1. Gene
  2. TSHZ2 - teashirt zinc finger homeobox 2 Gene

TSHZ2 - teashirt zinc finger homeobox 2 Gene

Homo sapiens

Also known as TSH2; ZABC2; ZNF218; OVC10-2; C20orf17

Gene ID: 128553 | Gene type: protein coding

About TSHZ2

Cytogenetic location: 20q13.2 Genomic coordinates (GRCh38): 20:52,972,358-53,495,330 (from NCBI)

This gene has 5 transcripts (splice variants), 204 orthologues and 2 paralogues. Ubiquitous expression in gall bladder (RPKM 3.9), ovary (RPKM 3.7) and 23 other tissues.

Summary

This gene is a member of the teashirt C2H2-type zinc-finger protein family of transcription factors. This gene encodes a protein with five C2H2-type zinc fingers, a homeobox DNA-binding domain and a coiled-coil domain. This nuclear protein is predicted to act as a transcriptional repressor. This gene is thought to play a role in the development and progression of breast and Other types of Cancer. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]

TSHZ2 Products(2)

mRNA Protein Name
NM_001193421.2 NP_001180350.1 teashirt homolog 2 isoform 2
NM_173485.6 NP_775756.3 teashirt homolog 2 isoform 1
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
24407287 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

TSHZ2 Protein Structure

zf-C2H2_2

zf-C2H2_2: C2H2 type zinc-finger (2 copies) (266 - 301)

zf-C2H2_2

zf-C2H2_2: C2H2 type zinc-finger (2 copies) (380 - 407)

zf-C2H2_2

zf-C2H2_2: C2H2 type zinc-finger (2 copies) (928 - 1023)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1034 a.a.
Protein Preferred Names Protein Names

teashirt homolog 2

cell growth-inhibiting protein 7

TSHZ2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
TSHZ2 Q9NRE2 CCDC57 Homo sapiens Q2TAC2-2 32296183
Intra
TSHZ2 Q9NRE2 CCDC57 Homo sapiens Q2TAC2-2 32296183
Intra
TSHZ2 Q9NRE2 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
TSHZ2 Q9NRE2 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
TSHZ2 Q9NRE2 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
TSHZ2 Q9NRE2 CRACR2B Homo sapiens Q8N4Y2-3 32296183
Intra
TSHZ2 Q9NRE2 CRACR2B Homo sapiens Q8N4Y2-3 32296183
Intra
TSHZ2 Q9NRE2 BACH2 Homo sapiens Q9BYV9 32296183
Intra
TSHZ2 Q9NRE2 BACH2 Homo sapiens Q9BYV9 32296183
Intra
TSHZ2 Q9NRE2 PNMA1 Homo sapiens Q8ND90 32296183
Intra
TSHZ2 Q9NRE2 PNMA1 Homo sapiens Q8ND90 32296183
Intra
TSHZ2 Q9NRE2 MCC Homo sapiens P23508 32296183
Intra
TSHZ2 Q9NRE2 MCC Homo sapiens P23508 32296183
Intra
TSHZ2 Q9NRE2 CCDC88B Homo sapiens A6NC98 32296183
Intra
TSHZ2 Q9NRE2 CCDC88B Homo sapiens A6NC98 32296183
Intra
TSHZ2 Q9NRE2 TRAF2 Homo sapiens Q12933 32296183
Intra
TSHZ2 Q9NRE2 TRAF2 Homo sapiens Q12933 32296183
Intra
TSHZ2 Q9NRE2 TRAF1 Homo sapiens Q13077 32296183
Intra
TSHZ2 Q9NRE2 TRAF1 Homo sapiens Q13077 32296183
Intra
TSHZ2 Q9NRE2 SPTA1 Homo sapiens P02549 32296183
Intra
TSHZ2 Q9NRE2 SPTA1 Homo sapiens P02549 32296183
Intra
TSHZ2 Q9NRE2 RABEP1 Homo sapiens Q15276 32296183
Intra
TSHZ2 Q9NRE2 RABEP1 Homo sapiens Q15276 32296183
Intra
TSHZ2 Q9NRE2 GOLGA2 Homo sapiens Q08379 32296183
Intra
TSHZ2 Q9NRE2 GOLGA2 Homo sapiens Q08379 32296183
Intra
TSHZ2 Q9NRE2 GRIPAP1 Homo sapiens Q4V328 32296183
Intra
TSHZ2 Q9NRE2 GRIPAP1 Homo sapiens Q4V328 32296183
Intra
TSHZ2 Q9NRE2 RINT1 Homo sapiens Q6NUQ1 32296183
Intra
TSHZ2 Q9NRE2 RINT1 Homo sapiens Q6NUQ1 32296183
Intra
TSHZ2 Q9NRE2 COG3 Homo sapiens Q96JB2-2 32296183
Intra
TSHZ2 Q9NRE2 COG3 Homo sapiens Q96JB2-2 32296183
Intra
TSHZ2 Q9NRE2 PHAF1 Homo sapiens Q9BSU1 32296183
Intra
TSHZ2 Q9NRE2 PHAF1 Homo sapiens Q9BSU1 32296183
Intra
TSHZ2 Q9NRE2 CNTROB Homo sapiens Q8N137 32296183
Intra
TSHZ2 Q9NRE2 CNTROB Homo sapiens Q8N137 32296183
Intra
TSHZ2 Q9NRE2 GIGYF1 Homo sapiens O75420 32296183
Intra
TSHZ2 Q9NRE2 GIGYF1 Homo sapiens O75420 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Autosomal Recessive Alport Syndrome

Alport Syndrome, Recessive Type

Alport Syndrome, Autosomal Recessive

Alport Syndrome Autosomal Recessive

Alport Syndrome Recessive Type

Nephropathy And Deafness

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 TSHZ2 VGNC VGNC:47904
Mus musculus TSHZ2 MGD MGI:2153084
Rattus norvegicus TSHZ2 RGD RGD:6490867
Macaca mulatta TSHZ2 VGNC VGNC:78875
Bos taurus TSHZ2 VGNC VGNC:59371
Felis catus TSHZ2 VGNC VGNC:66618