FIBCD1 (fibrinogen C domain containing 1)
Gene | |
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
84929 |
Gene name
Gene Name - the full gene name approved by the HGNC.
|
Fibrinogen C domain containing 1 |
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
|
FIBCD1 |
Synonyms (NCBI Gene)
Gene synonyms aliases
|
- |
Chromosome
Chromosome number
|
9 |
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
9q34.12 |
Summary
Summary of gene provided in NCBI Entrez Gene.
|
FIBCD1 is a conserved type II transmembrane endocytic receptor that binds chitin and is located primarily in the intestinal brush border (Schlosser et al., 2009 [PubMed 19710473]).[supplied by OMIM, Apr 2010] |
miRNA
miRNA information provided by mirtarbase database.
|
|||||||||||||||||||||||||
|
Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
|
|||||||||||||||||||||||||||||||
|
Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
|
|||||||
|
Protein | |||||||||||
UniProt ID | Q8N539 | ||||||||||
Protein name | Fibrinogen C domain-containing protein 1 | ||||||||||
Protein function | Acetyl group-binding receptor which shows a high-affinity and calcium-dependent binding to acetylated structures such as chitin, some N-acetylated carbohydrates, and amino acids, but not to their non-acetylated counterparts. Can facilitate the e | ||||||||||
PDB | 4M7F , 4M7H , 6ZQR , 6ZQX , 6ZQY , 6ZR0 , 6ZR3 , 6ZR4 | ||||||||||
Family and domains |
Pfam
|
||||||||||
Tissue specificity | TISSUE SPECIFICITY: Expressed in the small and large intestinal epithelial cells with a highly polarized localization to the apical surface corresponding to the brush border and in the ducts of the salivary gland. {ECO:0000269|PubMed:19710473}. | ||||||||||
Sequence |
|
||||||||||
Sequence length | 461 | ||||||||||
Interactions | View interactions |
Associated diseases
Disease information provided by ClinVar, GenCC, and GWAS databases.
|
|||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||
|