SBSN - suprabasin Gene

Homo sapiens

Also known as UNQ698

Gene ID: 374897 | Gene type: protein coding

About SBSN

Cytogenetic location: 19q13.12 Genomic coordinates (GRCh38): 19:35,523,367-35,528,311 (from NCBI)

This gene has 3 transcripts (splice variants) and 97 orthologues. Restricted expression toward skin (RPKM 753.6).

Located in extracellular exosome. [provided by Alliance of Genome Resources, Apr 2022]

mRNA	Protein	Name
NM_001166034.2	NP_001159506.1	suprabasin isoform 1 precursor
NM_001166035.2	NP_001159507.1	suprabasin isoform 3 precursor
NM_198538.4	NP_940940.1	suprabasin isoform 2 precursor

Protein Preferred Names

Protein Names

suprabasin

HLAR698

Diseases

Alias

Metal Allergy

Salivary Gland Adenoid Cystic Carcinoma

Cylindroma

Fuchs' Endothelial Dystrophy

Fuchs Endothelial Corneal Dystrophy	Fuchs Endothelial Dystrophy
Fuchs Dystrophy	Fced
Fuchs' Corneal Dystrophy	Fuchs' Endothelial Corneal Dystrophy
Fuchs Atrophy	Fuchs Corneal Dystrophy
Endoepithelial Corneal Dystrophy	Fecd
Late Hereditary Endothelial Dystrophy	Corneal Dystrophy, Fuchs Endothelial
Dystrophy, Corneal, Fuchs Endothelial	Corneal Dystrophy, Fuchs' Endothelial, 1

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-RS12471	SBSN Human Pre-designed siRNA Set A		/	Unkown

Species	Symbol	Source	ID
Rattus norvegicus	SBSN	RGD	RGD:1562305
Bos taurus	SBSN	VGNC	VGNC:34310
Mus musculus	SBSN	MGD	MGI:2446326
Felis catus	SBSN	VGNC	VGNC:64890

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