TEX28 - testis expressed 28 Gene

Homo sapiens

Also known as fTEX; MRX99; CXorf2; TEX28P1; TEX28P2

Gene ID: 1527 | Gene type: protein coding

About TEX28

Cytogenetic location: Xq28 Genomic coordinates (GRCh38): X:154,271,265-154,295,211 (from NCBI)

This gene has 4 transcripts (splice variants), 87 orthologues and 3 paralogues. Restricted expression toward testis (RPKM 2.4).

Summary

Predicted to be integral component of membrane. Predicted to be active in endomembrane system. [provided by Alliance of Genome Resources, Apr 2022]

TEX28 Products(2)

mRNA	Protein	Name
NM_001205201.2	NP_001192130.1	testis-specific protein TEX28
NM_001586.3	NP_001577.1	testis-specific protein TEX28

Gene Ontology

Molecular Function

Molecular Function GO Annotation	Evidence	Reference	Source
enables protein binding	IPI IPI: Inferred from physical interaction	28514442	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

TEX28 Protein Structure

Tmemb_cc2

0
100
200
300
410 a.a.

Protein Preferred Names

Protein Names

testis-specific protein TEX28

Related Diseases

Diseases

Alias

Colorblindness, Partial, Protan Series

Protanopia	Red Color Blindness
Protan Defect	CBP
Red Colorblindness	Colorblindness, Protan
Color Blindness, Red

Red-Green Color Blindness

Deutan Defect	Deuteranopia
Reduced Red-Green Discrimination	Color Blindness, Red-Green
Colorblindness, Partial, Deutan Series

Gene Duplication Disease

Gene Duplication Syndrome

Blue Cone Monochromacy

Blue Cone Monochromatism	BCM
Cbbm	Color Blindness Blue Mono Cone Monochromatic Type
Cone Dystrophy 5, X-Linked	Colorblindness, Blue-Mono-Cone-Monochromatic Type
Achromatopsia Incomplete X-Linked	Incomplete Achromatopsia X-Linked
X-Chromosome-Linked Achromatopsia	X-Linked Achromatopsia Incomplete
Atypical X-Linked Achromatopsia	Color Blindness, Blue Monocone Monochromatic Type
S Cone Monochromacy	S Cone Monochromatism
X-Linked Incomplete Achromatopsia	Colorblindness Blue-Mono-Cone-Monochromatic Type
Cone Dystrophy 5	COD5
Cone Dystrophy 5 X-Linked	Monochromacy, Blue Cone
Cone Monochromatism	Achromatopsia Incomplete, X-Linked

Myopia

Near-Sightedness	Short-Sightedness
Nearsightedness	Nearsighted
Near Vision	Close Sighted
Myopic	Short-Sighted
Near Sighted

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-RS14396	TEX28 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	TEX28	MGD	MGI:2686384
Macaca mulatta	TEX28	VGNC	VGNC:79524
Rattus norvegicus	TEX28	RGD	RGD:1582832
Bos taurus	TEX28	VGNC	VGNC:50110
Canis familiaris	TEX28	VGNC	VGNC:54606

Name
Email *

	Sorry, but the email address you supplied was invalid.