MIOX - myo-inositol oxygenase Gene

Homo sapiens

Also known as ALDRL6

Gene ID: 55586 | Gene type: protein coding

About MIOX

Cytogenetic location: 22q13.33 Genomic coordinates (GRCh38): 22:50,486,859-50,490,648 (from NCBI)

This gene has 4 transcripts (splice variants) and 194 orthologues. Restricted expression toward kidney (RPKM 162.3).

Summary

Enables ferric iron binding activity and inositol oxygenase activity. Involved in inositol catabolic process. Predicted to be located in cytoplasm and inclusion body. [provided by Alliance of Genome Resources, Apr 2022]

MIOX Products(1)

mRNA	Protein	Name
NM_017584.6	NP_060054.4	inositol oxygenase

MIOX Protein Structure

MIOX

0
100
200
285 a.a.

Protein Preferred Names

Protein Names

inositol oxygenase

MI oxygenase

Related Diseases

Diseases

Alias

Ichthyosis, Congenital, Autosomal Recessive 3

Autosomal Recessive Congenital Ichthyosis 3	ARCI3
Lamellar Ichthyosis 5	Collodion Baby, Self-Healing
Ichthyosis, Lamellar, 5, Formerly	Li5, Formerly
Li5	Self-Healing Collodion Baby
Ichthyosis, Congenital, Autosomal Recessive, Type 3

Hypoascorbemia

Scurvy	Ascorbic Acid Deficiency
Vitamin C Deficiency	Vitamin C, Inability To Synthesize
Deficiency Of Vitamin C	Scorbutus
Vitamin C

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-RS08459	MIOX Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	MIOX	MGD	MGI:1891725
Macaca mulatta	MIOX	VGNC	VGNC:74769
Bos taurus	MIOX	VGNC	VGNC:97286
Felis catus	MIOX	VGNC	VGNC:63515
Canis familiaris	MIOX	VGNC	VGNC:43240
Rattus norvegicus	MIOX	RGD	RGD:628739