1. Gene
  2. STAMBPL1 - STAM binding protein like 1 Gene

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

USP8_dimer: USP8 dimerisation domain (28 - 130)

JAB

JAB: JAB1/Mov34/MPN/PAD-1 ubiquitin protease (267 - 372)

  • 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

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