LAD1 - ladinin 1 Gene

Homo sapiens

Also known as LadA

Gene ID: 3898 | Gene type: protein coding

About LAD1

Cytogenetic location: 1q32.1 Genomic coordinates (GRCh38): 1:201,380,833-201,399,324 (from NCBI)

This gene has 7 transcripts (splice variants) and 115 orthologues. Biased expression in esophagus (RPKM 94.2), skin (RPKM 74.3) and 10 other tissues.

Summary

The protein encoded by this gene may be an anchoring filament that is a component of basement membranes. It may contribute to the stability of the association of the epithelial layers with the underlying mesenchyme. [provided by RefSeq, Jul 2008]

LAD1 Products(1)

mRNA	Protein	Name
NM_005558.4	NP_005549.2	ladinin-1

Protein Preferred Names

Protein Names

ladinin-1

lad-1

Related Diseases

Diseases

Alias

Epidermolysis Bullosa Acquisita

Acquired Epidermolysis Bullosa	Eb Acquisita
Eba	Eba - [Epidermolysis Bullosa Acquisita]

Cicatricial Pemphigoid

Mucous Membrane Pemphigoid	Ocular Pemphigoid
Benign Mucous Membrane Pemphigoid	Benign Mucous Membrane Pemphigoid With Ocular Involvement
Benign Mucosal Pemphigoid	Pemphigoid, Benign Mucous Membrane
Cicatricial Pemphigoid With Ocular Involvement	Ocular Pemphigus
Cicatricial Pemphigoid Disease	Mucosal Pemphigoid
Mucosynechial Pemphigoid	Pemphigoid Cicatricial
Cicatricial Pemphigoid Involving The Eye	Ocular Cicatricial Pemphigoid

Bullous Pemphigoid

Benign Pemphigus	Senile Dermatitis Herpetiformis
Old Age Pemphigus	Parapemphigus
Pemphigoid	Pemphigoid Bullous
Pemphigoid, Bullous

Epidermolysis Bullosa, Junctional 4, Intermediate

Gabeb	JEB4
Epidermolysis Bullosa, Junctional 4, Non-Herlitz Type	Epidermolysis Bullosa, Generalized Atrophic Benign
Epidermolysis Bullosa, Junctional, Localisata Variant

Pemphigus Gestationis

Pyloric Atresia

Epidermolysis Bullosa

Acantholysis Bullosa

Alzheimer Disease 18

AD18	Alzheimer'S Disease 18
Alzheimer Disease 18, Late-Onset	Alzheimer Disease 18, Susceptibility To
Alzheimer'S Disease 18, Late Onset	Alzheimer Disease 18 Late-Onset
Alzheimer Disease, Susceptibility To, Type 18

Junctional Epidermolysis Bullosa

Epidermolysis Bullosa, Junctional	Jeb
Epidermolysis Bullosa Atrophicans	Congenital Junctional Epidermolysis Bullosa
Epidermolysis Bullosa Junctional	Junctional Eb - [Epidermolysis Bullosa]
Jeb - [Junctional Epidermolysis Bullosa]	Lucidolytic Epidermolysis Bullosa

Skin Disease

Skin Diseases	Genodermatosis
Abnormality Of The Skin	Skin Diseases, Genetic
Skin And Subcutaneous Tissue Disease	Dermatologic Disorders

Myasthenic Syndrome, Congenital, 5

Endplate Acetylcholinesterase Deficiency	Congenital Myasthenic Syndrome 5
CMS5	Ead
Engel Congenital Myasthenic Syndrome	Myasthenic Syndrome, Congenital, Engel Type
Cms Ic	Congenital Myasthenic Syndrome Type Ic
Congenital Myasthenic Syndrome Type Ic, Formerly	Cms1c, Formerly
Cms Ic, Formerly	Congenital Myasthenic Syndrome Engel Type
End Plate Acetylcholinesterase Deficiency	Synaptic Congenital Myasthenic Syndromes
Cms1c	Cmse
Congenital Myasthenic Syndrome Type 1c	End-Plate Acetylcholinesterase Deficiency
Myasthenic Syndrome, Congenital, Type 5

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-RS07491	LAD1 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	LAD1	MGD	MGI:109343
Felis catus	LAD1	VGNC	VGNC:67999
Bos taurus	LAD1	VGNC	VGNC:30766
Rattus norvegicus	LAD1	RGD	RGD:1310652
Canis familiaris	LAD1	VGNC	VGNC:42561
Macaca fascicularis	LAD1	NCBI	NCBI:123566753
Others	LAD1	NCBI

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