1. Gene
  2. STAMBP - STAM binding protein Gene

STAMBP - STAM binding protein Gene

Homo sapiens

Also known as AMSH; MICCAP

Gene ID: 10617 | Gene type: protein coding

About STAMBP

Cytogenetic location: 2p13.1 Genomic coordinates (GRCh38): 2:73,828,961-73,873,656 (from NCBI)

This gene has 71 transcripts (splice variants), 209 orthologues, 1 paralogue and is associated with 3 phenotypes. Ubiquitous expression in thyroid (RPKM 4.9), brain (RPKM 4.5) and 25 other tissues.

Summary

Cytokine-mediated signal transduction in the JAK-STAT cascade requires the involvement of adaptor molecules. One such signal-transducing adaptor molecule contains an SH3 domain that is required for induction of MYC and cell growth. The protein encoded by this gene binds to the SH3 domain of the signal-transducing adaptor molecule, and plays a critical role in cytokine-mediated signaling for MYC induction and cell cycle progression. Multiple alternatively spliced transcript variants encoding the same protein isoform have been found for this gene. [provided by RefSeq, Jul 2008]

STAMBP Products(13)

mRNA Protein Name
NM_001353967.2 NP_001340896.1 STAM-binding protein isoform 1
NM_001353968.2 NP_001340897.1 STAM-binding protein isoform 1
NM_001353969.2 NP_001340898.1 STAM-binding protein isoform 2
NM_001353970.2 NP_001340899.1 STAM-binding protein isoform 2
NM_001353971.2 NP_001340900.1 STAM-binding protein isoform 3
NM_001353972.2 NP_001340901.1 STAM-binding protein isoform 3
NM_001353973.2 NP_001340902.1 STAM-binding protein isoform 3
NM_001353974.2 NP_001340903.1 STAM-binding protein isoform 3
NM_001353975.2 NP_001340904.1 STAM-binding protein isoform 3
NM_001353976.2 NP_001340905.1 STAM-binding protein isoform 4
NM_006463.6 NP_006454.1 STAM-binding protein isoform 1
NM_201647.4 NP_964010.1 STAM-binding protein isoform 1
NM_213622.4 NP_998787.1 STAM-binding protein isoform 1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables K63-linked deubiquitinase activity IDA
IDA: Inferred from direct assay
34425109 GOA
enables deubiquitinase activity IDA
IDA: Inferred from direct assay
18388320 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
10383417 GOA
enables protein domain specific binding IPI
IPI: Inferred from physical interaction
18395747 GOA
Biological Process GO Annotation Evidence Reference Source
acts upstream of or within mitotic cytokinesis IMP
IMP: Inferred from mutant phenotype
18388320 GOA
involved in negative regulation of Ras protein signal transduction IMP
IMP: Inferred from mutant phenotype
23542699 GOA
involved in negative regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction IMP
IMP: Inferred from mutant phenotype
23542699 GOA
acts upstream of or within protein deubiquitination IMP
IMP: Inferred from mutant phenotype
18388320 GOA
Cellular Component GO Annotation Evidence Reference Source
located in cleavage furrow IDA
IDA: Inferred from direct assay
18388320 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

STAMBP Protein Structure

USP8_dimer

USP8_dimer: USP8 dimerisation domain (13 - 116)

JAB

JAB: JAB1/Mov34/MPN/PAD-1 ubiquitin protease (254 - 360)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 424 a.a.
Protein Preferred Names Protein Names

STAM-binding protein

associated molecule with the SH3 domain of STAM

STAMBP Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
STAMBP O95630 JPH3 Homo sapiens Q8WXH2 32814053
Intra
STAMBP O95630 JPH3 Homo sapiens Q8WXH2 32814053
Intra
STAMBP O95630 JPH3 Homo sapiens Q8WXH2 32814053
Intra
STAMBP O95630 CHMP1A Homo sapiens Q9HD42 17711858
Intra
STAMBP O95630 CHMP1A Homo sapiens Q9HD42
Y2H
17711858
Intra
STAMBP O95630 CHMP1A Homo sapiens Q9HD42 33961781
Intra
STAMBP O95630 CHMP1A Homo sapiens Q9HD42 28514442
Intra
STAMBP O95630 APOBEC3A Homo sapiens P31941 32296183
Intra
STAMBP O95630 BMP2K Homo sapiens Q9NSY1 33961781
Intra
STAMBP O95630 BMP2K Homo sapiens Q9NSY1 28514442
Intra
STAMBP O95630 CHMP3 Homo sapiens Q9Y3E7-1 21827950
Intra
STAMBP O95630 CHMP1B Homo sapiens Q7LBR1
Y2H
21988832
Intra
STAMBP O95630 CHMP1B Homo sapiens Q7LBR1
Y2H
16730941
Intra
STAMBP O95630 CHMP1B Homo sapiens Q7LBR1 25416956
Intra
STAMBP O95630 CHMP1B Homo sapiens Q7LBR1 25416956
Intra
STAMBP O95630 CHMP1B Homo sapiens Q7LBR1 21827950
Intra
STAMBP O95630 CHMP1B Homo sapiens Q7LBR1 32296183
Intra
STAMBP O95630 CHMP1B Homo sapiens Q7LBR1
SPR
21827950
Intra
STAMBP O95630 CHMP3 Homo sapiens Q9Y3E7 28514442
Intra
STAMBP O95630 CHMP3 Homo sapiens Q9Y3E7 25416956
Intra
STAMBP O95630 CHMP3 Homo sapiens Q9Y3E7
Y2H
16730941
Intra
STAMBP O95630 CHMP3 Homo sapiens Q9Y3E7 17711858
Intra
STAMBP O95630 CHMP3 Homo sapiens Q9Y3E7 19615732
Intra
STAMBP O95630 CHMP3 Homo sapiens Q9Y3E7
Y2H
17711858
Intra
STAMBP O95630 PRKN Homo sapiens O60260-5 32814053
Intra
STAMBP O95630 PRKN Homo sapiens O60260-5 32814053
Intra
STAMBP O95630 PRKN Homo sapiens O60260-5 32814053
Intra
STAMBP O95630 CHMP2A Homo sapiens O43633 33961781
Intra
STAMBP O95630 CHMP2A Homo sapiens O43633 28514442
Intra
STAMBP O95630 CCT5 Homo sapiens P48643 32814053
Intra
STAMBP O95630 CCT5 Homo sapiens P48643 32814053
Intra
STAMBP O95630 CCT5 Homo sapiens P48643 32814053
Intra
STAMBP O95630 TRIP13 Homo sapiens Q15645 31515488
Intra
STAMBP O95630 TARDBP Homo sapiens Q13148 32814053
Intra
STAMBP O95630 TARDBP Homo sapiens Q13148 32814053
Intra
STAMBP O95630 TARDBP Homo sapiens Q13148 32814053
Intra
STAMBP O95630 STAM2 Homo sapiens O75886 19060904
Intra
STAMBP O95630 STAM2 Homo sapiens O75886 19060904
Intra
STAMBP O95630 RNF11 Homo sapiens Q9Y3C5 14755250
Intra
STAMBP O95630 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
STAMBP O95630 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
STAMBP O95630 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
STAMBP O95630 RNF11 Homo sapiens Q9Y3C5
Y2H
14755250
Intra
STAMBP O95630 GRB2 Homo sapiens P62993 25416956
Intra
STAMBP O95630 GRB2 Homo sapiens P62993 25416956
Intra
STAMBP O95630 GRB2 Homo sapiens P62993 19615732
Intra
STAMBP O95630 UBB Homo sapiens P0CG47 32814053
Intra
STAMBP O95630 UBB Homo sapiens P0CG47 32814053
Intra
STAMBP O95630 UBB Homo sapiens P0CG47 32814053
Intra
STAMBP O95630 SMAD6 Homo sapiens O43541-2
Y2H
11483516
Intra
STAMBP O95630 CHMP5 Homo sapiens Q9NZZ3
Y2H
21988832
Intra
STAMBP O95630 STAM Homo sapiens Q92783
ITC
17078930
Intra
STAMBP O95630 STAM Homo sapiens Q92783 10383417
Intra
STAMBP O95630 ATXN1 Homo sapiens P54253 32814053
Intra
STAMBP O95630 ATXN1 Homo sapiens P54253 32814053
Intra
STAMBP O95630 ATXN1 Homo sapiens P54253 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

STAMBP Antibodies

Cat. No. Product Name Application Reactivity
HY-P82962 AMSH Antibody (YA2707) WB Human

Related Diseases

Diseases Alias
Microcephaly-Capillary Malformation Syndrome

Mic-Cap Syndrome

MICCAP

Mic-Cm Syndrome

Microcephaly-Cutaneous Capillary Malformation Syndrome

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

Microcephaly

Microencephaly

Microcephalus

Microcephalic

Nanocephaly

Congenital Microcephaly

Brain Hypoplasia

Brain Nondevelopment

Cephalic Hypoplasia

Undeveloped Cerebrum

Undeveloped Brain

Micrencephalon

Micrencephaly

Epilepsy

Epilepsy Syndrome

Epileptic Syndrome

Epilepsies

Symptomatic Epilepsies

Post Traumatic Epilepsy

Traumatic Epilepsy

Traumatic Epileptic

Epilepsy Due To Hippocampal Sclerosis

Epilepsy With Ammon'S Horn Sclerosis

Epilepsy Due To Cortical Dysplasia

Epilepsy Due To Neuronal Migration Disorders

Congenital Nervous System Abnormality

Congenital Neurologic Anomaly

Congenital Nervous System Disorder

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
Macaca mulatta STAMBP VGNC VGNC:77935
Rattus norvegicus STAMBP RGD RGD:619963
Mus musculus STAMBP MGD MGI:1917777
Bos taurus STAMBP VGNC VGNC:35356
Felis catus STAMBP VGNC VGNC:65747
Others STAMBP NCBI