA Protein Name
NM_001410699.1 NP_001397628.1 transforming acidic coiled-coil-containing protein 3 isoform 2
NM_006342.3 NP_006333.1 transforming acidic coiled-coil-containing protein 3 isoform 1
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
20360068 GOA
Biological Process GO Annotation Evidence References Source
involved in metaphase/anaphase transition of mitotic cell cycle IMP
IMP: Inferred from mutant phenotype
23532825 GOA
involved in microtubule cytoskeleton organization involved in mitosis IMP
IMP: Inferred from mutant phenotype
23532825 GOA
involved in regulation of mitotic spindle organization IMP
IMP: Inferred from mutant phenotype
21297582 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

TACC3 Protein Structure

TACC

TACC: Transforming acidic coiled-coil-containing protein (TACC) (638 - 837)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 838 a.a.
Protein Preferred Names Protein Names

transforming acidic coiled-coil-containing protein 3

TACC3 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
TACC3 Q9Y6A5 CIB3 Homo sapiens Q96Q77 25416956
Intra
TACC3 Q9Y6A5 CIB3 Homo sapiens Q96Q77 32296183
Intra
TACC3 Q9Y6A5 CIB3 Homo sapiens Q96Q77 32296183
Intra
TACC3 Q9Y6A5 CLTA Homo sapiens P09496 21297582
Intra
TACC3 Q9Y6A5 ASPSCR1 Homo sapiens Q9BZE9 25416956
Intra
TACC3 Q9Y6A5 ASPSCR1 Homo sapiens Q9BZE9 25416956
Intra
TACC3 Q9Y6A5 IQCD Homo sapiens Q96DY2-2 32296183
Intra
TACC3 Q9Y6A5 IQCD Homo sapiens Q96DY2-2 32296183
Intra
TACC3 Q9Y6A5 VPS37C Homo sapiens A5D8V6 25416956
Intra
TACC3 Q9Y6A5 VPS37C Homo sapiens A5D8V6 25416956
Intra
TACC3 Q9Y6A5 EGFR Homo sapiens P00533 27956147
Intra
TACC3 Q9Y6A5 EGFR Homo sapiens P00533 27956147
Intra
TACC3 Q9Y6A5 CKAP5 Homo sapiens Q14008 33961781
Intra
TACC3 Q9Y6A5 CKAP5 Homo sapiens Q14008
IF
21297582
Intra
TACC3 Q9Y6A5 CKAP5 Homo sapiens Q14008 26496610
Intra
TACC3 Q9Y6A5 CKAP5 Homo sapiens Q14008 21297582
Intra
TACC3 Q9Y6A5 SNX20 Homo sapiens Q7Z614 25416956
Intra
TACC3 Q9Y6A5 SNX20 Homo sapiens Q7Z614 25416956
Intra
TACC3 Q9Y6A5 CEP55 Homo sapiens Q53EZ4
Y2H
27107012
Intra
TACC3 Q9Y6A5 CEP55 Homo sapiens Q53EZ4 33961781
Intra
TACC3 Q9Y6A5 CEP55 Homo sapiens Q53EZ4
SLC
27107012
Intra
TACC3 Q9Y6A5 TBC1D22B Homo sapiens Q9NU19 29892012
Intra
TACC3 Q9Y6A5 TBC1D22B Homo sapiens Q9NU19 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

TACC3 Antibodies

Cat. No. Product Name Application Reactivity
HY-P83176 TACC3 Antibody (YA2921) WB, IHC-P, ICC/IF Human, Mouse, Rat

Related Diseases

Diseases Alias
Gliosarcoma
  • Glioblastoma With Sarcomatous Component

  • Sarcomatous Glioblastoma

Giant Cell Glioblastoma
  • Monstrocellular Sarcoma

Developmental And Epileptic Encephalopathy 23
  • DEE23

  • Epileptic Encephalopathy, Early Infantile, 23

  • Eiee23

  • Early-Onset Epileptic Encephalopathy-Cortical Blindness-Intellectual Disability-Facial Dysmorphism Syndrome

  • Epilepsy-Cortical Blindness-Intellectual Disability-Facial Dysmorphism Syndrome

  • Developmental And Epileptic Encephalopathy, 23

  • Early Infantile Epileptic Encephalopathy 23

Thymus Lymphoma
  • Thymic Lymphoma

Bladder Cancer
  • Urinary Bladder Cancer

  • Bladder Carcinoma

  • Urinary Bladder Carcinoma

  • Bladder Neoplasm

  • Bladder Tumor

  • Cancer, Bladder

  • Malignant Neoplasm Of Urinary Bladder

  • Carcinoma Of Bladder

  • Bladder Cancer, Somatic

  • Tumor Of The Bladder

  • Carcinoma Of Urinary Bladder

  • Bladder Carcinoma Urinary

  • Cancer Of The Urinary Bladder

  • Cancer, Urinary Bladder

  • Malignant Bladder Neoplasm

  • Malignant Bladder Tumor

  • Neoplasm Of The Bladder

  • Neoplasm Of The Urinary Bladder

  • Tumor Of The Urinary Bladder

  • Urinary Bladder Neoplasm

  • BLC

  • Urothelial Carcinoma Of The Bladder

  • Bladder Tumors

  • Urinary Bladder Neoplasms

  • Bladder Cancer Nos

  • Vesical Cancer Nos

  • Malignant Neoplasm Of Bladder, Part Unspecified

  • Malignant Tumour Of Urinary Bladder

  • Primary Malignant Neoplasm Of Bladder

Wolf-Hirschhorn Syndrome
  • Pitt-Rogers-Danks Syndrome

  • WHS

  • Chromosome 4p16.3 Deletion Syndrome

  • Wittwer Syndrome

  • 4p- Syndrome

  • Pitt Syndrome

  • 4p Deletion Syndrome

  • Distal Deletion 4p

  • Distal Monosomy 4p

  • Telomeric Deletion 4p

  • Prds

  • 4p Syndrome

  • Chromosome 4p Syndrome

  • Microcephaly, Iugr, Hypertelorism, Ptosis, Iris Coloboma, Hooked Nose, External Ear Dysplasia, Psychomotor Retardation

  • Wolf Syndrome

  • Chromosome 4p Deletion Syndrome

  • Chromosome 4p Monosomy

  • Del Syndrome

  • Monosomy 4p

  • Partial Monosomy 4p

  • Chromosome 4 Short Arm Deletion

Fibrolamellar Carcinoma
  • Fibrolamellar Hepatocellular Carcinoma

  • Fhcc

  • Fibrolamellar Hepatocarcinoma

  • Hepatocellular Carcinoma, Fibrolamellar

  • Oncocytic Hepatocellular Tumor

  • Eosinophilic Glassy Cell Hepatoma

  • Eosinophilic Hepatocellular Carcinoma With Lamellar Fibrosis

  • Fl-Hcc

  • Fibrolamellar Oncocytic Hepatoma

  • Hepatocellular Carcinoma With Increased Stromal Fibrosis

  • Polygonal Cell Hepatocellular Carcinoma With Fibrous Stroma

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 TACC3 VGNC VGNC:53244
Bos taurus TACC3 VGNC VGNC:53778
Macaca mulatta TACC3 VGNC VGNC:78082
Rattus norvegicus TACC3 RGD RGD:1302948
Mus musculus TACC3 MGD MGI:1341163
Felis catus TACC3 VGNC VGNC:82312
Others TACC3 NCBI