INE1 - inactivation escape 1 Gene

Homo sapiens

Also known as NCRNA00010

Gene ID: 8552 | Gene type: ncRNA

About INE1

Cytogenetic location: Xp11.3 Genomic coordinates (GRCh38): X:47,204,848-47,205,861 (from NCBI)

This gene has 1 transcript (splice variant).

Summary

X chromosome inactivation provides dosage compensation for the expression level of X-linked genes from the single X in males and the two in females. This X chromosome gene is intronless and was identified because its transcription escapes X inactivation in females. This gene does not make a protein.[provided by RefSeq, May 2010]

Related Diseases

Diseases

Alias

Anal Carcinoma In Situ

Carcinoma In Situ Of Anal Canal	Carcinoma In Situ Of Anus
Anal Carcinoma Stage 0	Anal Intraepithelial Neoplasia Grade Iii
Intraepithelial Neoplasia Of Anal Canal, High Grade	Ain - [Anal Intraepithelial Neoplasia] High Grade

Chromosome Xp21 Deletion Syndrome

Complex Glycerol Kinase Deficiency	Xp21 Microdeletion Syndrome
Monosomy Xp21	Xp21 Deletion Syndrome
Complex Gkd	Del
Xp21 Contiguous Gene Deletion Syndrome	Glycerol Kinase Deficiency - Contiguous Gene Syndrome

Pericardial Tuberculosis

Pericarditis, Tuberculous	Tuberculous Pericarditis
Pericarditis Tuberculous

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-RS16346	INE1 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	INE1	NCBI

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