MYMX - myomixer, myoblast fusion factor Gene

Homo sapiens

Also known as CFZS2; MINION; hMINION

Gene ID: 101929726 | Gene type: protein coding

About MYMX

Cytogenetic location: 6p21.1 Genomic coordinates (GRCh38): 6:44,192,721-44,218,234 (from NCBI)

This gene has 2 transcripts (splice variants) and 62 orthologues. Biased expression in fat (RPKM 1.3), stomach (RPKM 0.3) and 7 other tissues.

Summary

Predicted to be involved in myoblast fusion involved in skeletal muscle regeneration; plasma membrane fusion; and skeletal muscle organ development. Predicted to be integral component of plasma membrane. Predicted to be active in Golgi membrane; endoplasmic reticulum membrane; and plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

MYMX Products(2)

mRNA	Protein	Name
NM_001315494.2	NP_001302423.1	protein myomixer precursor
NM_001347931.2	NP_001334860.1	protein myomixer precursor

Protein Preferred Names

Protein Names

protein myomixer

microprotein inducer of fusion

Related Diseases

Diseases

Alias

Carey-Fineman-Ziter Syndrome 2

CFZS2

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

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS08928	MYMX Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	MYMX	VGNC	VGNC:54973
Mus musculus	MYMX	MGD	MGI:3649059
Felis catus	MYMX	VGNC	VGNC:102473
Rattus norvegicus	MYMX	RGD	RGD:11426996