PTPN1 - protein tyrosine phosphatase non-receptor type 1 Gene

Also Known as PTP1B

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 5770

About PTPN1

Cytogenetic location: 20q13.13 Genomic coordinates (GRCh38): 20:50,510,383-50,585,241 (from NCBI)

This gene has 2 transcripts (splice variants), 209 orthologues, 35 paralogues and is associated with 1 phenotype. Ubiquitous expression in lymph node (RPKM 30.4), appendix (RPKM 29.5) and 25 other tissues.

Summary

The protein encoded by this gene is the founding member of the protein tyrosine Phosphatase (PTP) family, which was isolated and identified based on its enzymatic activity and amino acid sequence. PTPs catalyze the hydrolysis of the phosphate monoesters specifically on tyrosine residues. Members of the PTP family share a highly conserved catalytic motif, which is essential for the catalytic activity. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP has been shown to act as a negative regulator of Insulin signaling by dephosphorylating the phosphotryosine residues of Insulin Receptor kinase. This PTP was also reported to dephosphorylate epidermal growth factor receptor kinase, as well as JAK2 and Tyk2 kinases, which implicated the role of this PTP in cell growth control, and cell response to interferon stimulation. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2013]

PTPN1 Products (2)

mRNA Protein Name
NM_001278618.2 NP_001265547.1 tyrosine-protein phosphatase non-receptor type 1 isoform 2
NM_002827.4 NP_002818.1 tyrosine-protein phosphatase non-receptor type 1 isoform 1
Molecular Function GO Annotation Evidence References Source
enables enzyme binding IPI
IPI: Inferred from physical interaction
22169477 GOA
enables ephrin receptor binding IPI
IPI: Inferred from physical interaction
21135139 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
8702689 GOA
enables protein kinase binding IPI
IPI: Inferred from physical interaction
22169477 GOA
enables protein tyrosine phosphatase activity IDA
IDA: Inferred from direct assay
18074158 GOA
enables receptor tyrosine kinase binding IPI
IPI: Inferred from physical interaction
18819921 GOA
enables zinc ion binding IDA
IDA: Inferred from direct assay
18074158 GOA
Biological Process GO Annotation Evidence References Source
involved in actin cytoskeleton organization IMP
IMP: Inferred from mutant phenotype
21135139 GOA
involved in endoplasmic reticulum unfolded protein response IDA
IDA: Inferred from direct assay
22169477 GOA
involved in negative regulation of MAP kinase activity IMP
IMP: Inferred from mutant phenotype
22045810 GOA
involved in negative regulation of PERK-mediated unfolded protein response IDA
IDA: Inferred from direct assay
21216966 GOA
involved in peptidyl-tyrosine dephosphorylation IDA
IDA: Inferred from direct assay
21135139 GOA
involved in peptidyl-tyrosine dephosphorylation IMP
IMP: Inferred from mutant phenotype
14966296 GOA
involved in platelet-derived growth factor receptor-beta signaling pathway IMP
IMP: Inferred from mutant phenotype
14966296 GOA
involved in positive regulation of protein tyrosine kinase activity IDA
IDA: Inferred from direct assay
21216966 GOA
involved in positive regulation of receptor catabolic process IMP
IMP: Inferred from mutant phenotype
22045810 GOA
involved in protein dephosphorylation IMP
IMP: Inferred from mutant phenotype
22045810 GOA
involved in regulation of endocytosis IDA
IDA: Inferred from direct assay
21135139 GOA
involved in regulation of hepatocyte growth factor receptor signaling pathway IMP
IMP: Inferred from mutant phenotype
18819921 GOA
involved in regulation of intracellular protein transport IMP
IMP: Inferred from mutant phenotype
22045810 GOA
involved in regulation of signal transduction IMP
IMP: Inferred from mutant phenotype
21135139 GOA
Cellular Component GO Annotation Evidence References Source
located in cytoplasmic side of endoplasmic reticulum membrane IDA
IDA: Inferred from direct assay
1739967 GOA
located in early endosome IDA
IDA: Inferred from direct assay
21135139 GOA
colocalizes with plasma membrane IDA
IDA: Inferred from direct assay
21135139 GOA
part of protein-containing complex IDA
IDA: Inferred from direct assay
28246125 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

PTPN1 Protein Structure

Y_phosphatase

Y_phosphatase: Protein-tyrosine phosphatase (40 - 276)

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

tyrosine-protein phosphatase non-receptor type 1

  • protein tyrosine phosphatase, placental

PTPN1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
PTPN1 P18031 NTRK1 Homo sapiens P04629 12237455
Intra
PTPN1 P18031 TMEM41A Homo sapiens Q96HV5 32296183
Intra
PTPN1 P18031 TMEM41A Homo sapiens Q96HV5 32296183
Intra
PTPN1 P18031 TMEM41A Homo sapiens Q96HV5 32296183
Intra
PTPN1 P18031 LAT Homo sapiens O43561 12857726
Intra
PTPN1 P18031 AQP6 Homo sapiens Q13520 32296183
Intra
PTPN1 P18031 AQP6 Homo sapiens Q13520 32296183
Intra
PTPN1 P18031 AQP6 Homo sapiens Q13520 32296183
Intra
PTPN1 P18031 CAPN1 Homo sapiens P07384 9407132
Cross
PTPN1 P18031 Pdgfrb Mus musculus P05622 12614164
Cross
PTPN1 P18031 Pdgfrb Mus musculus P05622 18515860
Intra
PTPN1 P18031 INSR Homo sapiens P06213-1 16271887
Intra
PTPN1 P18031 PIGP Homo sapiens P57054 32296183
Intra
PTPN1 P18031 PIGP Homo sapiens P57054 32296183
Intra
PTPN1 P18031 PIGP Homo sapiens P57054 32296183
Intra
PTPN1 P18031 ELOVL4 Homo sapiens Q9GZR5 32296183
Intra
PTPN1 P18031 ELOVL4 Homo sapiens Q9GZR5 32296183
Intra
PTPN1 P18031 ELOVL4 Homo sapiens Q9GZR5 32296183
Intra
PTPN1 P18031 TMEM86B Homo sapiens Q8N661 32296183
Intra
PTPN1 P18031 TMEM86B Homo sapiens Q8N661 32296183
Intra
PTPN1 P18031 TMEM86B Homo sapiens Q8N661 32296183
Intra
PTPN1 P18031 GHR Homo sapiens P10912 12907755
Intra
PTPN1 P18031 GHR Homo sapiens P10912 12907755
Intra
PTPN1 P18031 EGFR Homo sapiens P00533 24658140
Intra
PTPN1 P18031 EGFR Homo sapiens P00533
IF
9050838
Intra
PTPN1 P18031 EGFR Homo sapiens P00533 9050838
Intra
PTPN1 P18031 EGFR Homo sapiens P00533 24658140
Intra
PTPN1 P18031 CTTN Homo sapiens Q14247 18387954
Intra
PTPN1 P18031 NTRK3 Homo sapiens Q16288 12237455
Cross
PTPN1 P18031 Cdh2 Mus musculus P15116 11106648
Intra
PTPN1 P18031 GRB2 Homo sapiens P62993 10660596
Intra
PTPN1 P18031 INSR Homo sapiens P06213 11579209
Intra
PTPN1 P18031 INSR Homo sapiens P06213 11506178
Intra
PTPN1 P18031 INSR Homo sapiens P06213 12237455
Intra
PTPN1 P18031 INSR Homo sapiens P06213 11579209
Intra
PTPN1 P18031 INSR Homo sapiens P06213 12237455
Intra
PTPN1 P18031 IGF1R Homo sapiens P08069 16926280
Intra
PTPN1 P18031 IGF1R Homo sapiens P08069 8999839
Intra
PTPN1 P18031 JAK2 Homo sapiens O60674 11694501
Intra
PTPN1 P18031 JAK2 Homo sapiens O60674 15821101
Intra
PTPN1 P18031 JAK2 Homo sapiens O60674 11970898
Intra
PTPN1 P18031 JAK2 Homo sapiens O60674 11970898
Intra
PTPN1 P18031 STAT3 Homo sapiens P40763 11970898
Intra
PTPN1 P18031 TXN Homo sapiens P10599 24976139
Intra
PTPN1 P18031 CAV1 Homo sapiens Q03135 16388599
Intra
PTPN1 P18031 CAV1 Homo sapiens Q03135 16388599
Intra
PTPN1 P18031 EPOR Homo sapiens P19235 14527337
Intra
PTPN1 P18031 SRC Homo sapiens P12931 16115959
Intra
PTPN1 P18031 SRC Homo sapiens P12931 15866871
Intra
PTPN1 P18031 SRC Homo sapiens P12931 9600099
Intra
PTPN1 P18031 SRC Homo sapiens P12931 17092689
Intra
PTPN1 P18031 SRC Homo sapiens P12931 16115959
Intra
PTPN1 P18031 TIMMDC1 Homo sapiens Q9NPL8 32296183
Intra
PTPN1 P18031 TIMMDC1 Homo sapiens Q9NPL8 32296183
Intra
PTPN1 P18031 TIMMDC1 Homo sapiens Q9NPL8 32296183
Intra
PTPN1 P18031 BCAR1 Homo sapiens P56945 15866871
Intra
PTPN1 P18031 ITGB3 Homo sapiens P05106 16115959
Intra
PTPN1 P18031 TRPV6 Homo sapiens Q9H1D0 15894168
Intra
PTPN1 P18031 TRPV6 Homo sapiens Q9H1D0 17197020
Intra
PTPN1 P18031 TRPV6 Homo sapiens Q9H1D0 15894168
Intra
PTPN1 P18031 STAT5A Homo sapiens P42229 12237455
Intra
PTPN1 P18031 STAT5A Homo sapiens P42229 12237455
Cross
PTPN1 P18031 Bcar1 Mus musculus Q61140 12023880
Cross
PTPN1 P18031 Bcar1 Mus musculus Q61140 16644720
Cross
PTPN1 P18031 Sumo1 Mus musculus P63166 17159996
Intra
PTPN1 P18031 BCR Homo sapiens P11274-1 9566916
Intra
PTPN1 P18031 BCR Homo sapiens P11274-1 9566916
Cross
PTPN1 P18031 Bcar1 Rattus norvegicus Q63767 8940134
Cross
PTPN1 P18031 Bcar1 Rattus norvegicus Q63767 8940134
Cross
PTPN1 P18031 Bcar1 Rattus norvegicus Q63767 8940134
Cross
PTPN1 P18031 Grb2 Rattus norvegicus P62994 8940134
Cross
PTPN1 P18031 Irs1 Rattus norvegicus P35570 10660596
Cross
PTPN1 P18031 Irs1 Rattus norvegicus P35570 10660596
Cross
PTPN1 P18031 Plcg1 Rattus norvegicus P10686 17128263
Cross
PTPN1 P18031 Src Rattus norvegicus Q9WUD9 31585087
Cross
PTPN1 P18031 Crk Rattus norvegicus Q63768 8940134
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant PTPN1 Proteins

Cat. No. Product Name Accession Purity
HY-P73685 PTP1B Protein, Human (His) P18031 (E2-N321) ≥ 95%, as determined by reducing SDS-PAGE.

PTPN1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P81300 Phospho-PTP1B (Ser352) Antibody (YA1027) WB, ICC/IF, IP Human
HY-P81300A Phospho-PTP1B (Ser378) Antibody (YA1028) WB, IHC-P Human
HY-P81300AA Phospho-PTP1B (Ser378) Antibody (YA1028)(PBS only) WB, IHC-P Human
HY-P82031 PTP1B Antibody (YA1776) WB, IHC-F, IHC-P, ICC/IF Human
HY-P82031A PTP1B Antibody (YA1776)(PBS only) WB, IHC-F, IHC-P, ICC/IF Human
HY-P84143 PTP1B Antibody (YA3840) WB, IHC-P, ICC/IF, FC, ELISA Human
HY-P84143A PTP1B Antibody (YA3840)(PBS only) WB, IHC-P, ICC/IF, FC, ELISA Human

Related Diseases

Diseases Alias
Type 2 Diabetes Mellitus
  • Insulin Resistance

  • NIDDM

  • Type 2 Diabetes

  • Diabetes Mellitus, Non-Insulin-Dependent

  • T2D

  • Noninsulin-Dependent Diabetes Mellitus

  • Diabetes Mellitus, Type Ii

  • Maturity-Onset Diabetes

  • Insulin Resistance, Severe, Digenic

  • Diabetes Mellitus, Type 2

  • Diabetes Mellitus, Noninsulin-Dependent

  • Diabetes Mellitus, Noninsulin-Dependent, Association With

  • Diabetes Mellitus, Noninsulin-Dependent, Late Onset

  • Hypertension, Insulin Resistance-Related, Susceptibility To

  • Insulin Resistance, Susceptibility To

  • Non-Insulin-Dependent Diabetes Mellitus

  • Type Ii Diabetes Mellitus

  • Adult-Onset Diabetes Mellitus

  • Maturity-Onset Diabetes Mellitus

  • Diabetes Mellitus Type 2

  • Type Ii Diabetes

  • Type 2 Diabetes Mellitus, Susceptibility To

  • Diabetes, Type 2

  • Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To

  • Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To

  • Diabetes Mellitus, Type 2, Susceptibility To

  • Diabetes Mellitus, Noninsulin-Dependent, 2

  • Diabetes Mellitus, Type Ii, Susceptibility To

  • Hypertension, Insulin Resistance-Related

  • Adult-Onset Diabetes

  • Aodm

  • Diabetes Mellitus, Adult-Onset

  • Diabetes Mellitus Type Ii

  • Diabetes Mellitus Type 2, Susceptibility To

  • Diabetes, Type Ii, Susceptibility To

  • Diabetes Type 2

  • Diabetes Mellitus

  • Adult Onset Diabetes

  • Maturity Onset Diabetes

  • Nonketotic Diabetes

  • Non-Insulin Dependent Diabetes Mellitus

  • T2dm - [Type 2 Diabetes Mellitus]

  • Niddm - [Non Insulin Dependent Diabetes Mellitus]

  • Dm2

  • Dm Type Ii

  • Diabetic Type 2

  • Insulin Requiring Type 2 Diabetes

  • Noninsulin Dependent Diabetes

  • Non-Insulin-Dependent Diabetes Mellitus Without Complications

  • Diabetes Due To Insulin Secretory Defect

  • Diabetes Mellitus Due To Insulin Secretory Defect

  • Non-Insulin-Dependent Diabetes Of The Young

  • Senile Diabetes

  • Nonketotic Hyperglycaemia

  • Stable Diabetes

Bubonic Plague
  • Black Death

  • Plague, Bubonic

  • Plague, Septicemic

  • Pestis Bubonica

Leptin Deficiency Or Dysfunction
  • Morbid Obesity

  • Obesity Due To Congenital Leptin Deficiency

  • LEPD

  • Congenital Leptin Deficiency

  • Obesity, Morbid

  • Obesity, Morbid, Due To Leptin Deficiency

  • Severe Obesity

  • Obesity, Morbid, Nonsyndromic 1

  • Leptin Deficiency

  • Obesity, Severe, Due To Leptin Deficiency

  • Leptin

  • Morbid Obesity Due To Leptin Deficiency

  • Obesity Morbid

  • Leptin Dysfunction

Body Mass Index Quantitative Trait Locus 11
  • OBESITY

  • Obesity, Susceptibility To

  • Leanness, Inherited

  • Obesity, Susceptibility To, Bmiq11

  • Obesity, Mild, Early-Onset

  • Obesity, Association With

  • Obesity, Early-Onset, Susceptibility To

  • Obesity, Severe

  • Obesity, Severe, And Type Ii Diabetes

  • Obesity, Late-Onset

  • Obesity , Susceptibility To

  • BMIQ11

  • Obesity Bmiq11

  • Obesity, Early-Onset

  • Simple Obesity Nos

  • Excess Fat

  • Obesity, Not Elsewhere Classified, Body Mass Index Not Elsewhere Classified

  • Adiposis

Diabetes Mellitus
  • Diabetes

Hepatic Adenomas, Familial
  • Hepatic Adenoma, Somatic

  • Familial Hepatic Adenoma

  • Familial Liver Cell Adenomas

  • Liver Cell Adenomas, Familial

  • Hepatic Adenomas Familial

  • HEPAF

  • Ha

  • Hepatocellular Adenomas

  • Hepatocellular Adenoma

Lipid Metabolism Disorder
  • Dyslipidemia

  • Disorder Of Fatty Acid Metabolism

  • Lipid Metabolism Disorders

  • Fatty Acid Metabolism Disorder

  • Disorder Of Lipid Metabolism

  • Abnormality Of Lipid Metabolism

  • Lipid Metabolism, Inborn Errors

  • Dyslipidemias

  • Disorders Of Lipid Metabolism

  • Congenital Disorders Of Lipid Metabolism

  • Inherited Disorders Of Lipid Metabolism

Rett Syndrome
  • Atypical Rett Syndrome

  • RTT

  • Rett Disorder

  • Rts

  • Autism, Dementia, Ataxia, And Loss Of Purposeful Hand Use

  • Rett Syndrome, Preserved Speech Variant

  • Rett Syndrome, Atypical

  • Rett'S Disorder

  • Rett Syndrome Variant

  • Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use Syndrome

  • Cerebroatrophic Hyperammonemia

  • Rett Like Syndrome

  • Rett'S Syndrome

  • Atypical Rtt

  • Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use

  • Rett Syndrome Preserved Speech Variant

  • Rett Syndrome Zappella Variant

  • Rett Syndrome, Zappella Variant

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

Noonan Syndrome With Multiple Lentigines
  • Leopard Syndrome

  • Multiple Lentigines Syndrome

  • Moynahan Syndrome

  • Cardiomyopathic Lentiginosis

  • Progressive Cardiomyopathic Lentiginosis

  • Cardio-Cutaneous Syndrome

  • Lentiginosis Profusa

  • Capute-Rimoin-Konigsmark-Esterly-Richardson Syndrome

  • Generalized Lentiginosis

  • Gorlin Syndrome Ii

  • Lentiginosis Profusa Syndrome

  • Lentigines, Electrocardiographic Conduction Abnormalities, Ocular Hypertelorism, Pulmonic Stenosis, Abnormal Genitalia, Retardation Of Growth, Deafnes

  • Diffuse Lentiginosis

  • Nsml

  • Familial Multiple Lentigines Syndrome

  • Alopecia-Epilepsy-Intellectual Disability Syndrome, Moynahan Type

  • Progressive Cardiomyopathic Lentiginosis Syndrome

  • Alopecia Epilepsy Oligophrenia Syndrome Of Moynahan

Rasopathy
  • Ras/Mitogen-Activated Protein Kinase Syndrome

Hypertension, Essential
  • Essential Hypertension

  • Hypertension

  • High Blood Pressure

  • Hypertension, Essential, Susceptibility To

  • Hypertensive Disease

  • Primary Hypertension

  • EHT

  • Hypertension, Salt-Sensitive Essential, Susceptibility To

  • Hyperpiesia

  • Idiopathic Hypertension

  • Hypertensive Disorder

  • Hypertension, Essential, Susceptibility To, 3

  • Hypertension, Essential 3

  • Hypertension, Essential, Salt-Sensitive

  • Hypertension, Essential, Susceptibility To, 6

  • Hypertension, Essential 6

  • Hypertension, Salt-Sensitive Essential

  • Hypertension, Susceptibility To

  • Hypertension, Essential, Susceptibility To, 4

  • Hypertension, Essential 4

  • Hypertension, Essential, Susceptibility To, 2

  • Hypertension, Essential 2

  • Hypertension, Essential, Susceptibility To, 1

  • Hypertension, Essential 1

  • Hypertension, Essential, Susceptibility To, 5

  • Hypertension, Essential 5

  • Htn

  • Vascular Hypertensive Disorder

  • Systemic Primary Arterial Hypertension

  • Hbp - [High Blood Pressure]

  • Systemic Arterial Hypertensive Disorder

  • Elevated Blood Pressure

  • Arterial Hypertension Nos

  • Hypertension Nos

  • Benign Hypertension

  • Systemic Arterial Hypertension

  • Systemic Hypertension

  • Artery Htn

  • Benign Htn

  • Vascular Htn

  • Vascular Hypertension

  • Cholesterol Hypertension

  • Cholesterol Htn

  • Idiopathic Htn

  • Malignant Hypertension

  • Malignant Htn

  • Raised Blood Pressure

  • Cardiovascular Hypertension

  • Primary Htn - [Hypertension]

  • High Arterial Tension

  • High Blood Pressure Disorder

  • Ht - [Hypertension]

  • Htn - [Hypertension]

  • Hypertensive Vascular Disease

  • Hypertensive Vascular Degeneration

Juvenile Myelomonocytic Leukemia
  • Leukemia, Juvenile Myelomonocytic

  • JMML

  • Leukemia, Juvenile Myelomonocytic, Somatic

  • Juvenile Chronic Myelomonocytic Leukemia

  • Juvenile Chronic Myelogenous Leukemia

  • Leukemia, Myelomonocytic, Juvenile

  • Juvenile Myelomonocytic Leukaemia Without Mention Of Remission

Leukemia, Chronic Myeloid
  • Chronic Myeloid Leukemia

  • Chronic Myelogenous Leukemia

  • CML

  • Chronic Granulocytic Leukemia

  • Leukemia, Philadelphia Chromosome-Positive, Resistant To Imatinib

  • Chronic Myeloid Leukaemia

  • Chronic Granulocytic Leukaemia

  • Chronic Myelogenous Leukaemia

  • Myeloid Leukemia, Chronic

  • Leukemia, Chronic Myelogenous

  • Leukemia, Chronic Myeloid, Philadelphia Chromosome Positive, Somatic

  • Cml - Chronic Myelogenous Leukemia

  • Cgl

  • Chronic Myelocytic Leukemia

  • Leukemia, Chronic Myeloid, Atypical

  • ACML

  • Atypical Chronic Myeloid Leukemia Bcr-Abl1 Negative

  • Myeloid Leukemia Chronic

  • Leukemia, Myeloid, Chronic

  • Leukemia, Myeloid, Chronic, Atypical, Bcr-Abl Negative

  • Cml- [Chronic Myeloid Leukaemia]

  • Cgl - [Chronic Granulocytic Leukaemia]

  • Chronic Myelocytic Leukaemia

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

Noonan Syndrome 1
  • Noonan Syndrome

  • NS1

  • Male Turner Syndrome

  • Female Pseudo-Turner Syndrome

  • Turner Phenotype With Normal Karyotype

  • Noonan Syndrome With Pigmented Villonodular Synovitis

  • Turner'S Phenotype, Karyotype Normal

  • Familial Turner Syndrome

  • Noonan'S Syndrome

  • Noonan-Ehmke Syndrome

  • Ns

  • Pseudo-Ullrich-Turner Syndrome

  • Turner Syndrome In Female With X Chromosome

  • Turner-Like Syndrome

  • Ullrich-Noonan Syndrome

  • Noonan-Like/Multiple Giant Cell Lesion Syndrome

  • Noonan Syndrome-Like Disorder With Multiple Giant Cell Lesions

  • Pterygium Colli Syndrome

  • Noonan Syndrome, Type 1

  • Turner Syndrome, Male

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 PTPN1 VGNC VGNC:45167
Macaca mulatta PTPN1 VGNC VGNC:76597
Rattus norvegicus PTPN1 RGD RGD:61965
Bos taurus PTPN1 VGNC VGNC:33529
Felis catus PTPN1 VGNC VGNC:69157
Mus musculus PTPN1 MGD MGI:97805
Others PTPN1 NCBI