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TP53

tumor protein p53

HCNC Approved Symbol
TP53 (HGNC:11998)
Genomic Coordinates
17:7,668,421 - 7,687,490 (17p13.1)
Synonyms
p53, LFS1
Disease Associations
This gene is associated with the following 12 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
{Adrenocortical carcinoma, pediatric}
202300AD
{Basal cell carcinoma 7}
614740AD
{Choroid plexus papilloma}
260500AD
{Colorectal cancer}
114500AD; SM
{Glioma susceptibility 1}
137800AD; SM
{Osteosarcoma}
259500SM
Bone marrow failure syndrome 5
618165AD
Breast cancer, somatic
114480-
Hepatocellular carcinoma, somatic
114550-
Li-Fraumeni syndrome
151623AD
Nasopharyngeal carcinoma, somatic
607107-
Pancreatic cancer, somatic
260350-

Diagnosed Cases

14Patients

In total, 14 patients were diagnosed with a variant in the TP53 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Breast carcinoma
 4 (28.6%)
Leukemia
 
2 (14.3%)
Hyperkeratosis
 
1 (7.1%)
Ichthyosis
 
1 (7.1%)
Basal cell carcinomas
 
1 (7.1%)