FER - FER tyrosine kinase Gene

Also Known as TYK3; PPP1R74; p94-Fer

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 2241

About FER

Cytogenetic location: 5q21.3 Genomic coordinates (GRCh38): 5:108,747,897-109,196,841 (from NCBI)

This gene has 9 transcripts (splice variants), 222 orthologues and 32 paralogues. Ubiquitous expression in thyroid (RPKM 2.8), testis (RPKM 2.2) and 25 other tissues.

Summary

The protein encoded by this gene is a member of the FPS/FES family of non-transmembrane Receptor Tyrosine Kinases. It regulates cell-cell adhesion and mediates signaling from the cell surface to the Cytoskeleton via growth factor receptors. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome X. [provided by RefSeq, Apr 2015]

FER Products (4)

mRNA Protein Name
NM_001308028.2 NP_001294957.1 tyrosine-protein kinase Fer isoform b
NM_001308031.2 NP_001294960.1 tyrosine-protein kinase Fer isoform c
NM_001308038.2 NP_001294967.1 tyrosine-protein kinase Fer isoform d
NM_005246.4 NP_005237.2 tyrosine-protein kinase Fer isoform a

FER Protein Structure

FCH

FCH: Fes/CIP4, and EFC/F-BAR homology domain (1 - 92)

SH2

SH2: SH2 domain (460 - 531)

Pkinase_Tyr

Pkinase_Tyr: Protein tyrosine kinase (565 - 814)

  • 0
  • 200
  • 400
  • 600
  • 822 a.a.
Protein Preferred Names Protein Names

tyrosine-protein kinase Fer

  • feline encephalitis virus-related kinase FER

FER Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Références
Intra
FER P16591 CDC37 Homo sapiens Q16543 25036637
Intra
FER P16591 CDC37 Homo sapiens Q16543 32707033
Intra
FER P16591 HSP90AB1 Homo sapiens P08238 32707033
Cross
FER P16591 Bcat Gallus gallus O42486 15226396
Cross: Cross-species interaction Intra: Intraspecies interaction

FER Anticorps

Cat. No. Nom du produit Application Reactivity
HY-P84133 FER Antibody (YA3830) WB, IHC-P, ICC/IF, ELISA Human, Mouse
HY-P84133A FER Antibody (YA3830)(PBS only) WB, IHC-P, ICC/IF, ELISA Human, Mouse
HY-P85158 FER Antibody (YA4850) WB, IHC-P, ICC/IF, ELISA Human, Mouse

Related Diseases

Diseases Alias
Sarcoma
  • Connective And Soft Tissue Neoplasm

  • Tumor Of Soft Tissue And Skeleton

  • Sarcomas

  • Sarcoma - Category

Trichothiodystrophy 5, Nonphotosensitive
  • TTD5

  • Nonphotosensitive Trichothiodystrophy 5

  • Trichothiodystrophy 5, Non-Photosensitive

Ceroid Lipofuscinosis, Neuronal, 6a
  • Neuronal Ceroid Lipofuscinosis 6

  • CLN6

  • Vlincl

  • Cln6 Disease

  • Ceroid Lipofuscinosis, Neuronal, 6

  • Late-Infantile Neuronal Ceroid Lipofuscinosis

  • CLN6A

  • Neuronal Ceroid Lipofuscinosis, Late Infantile, Variant

  • Neuronal Ceroid Lipofuscinosis 6a

  • Neuronal Ceroid Lipofuscinosis 6 Variable Age Of Onset

  • Cln6 Disease, Adult Kufs Type A

  • Cln6 Disease, Late Infantile

  • Neuronal Ceroid Lipofuscinosis, Gypsy/Indian Early Juvenile Variant

  • Ceroid Lipofuscinosis Neuronal 6

  • Cln6-Related Neuronal Ceroid Lipofuscinosis

  • Late Infantile Neuronal Ceroid Lipofuscinosis

  • Jansky-Bielschowsky Disease

  • Lincl

  • Late Infantile Ncl

  • Neuronal Ceroid Lipofuscinosis 6 With Variable Age At Onset

  • Variant Late-Onset Infantile Neuronal Ceroid Lipofuscinosis

  • Ceroid Lipofuscinosis, Neuronal, Late Infantile, Variant

  • Lipofuscinosis, Ceroid, Neuronal, Type 6

  • Ceroid Lipofuscinosis, Neuronal, 5

Leukemia, Acute Myeloid
  • Acute Myeloid Leukemia

  • Leukemia, Acute Myelogenous

  • Acute Myelogenous Leukemia

  • AML

  • Leukemia, Acute Myeloid, Susceptibility To

  • Acute Myeloblastic Leukemia

  • Leukemia, Acute Myeloid, Reduced Survival In, Somatic

  • Acute Myeloid Leukaemia

  • Leukemia, Myelocytic, Acute

  • Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome

  • Secondary Aml

  • Acute Myelocytic Leukemia

  • Acute Myeloid Leukemia, Somatic

  • Leukemia, Acute Myeloid, Somatic

  • Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic

  • Acute Myeloblastic Leukaemia

  • Acute Myelogenous Leukaemia

  • Aml - Acute Myeloid Leukemia

  • Acute Myeloid Leukemia With Cebpa Somatic Mutations

  • Aml With Cebpa Somatic Mutations

  • Inherited Acute Myeloid Leukemia

  • Familial Aml

  • Inherited Aml

  • Pure Familial Aml

  • Pure Familial Acute Myeloid Leukemia

  • Secondary Acute Myeloid Leukemia

  • Therapy-Related Aml And Myelodysplastic Syndrome

  • Acute Myeloid Leukemia, Secondary

  • Acute Non-Lymphoblastic Leukemia

  • Acute Non-Lymphocytic Leukemia

  • Acute Biphenotypic Leukemia

  • Acute Undifferentiated Leukemia

  • Acute Myeloblastic Leukaemia With Multilineage Dysplasia

  • Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission

  • Acute Myeloid Leukaemia With Myelodysplasia-Related Features

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