Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
146722
Gene name Gene Name - the full gene name approved by the HGNC.
CD300 molecule like family member f
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CD300LF
Synonyms (NCBI Gene) Gene synonyms aliases
CD300f, CLM-1, CLM1, IREM-1, IREM1, IgSF13, LMIR3, NKIR
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17q25.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the CD300 protein family. Members of this family are cell surface glycoproteins with a single IgV-like extracellular domain, and are involved in the regulation of immune response. The encoded protein is an inhibitory receptor
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT874949 hsa-miR-1299 CLIP-seq
MIRT874950 hsa-miR-132 CLIP-seq
MIRT874951 hsa-miR-194 CLIP-seq
MIRT874952 hsa-miR-204 CLIP-seq
MIRT874953 hsa-miR-211 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001786 Function Phosphatidylserine binding ISS
GO:0002376 Process Immune system process IEA
GO:0004888 Function Transmembrane signaling receptor activity IBA 21873635
GO:0005136 Function Interleukin-4 receptor binding ISS
GO:0005886 Component Plasma membrane IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
609807 29883 ENSG00000186074
Protein
UniProt ID Q8TDQ1
Protein name CMRF35-like molecule 1 (CLM-1) (CD300 antigen-like family member F) (Immune receptor expressed on myeloid cells 1) (IREM-1) (Immunoglobulin superfamily member 13) (IgSF13) (NK inhibitory receptor) (CD antigen CD300f)
Protein function Acts as an inhibitory receptor for myeloid cells and mast cells (PubMed:15549731). Positively regulates the phagocytosis of apoptotic cells (efferocytosis) via phosphatidylserine (PS) recognition; recognizes and binds PS as a ligand which is exp
PDB 2NMS
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07686 V-set 23 126 Immunoglobulin V-set domain Domain
PF15330 SIT 157 259 Family
Tissue specificity TISSUE SPECIFICITY: Highly expressed in spleen, peripheral blood leukocyte and monocyte, and lung. Weakly expressed in thymus, heart, brain, placenta, liver, skeletal muscle, kidney, pancreas, prostate, testis, ovary, small intestine or colon. Expressed s
Sequence
Sequence length 290
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Coronary artery disease Coronary Artery Disease rs137852988, rs121918313, rs121918529, rs121918531, rs137852340, rs1555800701, rs1215189537 29212778
Associations from Text Mining
Disease Name Relationship Type References
Autism Spectrum Disorder Stimulate 25601189
Autism Spectrum Disorder Associate 25601189
Behcet Syndrome Associate 36226612
Coronary Artery Disease Associate 34385509
Leukemia Associate 31338922
Leukemia Monocytic Acute Associate 21536801
Leukemia Myeloid Acute Associate 31338922
Leukemia Myeloid Acute Stimulate 35642341
Neoplasms Stimulate 35642341
Psoriasis Associate 20031577