CSF3R

GENERAL INFORMATION

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Gene name

CSF3R

Gene description

Colony stimulating factor 3 receptor (granulocyte)

Protein class

Cancer-related genes
CD markers
Disease related genes
FDA approved drug targets
Predicted intracellular proteins
Predicted membrane proteins

Predicted localization

Intracellular,Membrane

Number of transcripts

7
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (appendix, bone marrow, placenta)
GTEx:Group enriched (lung, spleen)

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic expression most abundant in placenta and a subset of leukocytes.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly consistent with RNA expression data.

Data reliability

Supportive based on 2 antibodies.
HPA048086 , CAB017116
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis

Placenta



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (appendix, bone marrow, placenta)

Organ

Expression

GTEx dataset
RNA tissue category:  Group enriched (lung, spleen)

Organ

Expression



GENE INFORMATION

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Gene name

CSF3R (HGNC Symbol)

Synonyms

CD114, GCSFR

Description

Colony stimulating factor 3 receptor (granulocyte) (HGNC Symbol)

Entrez gene summary

The protein encoded by this gene is the receptor for colony stimulating factor 3, a cytokine that controls the production, differentiation, and function of granulocytes. The encoded protein, which is a member of the family of cytokine receptors, may also function in some cell surface adhesion or recognition processes. Alternatively spliced transcript variants have been described. Mutations in this gene are a cause of Kostmann syndrome, also known as severe congenital neutropenia. [provided by RefSeq, Aug 2010]

Chromosome

1

Cytoband

p34.3

Chromosome location (bp)

36466043 - 36483278

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000119535 (version 78.38)

Entrez gene

1441

UniProt

Q99062 (UniProt - Evidence at protein level)

neXtProt

NX_Q99062

Antibodypedia

CSF3R antibodies


PROTEIN BROWSER

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ENST00000331941
 
ENST00000361632
 
ENST00000373103
 
ENST00000373104
 
ENST00000373106
 
ENST00000464465
 
ENST00000533491
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

CSF3R-001 ENSP00000362198
ENST00000373106
Q99062
Show all »
Show » Show » 836 92.2 Yes 1
CSF3R-003 ENSP00000362196
ENST00000373104
Q99062
Show all »
Show » Show » 783 86.6 Yes 1
CSF3R-004 ENSP00000362195
ENST00000373103
Q99062
Show all »
Show » Show » 863 95.1 Yes 1
CSF3R-018 ENSP00000435218
ENST00000464465
Show » Show » 388 42 No 1
CSF3R-019 ENSP00000431639
ENST00000533491
E9PK56
Show all »
Show » 21 2.2 No 0
CSF3R-201 ENSP00000332180
ENST00000331941
Q99062
Show all »
Show » Show » 783 86.6 Yes 1
CSF3R-202 ENSP00000355406
ENST00000361632
Q99062
Show all »
Show » Show » 836 92.2 Yes 1