HRAS - Gene browser

HRAS

HRas proto-oncogene, GTPase

HCNC Approved Symbol: HRAS (HGNC:5173)
Genomic Coordinates: 11:532,242 - 535,576 (11p15.5)
Synonyms: HRAS1
Disease Associations: This gene is associated with the following 7 diseases in OMIM.

Diagnosed Cases

18Patients

In total, 18 patients were diagnosed with a variant in the HRAS gene.

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

018
Patient count

Global developmental delay: 5 (27.8%)
Patient Count: 5 (27.8%)
% of total patients presenting each phenotype is shown in parentheses.
5 (27.8%)
Coarse facies: 4 (22.2%)
Patient Count: 4 (22.2%)
% of total patients presenting each phenotype is shown in parentheses.
4 (22.2%)
Failure to thrive: 4 (22.2%)
Patient Count: 4 (22.2%)
% of total patients presenting each phenotype is shown in parentheses.
4 (22.2%)
Low set ears: 4 (22.2%)
Patient Count: 4 (22.2%)
% of total patients presenting each phenotype is shown in parentheses.
4 (22.2%)
Relative macrocephaly: 4 (22.2%)
Patient Count: 4 (22.2%)
% of total patients presenting each phenotype is shown in parentheses.
4 (22.2%)