1. Gene
  2. PTPRD - protein tyrosine phosphatase receptor type D Gene

PTPRD - protein tyrosine phosphatase receptor type D Gene

Homo sapiens

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

Gene ID: 5789 | Gene type: protein coding

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

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)

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  • 1800
  • 1912 a.a.
Protein Preferred Names Protein Names

receptor-type tyrosine-protein phosphatase delta

protein tyrosine phosphatase, receptor type, delta polypeptide

Recombinant PTPRD Proteins

Cat. No. Product Name Accession Purity
HY-P78721 PTPRD Protein, Human (HEK293, His) P23468 (E21-E1265) ≥95%
HY-P79442 PTPRD Protein, Human (HEK293, hFc) P23468 (E21-S1174) ≥95%

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