STAMBPL1 - STAM binding protein like 1 Gene

Homo sapiens

Also known as AMSH-FP; AMSH-LP; ALMalpha; bA399O19.2

Gene ID: 57559 | Gene type: protein coding

About STAMBPL1

Cytogenetic location: 10q23.31 Genomic coordinates (GRCh38): 10:88,880,245-88,923,487 (from NCBI)

This gene has 6 transcripts (splice variants), 206 orthologues and 1 paralogue. Broad expression in adrenal (RPKM 7.5), testis (RPKM 6.2) and 22 other tissues.

Summary

Predicted to enable Lys63-specific Deubiquitinase activity and thiol-dependent Deubiquitinase. Predicted to be involved in protein K63-linked deubiquitination. Located in membrane. [provided by Alliance of Genome Resources, Apr 2022]

STAMBPL1 Products(1)

mRNA	Protein	Name
NM_020799.4	NP_065850.1	AMSH-like protease

STAMBPL1 Protein Structure

USP8_dimer

JAB

0
100
200
300
400
436 a.a.

Protein Preferred Names

Protein Names

AMSH-like protease

associated molecule with the SH3 domain of STAM (AMSH) - Family Protein

Related Diseases

Diseases

Alias

Hermansky-Pudlak Syndrome 3

HPS3	Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial
Delta Storage Pool Disease	Hermansky-Pudlak Syndrome, Type 3
Platelet Storage Pool Deficiency	Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells

Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome

Jacobs Syndrome	Arthropathy-Camptodactyly Syndrome
Pericarditis-Arthropathy-Camptodactyly Syndrome	Xyy Syndrome
Pac Syndrome	Cacp Syndrome
CACP	Fibrosing Serositis, Familial
Camptodactyly-Arthropathy-Pericarditis Syndrome	Cap Syndrome
47, Xyy Syndrome	47,Xyy Syndrome
Double Y Syndrome	Camptodactyly-Arthropathy-Coxa-Vara-Pericarditis Syndrome
Hypertrophic Synovitis, Congenital Familial	Congenital Familial Hypertrophic Synovitis
Xyy Karyotype	Y Disomy
Yy Syndrome	Familial Fibrosing Serositis
Disomy Y	Double Y
Camptodactyly Arthropathy Coxa Vara Pericarditis Syndrome	Arthropathy Camptodactyly Syndrome
Camptodactyly Arthropathy Pericarditis Syndrome	Pericarditis Arthropathy Camptodactyly Syndrome
Jacob'S Syndrome	47,Xyy
Cdags Syndrome

Autosomal Dominant Cerebellar Ataxia

Spinocerebellar Ataxia	Adca
Pierre Marie Cerebellar Ataxia	Ataxia, Spinocerebellar
Sca	Autosomal Dominant Spinocerebellar Ataxia
Spinocerebellar Ataxias

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-RS13872	STAMBPL1 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	STAMBPL1	MGD	MGI:1923880
Bos taurus	STAMBPL1	VGNC	VGNC:35357
Felis catus	STAMBPL1	VGNC	VGNC:65748
Rattus norvegicus	STAMBPL1	RGD	RGD:1583011
Macaca mulatta	STAMBPL1	VGNC	VGNC:77982
Canis familiaris	STAMBPL1	VGNC	VGNC:46877
Others	STAMBPL1	NCBI

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