PTPRD - protein tyrosine phosphatase receptor type D Gene

Also Known as HPTP; PTPD; HPTPD; HPTPDELTA; RPTPDELTA; R-PTP-delta

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 5789

About PTPRD

Cytogenetic location: 9p24.1-p23 Genomic coordinates (GRCh38): 9:8,314,246-10,613,002 (from NCBI)

This gene has 16 transcripts (splice variants), 1 gene allele, 274 orthologues, 35 paralogues and is associated with 129 phenotypes. Broad expression in brain (RPKM 18.0), kidney (RPKM 8.8) and 14 other tissues.

Summary

The protein encoded by this gene is a member of the protein tyrosine Phosphatase (PTP) family. 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 contains an extracellular region, a single transmembrane segment and two tandem intracytoplasmic catalytic domains, and thus represents a receptor-type PTP. The extracellular region of this protein is composed of three Ig-like and eight fibronectin type III-like domains. Studies of the similar genes in chicken and fly suggest the role of this PTP is in promoting neurite growth, and regulating neurons axon guidance. Multiple alternatively spliced transcript variants of this gene have been reported. A related pseudogene has been identified on chromosome 5. [provided by RefSeq, Jan 2010]

PTPRD Products (10)

mRNA Protein Name
NM_001040712.2 NP_001035802.1 receptor-type tyrosine-protein phosphatase delta isoform 5 precursor
NM_001171025.2 NP_001164496.1 receptor-type tyrosine-protein phosphatase delta isoform 6 precursor
NM_001377946.1 NP_001364875.1 receptor-type tyrosine-protein phosphatase delta isoform 7 precursor
NM_001377947.1 NP_001364876.1 receptor-type tyrosine-protein phosphatase delta isoform 8 precursor
NM_001377958.1 NP_001364887.1 receptor-type tyrosine-protein phosphatase delta isoform 9 precursor
NM_001378058.1 NP_001364987.1 receptor-type tyrosine-protein phosphatase delta isoform 10 precursor
NM_002839.4 NP_002830.1 receptor-type tyrosine-protein phosphatase delta isoform 1 precursor
NM_130391.4 NP_569075.2 receptor-type tyrosine-protein phosphatase delta isoform 2 precursor
NM_130392.3 NP_569076.2 receptor-type tyrosine-protein phosphatase delta isoform 3 precursor
NM_130393.3 NP_569077.2 receptor-type tyrosine-protein phosphatase delta isoform 4 precursor
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
12570871 GOA
Biological Process GO Annotation Evidence References Source
involved in presynapse assembly IDA
IDA: Inferred from direct assay
21926414 GOA
involved in presynapse assembly IMP
IMP: Inferred from mutant phenotype
21926414 GOA
involved in synaptic membrane adhesion IDA
IDA: Inferred from direct assay
23345436 GOA
involved in synaptic membrane adhesion IMP
IMP: Inferred from mutant phenotype
23345436 GOA
involved in trans-synaptic signaling by trans-synaptic complex IDA
IDA: Inferred from direct assay
21926414 GOA
involved in trans-synaptic signaling by trans-synaptic complex IMP
IMP: Inferred from mutant phenotype
21926414 GOA
Cellular Component GO Annotation Evidence References Source
is active in glutamatergic synapse IDA
IDA: Inferred from direct assay
21926414 GOA
is active in glutamatergic synapse IMP
IMP: Inferred from mutant phenotype
21926414 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

PTPRD Protein Structure

I-set

I-set: Immunoglobulin I-set domain (24 - 115)

I-set

I-set: Immunoglobulin I-set domain (127 - 216)

I-set

I-set: Immunoglobulin I-set domain (236 - 319)

fn3

fn3: Fibronectin type III domain (325 - 405)

fn3

fn3: Fibronectin type III domain (419 - 504)

fn3

fn3: Fibronectin type III domain (518 - 595)

fn3

fn3: Fibronectin type III domain (612 - 699)

fn3

fn3: Fibronectin type III domain (714 - 812)

fn3

fn3: Fibronectin type III domain (830 - 906)

fn3

fn3: Fibronectin type III domain (922 - 1006)

Y_phosphatase

Y_phosphatase: Protein-tyrosine phosphatase (1380 - 1611)

Y_phosphatase

Y_phosphatase: Protein-tyrosine phosphatase (1669 - 1902)

  • 0
  • 300
  • 600
  • 900
  • 1200
  • 1500
  • 1800
  • 1912 a.a.
Protein Preferred Names Protein Names

receptor-type tyrosine-protein phosphatase delta

  • protein tyrosine phosphatase, receptor type, delta polypeptide

PTPRD Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
PTPRD P23468 AURKA Homo sapiens O14965 22305495
Intra
PTPRD P23468 AURKA Homo sapiens O14965 22305495
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant PTPRD Proteins

Cat. No. Product Name Accession Purity
HY-P78721 PTPRD Protein, Human (HEK293, His) P23468-1 (E21-E1265) ≥ 90%, as determined by reducing SDS-PAGE.

PTPRD Antibodies

Cat. No. Product Name Application Reactivity
HY-P84196 PTPRD Antibody (YA3893) FC, ELISA Human
HY-P84196A PTPRD Antibody (YA3893)(PBS only) FC, ELISA Human

Related Diseases

Diseases Alias
Restless Legs Syndrome
  • Wed

  • Willis-Ekbom Disease

  • Restless Leg Syndrome

  • Ekbom Syndrome

  • Wittmaack-Ekbom Syndrome

  • Willis Ekbom Disease

  • Ekbom'S Syndrome

  • Rls

  • Restless Legs

  • Restless Legs Syndrome, Susceptibility To

Chromosome 9p Deletion Syndrome
  • Monosomy 9p

  • Monosomy 9p Syndrome

  • Alfi Syndrome

  • 9p Syndrome

  • Chromosome 9p Deletion

  • 9p Deletion

  • 9p Monosomy

  • Deletion 9p

  • Partial Monosomy 9p

  • 9p Deletion Syndrome

  • 9p- Syndrome

  • Alfi'S Syndrome

  • Chromosome 9, Partial Trisomy 9p

Obsessive-Compulsive Disorder
  • OCD

  • Obsessive-Compulsive Disorder, Susceptibility To

  • Anancastic Neurosis

  • Obsessive Compulsive Disorder

  • Anankastic Neurosis

  • Obsessive-Compulsive Neurosis

  • Obsessive Compulsive Behavior

Hypermethioninemia Due To Adenosine Kinase Deficiency
  • Adk Hypermethioninemia

  • Hypermethioninemia Encephalopathy Due To Adenosine Kinase Deficiency

  • Hypermethioninemia Encephalopathy Due To Adk Deficiency

  • Mrt8

  • Mental Retardation, Autosomal Recessive 8, Formerly

  • Mrt8, Formerly

  • HMAKD

  • Mental Retardation, Autosomal Recessive 8

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

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
Felis catus PTPRD VGNC VGNC:69171
Bos taurus PTPRD VGNC VGNC:33548
Canis familiaris PTPRD VGNC VGNC:45185
Mus musculus PTPRD MGD MGI:97812
Rattus norvegicus PTPRD RGD RGD:1561090
Macaca mulatta PTPRD VGNC VGNC:76614
Others PTPRD NCBI