1. Gene
  2. STUB1 - STIP1 homology and U-box containing protein 1 Gene

STUB1 - STIP1 homology and U-box containing protein 1 Gene

Homo sapiens

Also known as CHIP; SCA48; UBOX1; SCAR16; HSPABP2; NY-CO-7; SDCCAG7

Gene ID: 10273 | Gene type: protein coding

About STUB1

Cytogenetic location: 16p13.3 Genomic coordinates (GRCh38): 16:680,410-682,801 (from NCBI)

This gene has 11 transcripts (splice variants), 236 orthologues, 18 paralogues and is associated with 3 phenotypes. Ubiquitous expression in fat (RPKM 42.9), kidney (RPKM 39.1) and 25 other tissues.

Summary

This gene encodes a protein containing tetratricopeptide repeat and a U-box that functions as a ubiquitin Ligase/cochaperone. The encoded protein binds to and ubiquitinates shock cognate 71 kDa protein (Hspa8) and DNA Polymerase beta (Polb), among Other targets. Mutations in this gene cause spinocerebellar ataxia, autosomal recessive 16. Alternative splicing results in multiple transcript variants. There is a pseudogene for this gene on chromosome 2. [provided by RefSeq, Jun 2014]

STUB1 Products(2)

mRNA Protein Name
NM_001293197.2 NP_001280126.1 E3 ubiquitin-protein ligase CHIP isoform b
NM_005861.4 NP_005852.2 E3 ubiquitin-protein ligase CHIP isoform a
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables G protein-coupled receptor binding IPI
IPI: Inferred from physical interaction
12150907 GOA
enables Hsp70 protein binding IDA
IDA: Inferred from direct assay
10330192 GOA
enables Hsp70 protein binding IPI
IPI: Inferred from physical interaction
24613385 GOA
enables Hsp90 protein binding IDA
IDA: Inferred from direct assay
11146632 GOA
enables R-SMAD binding IPI
IPI: Inferred from physical interaction
15781469 GOA
enables SMAD binding IPI
IPI: Inferred from physical interaction
24613385 GOA
enables TPR domain binding IDA
IDA: Inferred from direct assay
11146632 GOA
enables enzyme binding IPI
IPI: Inferred from physical interaction
16280320 GOA
enables heat shock protein binding IPI
IPI: Inferred from physical interaction
16207813 GOA
enables kinase binding IPI
IPI: Inferred from physical interaction
17512523 GOA
enables misfolded protein binding IDA
IDA: Inferred from direct assay
16831871 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
11146632 GOA
enables protein homodimerization activity IPI
IPI: Inferred from physical interaction
23990462 GOA
enables protein-folding chaperone binding IPI
IPI: Inferred from physical interaction
16207813 GOA
enables ubiquitin protein ligase activity IDA
IDA: Inferred from direct assay
14610072 GOA
enables ubiquitin protein ligase activity IGI
IGI: Inferred from genetic interaction
16207813 GOA
enables ubiquitin protein ligase activity IMP
IMP: Inferred from mutant phenotype
15781469 GOA
enables ubiquitin protein ligase binding IPI
IPI: Inferred from physical interaction
12150907 GOA
enables ubiquitin-protein transferase activity IDA
IDA: Inferred from direct assay
15466472 GOA
enables ubiquitin-protein transferase activity IMP
IMP: Inferred from mutant phenotype
19713937 GOA
Biological Process GO Annotation Evidence Reference Source
involved in ERAD pathway IMP
IMP: Inferred from mutant phenotype
23990462 GOA
involved in cellular response to misfolded protein IDA
IDA: Inferred from direct assay
16831871 GOA
involved in negative regulation of smooth muscle cell apoptotic process IMP
IMP: Inferred from mutant phenotype
20724525 GOA
involved in negative regulation of transforming growth factor beta receptor signaling pathway IMP
IMP: Inferred from mutant phenotype
15781469 GOA
involved in positive regulation of ERAD pathway IMP
IMP: Inferred from mutant phenotype
26265139 GOA
involved in positive regulation of chaperone-mediated protein complex assembly IDA
IDA: Inferred from direct assay
16831871 GOA
involved in positive regulation of proteasomal ubiquitin-dependent protein catabolic process IDA
IDA: Inferred from direct assay
11146632 GOA
involved in positive regulation of protein ubiquitination IDA
IDA: Inferred from direct assay
11146632 GOA
involved in positive regulation of proteolysis IMP
IMP: Inferred from mutant phenotype
26634371 GOA
involved in proteasome-mediated ubiquitin-dependent protein catabolic process IDA
IDA: Inferred from direct assay
15781469 GOA
involved in proteasome-mediated ubiquitin-dependent protein catabolic process IMP
IMP: Inferred from mutant phenotype
29883609 GOA
involved in protein K63-linked ubiquitination IDA
IDA: Inferred from direct assay
16307917 GOA
involved in protein autoubiquitination IDA
IDA: Inferred from direct assay
16307917 GOA
involved in protein monoubiquitination IDA
IDA: Inferred from direct assay
24043303 GOA
involved in protein polyubiquitination IDA
IDA: Inferred from direct assay
15781469 GOA
involved in protein polyubiquitination IMP
IMP: Inferred from mutant phenotype
19713937 GOA
involved in protein quality control for misfolded or incompletely synthesized proteins IDA
IDA: Inferred from direct assay
16831871 GOA
involved in protein stabilization IDA
IDA: Inferred from direct assay
24043303 GOA
involved in protein ubiquitination IDA
IDA: Inferred from direct assay
14610072 GOA
involved in protein ubiquitination IMP
IMP: Inferred from mutant phenotype
16809764 GOA
involved in regulation of glucocorticoid metabolic process IDA
IDA: Inferred from direct assay
11146632 GOA
involved in regulation of protein stability IDA
IDA: Inferred from direct assay
16809764 GOA
involved in ubiquitin-dependent protein catabolic process IGI
IGI: Inferred from genetic interaction
18292230 GOA
involved in ubiquitin-dependent protein catabolic process IMP
IMP: Inferred from mutant phenotype
19713937 GOA
Cellular Component GO Annotation Evidence Reference Source
located in cytoplasm IDA
IDA: Inferred from direct assay
10330192 GOA
located in endoplasmic reticulum IDA
IDA: Inferred from direct assay
12150907 GOA
located in nuclear inclusion body IDA
IDA: Inferred from direct assay
16831871 GOA
is active in nucleus IDA
IDA: Inferred from direct assay
23973223 GOA
part of protein folding chaperone complex IPI
IPI: Inferred from physical interaction
16207813 GOA
part of ubiquitin ligase complex IDA
IDA: Inferred from direct assay
12150907 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

STUB1 Protein Structure

TPR_11

TPR_11: TPR repeat (26 - 90)

TPR_1

TPR_1: Tetratricopeptide repeat (94 - 123)

U-box

U-box: U-box domain (227 - 299)

  • 0
  • 100
  • 200
  • 303 a.a.
Protein Preferred Names Protein Names

E3 ubiquitin-protein ligase CHIP

CLL-associated antigen KW-8

STUB1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
STUB1 Q9UNE7 NF2 Homo sapiens P35240 32814053
Intra
STUB1 Q9UNE7 NF2 Homo sapiens P35240 32814053
Intra
STUB1 Q9UNE7 NF2 Homo sapiens P35240 32814053
Intra
STUB1 Q9UNE7 OLFM3 Homo sapiens Q96PB7 25416956
Intra
STUB1 Q9UNE7 BAG1 Homo sapiens Q99933 25036637
Intra
STUB1 Q9UNE7 CISD2 Homo sapiens Q8N5K1 32814053
Intra
STUB1 Q9UNE7 CISD2 Homo sapiens Q8N5K1 32814053
Intra
STUB1 Q9UNE7 CISD2 Homo sapiens Q8N5K1 32814053
Intra
STUB1 Q9UNE7 MLF2 Homo sapiens Q15773 25036637
Intra
STUB1 Q9UNE7 MLF2 Homo sapiens Q15773 33961781
Intra
STUB1 Q9UNE7 MLF2 Homo sapiens Q15773 25036637
Intra
STUB1 Q9UNE7 UBE2N Homo sapiens P61088 25036637
Intra
STUB1 Q9UNE7 RAB7A Homo sapiens P51149 32814053
Intra
STUB1 Q9UNE7 RAB7A Homo sapiens P51149 32814053
Intra
STUB1 Q9UNE7 RAB7A Homo sapiens P51149 32814053
Intra
STUB1 Q9UNE7 DMWD Homo sapiens G5E9A7 32814053
Intra
STUB1 Q9UNE7 DMWD Homo sapiens G5E9A7 32814053
Intra
STUB1 Q9UNE7 DMWD Homo sapiens G5E9A7 32814053
Intra
STUB1 Q9UNE7 SEPTIN2 Homo sapiens Q15019-2 32814053
Intra
STUB1 Q9UNE7 SEPTIN2 Homo sapiens Q15019-2 32814053
Intra
STUB1 Q9UNE7 SEPTIN2 Homo sapiens Q15019-2 32814053
Intra
STUB1 Q9UNE7 BSCL2 Homo sapiens J3KQ12 32814053
Intra
STUB1 Q9UNE7 BSCL2 Homo sapiens J3KQ12 32814053
Intra
STUB1 Q9UNE7 BSCL2 Homo sapiens J3KQ12 32814053
Intra
STUB1 Q9UNE7 CAMK2A Homo sapiens Q9UQM7 32814053
Intra
STUB1 Q9UNE7 CAMK2A Homo sapiens Q9UQM7 32814053
Intra
STUB1 Q9UNE7 CAMK2A Homo sapiens Q9UQM7 32814053
Intra
STUB1 Q9UNE7 NGFR Homo sapiens P08138 32814053
Intra
STUB1 Q9UNE7 NGFR Homo sapiens P08138 32814053
Intra
STUB1 Q9UNE7 NGFR Homo sapiens P08138 32814053
Intra
STUB1 Q9UNE7 MOS Homo sapiens P00540 25036637
Intra
STUB1 Q9UNE7 UBE2Q1 Homo sapiens Q7Z7E8 16275660
Intra
STUB1 Q9UNE7 UBE2Q1 Homo sapiens Q7Z7E8 16275660
Intra
STUB1 Q9UNE7 ATCAY Homo sapiens Q86WG3 16275660
Intra
STUB1 Q9UNE7 ATCAY Homo sapiens Q86WG3 16275660
Intra
STUB1 Q9UNE7 GLE1 Homo sapiens Q53GS7 32814053
Intra
STUB1 Q9UNE7 GLE1 Homo sapiens Q53GS7 32814053
Intra
STUB1 Q9UNE7 GLE1 Homo sapiens Q53GS7 32814053
Intra
STUB1 Q9UNE7 MPO Homo sapiens P05164 32814053
Intra
STUB1 Q9UNE7 MPO Homo sapiens P05164 32814053
Intra
STUB1 Q9UNE7 MPO Homo sapiens P05164 32814053
Intra
STUB1 Q9UNE7 COL25A1 Homo sapiens Q8NE08 32814053
Intra
STUB1 Q9UNE7 COL25A1 Homo sapiens Q8NE08 32814053
Intra
STUB1 Q9UNE7 COL25A1 Homo sapiens Q8NE08 32814053
Intra
STUB1 Q9UNE7 PEX7 Homo sapiens O00628-2 32814053
Intra
STUB1 Q9UNE7 PEX7 Homo sapiens O00628-2 32814053
Intra
STUB1 Q9UNE7 PEX7 Homo sapiens O00628-2 32814053
Intra
STUB1 Q9UNE7 SPTLC1 Homo sapiens O15269-2 32814053
Intra
STUB1 Q9UNE7 SPTLC1 Homo sapiens O15269-2 32814053
Intra
STUB1 Q9UNE7 SPTLC1 Homo sapiens O15269-2 32814053
Intra
STUB1 Q9UNE7 ALS2 Homo sapiens A0A0S2Z5Q7 32814053
Intra
STUB1 Q9UNE7 ALS2 Homo sapiens A0A0S2Z5Q7 32814053
Intra
STUB1 Q9UNE7 ALS2 Homo sapiens A0A0S2Z5Q7 32814053
Intra
STUB1 Q9UNE7 PANK2 Homo sapiens Q9BZ23-2 32814053
Intra
STUB1 Q9UNE7 PANK2 Homo sapiens Q9BZ23-2 32814053
Intra
STUB1 Q9UNE7 PANK2 Homo sapiens Q9BZ23-2 32814053
Intra
STUB1 Q9UNE7 NCAM1 Homo sapiens P13591 32814053
Intra
STUB1 Q9UNE7 NCAM1 Homo sapiens P13591 32814053
Intra
STUB1 Q9UNE7 NCAM1 Homo sapiens P13591 32814053
Intra
STUB1 Q9UNE7 TXN2 Homo sapiens Q99757 25416956
Intra
STUB1 Q9UNE7 HSP90AA1 Homo sapiens P07900 16307917
Intra
STUB1 Q9UNE7 HSP90AA1 Homo sapiens P07900
Y2H
16275660
Intra
STUB1 Q9UNE7 EGFR Homo sapiens P00533 20029029
Intra
STUB1 Q9UNE7 EGFR Homo sapiens P00533 24658140
Intra
STUB1 Q9UNE7 SQSTM1 Homo sapiens Q13501 32814053
Intra
STUB1 Q9UNE7 SQSTM1 Homo sapiens Q13501 32814053
Intra
STUB1 Q9UNE7 SQSTM1 Homo sapiens Q13501 32814053
Intra
STUB1 Q9UNE7 HSPA8 Homo sapiens P11142
Y2H
16275660
Intra
STUB1 Q9UNE7 HSPA8 Homo sapiens P11142 16293251
Intra
STUB1 Q9UNE7 HSPA8 Homo sapiens P11142 33961781
Intra
STUB1 Q9UNE7 HSP90AB1 Homo sapiens P08238 16293251
Intra
STUB1 Q9UNE7 HSP90AB1 Homo sapiens P08238
ITC
20618441
Intra
STUB1 Q9UNE7 HSPB1 Homo sapiens P04792 32814053
Intra
STUB1 Q9UNE7 HSPB1 Homo sapiens P04792 32814053
Intra
STUB1 Q9UNE7 HSPB1 Homo sapiens P04792 25277244
Intra
STUB1 Q9UNE7 HSPB1 Homo sapiens P04792 32814053
Intra
STUB1 Q9UNE7 BAG2 Homo sapiens O95816 25036637
Intra
STUB1 Q9UNE7 MAP3K2 Homo sapiens Q9Y2U5 20588253
Intra
STUB1 Q9UNE7 MAP3K2 Homo sapiens Q9Y2U5 20588253
Intra
STUB1 Q9UNE7 DAPK1 Homo sapiens P53355 29513927
Intra
STUB1 Q9UNE7 RAF1 Homo sapiens P04049 25036637
Intra
STUB1 Q9UNE7 MAPT Homo sapiens P10636 16275660
Intra
STUB1 Q9UNE7 MAPT Homo sapiens P10636 16275660
Intra
STUB1 Q9UNE7 RGS17 Homo sapiens Q9UGC6 32296183
Intra
STUB1 Q9UNE7 RGS17 Homo sapiens Q9UGC6 32296183
Intra
STUB1 Q9UNE7 PRKACA Homo sapiens P17612 32814053
Intra
STUB1 Q9UNE7 PRKACA Homo sapiens P17612 32814053
Intra
STUB1 Q9UNE7 PRKACA Homo sapiens P17612 32814053
Intra
STUB1 Q9UNE7 FYN Homo sapiens P06241 32814053
Intra
STUB1 Q9UNE7 FYN Homo sapiens P06241 32814053
Intra
STUB1 Q9UNE7 FYN Homo sapiens P06241 32814053
Intra
STUB1 Q9UNE7 SPRED1 Homo sapiens Q7Z699 32814053
Intra
STUB1 Q9UNE7 SPRED1 Homo sapiens Q7Z699 32814053
Intra
STUB1 Q9UNE7 SPRED1 Homo sapiens Q7Z699 32814053
Intra
STUB1 Q9UNE7 LRRK2 Homo sapiens Q5S007 29513927
Intra
STUB1 Q9UNE7 RUSC1 Homo sapiens Q9BVN2 25416956
Intra
STUB1 Q9UNE7 RUSC1 Homo sapiens Q9BVN2 25416956
Intra
STUB1 Q9UNE7 HSPA1A Homo sapiens P08107 25036637
Intra
STUB1 Q9UNE7 HSPA1A Homo sapiens P08107
Y2H
16275660
Intra
STUB1 Q9UNE7 HSPA1A Homo sapiens P08107
GMS
20618441
Intra
STUB1 Q9UNE7 HSPA1A Homo sapiens P08107 16275660
Intra
STUB1 Q9UNE7 A2M Homo sapiens P01023 32814053
Intra
STUB1 Q9UNE7 A2M Homo sapiens P01023 32814053
Intra
STUB1 Q9UNE7 A2M Homo sapiens P01023 32814053
Intra
STUB1 Q9UNE7 GAL Homo sapiens P22466 32814053
Intra
STUB1 Q9UNE7 GAL Homo sapiens P22466 32814053
Intra
STUB1 Q9UNE7 GAL Homo sapiens P22466 32814053
Intra
STUB1 Q9UNE7 UBE2L3 Homo sapiens P68036 32814053
Intra
STUB1 Q9UNE7 UBE2L3 Homo sapiens P68036 32814053
Intra
STUB1 Q9UNE7 UBE2L3 Homo sapiens P68036 32814053
Intra
STUB1 Q9UNE7 ACD Homo sapiens Q96AP0 21044950
Intra
STUB1 Q9UNE7 ACD Homo sapiens Q96AP0 21044950
Intra
STUB1 Q9UNE7 WFS1 Homo sapiens O76024 32814053
Intra
STUB1 Q9UNE7 WFS1 Homo sapiens O76024 32814053
Intra
STUB1 Q9UNE7 WFS1 Homo sapiens O76024 32814053
Intra
STUB1 Q9UNE7 MLF1 Homo sapiens P58340 25036637
Intra
STUB1 Q9UNE7 MLF1 Homo sapiens P58340 33961781
Intra
STUB1 Q9UNE7 BAG3 Homo sapiens O95817 25036637
Intra
STUB1 Q9UNE7 CCL28 Homo sapiens Q9NRJ3 25416956
Intra
STUB1 Q9UNE7 CCL28 Homo sapiens Q9NRJ3 25416956
Intra
STUB1 Q9UNE7 CCL28 Homo sapiens Q9NRJ3 25416956
Intra
STUB1 Q9UNE7 REC8 Homo sapiens O95072 25036637
Intra
STUB1 Q9UNE7 FOXP3 Homo sapiens Q9BZS1 23973223
Intra
STUB1 Q9UNE7 CYTH1 Homo sapiens Q15438 32814053
Intra
STUB1 Q9UNE7 CYTH1 Homo sapiens Q15438 32814053
Intra
STUB1 Q9UNE7 CYTH1 Homo sapiens Q15438 32814053
Cross
STUB1 Q9UNE7 Bag5 Rattus norvegicus Q5QJC9 21358815
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant STUB1 Proteins

Cat. No. Product Name Accession Purity
HY-P71340 STUB1 Protein, Human Q9UNE7 (M1-Y303) ≥95%

STUB1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P82351 STUB1 Antibody (YA2096) WB, ICC/IF, IP Human, Mouse, Rat

Related Diseases

Diseases Alias
Spinocerebellar Ataxia, Autosomal Recessive 16

Autosomal Recessive Spinocerebellar Ataxia 16

SCAR16

Autosomal Recessive Cerebellar Ataxia Due To Stub1 Deficiency

Spinocerebellar Ataxia Autosomal Recessive Type 16

Spinocerebellar Ataxia, Autosomal Recessive, 16

Ataxia, Spinocerebellar, Autosomal Recessive, Type 16

Spinocerebellar Ataxia 48

SCA48

Cerebellar Ataxia Type 48

Sca48

Gordon Holmes Syndrome

Cerebellar Ataxia And Hypogonadotropic Hypogonadism

Lhrh Deficiency And Ataxia

Cerebellar Ataxia-Hypogonadism Syndrome

GDHS

Cahh

Luteinizing Hormone-Releasing Hormone Deficiency With Ataxia

Gordon-Holmes Syndrome

Deficiency Of Luteinizing Hormone-Releasing Hormone With Ataxia

Luteinizing Hormone-Releasing Hormone, Deficiency Of, With Ataxia

Cerebellar Ataxia - Hypogonadism

Luteinizing Hormone Releasing Hormone, Deficiency Of With Ataxia

Ataxia, Cerebellar, And Hypogonadotropic Hypogonadism

Spinocerebellar Ataxia 15

SCA15

Spinocerebellar Ataxia Type 15

Spinocerebellar Ataxia Type 16

Sca16

Spinocerebellar Ataxia Type 15/16

Spinocerebellar Ataxia 16, Formerly

Sca16, Formerly

Spinocerebellar Ataxia 16

Sca15/16

Ataxia, Spinocerebellar, Type 15

Siderosis

Pulmonary Siderosis

Deposition Of Iron

Arc-Welders' Disease

Arc-Welders' Lung

Arc-Welders' Nodulation

Arc-Welders' Pneumoconiosis

Iron Oxide Lung

Iron Pneumoconiosis

Pneumoconiosis Siderotico

Siderotic Lung Disease

Steel Grinders' Disease

Welders' Lung

Welders' Siderosis

Lung Fibrosis With Siderosis

Dyslexia
Colorectal Cancer

Colon Cancer

Colorectal Carcinoma

Colon Carcinoma

Colorectal Cancer, Susceptibility To

Carcinoma Of Colon

CRC

Colorectal Cancer With Chromosomal Instability, Somatic

Colon Cancer, Somatic

Colon Cancer, Susceptibility To

Colonic Neoplasms

Colorectal Neoplasms

Colorectal Cancer, Somatic

Colon Cancer, Advanced, Somatic

Colonic Carcinoma

Colorectal Carcinomas

Colon Cancers

Colorectal Cancers

Cancer, Colorectal, Somatic

Cancer, Colon

Cancer, Colorectal, Susceptibility To

Colorectal Neoplasm

Colonic Neoplasm

Malignant Tumor Of Colon

Parkinson Disease, Late-Onset

Parkinson Disease

Parkinson'S Disease

PD

PARK

Parkinson Disease, Susceptibility To

Late Onset Parkinson'S Disease

Late Onset Parkinson Disease

Paralysis Agitans

Primary Parkinsonism

Idiopathic Parkinson Disease

Parkinson'S

Parkinson Disease, Late-Onset, Susceptibility To

Parkinson Disease, Age Of Onset, Modifier

Lewy Body Parkinson Disease

Idiopathic Parkinson'S Disease

Pd - [Parkinson Disease]

Parkinson Disease Nos

Parkinson, Nos

Primary Parkinson Disease

Hematuria, Benign Familial

Benign Familial Hematuria

BFH

Thin Membrane Nephropathy

Tmn

Thin Basement Membrane Nephropathy

Thin-Basement-Membrane Nephropathy

Hematuria, Familial Benign

Hematuria Benign Familial

Hematuria, Benign, Familial

Thin Basement Membrane Disease

Acute Tympanitis

Acute Myringitis

Spinal And Bulbar Muscular Atrophy, X-Linked 1

Kennedy Disease

Sbma

Spinal And Bulbar Muscular Atrophy

Kennedy'S Disease

X-Linked Spinal And Bulbar Muscular Atrophy

SMAX1

Kd

Kennedy Spinal And Bulbar Muscular Atrophy

Spinobulbar Muscular Atrophy

Bulbospinal Muscular Atrophy, X-Linked

Bulbospinal Neuronopathy, X-Linked Recessive

Xbsn

Spinal And Bulbar Muscular Atrophy Of Kennedy

Bulbospinal Muscular Atrophy

X-Linked Bulbospinal Amyotrophy

Bulbo-Spinal Atrophy, X-Linked

Spinal Bulbar Muscular Atrophy

X-Linked Bulbo-Spinal Atrophy

X-Linked Spinal Bulbar Muscular Atrophy

X-Linked Bsma

X-Linked Bulbospinal Muscular Atrophy

Spinal And Bulbar Muscular Atrophy X-Linked 1

Bulbospinal Muscular Atrophy X-Linked

Bulbospinal Neuronopathy X-Linked Recessive

Kennedy Disease)

Kennedy Syndrome

Atrophy, Muscular, Spinal And Bulbar, Kennedy Type

Atrophy, Muscular, Spinobulbar

Bulbospinal Neuronopathy

Cystic Fibrosis

Mucoviscidosis

CF

Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis

Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis

Cystic Fibrosis Lung Disease, Modifier Of

Cystic Fibrosis Of Pancreas

Fibrocystic Disease Of Pancreas

Cf - [Cystic Fibrosis]

Cystic Fibrosis Nos

Fibrocystic Disease

Fibrocystic Disease Of The Pancreas

Mucoviscidosis Of Pancreas

Nonproliferative Fibrocystic Disease

Pancreatic Cystic Fibrosis

Spondylocostal Dysostosis 3, Autosomal Recessive

SCDO3

Spondylocostal Dysostosis, Autosomal Recessive 3

Spondylocostal Dysostosis 3

Autosomal Recessive Spondylocostal Dysostosis 3

Doid:0112361

Dysostosis, Spondylocostal, Autosomal Recessive, Type 3

Jarcho-Levin Syndrome

Dystonia

Dystonic Disease

Dystonic Disorder

Dystonia Disorders

Neuroleptic Dyskinesia

Autosomal Dominant Cerebellar Ataxia

Spinocerebellar Ataxia

Adca

Pierre Marie Cerebellar Ataxia

Ataxia, Spinocerebellar

Sca

Autosomal Dominant Spinocerebellar Ataxia

Spinocerebellar Ataxias

Myelodysplastic Syndrome

Myelodysplastic Syndromes

Myelodysplasia

MDS

Myelodysplastic Syndrome Included

Myelodysplastic Syndrome, Susceptibility To, Included

Myelodysplastic Syndrome, Somatic

Myelodysplastic Syndrome, Susceptibility To

Alzheimer Disease, Familial, 1

Alzheimer Disease

Alzheimer'S Disease

Presenile And Senile Dementia

AD1

Alzheimer Disease, Susceptibility To

Alzheimer Disease, Late-Onset, Susceptibility To

Alzheimer Disease 1, Familial

AD

Familial Alzheimer Disease

Alzheimer Disease, Late-Onset

Alzheimers Dementia

Alzheimer Dementia

Alzheimer Sclerosis

Alzheimer Syndrome

Alzheimer-Type Dementia

Dat

Primary Senile Degenerative Dementia

Sdat

Alzheimer Disease 1

Autosomal Dominant Alzheimer Disease

Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy

Late Onset Alzheimer Disease

Alzheimers Disease

Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy

Late-Onset Alzheimers Disease

Alzheimer'S Disease Pathway Kegg

Dementia Due To Alzheimer'S Disease

Alzheimer Disease Type 1

Alzheimers

Attention Deficit-Hyperactivity Disorder

Attention Deficit Hyperactivity Disorder

ADHD

Attention Deficit Disorder

Attention Deficit-Hyperactivity Disorder, Susceptibility To

Attention Deficit Disorder With Hyperactivity

Hyperkinetic Disorder

Hyperactivity Of Childhood

Attention-Deficit/Hyperactivity Disorder

Add

Addh

Attention Deficit

Attention Deficit Disorder Of Childhood With Hyperactivity

Attention Deficit Disorder With Hyperactivity Syndrome

Hyperkinetic Syndrome

Attention-Deficit Hyperactivity Disorder

Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type

Disturbance Of Activity And Attention

Disorder Of Activity And Attention

Adhd - [Attention Deficit Hyperactivity Disorder]

Hyperkinetic Disorders

Disorder Of Activity And Attention With Hyperkinesia

Attention Deficit Syndrome With Hyperactivity

Leukemia, Acute Myeloid

Acute Myeloid Leukemia

Leukemia, Acute Myelogenous

Acute Myelogenous Leukemia

AML

Leukemia, Acute Myeloid, Susceptibility To

Acute Myeloblastic Leukemia

Leukemia, Acute Myeloid, Reduced Survival In, Somatic

Acute Myeloid Leukaemia

Leukemia, Myelocytic, Acute

Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome

Secondary Aml

Acute Myelocytic Leukemia

Acute Myeloid Leukemia, Somatic

Leukemia, Acute Myeloid, Somatic

Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic

Acute Myeloblastic Leukaemia

Acute Myelogenous Leukaemia

Aml - Acute Myeloid Leukemia

Acute Myeloid Leukemia With Cebpa Somatic Mutations

Aml With Cebpa Somatic Mutations

Inherited Acute Myeloid Leukemia

Familial Aml

Inherited Aml

Pure Familial Aml

Pure Familial Acute Myeloid Leukemia

Secondary Acute Myeloid Leukemia

Therapy-Related Aml And Myelodysplastic Syndrome

Acute Myeloid Leukemia, Secondary

Acute Non-Lymphoblastic Leukemia

Acute Non-Lymphocytic Leukemia

Acute Biphenotypic Leukemia

Acute Undifferentiated Leukemia

Acute Myeloblastic Leukaemia With Multilineage Dysplasia

Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission

Acute Myeloid Leukaemia With Myelodysplasia-Related Features

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
Bos taurus STUB1 VGNC VGNC:58615
Rattus norvegicus STUB1 RGD RGD:1306167
Canis familiaris STUB1 VGNC VGNC:54073
Macaca mulatta STUB1 VGNC VGNC:99598
Felis catus STUB1 VGNC VGNC:65805
Mus musculus STUB1 MGD MGI:1891731
Others STUB1 NCBI