CRNN (cornulin)
Gene | |
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
49860 |
Gene name
Gene Name - the full gene name approved by the HGNC.
|
Cornulin |
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
|
CRNN |
Synonyms (NCBI Gene)
Gene synonyms aliases
|
C1orf10, DRC1, PDRC1, SEP53 |
Chromosome
Chromosome number
|
1 |
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
1q21.3 |
Summary
Summary of gene provided in NCBI Entrez Gene.
|
This gene encodes a member of the "fused gene" family of proteins, which contain N-terminus EF-hand domains and multiple tandem peptide repeats. The encoded protein contains two EF-hand Ca2+ binding domains in its N-terminus and two glutamine- and threoni |
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 | Q9UBG3 | ||||||||||
Protein name | Cornulin (53 kDa putative calcium-binding protein) (53 kDa squamous epithelial-induced stress protein) (58 kDa heat shock protein) (Squamous epithelial heat shock protein 53) (Tumor-related protein) | ||||||||||
Protein function | Promotes cell proliferation, G1/S cell cycle progression and induces expression of the cell cycle regulator CCND1 (PubMed:30009832). Regulates proliferation induced by pro-inflammatory cytokine response via activation of NFKB1 and PI3K/AKT signa | ||||||||||
Family and domains |
Pfam
|
||||||||||
Tissue specificity | TISSUE SPECIFICITY: Expressed in the basal skin layer (at protein level) (PubMed:30009832). Squamous epithelia cell-specific. Expressed in the esophagus (periphery of the cells of the granular and the upper spinous layers), foreskin (granular and lower co | ||||||||||
Sequence |
|
||||||||||
Sequence length | 495 | ||||||||||
Interactions | View interactions |
Associated diseases
Disease information provided by ClinVar, GenCC, and GWAS databases.
|
|||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||
|