TSG101 - tumor susceptibility 101 Gene

Also Known as TSG10; VPS23

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 7251

About TSG101

Cytogenetic location: 11p15.1 Genomic coordinates (GRCh38): 11:18,480,311-18,526,942 (from NCBI)

This gene has 12 transcripts (splice variants), 227 orthologues and 1 paralogue. Ubiquitous expression in testis (RPKM 34.7), adrenal (RPKM 31.6) and 25 other tissues.

Summary

The protein encoded by this gene belongs to a group of apparently inactive homologs of ubiquitin-conjugating Enzymes. The gene product contains a coiled-coil domain that interacts with stathmin, a cytosolic phosphoprotein implicated in tumorigenesis. The protein may play a role in cell growth and differentiation and act as a negative growth regulator. In vitro steady-state expression of this tumor susceptibility gene appears to be important for maintenance of genomic stability and cell cycle regulation. Mutations and alternative splicing in this gene occur in high frequency in breast Cancer and suggest that defects occur during breast Cancer tumorigenesis and/or progression. [provided by RefSeq, Jul 2008]

TSG101 Products (1)

mRNA Protein Name
NM_006292.4 NP_006283.1 tumor susceptibility gene 101 protein
Molecular Function GO Annotation Evidence References Source
enables calcium-dependent protein binding IPI
IPI: Inferred from physical interaction
19520058 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
12802020 GOA
enables protein homodimerization activity IPI
IPI: Inferred from physical interaction
14519844 GOA
enables protein-containing complex binding IDA
IDA: Inferred from direct assay
16973552 GOA
enables ubiquitin binding IDA
IDA: Inferred from direct assay
11595185 GOA
enables ubiquitin protein ligase binding IPI
IPI: Inferred from physical interaction
17229889 GOA
enables virion binding IDA
IDA: Inferred from direct assay
11595185 GOA
Cellular Component GO Annotation Evidence References Source
part of ESCRT I complex IDA
IDA: Inferred from direct assay
18005716 GOA
part of ESCRT I complex IPI
IPI: Inferred from physical interaction
18005716 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
18077552 GOA
located in early endosome IDA
IDA: Inferred from direct assay
11916981 GOA
located in endosome IDA
IDA: Inferred from direct assay
17940959 GOA
located in extracellular exosome IDA
IDA: Inferred from direct assay
15326289 GOA
located in late endosome IMP
IMP: Inferred from mutant phenotype
15126635 GOA
located in plasma membrane IDA
IDA: Inferred from direct assay
17940959 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

TSG101 Protein Structure

UEV

UEV: UEV domain (22 - 141)

Vps23_core

Vps23_core: Vps23 core domain (315 - 379)

  • 0
  • 100
  • 200
  • 300
  • 390 a.a.
Protein Preferred Names Protein Names

tumor susceptibility gene 101 protein

  • ESCRT-I complex subunit TSG101

TSG101 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
TSG101 Q99816 ZWINT Homo sapiens O95229 32296183
Intra
TSG101 Q99816 ZWINT Homo sapiens O95229 32296183
Intra
TSG101 Q99816 KRT13 Homo sapiens A1A4E9 25416956
Intra
TSG101 Q99816 KRT13 Homo sapiens A1A4E9 25416956
Intra
TSG101 Q99816 FAM9B Homo sapiens Q8IZU0 25416956
Intra
TSG101 Q99816 FAM9B Homo sapiens Q8IZU0 25416956
Intra
TSG101 Q99816 VPS37A Homo sapiens Q8NEZ2-2 25416956
Intra
TSG101 Q99816 KRT34 Homo sapiens O76011 32296183
Intra
TSG101 Q99816 KRT34 Homo sapiens O76011 32296183
Intra
TSG101 Q99816 KRT35 Homo sapiens Q92764 32296183
Intra
TSG101 Q99816 KRT35 Homo sapiens Q92764 32296183
Intra
TSG101 Q99816 GLI2 Homo sapiens P10070 35044719
Intra
TSG101 Q99816 PPP1R13B Homo sapiens Q96KQ4 32296183
Intra
TSG101 Q99816 PPP1R13B Homo sapiens Q96KQ4 32296183
Intra
TSG101 Q99816 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
TSG101 Q99816 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
TSG101 Q99816 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
TSG101 Q99816 TRIML2 Homo sapiens Q8N7C3 32296183
Intra
TSG101 Q99816 TRIML2 Homo sapiens Q8N7C3 32296183
Intra
TSG101 Q99816 CEP63 Homo sapiens Q96MT8-3 32296183
Intra
TSG101 Q99816 CEP63 Homo sapiens Q96MT8-3 32296183
Intra
TSG101 Q99816 CAGE1 Homo sapiens Q8TC20-4 32296183
Intra
TSG101 Q99816 CAGE1 Homo sapiens Q8TC20-4 32296183
Intra
TSG101 Q99816 LCN2 Homo sapiens P80188 32296183
Intra
TSG101 Q99816 LCN2 Homo sapiens P80188 32296183
Intra
TSG101 Q99816 VPS28 Homo sapiens Q9UK41-2 32296183
Intra
TSG101 Q99816 VPS28 Homo sapiens Q9UK41-2 32296183
Intra
TSG101 Q99816 VPS28 Homo sapiens Q9UK41-2 32296183
Intra
TSG101 Q99816 VPS28 Homo sapiens Q9UK41-2 31515488
Intra
TSG101 Q99816 SCARA5 Homo sapiens Q6ZMJ2-2 32296183
Intra
TSG101 Q99816 SCARA5 Homo sapiens Q6ZMJ2-2 32296183
Intra
TSG101 Q99816 FAM110A Homo sapiens Q9BQ89 32296183
Intra
TSG101 Q99816 MGRN1 Homo sapiens O60291 37219487
Intra
TSG101 Q99816 TRIM54 Homo sapiens Q9BYV2 32296183
Intra
TSG101 Q99816 TRIM54 Homo sapiens Q9BYV2 32296183
Intra
TSG101 Q99816 TRIM54 Homo sapiens Q9BYV2 32296183
Intra
TSG101 Q99816 BRPF3 Homo sapiens Q9ULD4-2 32296183
Intra
TSG101 Q99816 BRPF3 Homo sapiens Q9ULD4-2 32296183
Intra
TSG101 Q99816 BRPF3 Homo sapiens Q9ULD4-2 32296183
Intra
TSG101 Q99816 HAUS1 Homo sapiens Q96CS2 25416956
Intra
TSG101 Q99816 HAUS1 Homo sapiens Q96CS2 32296183
Intra
TSG101 Q99816 HAUS1 Homo sapiens Q96CS2 32296183
Intra
TSG101 Q99816 VPS37C Homo sapiens A5D8V6 25416956
Intra
TSG101 Q99816 VPS37C Homo sapiens A5D8V6 32296183
Intra
TSG101 Q99816 VPS37C Homo sapiens A5D8V6 25416956
Intra
TSG101 Q99816 VPS37C Homo sapiens A5D8V6 35271311
Intra
TSG101 Q99816 VPS37C Homo sapiens A5D8V6 32296183
Intra
TSG101 Q99816 PRRC1 Homo sapiens Q96M27 35044719
Intra
TSG101 Q99816 PKNOX2 Homo sapiens Q96KN3 32296183
Intra
TSG101 Q99816 PKNOX2 Homo sapiens Q96KN3 32296183
Intra
TSG101 Q99816 VPS37A Homo sapiens Q8NEZ2 25416956
Intra
TSG101 Q99816 VPS37A Homo sapiens Q8NEZ2 32296183
Intra
TSG101 Q99816 VPS37A Homo sapiens Q8NEZ2 35271311
Intra
TSG101 Q99816 VPS37A Homo sapiens Q8NEZ2 32296183
Intra
TSG101 Q99816 BAG4 Homo sapiens O95429 32296183
Intra
TSG101 Q99816 BAG4 Homo sapiens O95429 32296183
Intra
TSG101 Q99816 KRT75 Homo sapiens O95678 32296183
Intra
TSG101 Q99816 KRT75 Homo sapiens O95678 32296183
Intra
TSG101 Q99816 SNAPIN Homo sapiens O95295 32296183
Intra
TSG101 Q99816 SNAPIN Homo sapiens O95295 32296183
Intra
TSG101 Q99816 IQGAP1 Homo sapiens P46940
Y2H
17853893
Intra
TSG101 Q99816 KRT18 Homo sapiens P05783 32296183
Intra
TSG101 Q99816 KRT18 Homo sapiens P05783
Y2H
19549727
Intra
TSG101 Q99816 KRT18 Homo sapiens P05783 32296183
Intra
TSG101 Q99816 CD2AP Homo sapiens Q9Y5K6 17853893
Intra
TSG101 Q99816 PDCD6IP Homo sapiens Q8WUM4 37219487
Intra
TSG101 Q99816 PDCD6IP Homo sapiens Q8WUM4
SPR
17350572
Intra
TSG101 Q99816 KIAA1328 Homo sapiens Q86T90 32296183
Intra
TSG101 Q99816 KIAA1328 Homo sapiens Q86T90 32296183
Intra
TSG101 Q99816 CCDC88B Homo sapiens A6NC98 32296183
Intra
TSG101 Q99816 CCDC88B Homo sapiens A6NC98 32296183
Intra
TSG101 Q99816 PDLIM7 Homo sapiens Q9NR12 32296183
Intra
TSG101 Q99816 PDLIM7 Homo sapiens Q9NR12 32296183
Intra
TSG101 Q99816 PDLIM7 Homo sapiens Q9NR12 25416956
Intra
TSG101 Q99816 PDLIM7 Homo sapiens Q9NR12 32296183
Intra
TSG101 Q99816 KRT16 Homo sapiens P08779 32296183
Intra
TSG101 Q99816 KRT16 Homo sapiens P08779 32296183
Intra
TSG101 Q99816 TNIP1 Homo sapiens Q15025 32296183
Intra
TSG101 Q99816 TNIP1 Homo sapiens Q15025 32296183
Intra
TSG101 Q99816 HSH2D Homo sapiens Q96JZ2 32296183
Intra
TSG101 Q99816 HSH2D Homo sapiens Q96JZ2 32296183
Intra
TSG101 Q99816 VPS37B Homo sapiens Q9H9H4 35271311
Intra
TSG101 Q99816 VPS37B Homo sapiens Q9H9H4 32296183
Intra
TSG101 Q99816 VPS37B Homo sapiens Q9H9H4 32296183
Intra
TSG101 Q99816 VPS37B Homo sapiens Q9H9H4 32296183
Intra
TSG101 Q99816 TAX1BP1 Homo sapiens Q86VP1 25416956
Intra
TSG101 Q99816 TAX1BP1 Homo sapiens Q86VP1 25416956
Intra
TSG101 Q99816 TAX1BP1 Homo sapiens Q86VP1 25416956
Intra
TSG101 Q99816 TAX1BP1 Homo sapiens Q86VP1 32296183
Intra
TSG101 Q99816 TAX1BP1 Homo sapiens Q86VP1 32296183
Intra
TSG101 Q99816 INCA1 Homo sapiens Q0VD86 32296183
Intra
TSG101 Q99816 INCA1 Homo sapiens Q0VD86 32296183
Intra
TSG101 Q99816 SYCE1 Homo sapiens Q8N0S2 32296183
Intra
TSG101 Q99816 SYCE1 Homo sapiens Q8N0S2 32296183
Intra
TSG101 Q99816 GOLM1 Homo sapiens Q8NBJ4 32296183
Intra
TSG101 Q99816 GOLM1 Homo sapiens Q8NBJ4 32296183
Intra
TSG101 Q99816 TOM1L1 Homo sapiens O75674
Y2H
15611048
Intra
TSG101 Q99816 TOM1L1 Homo sapiens O75674 37219487
Intra
TSG101 Q99816 LRSAM1 Homo sapiens Q6UWE0 16189514
Intra
TSG101 Q99816 LRSAM1 Homo sapiens Q6UWE0 25416956
Intra
TSG101 Q99816 LRSAM1 Homo sapiens Q6UWE0 25416956
Intra
TSG101 Q99816 LRSAM1 Homo sapiens Q6UWE0 32296183
Intra
TSG101 Q99816 LRSAM1 Homo sapiens Q6UWE0 32296183
Intra
TSG101 Q99816 MZB1 Homo sapiens Q8WU39 32296183
Intra
TSG101 Q99816 MZB1 Homo sapiens Q8WU39 32296183
Intra
TSG101 Q99816 ITPRID2 Homo sapiens P28290 35044719
Intra
TSG101 Q99816 ITPRID2 Homo sapiens P28290 37219487
Intra
TSG101 Q99816 PTPN23 Homo sapiens Q9H3S7 17174262
Intra
TSG101 Q99816 PTPN23 Homo sapiens Q9H3S7
Y2H
17174262
Intra
TSG101 Q99816 LITAF Homo sapiens Q99732 16118794
Intra
TSG101 Q99816 VPS28 Homo sapiens Q9UK41 35271311
Intra
TSG101 Q99816 VPS28 Homo sapiens Q9UK41 16189514
Intra
TSG101 Q99816 VPS28 Homo sapiens Q9UK41 25416956
Intra
TSG101 Q99816 LNX1 Homo sapiens Q8TBB1 32296183
Intra
TSG101 Q99816 LNX1 Homo sapiens Q8TBB1 32296183
Intra
TSG101 Q99816 HGS Homo sapiens O14964
Y2H
12802020
Intra
TSG101 Q99816 HGS Homo sapiens O14964 16189514
Intra
TSG101 Q99816 HGS Homo sapiens O14964 35271311
Intra
TSG101 Q99816 CEP55 Homo sapiens Q53EZ4
SLC
27107012
Intra
TSG101 Q99816 CEP55 Homo sapiens Q53EZ4 32296183
Intra
TSG101 Q99816 CEP55 Homo sapiens Q53EZ4 17853893
Intra
TSG101 Q99816 CEP55 Homo sapiens Q53EZ4 27107012
Intra
TSG101 Q99816 CEP55 Homo sapiens Q53EZ4
Y2H
19549727
Intra
TSG101 Q99816 CEP55 Homo sapiens Q53EZ4 16189514
Intra
TSG101 Q99816 CEP55 Homo sapiens Q53EZ4
Y2H
27107012
Intra
TSG101 Q99816 CEP55 Homo sapiens Q53EZ4 17853893
Intra
TSG101 Q99816 CEP55 Homo sapiens Q53EZ4 25416956
Intra
TSG101 Q99816 CEP55 Homo sapiens Q53EZ4
IF
17853893
Intra
TSG101 Q99816 CEP55 Homo sapiens Q53EZ4 32296183
Intra
TSG101 Q99816 CEP55 Homo sapiens Q53EZ4
Y2H
17853893
Intra
TSG101 Q99816 CEP55 Homo sapiens Q53EZ4 25416956
Intra
TSG101 Q99816 DAXX Homo sapiens Q9UER7 15033475
Intra
TSG101 Q99816 CBY1 Homo sapiens Q9Y3M2 32296183
Intra
TSG101 Q99816 CBY1 Homo sapiens Q9Y3M2 32296183
Intra
TSG101 Q99816 CBY1 Homo sapiens Q9Y3M2 32296183
Intra
TSG101 Q99816 KRT31 Homo sapiens Q15323 32296183
Intra
TSG101 Q99816 KRT31 Homo sapiens Q15323 32296183
Intra
TSG101 Q99816 KRT31 Homo sapiens Q15323 25416956
Intra
TSG101 Q99816 AJUBA Homo sapiens Q96IF1 32296183
Intra
TSG101 Q99816 AJUBA Homo sapiens Q96IF1 37219487
Intra
TSG101 Q99816 AJUBA Homo sapiens Q96IF1 32296183
Cross
TSG101 Q99816 gag Human immunodeficiency virus P18095
FPS
37219487
Cross
TSG101 Q99816 gag Human immunodeficiency virus P18095
FPS
37100772
Cross: Cross-species interaction Intra: Intraspecies interaction

TSG101 Antibodies

Cat. No. Product Name Application Reactivity
HY-P80924 TSG101 Antibody (YA025) WB, IHC-F, IHC-P, ICC/IF Human, Mouse, Rat
HY-P80924A TSG101 Antibody (YA025)(PBS only) WB, IHC-F, IHC-P, ICC/IF Human, Mouse, Rat
HY-P84757 TSG101 Antibody (YA4454) IHC-P, FC, ELISA Human
HY-P84757A TSG101 Antibody (YA4454)(PBS only) IHC-P, FC, ELISA Human
HY-P86564 TSG101 Antibody (YA6256) WB, ICC/IF, IP, ELISA Human, Mouse, Rat

Related Diseases

Diseases Alias
Hepatitis E
Charcot-Marie-Tooth Disease, Axonal, Type 2p
  • CMT2P

  • Charcot-Marie-Tooth Disease Axonal Type 2p

  • Charcot-Marie-Tooth Disease Type 2p

  • Charcot-Marie-Tooth Neuropathy, Type 2p

  • Charcot-Marie-Tooth Disease, Axonal, Type 2g, Formerly

  • Cmt2g, Formerly

  • Charcot-Marie-Tooth Neuropathy Type 2p

  • Charcot-Marie-Toothe Disease, Axonal, Type 2p

  • Charcot-Marie-Tooth Disease 2p

  • Charcot-Marie-Tooth Disease, Axonal Type 2g

  • Charcot-Marie-Tooth Neuropathy Axonal Type 2p

  • Cmt2g

  • Charcot-Marie-Tooth Disease, Type 2p

  • Charcot-Marie-Tooth Disease, Axonal, Type 2g

Breast Cancer
  • Breast Carcinoma

  • Male Breast Cancer

  • Breast Cancer, Familial

  • Malignant Neoplasm Of Breast

  • Breast Cancer, Susceptibility To

  • Breast Cancer, Early-Onset

  • Malignant Tumor Of Breast

  • Carcinoma Of Male Breast

  • Breast Cancer, Invasive Ductal

  • Breast Cancer, Protection Against

  • Breast Cancer, Somatic

  • Breast Cancer, Male

  • Breast Cancer, Lobular, Somatic

  • Breast Tumor

  • Mammary Cancer

  • Mammary Tumor

  • Malignant Neoplasm Of Male Breast

  • Mammary Carcinoma

  • Male Breast Carcinoma

  • Familial Cancer Of Breast

  • Invasive Ductal Breast Carcinoma

  • Breast Cancer Susceptibility

  • Breast Cancer, Male, Susceptibility To

  • Breast Cancer, Early-Onset, Susceptibility To

  • Malignant Tumor Of The Breast

  • Mammary Neoplasm

  • Primary Breast Cancer

  • Neoplasm Of Male Breast

  • Carcinoma Of Breast

  • Breast Cancer In Men

  • Familial Breast Cancer

  • Cancer Of Breast

  • BC

  • Breast Cancer Familial

  • Breast Cancer Familial Male

  • Breast Cancer, Familial Male

  • Breast Male Carcinoma

  • Breast Neoplasms

  • Breast Neoplasms, Male

  • Mammary Tumors

  • Mammary Carcinomas

  • Cancer, Breast

  • Cancer, Breast, Susceptibility

  • Invasive Breast Ductal Carcinoma

  • Breast Neoplasm

  • Susceptibility To Breast Cancer

  • Mammary Neoplasms

  • Animal Mammary Neoplasms

  • Primary Malignant Neoplasm Of Breast

  • Infiltrating Ductal Carcinoma Of Breast

  • Infiltrating Duct Carcinoma Of Unspecified Site

  • Infiltrating Ductular Carcinoma Of Unspecified Site

  • Invasive Breast Carcinoma Of No Special Type

  • Microinvasive Carcinoma Of Breast

  • Carcinoma With Apocrine Differentiation

Charcot-Marie-Tooth Disease
  • Cmt

  • Hmsn

  • Hereditary Motor And Sensory Neuropathy

  • Pma

  • Cmt - Charcot-Marie-Tooth Disease

  • Charcot Marie Tooth Disease

  • Charcot-Marie-Tooth Hereditary Neuropathy

  • Charcot-Marie-Tooth Syndrome

  • Peroneal Muscular Atrophy

  • Hereditary Motor And Sensory Neuropathies

Charcot-Marie-Tooth Disease, Demyelinating, Type 1c
  • Charcot-Marie-Tooth Disease Type 1c

  • CMT1C

  • Hmsn1c

  • Hmsn Ic

  • Charcot-Marie-Tooth Disease, Type 1c

  • Charcot-Marie-Tooth Neuropathy Type 1c

  • Cmt, Slow Nerve Conduction Type C

  • Charcot-Marie-Tooth Neuropathy, Type 1c

  • Neuropathy, Hereditary Motor And Sensory, Type Ic

  • Cmt Slow Nerve Conduction Type C

  • Neuropathy Hereditary Motor And Sensory Type 1c

  • Charcot-Marie-Tooth Disease 1c

  • Charcot-Marie-Tooth Disease Demyelinating Type 1c

  • Hereditary Motor And Sensory Neuropathy Ic

  • Charcot-Marie-Tooth Disease, Type Ic

Immune Deficiency Disease
  • Immunodeficiency

  • Primary Immunodeficiency

  • Primary Immunodeficiency Disease

  • Immunologic Deficiency Syndromes

  • Hypoimmunity

  • Immune Deficiency Disorder

  • Immunodeficiency Syndrome

  • Immune Disorder

  • Primary Immune Deficiency Disorder

  • Immune System Diseases

  • Human Immunodeficiency Virus Infection

  • Hiv - [Human Immunodeficiency Virus Infection]

  • Hiv Positive Nos

  • Hiv Disease

  • Acquired Immune Deficiency Syndrome-Related Complex

  • Aids-Like Syndrome

  • Aids-Related Complex Nos

  • Arc - [Aids-Related Complex]

  • Immunodeficiency Due To Human Immunodeficiency Virus Infection

  • Unspecified Human Immunodeficiency Virus Disease

  • Hiv Disease Nos

  • Human Immunodeficiency Virus Positive Nos

  • Hiv Nos

  • Deficiency Of Complement Initial Pathway

  • Deficiency Of Complement Terminal Pathway

  • Cfdd - [Complement Factor D Deficiency]

  • Immunodeficiency With Nk-Cell - [Natural-Killer Cell] Deficiency

  • Nonfamilial Hypogammaglobulinaemia

  • Common Variable Immune Deficiency

  • Nonfamilial Agammaglobulinaemia

  • Common Variable Agammaglobulinaemia

  • Agammaglobulinaemia Nos

  • Agammaglobulinaemia Antibody Deficiency Syndrome

  • Hypogammaglobulinaemia Antibody Deficiency Syndrome

  • Acquired Agammaglobulinaemia Nos

  • Hypogammaglobulinaemia Nos

  • Hyper Igm

Human Immunodeficiency Virus Type 1
  • Aids

  • Hiv/Aids

  • Aids, Delayed/Rapid Progression To

  • Hiv-1, Susceptibility To

  • Hiv-1 Viremia, Susceptibility To

  • Human Immunodeficiency Virus Type 1, Susceptibility To

  • Hiv-1

  • Aids, Slow Progression To

  • Rapid Progression To Aids From Hiv1 Infection

  • Hiv1 Infection, Resistance To

  • Hiv1 Infection

  • Hiv-1 Viremia

  • Aids, Resistance To

  • Aids, Rapid Progression To

  • Hiv/Aids, Susceptibility To

  • Hiv-1, Resistance To

  • Hiv1, Resistance To

  • Hiv1

  • Hiv-1 Disease, Delayed Progression Of

  • Hiv-1 Disease, Rapid Progression Of

  • Hiv Infection, Resistance To

  • Hiv Type 1, Susceptibility To

  • Hiv Type 1

  • Hiv-1 Infection

  • Human Immunodeficiency Virus I Infection

  • Acquired Immunodeficiency Syndrome

  • Hiv-Infection/Aids

Prostate Cancer
  • Prostate Carcinoma

  • Prostate Cancer, Familial

  • Prostate Neoplasm

  • Prostate Cancer, Somatic

  • Prostate Cancer, Susceptibility To

  • Prostatic Cancer

  • Prostatic Neoplasms

  • Hereditary Prostate Cancer

  • Prostatic Neoplasm

  • Cancer Of Prostate

  • Carcinoma Of Prostate

  • Familial Prostate Cancer

  • Familial Prostate Carcinoma

  • Malignant Tumor Of Prostate

  • Malignant Neoplasm Of Prostate

  • Prostate Cancer, Familial, Susceptibility To

  • Malignant Tumor Of The Prostate

  • Ngp - New Growth Of Prostate

  • Tumor Of The Prostate

  • Prostate Cancer, Hereditary

  • Cancer Of The Prostate

  • Malignant Neoplasm Of The Prostate

  • Prostatic Carcinoma

  • PC

  • Prca

  • Cancer, Prostate

  • Malignant Prostatic Tumour

  • Malignant Tumour Of Prostate

  • Primary Prostate Cancer

  • Primary Malignant Neoplasm Of Prostate

  • Prostate Gland Cancer

Ovarian Cancer
  • Ovarian Carcinoma

  • Ovarian Neoplasm

  • Malignant Tumour Of Ovary

  • Cancer Of The Ovary

  • Epithelial Ovarian Cancer

  • Neoplasm Of Ovary

  • Ovarian Neoplasms

  • Ovarian Cancers

  • Malignant Neoplasm Of Ovary

  • Primary Malignant Neoplasm Of Ovary

  • Ovarian Cancer, Somatic

  • Malignant Ovarian Tumor

  • Ovary Neoplasm

  • Primary Ovarian Cancer

  • Tumor Of The Ovary

  • Malignant Neoplasm Of The Ovary

  • Malignant Tumor Of The Ovary

  • Ovarian Malignant Tumor

  • OC

  • Ovarian Carcinomas

  • Cancer, Ovarian

  • Cancer Of Ovary

  • Ovary Cancer

  • Ca Ovary

T-Cell Acute Lymphoblastic Leukemia
  • T-Cell Leukemia

  • Acute T Cell Leukemia

  • Precursor T Lymphoblastic Leukemia

  • Precursor T-Lymphoblastic Lymphoma/Leukemia

  • T Acute Lymphoblastic Leukemia

  • T-Cell Acute Lymphocytic Leukaemia

  • T-Cell Lymphoblastic Leukemia/Lymphoma

  • Leukemia T-Cell

  • Leukemia, T-Cell

  • Leukemia, Acute, Lymphoblastic, T-Cell

  • Leukemia, T-Cell Acute Lymphoblastic

  • Leukemia, Acute T-Cell

  • Precursor T-Cell Lymphoblastic Leukemia-Lymphoma

  • Precursor T-Cell Lymphoblastic Lymphoma

  • Precursor T Cell Lymphoblastic Leukemia/Lymphoblastic Lymphoma

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
Canis familiaris TSG101 VGNC VGNC:47898
Macaca mulatta TSG101 VGNC VGNC:78998
Felis catus TSG101 VGNC VGNC:66613
Bos taurus TSG101 VGNC VGNC:36414
Mus musculus TSG101 MGD MGI:106581
Rattus norvegicus TSG101 RGD RGD:3909
Others TSG101 NCBI