DRGX - dorsal root ganglia homeobox Gene

Homo sapiens

Also known as DRG11; PRRXL1

Gene ID: 644168 | Gene type: protein coding

About DRGX

Cytogenetic location: 10q11.23 Genomic coordinates (GRCh38): 10:49,364,066-49,396,089 (from NCBI)

This gene has 1 transcript (splice variant), 204 orthologues and 50 paralogues. Biased expression in adrenal (RPKM 3.2) and skin (RPKM 0.2).

Summary

Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within several processes, including detection of temperature stimulus; nervous system development; and sensory perception of mechanical stimulus. Predicted to be located in nucleus. Predicted to be part of chromatin. [provided by Alliance of Genome Resources, Apr 2022]

DRGX Products(1)

mRNA	Protein	Name
NM_001276451.2	NP_001263380.1	dorsal root ganglia homeobox protein

DRGX Protein Structure

Homeobox

OAR

0
100
200
263 a.a.

Protein Preferred Names

Protein Names

dorsal root ganglia homeobox protein

paired related homeobox-like 1

Related Diseases

Diseases

Alias

Chromosome 16p12.2-P11.2 Deletion Syndrome, 7.1- To 8.7-Mb

Chromosome 16p12.2-P11.2 Deletion Syndrome	16p11.2p12.2 Microdeletion Syndrome
16p11.2-P12.2 Microdeletion Syndrome	Del(16)(P11.2p12.2)
Monosomy 16p11.2p12.2	Chromosome Deletion Syndrome 16p12.2-P11.2

Myasthenic Syndrome, Congenital, 6, Presynaptic

Familial Infantile Myasthenia	CMS6
Cmsea	Congenital Myasthenic Syndrome 6
Familial Infantile Myasthenia Gravis 2	Fimg2
Myasthenic Syndrome, Congenital, Associated With Episodic Apnea	Myasthenic Syndrome, Presynaptic, Congenital, Associated With Episodic Apnea
Congenital Myasthenic Syndrome Type Ia2, Formerly	Cms1a2, Formerly
Cms Ia2, Formerly	Myasthenia, Familial Infantile, Formerly
Fim, Formerly	Myasthenia Gravis, Familial Infantile, 2, Formerly
Fimg2, Formerly	Cms Ia2
Cms1a2	Congenital Myasthenic Syndrome 6, Presynaptic
Congenital Myasthenic Syndrome Type Ia2	Congenital Presynaptic Myasthenic Syndrome Associated With Episodic Apnea
Fim	Cms1a
Cms-Ea	Cms Ia
Congenital Myasthenic Syndrome Pre-Synaptic Associated With Episodic Apnea	Congenital Myasthenic Syndrome Type 1a
Congenital Myasthenic Syndrome Type Ia	Myasthenic Syndrome, Congenital, Type 6, Presynaptic

Developmental And Epileptic Encephalopathy 28

DEE28	Epileptic Encephalopathy, Early Infantile, 28
Eiee28	Developmental And Epileptic Encephalopathy, 28
Early Infantile Epileptic Encephalopathy 28	Encephalopathy, Epileptic, Early Infantile, Type 28

Spinocerebellar Ataxia, Autosomal Recessive 12

Autosomal Recessive Spinocerebellar Ataxia 12	SCAR12
Spinocerebellar Ataxia With Mental Retardation And Epilepsy	Autosomal Recessive Cerebellar Ataxia-Epilepsy-Intellectual Disability Syndrome Due To Wwox Deficiency
Autosomal Recessive Spinocerebellar Ataxia Type 12	Spinocerebellar Ataxia, Autosomal Recessive, 12
Ataxia, Spinocerebellar, Autosomal Recessive, Type 12

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-RS04011	DRGX Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	DRGX	RGD	RGD:628616
Bos taurus	DRGX	VGNC	VGNC:28210
Macaca mulatta	DRGX	VGNC	VGNC:106037
Canis familiaris	DRGX	VGNC	VGNC:40099
Mus musculus	DRGX	MGD	MGI:2148204

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