TSHZ1 - teashirt zinc finger homeobox 1 Gene

Homo sapiens

Also known as CAA; TSH1; NY-CO-33; SDCCAG33

Gene ID: 10194 | Gene type: protein coding

About TSHZ1

Cytogenetic location: 18q22.3 Genomic coordinates (GRCh38): 18:75,210,797-75,289,944 (from NCBI)

This gene has 5 transcripts (splice variants), 267 orthologues, 2 paralogues and is associated with 3 phenotypes. Ubiquitous expression in ovary (RPKM 18.5), placenta (RPKM 15.6) and 24 other tissues.

Summary

This gene encodes a colon Cancer antigen that was defined by serological analysis of recombinant cDNA expression libraries. The encoded protein is a member of the teashirt C2H2-type zinc-finger protein family and may be involved in transcriptional regulation of developmental processes. Mutations in this gene may be associated with congenital aural atresia syndrome. [provided by RefSeq, Jan 2012]

TSHZ1 Products(2)

mRNA	Protein	Name
NM_001308210.2	NP_001295139.1	teashirt homolog 1 isoform 1
NM_005786.6	NP_005777.3	teashirt homolog 1 isoform 2

TSHZ1 Protein Structure

zf-C2H2_2

0
200
400
600
800
1000
1077 a.a.

Protein Preferred Names

Protein Names

teashirt homolog 1

antigen NY-CO-33

Related Diseases

Diseases

Alias

Aural Atresia, Congenital

CAA	Aural Atresia, Congenital, With Hyposmia

External Auditory Canal Aplasia/Hypoplasia

External Auditory Canal Stenosis/Atresia

Anomaly Of Osseous Meatus

Vertical Talus, Congenital

Congenital Vertical Talus	CVT
Congenital Convex Pes Valgus	Rocker-Bottom Foot Deformity
Vertical Talus	Pes Valgus, Congenital Convex
Congenital Convex Foot	Congenital Rocker-Bottom Foot
Rocker Bottom Foot	Flatfoot
Rocker-Bottom Foot	Charcot-Marie-Tooth Disease, Foot Deformity Of

Chromosome 18q Deletion Syndrome

18q- Syndrome	Monosomy 18q
Deletion Of Long Arm Of Chromosome 18	Chromosome 18q- Syndrome
Deletion 18q	18q Deletion Syndrome
Distal 18q Deletion Syndrome	Chromosome 18 Long Arm Deletion Syndrome
Chromosome 18q Monosomy	Del Syndrome
Chromosome 18 Deletion Syndrome

Valproate Embryopathy

Fetal Valproate Syndrome	Fetal Valproic Acid Syndrome
Fvs	Valproic Acid Embryopathy
Fetal Valproate Spectrum Disorder	Valproate Embryopathy, Susceptibility To
Foetal Valproate Syndrome	Foetal Valproic Acid Syndrome
Susceptibility To Valproate Embryopathy	Valproic Acid Antenatal Infection

Hypertrichosis Universalis Congenita, Ambras Type

Ambras Syndrome	Hypertrichosis, Congenital Generalized
HTC1	HTC2
Chromosome Xq27.1 Interchromosomal Insertion Syndrome	Cgh
Hcg	Ambras Type Hypertrichosis Universalis Congenita
X-Linked Congenital Generalized Hypertrichosis	Congenital Generalized Hypertrichosis, Macias-Flores Type
Macias Flores-Garcia Cruz-Rivera Syndrome	Htc 1
Hypertrichosis Universalis Congenita Ambras Type	Hypertrichosis Congenital Generalized X-Linked
Macias-Flores Garcia-Cruz Rivera Syndrome	Congenital Generalized Hypertrichosis, Ambras Type

Substance-Induced Psychosis

Cleft Soft Palate

Cleft Velum	Cleft Velum Palatinum
Soft Cleft Palate	Soft Palate Perforation

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

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS15148	TSHZ1 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	TSHZ1	VGNC	VGNC:47903
Macaca mulatta	TSHZ1	VGNC	VGNC:78553
Felis catus	TSHZ1	VGNC	VGNC:80541
Mus musculus	TSHZ1	MGD	MGI:1346031
Rattus norvegicus	TSHZ1	RGD	RGD:1311684
Bos taurus	TSHZ1	VGNC	VGNC:56375

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