MYORG - myogenesis regulating glycosidase (putative) Gene

Homo sapiens

Also known as IBGC7; NET37; KIAA1161

Gene ID: 57462 | Gene type: protein coding

About MYORG

Cytogenetic location: 9p13.3 Genomic coordinates (GRCh38): 9:34,366,666-34,376,898 (from NCBI)

This gene has 2 transcripts (splice variants), 281 orthologues, 6 paralogues and is associated with 2 phenotypes. Broad expression in duodenum (RPKM 7.6), small intestine (RPKM 7.3) and 18 other tissues.

Summary

Predicted to enable hydrolase activity, hydrolyzing O-glycosyl compounds. Involved in skeletal muscle fiber development. Predicted to be located in endoplasmic reticulum membrane and nuclear membrane. Implicated in basal ganglia calcification. [provided by Alliance of Genome Resources, Apr 2022]

MYORG Products(1)

mRNA	Protein	Name
NM_020702.5	NP_065753.2	myogenesis-regulating glycosidase

MYORG Protein Structure

Glyco_hydro_31

0
200
400
600
680 a.a.

Protein Preferred Names

Protein Names

myogenesis-regulating glycosidase

Related Diseases

Diseases

Alias

Basal Ganglia Calcification, Idiopathic, 7, Autosomal Recessive

IBGC7

Basal Ganglia Calcification, Idiopathic, 1

Primary Familial Brain Calcification	Pfbc
Bspdc	Bilateral Striopallidodentate Calcinosis
Cerebrovascular Ferrocalcinosis	IBGC1
Familial Idiopathic Basal Ganglia Calcification	Idiopathic Basal Ganglia Calcification 1
Striopallidodentate Calcinosis, Bilateral	Striopallidodentate Calcinosis, Autosomal Dominant, Adult-Onset
Cerebral Calcification, Nonarteriosclerotic, Idiopathic, Adult-Onset	Ferrocalcinosis, Cerebrovascular
Fahr Disease, Familial, Formerly	Basal Ganglia Calcification, Idiopathic, 3, Formerly
Ibgc3, Formerly	Basal Ganglia Calcification, Idiopathic, 2, Formerly
Ibgc2, Formerly	Fibgc
Striopallidodentate Calcinosis	Idiopathic Basal Ganglia Calcification
Ferrocalcinosis Cerebro Vascular	Autosomal Dominant Adult-Onset Striopallidodentate Calcinosis
Familial Fahr Disease	Ibgc2
Ibgc3	Idiopathic Basal Ganglia Calcification 2
Idiopathic Basal Ganglia Calcification 3	Non-Arteriosclerotic, Idiopathic, Adult-Onset Cerebral Calcification
Basal Ganglia Calcification, Idiopathic	Calcification, Basal Ganglia, Idiopathic
Calcification, Basal Ganglia, Idiopathic, Type 1	Fahr'S Syndrome

Basal Ganglia Calcification

Fahr'S Syndrome	Fahr'S Disease
Fahr Disease

Basal Ganglia Disease

Basal Ganglia Diseases	Basal Ganglia Disorders
Abnormality Of The Basal Ganglia

Optic Disk Drusen

Optic Disc Drusen	Drusen Of Optic Disc
Optic Nerve Head Drusen	Drusen Optic Disc

Parkinsonism

Parkinsonism-Plus	Idiopathic Parkinsonism
Primary Parkinsonism	Paralysis Agitans Syndrome
Parkinsonian Syndrome	Trembling Paralysis
Paralysis Agitans	Shaking Palsy
Shaking Paralysis

Lingual-Facial-Buccal Dyskinesia

Orofacial Dyskinesia	Oro-Facial Dyskinesia
Dyskinesias

Dystonia

Dystonic Disease	Dystonic Disorder
Dystonia Disorders	Neuroleptic Dyskinesia

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-RS08963	MYORG Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	MYORG	VGNC	VGNC:55157
Mus musculus	MYORG	MGD	MGI:2140300
Felis catus	MYORG	VGNC	VGNC:102953
Rattus norvegicus	MYORG	RGD	RGD:1309821
Macaca mulatta	MYORG	VGNC	VGNC:103279

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