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UMOD gene

uromodulin

Key facts

Official symbol
UMOD
Full name
UMOD
Chromosome
16
Map location
16p12.3
Organism
Homo sapiens
NCBI Gene ID
7369
Also known as
ADMCKD2, ADTKD1, FJHN, HNFJ, HNFJ1, MCKD2

Function summary

The protein encoded by this gene is the most abundant protein in mammalian urine under physiological conditions. Its excretion in urine follows proteolytic cleavage of the ectodomain of its glycosyl phosphatidylinosital-anchored counterpart that is situated on the luminal cell surface of the loop of Henle. This protein may act as a constitutive inhibitor of calcium crystallization in renal fluids. Excretion of this protein in urine may provide defense against urinary tract infections caused by uropathogenic bacteria. Defects in this gene are associated with the renal disorders medullary cystic kidney disease-2 (MCKD2), glomerulocystic kidney disease with hyperuricemia and isosthenuria (GCKDHI), and familial juvenile hyperuricemic nephropathy (FJHN). Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2013].

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Data source: NCBI Gene · alsesAI Gene Library