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FLASH GENE
Symbol GREM1 contributors: mct/npt/pgu - updated : 27-08-2015
HGNC name gremlin 1, cysteine knot superfamily, homolog (Xenopus laevis)
HGNC id 2001
ASSOCIATED DISORDERS
corresponding disease(s)
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
tumoral     --low  
associated with tumor progression
tumoral     --other  
aberrantly expressed by cancer-associated stromal cells (basal cell carcinoma)
constitutional     --over  
overexpression causes osteopenia
constitutional   deletion    
causes increased trabecular bone volume secondary to increased bone formation and osteoblastic activity
constitutional   deletion    
has a major impact in the early phases of bone acquisition, and are in accordance with the role of BMPs during skeletal development
tumoral     --low  
by hypermethylation in renal cell carcinoma
constitutional germinal mutation      
in isolated Congenital anomalies of the kidney and urinary tract (CAKUT)
constitutional     --over  
in rheumatoid arthritis (RA) joints
Susceptibility to colorectal cancer (CRC)
Variant & Polymorphism other SNPs near GREM1 were strongly associated with increased CRC risk
Candidate gene
Marker
Therapy target
SystemTypeDisorderPubmed
neurosensorialvisualanterior chamber
modulation of the extracellular matrix via gremlin provides a novel therapeutic target for glaucoma
ANIMAL & CELL MODELS