Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1436
Gene name Gene Name - the full gene name approved by the HGNC.
Colony stimulating factor 1 receptor
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CSF1R
Synonyms (NCBI Gene) Gene synonyms aliases
BANDDOS, C-FMS, CD115, CSF-1R, CSFR, FIM2, FMS, GPSC, HDLS, HDLS1, M-CSF-R
Chromosome Chromosome number
5
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
5q32
Summary Summary of gene provided in NCBI Entrez Gene.
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. Li
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs1801271 T>A,C Likely-pathogenic Coding sequence variant, non coding transcript variant, missense variant
rs121913390 A>G,T Likely-pathogenic Missense variant, coding sequence variant, stop gained, non coding transcript variant
rs121913392 A>C,T Likely-pathogenic Stop gained, coding sequence variant, non coding transcript variant
rs121913393 A>G Likely-pathogenic Missense variant, coding sequence variant, non coding transcript variant
rs143025739 G>A Conflicting-interpretations-of-pathogenicity, likely-benign Non coding transcript variant, missense variant, coding sequence variant, 5 prime UTR variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT006103 hsa-miR-155-5p ELISA, Luciferase reporter assay, qRT-PCR, Western blot 21355095
MIRT006103 hsa-miR-155-5p ELISA, Luciferase reporter assay, qRT-PCR, Western blot 21355095
MIRT006103 hsa-miR-155-5p ELISA, Luciferase reporter assay, qRT-PCR, Western blot 21355095
MIRT006103 hsa-miR-155-5p Other 20584899
MIRT438232 hsa-miR-22-3p Luciferase reporter assay, qRT-PCR 24198819
Transcription factors
Transcription factor Regulation Reference
NR3C1 Unknown 11891846
RUNX1 Unknown 8585955;9209363
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0001934 Process Positive regulation of protein phosphorylation IMP 20504948
GO:0002376 Process Immune system process IEA
GO:0002573 Process Myeloid leukocyte differentiation IEA
GO:0002931 Process Response to ischemia IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
164770 2433 ENSG00000182578
Protein
UniProt ID P07333
Protein name Macrophage colony-stimulating factor 1 receptor (CSF-1 receptor) (CSF-1-R) (CSF-1R) (M-CSF-R) (EC 2.7.10.1) (Proto-oncogene c-Fms) (CD antigen CD115)
Protein function Tyrosine-protein kinase that acts as a cell-surface receptor for CSF1 and IL34 and plays an essential role in the regulation of survival, proliferation and differentiation of hematopoietic precursor cells, especially mononuclear phagocytes, such
PDB 2I0V , 2I0Y , 2I1M , 2OGV , 3BEA , 3DPK , 3KRJ , 3KRL , 3LCD , 3LCO , 4DKD , 4HW7 , 4LIQ , 4R7H , 4R7I , 4WRL , 4WRM , 6IG8 , 6N33 , 6T2W , 6WXJ , 7MFC , 8CGC , 8JOT , 8W1L
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00047 ig 207 293 Immunoglobulin domain Domain
PF13927 Ig_3 397 489 Domain
PF07714 PK_Tyr_Ser-Thr 582 910 Protein tyrosine and serine/threonine kinase Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in bone marrow and in differentiated blood mononuclear cells.
Sequence
MGPGVLLLLLVATAWHGQGIPVIEPSVPELVVKPGATVTLRCVGNGSVEWDGPPSPHWTL
YSDGSSSILSTNNATFQNTGTYRCTEPGDPLGGSAAIHLYVKDPARPWNVLAQEVVVFED
QDALLPCLLTDPVLEAGVSLVRVRGRPLMRHTNYSFSPWHGFTIHRAKFIQSQDYQCSAL
MGGRKVMSISIRLKVQKVIPGPPALTLVPAELVRIRGEAAQIVCSASSVDVNFDVFLQHN
NTKLAIPQQSDFHNNRYQKVLTLNLDQVDFQHAGNYSCVASNVQGKHSTSMFF
RVVESAY
LNLSSEQNLIQEVTVGEGLNLKVMVEAYPGLQGFNWTYLGPFSDHQPEPKLANATTKDTY
RHTFTLSLPRLKPSEAGRYSFLARNPGGWRALTFELTLRYPPEVSVIWTFINGSGTLLCA
ASGYPQPNVTWLQCSGHTDRCDEAQVLQVWDDPYPEVLSQEPFHKVTVQSLLTVETLEHN
QTYECRAHN
SVGSGSWAFIPISAGAHTHPPDEFLFTPVVVACMSIMALLLLLLLLLLYKY
KQKPKYQVRWKIIESYEGNSYTFIDPTQLPYNEKWEFPRNNLQFGKTLGAGAFGKVVEAT
AFGLGKEDAVLKVAVKMLKSTAHADEKEALMSELKIMSHLGQHENIVNLLGACTHGGPVL
VITEYCCYGDLLNFLRRKAEAMLGPSLSPGQDPEGGVDYKNIHLEKKYVRRDSGFSSQGV
DTYVEMRPVSTSSNDSFSEQDLDKEDGRPLELRDLLHFSSQVAQGMAFLASKNCIHRDVA
ARNVLLTNGHVAKIGDFGLARDIMNDSNYIVKGNARLPVKWMAPESIFDCVYTVQSDVWS
YGILLWEIFSLGLNPYPGILVNSKFYKLVKDGYQMAQPAFAPKNIYSIMQACWALEPTHR
PTFQQICSFL
QEQAQEDRRERDYTNLPSSSRSGGSGSSSSELEEESSSEHLTCCEQGDIA
QPLLQPNNYQFC
Sequence length 972
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  MAPK signaling pathway
Ras signaling pathway
Rap1 signaling pathway
Cytokine-cytokine receptor interaction
Viral protein interaction with cytokine and cytokine receptor
PI3K-Akt signaling pathway
Osteoclast differentiation
Hematopoietic cell lineage
Pathways in cancer
Transcriptional misregulation in cancer
Acute myeloid leukemia
  Other interleukin signaling
Transcriptional Regulation by VENTX
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Hereditary Diffuse Leukoencephalopathy With Spheroids hereditary diffuse leukoencephalopathy with spheroids, Leukoencephalopathy, diffuse hereditary, with spheroids 1 rs281860267, rs690016556, rs281860274, rs690016562, rs690016564, rs387906662, rs690016548, rs281860281, rs397515556, rs917027829, rs397515557, rs1561904557, rs587777245, rs281860279, rs587777246
View all (3 more)
N/A
alzheimer disease Alzheimer disease rs1561901881, rs1561905293 N/A
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Calcifying Leukoencephalopathy-Skeletal Dysplasia early-onset calcifying leukoencephalopathy-skeletal dysplasia N/A N/A GenCC
Dysosteosclerosis brain abnormalities, neurodegeneration, and dysosteosclerosis N/A N/A GenCC
Frontotemporal dementia frontotemporal dementia N/A N/A ClinVar
Gout Gout N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
AA amyloidosis Associate 33350588
Adenocarcinoma of Lung Associate 35946526
Agenesis of Corpus Callosum Associate 31520500, 39374256
Alcohol Related Disorders Associate 39217398
Alcoholism Associate 24428556
Alzheimer Disease Associate 29486463, 30917570, 31182772, 33350588, 36042609, 36189598
Arthritis Associate 24100919
Arthritis Juvenile Associate 37904379
Arthritis Psoriatic Associate 24100919
Arthritis Rheumatoid Associate 28659662, 35304503