LY86 - lymphocyte antigen 86 Gene

Homo sapiens

Also known as MD1; MD-1; MMD-1; dJ80N2.1

Gene ID: 9450 | Gene type: protein coding

About LY86

Cytogenetic location: 6p25.1 Genomic coordinates (GRCh38): 6:6,588,720-6,654,982 (from NCBI)

This gene has 2 transcripts (splice variants) and 130 orthologues. Biased expression in lymph node (RPKM 17.5), spleen (RPKM 16.2) and 13 other tissues.

Summary

Acts upstream of or within positive regulation of lipopolysaccharide-mediated signaling pathway. Predicted to be located in extracellular space. [provided by Alliance of Genome Resources, Apr 2022]

LY86 Products(1)

mRNA	Protein	Name
NM_004271.4	NP_004262.1	lymphocyte antigen 86 precursor

LY86 Protein Structure

E1_DerP2_DerF2

0
100
162 a.a.

Protein Preferred Names

Protein Names

lymphocyte antigen 86

MD-1, RP105-associated

Recombinant LY86 Proteins

Cat. No.	Product Name	Accession	Purity
HY-P70223	Lymphocyte antigen 86/LY86 Protein, Human (HEK293, Fc)	O95711 (G21-S162)	≥95%

Related Diseases

Diseases

Alias

Muscular Dystrophy, Duchenne Type

Duchenne Muscular Dystrophy	DMD
Muscular Dystrophy, Duchenne	Muscular Dystrophy, Pseudohypertrophic Progressive, Duchenne Type
Severe Dystrophinopathy, Duchenne Type	Muscular Dystrophy Duchenne
Dystrophy, Muscular, Duchenne Type	Benign Duchenne Muscular Dystrophy
Duchenne Motor Neuron Disease	Duchenne Type Dystrophy
Duchenne-Griesinger Disease

Mediastinal Lipomatosis

Myotonic Disease

Myotonic Disorders	Myotonic Syndrome
Symptomatic Myotonia

Frontometaphyseal Dysplasia 1

FMD1

Fmd

Dilated Cardiomyopathy 1t

Cmd1t

Cardiomyopathy, Dilated, 1t

Splenic Flexure Cancer

Ca Splenic Flexure - Colon	Malignant Neoplasm Of Splenic Flexure
Malignant Tumor Of Splenic Flexure	Malignant Neoplasm Of Splenic Flexure Of Colon

Niemann-Pick Disease, Type C2

NPC2	Niemann-Pick Disease Type C2
Niemann-Pick C2 Disease	Niemann-Pick Disease C2

Myotonic Dystrophy 1

Myotonic Dystrophy	Dystrophia Myotonica
Steinert Disease	Myotonic Dystrophy Type 1
Myotonia Atrophica	DM1
Congenital Myotonic Dystrophy	Myotonia Dystrophica
Steinert Myotonic Dystrophy	Dystrophia Myotonica 1
Dm	Steinert'S Disease
Steinert Myotonic Dystrophy Syndrome	Myotonic Dystrophy Of Steinert
Dystrophia Myotonica Type 1	Myotonic Dystrophy Congenital
Dystrophy, Myotonic, Type 1	Dm - [Dystrophia Myotonica]
Myotonic Muscular Dystrophy

Gaucher Disease, Type Ii

GD2	Gd Ii
Gaucher Disease, Acute Neuronopathic Type	Gaucher Disease Type 2
Gaucher Disease Type Ii	Gaucher'S Disease Type Ii
Infantile Cerebral Gaucher Disease	Acute Neuronopathic Gaucher Disease
Gd 2	Gaucher Disease, Infantile Cerebral
Gaucher Disease 2	Type 2 Gaucher Disease
Gaucher Disease, Type 2

Frontometaphyseal Dysplasia

Fmd	Dysplasia, Frontometaphyseal

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-RS07906	LY86 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Bos taurus	LY86	VGNC	VGNC:31093
Rattus norvegicus	LY86	RGD	RGD:1309936
Canis familiaris	LY86	VGNC	VGNC:42876
Felis catus	LY86	VGNC	VGNC:102454
Mus musculus	LY86	MGD	MGI:1321404
Macaca mulatta	LY86	VGNC	VGNC:104410
Others	LY86	NCBI

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