Gene Gene information from NCBI Gene database.
Entrez ID 64581
Gene name C-type lectin domain containing 7A
Gene symbol CLEC7A
Synonyms (NCBI Gene)
BGRCANDF4CD369CLECSF12DECTIN1SCARE2
Chromosome 12
Chromosome location 12p13.2
Summary This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. The encoded glycoprotein is a small type II membrane receptor with an extracellular C-type lectin-like domain fold and a cytoplasmic domain with an immunorec
miRNA miRNA information provided by mirtarbase database.
344
miRTarBase ID miRNA Experiments Reference
MIRT711136 hsa-miR-4777-3p HITS-CLIP 19536157
MIRT711135 hsa-miR-4768-5p HITS-CLIP 19536157
MIRT711134 hsa-miR-6833-3p HITS-CLIP 19536157
MIRT711133 hsa-miR-6809-3p HITS-CLIP 19536157
MIRT711136 hsa-miR-4777-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
95
GO ID Ontology Definition Evidence Reference
GO:0001775 Process Cell activation ISS
GO:0001872 Function (1->3)-beta-D-glucan binding IBA
GO:0001872 Function (1->3)-beta-D-glucan binding IDA 22267217, 24721111
GO:0001872 Function (1->3)-beta-D-glucan binding IEA
GO:0001872 Function (1->3)-beta-D-glucan binding ISS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
606264 14558 ENSG00000172243
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BXN2
Protein name C-type lectin domain family 7 member A (Beta-glucan receptor) (C-type lectin superfamily member 12) (Dendritic cell-associated C-type lectin 1) (DC-associated C-type lectin 1) (Dectin-1) (CD antigen CD369)
Protein function Lectin that functions as a pattern recognizing receptor (PRR) specific for beta-1,3-linked and beta-1,6-linked glucans, which constitute cell wall constituents from pathogenic bacteria and fungi (PubMed:11567029, PubMed:12423684). Necessary for
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00059 Lectin_C 137 243 Lectin C-type domain Domain
Tissue specificity TISSUE SPECIFICITY: Highly expressed in peripheral blood leukocytes and dendritic cells. Detected in spleen, bone marrow, lung, muscle, stomach and placenta. {ECO:0000269|PubMed:11470510, ECO:0000269|PubMed:11491532, ECO:0000269|PubMed:11567029, ECO:00002
Sequence
MEYHPDLENLDEDGYTQLHFDSQSNTRIAVVSEKGSCAASPPWRLIAVILGILCLVILVI
AVVLGTMAIWRSNSGSNTLENGYFLSRNKENHSQPTQSSLEDSVTPTKAVKTTGVLSSPC
PPNWIIYEKSCYLFSMSLNSWDGSKRQCWQLGSNLLKIDSSNELGFIVKQVSSQPDNSFW
IGLSRPQTEVPWLWEDGSTFSSNLFQIRTTATQENPSPNCVWIHVSVIYDQLCSVPSYSI
CEK
KFSM
Sequence length 247
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Phagosome
Neutrophil extracellular trap formation
C-type lectin receptor signaling pathway
Tuberculosis
  CLEC7A (Dectin-1) signaling
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
16
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Aspergillosis, susceptibility to Benign; Likely benign; Uncertain significance rs16910526, rs143893294, rs144190589 RCV000023528
RCV003224435
RCV002503078
CLEC7A-related disorder Benign; Likely benign rs16910526, rs369160278, rs191421705, rs151164069 RCV003974796
RCV003912231
RCV003941582
RCV003968136
Familial chronic mucocutaneous candidiasis Uncertain significance; Benign; Likely benign rs1948157159, rs16910526, rs143893294, rs144190589 RCV001329912
RCV000004721
RCV000768185
RCV002503078
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Arthritis Psoriatic Stimulate 20631729
Arthritis Rheumatoid Associate 20158887
Asperger Syndrome Associate 26352598
Aspergillosis Associate 29118175
Autism Spectrum Disorder Associate 26352598
Autoimmune Diseases Stimulate 25474109
Bone Diseases Associate 20158887
Brain Injuries Traumatic Associate 35819574
Bronchiolitis Obliterans Syndrome Associate 31613800
Carcinoma Pancreatic Ductal Associate 40269781