TSHZ3 - teashirt zinc finger homeobox 3 Gene

Also Known as TSH3; ZNF537

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 57616

About TSHZ3

Cytogenetic location: 19q12 Genomic coordinates (GRCh38): 19:31,149,876-31,350,877 (from NCBI)

This gene has 4 transcripts (splice variants), 206 orthologues and 2 paralogues. Broad expression in ovary (RPKM 16.6), endometrium (RPKM 15.6) and 19 other tissues.

Summary

This gene encodes a zinc-finger transcription factor that regulates smooth muscle cell differentiation in the developing urinary tract. Consistent with this role, mice in which this gene has been inactivated exhibit abnormal gene expression in urinary tract smooth muscle cell precursors and kidney defects including hydronephrosis. The encoded transcription factor comprises a gene silencing complex that inhibits Caspase expression. Reduced expression of this gene and consequent Caspase upregulation may be correlated with progression of Alzheimer's disease in human patients. [provided by RefSeq, Jul 2016]

TSHZ3 Products (1)

mRNA Protein Name
NM_020856.4 NP_065907.2 teashirt homolog 3
Molecular Function GO Annotation Evidence References Source
enables chromatin binding IDA
IDA: Inferred from direct assay
19343227 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
19343227 GOA
Biological Process GO Annotation Evidence References Source
involved in negative regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
19343227 GOA
Cellular Component GO Annotation Evidence References Source
located in nucleus IDA
IDA: Inferred from direct assay
19343227 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

TSHZ3 Protein Structure

zf-C2H2_2

zf-C2H2_2: C2H2 type zinc-finger (2 copies) (213 - 245)

zf-C2H2_2

zf-C2H2_2: C2H2 type zinc-finger (2 copies) (272 - 301)

zf-C2H2_2

zf-C2H2_2: C2H2 type zinc-finger (2 copies) (386 - 412)

zf-C2H2_4

zf-C2H2_4: C2H2-type zinc finger (1041 - 1064)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1000
  • 1081 a.a.
Protein Preferred Names Protein Names

teashirt homolog 3

  • teashirt family zinc finger 3

TSHZ3 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
TSHZ3 Q63HK5 KRT40 Homo sapiens Q6A162 25416956
Intra
TSHZ3 Q63HK5 KRT40 Homo sapiens Q6A162 25416956
Intra
TSHZ3 Q63HK5 CTBP1 Homo sapiens Q13363-2 25416956
Intra
TSHZ3 Q63HK5 CTBP2 Homo sapiens P56545-3 32296183
Intra
TSHZ3 Q63HK5 CTBP2 Homo sapiens P56545-3 32296183
Intra
TSHZ3 Q63HK5 CCHCR1 Homo sapiens Q8TD31-3 32296183
Intra
TSHZ3 Q63HK5 CCHCR1 Homo sapiens Q8TD31-3 32296183
Intra
TSHZ3 Q63HK5 CCHCR1 Homo sapiens Q8TD31-3 32296183
Intra
TSHZ3 Q63HK5 ANKRA2 Homo sapiens Q9H9E1 32296183
Intra
TSHZ3 Q63HK5 ANKRA2 Homo sapiens Q9H9E1 32296183
Intra
TSHZ3 Q63HK5 ANKRA2 Homo sapiens Q9H9E1 32296183
Intra
TSHZ3 Q63HK5 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
TSHZ3 Q63HK5 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
TSHZ3 Q63HK5 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
TSHZ3 Q63HK5 TFIP11 Homo sapiens Q9UBB9 31515488
Intra
TSHZ3 Q63HK5 TFIP11 Homo sapiens Q9UBB9 25416956
Intra
TSHZ3 Q63HK5 TEPSIN Homo sapiens Q96N21 32296183
Intra
TSHZ3 Q63HK5 TEPSIN Homo sapiens Q96N21 32296183
Intra
TSHZ3 Q63HK5 TEPSIN Homo sapiens Q96N21 32296183
Intra
TSHZ3 Q63HK5 MTUS2 Homo sapiens Q5JR59-3 32296183
Intra
TSHZ3 Q63HK5 MTUS2 Homo sapiens Q5JR59-3 32296183
Intra
TSHZ3 Q63HK5 LRRC73 Homo sapiens Q5JTD7 32296183
Intra
TSHZ3 Q63HK5 LRRC73 Homo sapiens Q5JTD7 32296183
Intra
TSHZ3 Q63HK5 TSC1 Homo sapiens Q86WV8 32296183
Intra
TSHZ3 Q63HK5 TSC1 Homo sapiens Q86WV8 32296183
Intra
TSHZ3 Q63HK5 TSC1 Homo sapiens Q86WV8 32296183
Intra
TSHZ3 Q63HK5 ROPN1 Homo sapiens Q9HAT0 32296183
Intra
TSHZ3 Q63HK5 ROPN1 Homo sapiens Q9HAT0 32296183
Intra
TSHZ3 Q63HK5 ROPN1 Homo sapiens Q9HAT0 32296183
Intra
TSHZ3 Q63HK5 PIBF1 Homo sapiens Q4G0R1 32296183
Intra
TSHZ3 Q63HK5 PIBF1 Homo sapiens Q4G0R1 32296183
Intra
TSHZ3 Q63HK5 TRIM54 Homo sapiens Q9BYV2 32296183
Intra
TSHZ3 Q63HK5 TRIM54 Homo sapiens Q9BYV2 32296183
Intra
TSHZ3 Q63HK5 TRIM54 Homo sapiens Q9BYV2 32296183
Intra
TSHZ3 Q63HK5 TRAF2 Homo sapiens Q12933 25416956
Intra
TSHZ3 Q63HK5 TRAF2 Homo sapiens Q12933 25416956
Intra
TSHZ3 Q63HK5 COG6 Homo sapiens Q9Y2V7 32296183
Intra
TSHZ3 Q63HK5 COG6 Homo sapiens Q9Y2V7 32296183
Intra
TSHZ3 Q63HK5 COG6 Homo sapiens Q9Y2V7 32296183
Intra
TSHZ3 Q63HK5 SPAG5 Homo sapiens Q96R06 25416956
Intra
TSHZ3 Q63HK5 SPAG5 Homo sapiens Q96R06 25416956
Intra
TSHZ3 Q63HK5 TAX1BP1 Homo sapiens Q86VP1 25416956
Intra
TSHZ3 Q63HK5 GOLGA2 Homo sapiens Q08379 32296183
Intra
TSHZ3 Q63HK5 GOLGA2 Homo sapiens Q08379 32296183
Intra
TSHZ3 Q63HK5 HSF2BP Homo sapiens O75031 32296183
Intra
TSHZ3 Q63HK5 HSF2BP Homo sapiens O75031 32296183
Intra
TSHZ3 Q63HK5 TRIM27 Homo sapiens P14373 25416956
Intra
TSHZ3 Q63HK5 TRIM27 Homo sapiens P14373 25416956
Intra
TSHZ3 Q63HK5 MRPL28 Homo sapiens Q13084 32296183
Intra
TSHZ3 Q63HK5 MRPL28 Homo sapiens Q13084 32296183
Intra
TSHZ3 Q63HK5 RINT1 Homo sapiens Q6NUQ1 32296183
Intra
TSHZ3 Q63HK5 RINT1 Homo sapiens Q6NUQ1 32296183
Intra
TSHZ3 Q63HK5 RINT1 Homo sapiens Q6NUQ1 32296183
Intra
TSHZ3 Q63HK5 CEP70 Homo sapiens Q8NHQ1 25416956
Intra
TSHZ3 Q63HK5 CEP70 Homo sapiens Q8NHQ1 25416956
Intra
TSHZ3 Q63HK5 TRIM23 Homo sapiens P36406 25416956
Intra
TSHZ3 Q63HK5 TRIM23 Homo sapiens P36406 25416956
Intra
TSHZ3 Q63HK5 CEP63 Homo sapiens Q96MT8 25416956
Intra
TSHZ3 Q63HK5 CEP63 Homo sapiens Q96MT8 25416956
Intra
TSHZ3 Q63HK5 APEX2 Homo sapiens Q9UBZ4 32296183
Intra
TSHZ3 Q63HK5 APEX2 Homo sapiens Q9UBZ4 32296183
Intra
TSHZ3 Q63HK5 APEX2 Homo sapiens Q9UBZ4 32296183
Intra
TSHZ3 Q63HK5 MAD1L1 Homo sapiens Q9Y6D9 25416956
Intra
TSHZ3 Q63HK5 MTUS2 Homo sapiens Q5JR59 25416956
Intra
TSHZ3 Q63HK5 MTUS2 Homo sapiens Q5JR59 25416956
Intra
TSHZ3 Q63HK5 KRT31 Homo sapiens Q15323 32296183
Intra
TSHZ3 Q63HK5 KRT31 Homo sapiens Q15323 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Hydronephrosis
  • Stricture Of Ureteropelvic Junction With Hydronephrosis

  • Hydronephrosis With Ureteral Stricture, Not Elsewhere Classified

Prune Belly Syndrome
  • Eagle-Barrett Syndrome

  • Abdominal Muscle Deficiency Syndrome

  • PBS

  • Abdominal Muscles, Absence Of, With Urinary Tract Abnormality And Cryptorchidism

  • Egbrs

  • Eagle-Barret Syndrome

  • Urethral Obstruction Sequence

  • Obrinsky Syndrome

  • Triad Syndrome

  • Obrisnksy Syndrome

  • Euos

  • Early Urethral Obstruction Sequence

  • Renal Dysplasia Or Hydronephrosis, Oligohydramnios And Subsequent Lung Hypoplasia Due To Urethral Obstruction

  • Absence Of Abdominal Muscles With Urinary Tract Abnormality And Cryptorchidism

  • Abdomen Muscle Deficiency Syndrome

  • Abdomen Muscular Deficiency Syndrome

  • Abdominal Muscular Deficiency Syndrome

  • Abdominal Muscle Aplasia Syndrome

Calvarial Doughnut Lesions With Bone Fragility
  • Calvarial Doughnut Lesions With Bone Fragility With Or Without Spondylometaphyseal Dysplasia

  • Calvarial Doughnut Lesions-Bone Fragility Syndrome

  • CDL

  • Doughnut Lesions Of Skull, Familial

  • Calvarial Doughnut Lesions With Bone Fragility And Spondylometaphyseal Dysplasia

  • Familial Doughnut Lesions Of Skull

  • CDLSMD

Urofacial Syndrome 1
  • Urofacial Syndrome

  • Ochoa Syndrome

  • Hydronephrosis With Peculiar Facial Expression

  • Ufs

  • Inverted Smile And Occult Neuropathic Bladder

  • Partial Facial Palsy With Urinary Abnormalities

  • UFS1

  • Urofacial Ochoa'S Syndrome

  • Urofacial Syndrome Type 1

  • Facial Palsy, Partial, With Urinary Abnormalities

  • Hydronephrosis-Inverted Smile

  • Inverted Smile-Neurogenic Bladder

  • Hydronephrosis-Inverted Smile Syndrome

  • Inverted Smile-Neurogenic Bladder Syndrome

  • Partial Facial Palsy Partial With Urinary Abnormalities

  • Urologic Diseases

Lagophthalmos
  • Defective Lid Closure

  • Poor Closure Eyelids

Autism Spectrum Disorder
  • Asd

  • Autism Spectrum Disorders

  • Autistic Continuum

  • Pervasive Developmental Disorder

  • Pervasive Development Disorder

  • Autistic Behavior

  • Autistic Disorder

  • Autistic

  • Autistic Disorder Of Childhood Onset

  • Infantile Autism

  • Childhood Autism

  • Kanner Syndrome

  • Pervasive Developmental Delay Nos

  • Pervasive Developmental Disorder, Not Otherwise Specified

Autism
  • Autistic Disorder

  • Autism Susceptibility 1

  • Childhood Autism

  • Autistic Disorder Of Childhood Onset

  • Infantile Autism

  • Kanner'S Syndrome

  • Autistic

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 TSHZ3 VGNC VGNC:47905
Mus musculus TSHZ3 MGD MGI:2442819
Felis catus TSHZ3 VGNC VGNC:66619
Rattus norvegicus TSHZ3 RGD RGD:1306322
Macaca mulatta TSHZ3 VGNC VGNC:79866
Bos taurus TSHZ3 VGNC VGNC:36420