Selected-GenAtlas references SOURCE GeneCards NCBI Gene Swiss-Prot Ensembl
HGNC UniGene Nucleotide OMIM UCSC
Home Page
FLASH GENE
Symbol C19orf33 contributors: - updated : 07-02-2006
HGNC name chromosome 19 open reading frame 33
HGNC id 16668
ASSOCIATED DISORDERS
corresponding disease(s)
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
tumoral fusion      
with SPINT2, in several tissues (in the kidney, prostate, and placenta )
tumoral     --over  
in ovarian tumors
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS