CSF1R Chromosome 5

Colony stimulating factor 1 receptor
128 variants 128 Health Risk

Upload your DNA to see your personal genotypes for variants in CSF1R.

What This Gene Does
The protein encoded by this gene is the receptor for colony stimulating factor 1, a cytokine which controls the production, differentiation, and function of macrophages. This receptor mediates most if not all of the biological effects of this cytokine. Ligand binding activates the receptor kinase through a process of oligomerization and transphosphorylation. The encoded protein is a tyrosine kinase transmembrane receptor and member of the CSF1/PDGF receptor family of tyrosine-protein kinases. Mutations in this gene have been associated with a predisposition to myeloid malignancy. The first intron of this gene contains a transcriptionally inactive ribosomal protein L7 processed pseudogene oriented in the opposite direction. Alternative splicing results in multiple transcript variants. Expression of a splice variant from an LTR promoter has been found in Hodgkin lymphoma (HL), HL cell lines and anaplastic large cell lymphoma. [provided by RefSeq, Mar 2017]
Gene Info
Gene Group
"Receptor tyrosine kinases|CD molecules|Immunoglobulin like domain containing"
Locus Type
gene with protein product
Location
5q32
Ensembl
ENSG00000182578
Associated Conditions (16)
Inborn genetic diseases
CSF1R-related disorder
Leukoencephalopathy
diffuse hereditary
with spheroids 1
Brain abnormalities
neurodegeneration
and dysosteosclerosis
Hereditary diffuse leukoencephalopathy with spheroids
Acute myeloid leukemia
Colon adenocarcinoma
Frontotemporal dementia
CSF1R-Related Adult-Onset Leukoencephalopathy
Parkinsonian disorder
Alzheimer disease
CSF1R-related leukoencephalopathy
Key Variants
RS1037469343
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1161693014
Conflicting classifications of pathogenicity
Health Risk
RS1209791630
Conflicting classifications of pathogenicity
CSF1R-related disorder, CSF1R-related disorder
Health Risk
RS1256984931
Conflicting classifications of pathogenicity
Health Risk
RS1275309683
Conflicting classifications of pathogenicity
Leukoencephalopathy, diffuse hereditary, with spheroids 1
Health Risk
RS139635308
Conflicting classifications of pathogenicity
Brain abnormalities, neurodegeneration, and dysosteosclerosis
Health Risk
RS140815605
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS141621829
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS142435467
Conflicting classifications of pathogenicity
Hereditary diffuse leukoencephalopathy with spheroids, Inborn genetic diseases, Hereditary diffuse leukoencephalopathy with spheroids
Health Risk
RS142543645
Conflicting classifications of pathogenicity
CSF1R-related disorder, Inborn genetic diseases, CSF1R-related disorder
Health Risk
RS143025739
Conflicting classifications of pathogenicity
Hereditary diffuse leukoencephalopathy with spheroids, Inborn genetic diseases, Hereditary diffuse leukoencephalopathy with spheroids
Health Risk
RS144414073
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
All Variants (128)
RSID Category Clinical Significance Conditions
RS1037469343 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1161693014 Health Risk Conflicting classifications of pathogenicity
RS1209791630 Health Risk Conflicting classifications of pathogenicity CSF1R-related disorder, CSF1R-related disorder
RS1256984931 Health Risk Conflicting classifications of pathogenicity
RS1275309683 Health Risk Conflicting classifications of pathogenicity Leukoencephalopathy, diffuse hereditary, with spheroids 1
RS139635308 Health Risk Conflicting classifications of pathogenicity Brain abnormalities, neurodegeneration, and dysosteosclerosis
RS140815605 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS141621829 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS142435467 Health Risk Conflicting classifications of pathogenicity Hereditary diffuse leukoencephalopathy with spheroids, Inborn genetic diseases, Hereditary diffuse leukoencephalopathy with spheroids
RS142543645 Health Risk Conflicting classifications of pathogenicity CSF1R-related disorder, Inborn genetic diseases, CSF1R-related disorder
RS143025739 Health Risk Conflicting classifications of pathogenicity Hereditary diffuse leukoencephalopathy with spheroids, Inborn genetic diseases, Hereditary diffuse leukoencephalopathy with spheroids
RS144414073 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS146145627 Health Risk Conflicting classifications of pathogenicity CSF1R-related disorder, CSF1R-related disorder
RS146406037 Health Risk Conflicting classifications of pathogenicity Hereditary diffuse leukoencephalopathy with spheroids, Inborn genetic diseases, CSF1R-related disorder
RS1465872803 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS148357861 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS149168939 Health Risk Conflicting classifications of pathogenicity Hereditary diffuse leukoencephalopathy with spheroids, CSF1R-related disorder, Acute myeloid leukemia
RS149753251 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1757092904 Health Risk Conflicting classifications of pathogenicity Frontotemporal dementia, Frontotemporal dementia
RS1758508357 Health Risk Conflicting classifications of pathogenicity Hereditary diffuse leukoencephalopathy with spheroids, Hereditary diffuse leukoencephalopathy with spheroids
RS17854478 Health Risk Conflicting classifications of pathogenicity
RS191994354 Health Risk Conflicting classifications of pathogenicity
RS200702302 Health Risk Conflicting classifications of pathogenicity
RS200788902 Health Risk Conflicting classifications of pathogenicity
RS201569135 Health Risk Conflicting classifications of pathogenicity Hereditary diffuse leukoencephalopathy with spheroids, CSF1R-related disorder, Inborn genetic diseases
RS2113776541 Health Risk Conflicting classifications of pathogenicity Hereditary diffuse leukoencephalopathy with spheroids, Hereditary diffuse leukoencephalopathy with spheroids
RS2113778146 Health Risk Conflicting classifications of pathogenicity Leukoencephalopathy, diffuse hereditary, with spheroids 1
RS2113779247 Health Risk Conflicting classifications of pathogenicity CSF1R-Related Adult-Onset Leukoencephalopathy, CSF1R-Related Adult-Onset Leukoencephalopathy
RS281860275 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS281860278 Health Risk Conflicting classifications of pathogenicity Hereditary diffuse leukoencephalopathy with spheroids, Leukoencephalopathy, diffuse hereditary
RS369678672 Health Risk Conflicting classifications of pathogenicity Hereditary diffuse leukoencephalopathy with spheroids, Hereditary diffuse leukoencephalopathy with spheroids
RS370361925 Health Risk Conflicting classifications of pathogenicity Hereditary diffuse leukoencephalopathy with spheroids, CSF1R-related disorder, Hereditary diffuse leukoencephalopathy with spheroids
RS370648666 Health Risk Conflicting classifications of pathogenicity Hereditary diffuse leukoencephalopathy with spheroids, CSF1R-related disorder, Hereditary diffuse leukoencephalopathy with spheroids
RS372068592 Health Risk Conflicting classifications of pathogenicity CSF1R-related disorder, CSF1R-related disorder
RS372210450 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS372924085 Health Risk Conflicting classifications of pathogenicity Hereditary diffuse leukoencephalopathy with spheroids, Hereditary diffuse leukoencephalopathy with spheroids
RS528081931 Health Risk Conflicting classifications of pathogenicity
RS535129002 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS556530627 Health Risk Conflicting classifications of pathogenicity Hereditary diffuse leukoencephalopathy with spheroids, CSF1R-related disorder, Hereditary diffuse leukoencephalopathy with spheroids
RS560352241 Health Risk Conflicting classifications of pathogenicity CSF1R-related disorder, CSF1R-related disorder
RS56059682 Health Risk Conflicting classifications of pathogenicity Hereditary diffuse leukoencephalopathy with spheroids, Inborn genetic diseases, CSF1R-related disorder
RS570645140 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS690016551 Health Risk Conflicting classifications of pathogenicity Hereditary diffuse leukoencephalopathy with spheroids, Hereditary diffuse leukoencephalopathy with spheroids
RS690016564 Health Risk Conflicting classifications of pathogenicity Hereditary diffuse leukoencephalopathy with spheroids, Brain abnormalities, neurodegeneration
RS748228488 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS748641028 Health Risk Conflicting classifications of pathogenicity Brain abnormalities, neurodegeneration, and dysosteosclerosis
RS750413238 Health Risk Conflicting classifications of pathogenicity Parkinsonian disorder, Inborn genetic diseases, Parkinsonian disorder
RS751675713 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS754023795 Health Risk Conflicting classifications of pathogenicity Hereditary diffuse leukoencephalopathy with spheroids, Hereditary diffuse leukoencephalopathy with spheroids
RS755134660 Health Risk Conflicting classifications of pathogenicity
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