Gene Gene information from NCBI Gene database.
Entrez ID 2217
Gene name Fc gamma receptor and transporter
Gene symbol FCGRT
Synonyms (NCBI Gene)
FCRNFcgammaRnalpha-chain
Chromosome 19
Chromosome location 19q13.33
Summary This gene encodes a receptor that binds the Fc region of monomeric immunoglobulin G. The encoded protein transfers immunoglobulin G antibodies from mother to fetus across the placenta. This protein also binds immunoglobulin G to protect the antibody from
miRNA miRNA information provided by mirtarbase database.
91
miRTarBase ID miRNA Experiments Reference
MIRT017375 hsa-miR-335-5p Microarray 18185580
MIRT2428853 hsa-miR-146a CLIP-seq
MIRT2428854 hsa-miR-146b-5p CLIP-seq
MIRT2428855 hsa-miR-3136-3p CLIP-seq
MIRT2428856 hsa-miR-3181 CLIP-seq
Transcription factors Transcription factors information provided by TRRUST V2 database.
1
Transcription factor Regulation Reference
STAT1 Repression 18566411
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
14
GO ID Ontology Definition Evidence Reference
GO:0002416 Process IgG immunoglobulin transcytosis in epithelial cells mediated by FcRn immunoglobulin receptor NAS 7964511
GO:0005515 Function Protein binding IPI 32296183
GO:0005615 Component Extracellular space IBA
GO:0005768 Component Endosome IEA
GO:0005886 Component Plasma membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
601437 3621 ENSG00000104870
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P55899
Protein name IgG receptor FcRn large subunit p51 (FcRn) (IgG Fc fragment receptor transporter alpha chain) (Neonatal Fc receptor)
Protein function Cell surface receptor that transfers passive humoral immunity from the mother to the newborn. Binds to the Fc region of monomeric immunoglobulin gamma and mediates its selective uptake from milk (PubMed:10933786, PubMed:7964511). IgG in the milk
PDB 1EXU , 3M17 , 3M1B , 4K71 , 4N0F , 4N0U , 5BJT , 5BXF , 5WHK , 6C97 , 6C98 , 6C99 , 6FGB , 6ILM , 6LA6 , 6LA7 , 6NHA , 6QIO , 6QIP , 6WNA , 6WOL , 7B5F , 7C9V , 7Q15 , 7XXA , 9MI6
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00129 MHC_I 26 197 Class I Histocompatibility antigen, domains alpha 1 and 2 Domain
PF07654 C1-set 207 282 Immunoglobulin C1-set domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in full-term placenta, heart, lung, liver, muscle, kidney, pancreas, and both fetal and adult small intestine. {ECO:0000269|PubMed:28330995, ECO:0000269|PubMed:7964511}.
Sequence
Sequence length 365
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
NON-MELANOMA SKIN CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Acquired Hypogammaglobulinemia Common Variable Immunodeficiency BEFREE 23286945
★☆☆☆☆
Found in Text Mining only
Acute lymphocytic leukemia Lymphocytic Leukemia BEFREE 3500187
★☆☆☆☆
Found in Text Mining only
Acute monocytic leukemia Monocytic Leukemia BEFREE 1387692
★☆☆☆☆
Found in Text Mining only
Adult Acute Lymphocytic Leukemia Lymphocytic Leukemia BEFREE 3500187
★☆☆☆☆
Found in Text Mining only
Adult T-Cell Lymphoma/Leukemia T-Cell Lymphoma/Leukemia BEFREE 1984842, 2895757
★☆☆☆☆
Found in Text Mining only
Afibrinogenemia Afibrinogenemia BEFREE 17179831, 18388508
★☆☆☆☆
Found in Text Mining only
alpha^+^ Thalassemia alpha Thalassemia BEFREE 747178
★☆☆☆☆
Found in Text Mining only
Alport Syndrome Alport Syndrome BEFREE 11423936
★☆☆☆☆
Found in Text Mining only
Amyloid nephropathy Amyloid Nephropathy BEFREE 19073821, 8639778
★☆☆☆☆
Found in Text Mining only
Amyloidosis Amyloidosis BEFREE 8113408, 8639778
★☆☆☆☆
Found in Text Mining only