MAN1A1 - mannosidase alpha class 1A member 1 Gene

Homo sapiens

Also known as MAN9; HUMM3; HUMM9

Gene ID: 4121 | Gene type: protein coding

About MAN1A1

Cytogenetic location: 6q22.31 Genomic coordinates (GRCh38): 6:119,177,205-119,350,605 (from NCBI)

This gene has 1 transcript (splice variant), 222 orthologues and 6 paralogues. Ubiquitous expression in fat (RPKM 62.7), liver (RPKM 46.9) and 25 other tissues.

Summary

This gene encodes a class I mammalian Golgi 1,2-mannosidase which is a type II transmembrane protein. This protein catalyzes the hydrolysis of three terminal mannose residues from peptide-bound Man(9)-GlcNAc(2) oligosaccharides and belongs to family 47 of glycosyl hydrolases. [provided by RefSeq, Jul 2012]

MAN1A1 Products(1)

mRNA	Protein	Name
NM_005907.4	NP_005898.2	mannosyl-oligosaccharide 1,2-alpha-mannosidase IA

MAN1A1 Protein Structure

Glyco_hydro_47

0
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653 a.a.

Protein Preferred Names

Protein Names

mannosyl-oligosaccharide 1,2-alpha-mannosidase IA

Man9-mannosidase

Recombinant MAN1A1 Proteins

Cat. No.	Product Name	Accession	Purity
HY-P79040	MAN1A1 Protein, Human (CHO, His)	P33908 (P63-E653 )	≥95%

Related Diseases

Diseases

Alias

Congenital Disorder Of Glycosylation, Type In

Congenital Disorder Of Glycosylation	CDG1N
Congenital Disorders Of Glycosylation	Cdg In
Cdgin	Congenital Disorder Of Glycosylation 1n
Carbohydrate-Deficient Glycoprotein Syndrome	Cdg
Rft1-Cdg	Cdg-In
Congenital Disorder Of Glycosylation Type In	Carbohydrate Deficient Glycoprotein Syndrome
Cdg Syndrome	Congenital Disorder Of Glycosylation In
Carbohydrate-Deficient Glycoprotein Syndromes	Cdg Syndrome Type In
Carbohydrate Deficient Glycoprotein Syndrome Type In	Congenital Disorder Of Glycosylation Type 1n
Man5glcnac2-Pp-Dol Flippase Deficiency	Glycosylation, Congenital Disorder Of
Glycosylation, Congenital Disorder Of, Type In

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 (3)

Cat. No.	Product Name	Purity	Rare Diseases
HY-RS08004	MAN1A1 Human Pre-designed siRNA Set A	/	Unkown
HY-RS08006	MAN1B1 Human Pre-designed siRNA Set A	/	Unkown
HY-RS08007	MAN1C1 Human Pre-designed siRNA Set A	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	MAN1A1	MGD	MGI:104677
Bos taurus	MAN1A1	VGNC	VGNC:31161
Felis catus	MAN1A1	VGNC	VGNC:68144
Canis familiaris	MAN1A1	VGNC	VGNC:42942
Rattus norvegicus	MAN1A1	RGD	RGD:1310891
Macaca mulatta	MAN1A1	VGNC	VGNC:74483

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