1. Gene
  2. PTK7 - protein tyrosine kinase 7 (inactive) Gene

PTK7 - protein tyrosine kinase 7 (inactive) Gene

Homo sapiens

Also known as CCK4; CCK-4

Gene ID: 5754 | Gene type: protein coding

About PTK7

Cytogenetic location: 6p21.1 Genomic coordinates (GRCh38): 6:43,076,314-43,161,715 (from NCBI)

This gene has 20 transcripts (splice variants) and 229 orthologues. Broad expression in endometrium (RPKM 43.5), ovary (RPKM 31.2) and 19 other tissues.

Summary

This gene encodes a member of the receptor protein tyrosine kinase family of proteins that transduce extracellular signals across the cell membrane. The encoded protein lacks detectable catalytic tyrosine kinase activity, is involved in the Wnt signaling pathway and plays a role in multiple cellular processes including polarity and adhesion. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]

PTK7 Products(5)

mRNA Protein Name
NM_001270398.2 NP_001257327.1 inactive tyrosine-protein kinase 7 isoform e
NM_002821.5 NP_002812.2 inactive tyrosine-protein kinase 7 isoform a precursor
NM_152880.4 NP_690619.1 inactive tyrosine-protein kinase 7 isoform b precursor
NM_152881.4 NP_690620.1 inactive tyrosine-protein kinase 7 isoform c precursor
NM_152882.4 NP_690621.1 inactive tyrosine-protein kinase 7 isoform d precursor
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
21132015 GOA
Biological Process GO Annotation Evidence Reference Source
involved in actin cytoskeleton organization IMP
IMP: Inferred from mutant phenotype
20837484 GOA
involved in cell migration IMP
IMP: Inferred from mutant phenotype
20837484 GOA
involved in cellular response to retinoic acid IMP
IMP: Inferred from mutant phenotype
17910947 GOA
involved in positive regulation of canonical Wnt signaling pathway IMP
IMP: Inferred from mutant phenotype
21132015 GOA
involved in positive regulation of neuron projection development IMP
IMP: Inferred from mutant phenotype
17910947 GOA
Cellular Component GO Annotation Evidence Reference Source
located in cell-cell junction IDA
IDA: Inferred from direct assay
20837484 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

PTK7 Protein Structure

I-set

I-set: Immunoglobulin I-set domain (33 - 114)

Ig_2

Ig_2: Immunoglobulin domain (137 - 217)

I-set

I-set: Immunoglobulin I-set domain (229 - 302)

I-set

I-set: Immunoglobulin I-set domain (347 - 408)

I-set

I-set: Immunoglobulin I-set domain (415 - 498)

I-set

I-set: Immunoglobulin I-set domain (503 - 588)

I-set

I-set: Immunoglobulin I-set domain (593 - 679)

Pkinase_Tyr

Pkinase_Tyr: Protein tyrosine kinase (799 - 1061)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1000
  • 1070 a.a.
Protein Preferred Names Protein Names

inactive tyrosine-protein kinase 7

PTK7 protein tyrosine kinase 7

Recombinant PTK7 Proteins

Cat. No. Product Name Accession Purity
HY-P71821 PTK7 Protein, Human (P.pastoris, His) Q13308-1 (A31-T704) ≥95%
HY-P78398 PTK7 Protein, Human (HEK293, His) Q13308-1 (A31-T704) ≥95%

Related Diseases

Diseases Alias
Panic Disorder

Panic Anxiety Syndrome

Panic

Panic Disorder 1

Episodic Paroxysmal Anxiety Disorder

Anxiety

Anxiety Disorder

Anxiety Disorders

Anxiety State

Anxieties

Anxiety Neurosis

Agoraphobia

Fear Of Open Spaces

Phobia Of Going Out

Neural Tube Defects

Spina Bifida

Neural Tube Defect

NTD

Neural Tube Defects, Susceptibility To

Spinal Dysraphism

Spina Bifida, Susceptibility To

Rachischisis

Cleft Spine

Open Spine

Hydrocele Spinalis

Neural Tube Defect Nos

Sb - [Spina Bifida]

Spinal Hernia Nos

Spinal Fissure Nos

Scoliosis
Myelomeningocele

Meningomyelocele

Phobic Disorder

Phobic Disorders

Phobic Anxiety Disorder

Syringomyelia

Hydromyelia

Strabismus

Strabismus, Susceptibility To

Strabismus, Susceptibility To, 1

Strabismus 1

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 PTK7 VGNC VGNC:54670
Felis catus PTK7 VGNC VGNC:102498
Macaca mulatta PTK7 VGNC VGNC:83451
Mus musculus PTK7 MGD MGI:1918711
Rattus norvegicus PTK7 RGD RGD:1310472
Macaca fascicularis PTK7 NCBI NCBI:102126644
Leporidae PTK7 NCBI
Others PTK7 NCBI