OTC Chromosome X

Ornithine transcarbamylase
368 variants 368 Health Risk

Upload your DNA to see your personal genotypes for variants in OTC.

What This Gene Does
This nuclear gene encodes a mitochondrial matrix enzyme. The encoded protein is involved in the urea cycle which functions to detoxify ammonia into urea for excretion. Mutations in this enzyme lead to ornithine transcarbamylase deficiency, which causes hyperammonemia. [provided by RefSeq, May 2022]
Associated Conditions (14)
Ornithine carbamoyltransferase deficiency
Inborn genetic diseases
OTC-related disorder
Global developmental delay
Hyperammonemia
Likely inborn error of metabolism
Thyroid cancer
nonmedullary
1
Nonpapillary renal cell carcinoma
See cases
Abnormal circulating ornithine concentration
Protein avoidance
Squamous cell carcinoma of the head and neck
Key Variants
RS1051365488
Conflicting classifications of pathogenicity
Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency
Health Risk
RS1052206430
Conflicting classifications of pathogenicity
Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency
Health Risk
RS1168053730
Conflicting classifications of pathogenicity
Ornithine carbamoyltransferase deficiency, Inborn genetic diseases, Ornithine carbamoyltransferase deficiency
Health Risk
RS1357402422
Conflicting classifications of pathogenicity
Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency
Health Risk
RS137899554
Conflicting classifications of pathogenicity
Ornithine carbamoyltransferase deficiency, Inborn genetic diseases, Ornithine carbamoyltransferase deficiency
Health Risk
RS141273695
Conflicting classifications of pathogenicity
OTC-related disorder, Ornithine carbamoyltransferase deficiency, Inborn genetic diseases
Health Risk
RS1461226043
Conflicting classifications of pathogenicity
Ornithine carbamoyltransferase deficiency, Inborn genetic diseases, Ornithine carbamoyltransferase deficiency
Health Risk
RS148660170
Conflicting classifications of pathogenicity
Ornithine carbamoyltransferase deficiency, Inborn genetic diseases, Ornithine carbamoyltransferase deficiency
Health Risk
RS1555972495
Conflicting classifications of pathogenicity
Health Risk
RS1555972538
Conflicting classifications of pathogenicity
Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency, Inborn genetic diseases
Health Risk
RS1555975685
Conflicting classifications of pathogenicity
Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency
Health Risk
RS184053962
Conflicting classifications of pathogenicity
Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency
Health Risk
All Variants (368)
RSID Category Clinical Significance Conditions
RS72552295 Health Risk Pathogenic Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency
RS72552296 Health Risk Pathogenic Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency
RS72552297 Health Risk Pathogenic Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency
RS72552298 Health Risk Pathogenic
RS72552299 Health Risk Pathogenic
RS72552300 Health Risk Pathogenic Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency
RS72552301 Health Risk Pathogenic
RS72554303 Health Risk Pathogenic
RS72554304 Health Risk Pathogenic
RS72554305 Health Risk Pathogenic
RS72554306 Health Risk Pathogenic
RS72554309 Health Risk Pathogenic
RS72554310 Health Risk Pathogenic Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency
RS72554311 Health Risk Pathogenic Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency
RS72554313 Health Risk Pathogenic Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency
RS72554315 Health Risk Pathogenic
RS72554317 Health Risk Pathogenic
RS72554319 Health Risk Pathogenic
RS72554321 Health Risk Pathogenic
RS72554322 Health Risk Pathogenic Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency
RS72554323 Health Risk Pathogenic Ornithine carbamoyltransferase deficiency, Inborn genetic diseases, Ornithine carbamoyltransferase deficiency
RS72554325 Health Risk Pathogenic
RS72554326 Health Risk Pathogenic Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency
RS72554327 Health Risk Pathogenic Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency
RS72554329 Health Risk Pathogenic Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency
RS72554330 Health Risk Pathogenic Nonpapillary renal cell carcinoma, Nonpapillary renal cell carcinoma
RS72554332 Health Risk Pathogenic Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency
RS72554333 Health Risk Pathogenic
RS72554334 Health Risk Pathogenic
RS72554335 Health Risk Pathogenic
RS72554336 Health Risk Pathogenic
RS72554337 Health Risk Pathogenic
RS72554338 Health Risk Pathogenic Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency
RS72554339 Health Risk Pathogenic
RS72554340 Health Risk Pathogenic
RS72554341 Health Risk Pathogenic
RS72554342 Health Risk Pathogenic
RS72554343 Health Risk Pathogenic
RS72554344 Health Risk Pathogenic
RS72554345 Health Risk Pathogenic Ornithine carbamoyltransferase deficiency, Ornithine carbamoyltransferase deficiency
RS72554346 Health Risk Pathogenic
RS72554349 Health Risk Pathogenic
RS72554350 Health Risk Pathogenic
RS72554351 Health Risk Pathogenic
RS72554352 Health Risk Pathogenic
RS72554353 Health Risk Pathogenic
RS72554354 Health Risk Pathogenic
RS72554357 Health Risk Pathogenic
RS72554359 Health Risk Pathogenic Nonpapillary renal cell carcinoma, Nonpapillary renal cell carcinoma
RS72556251 Health Risk Pathogenic
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