PRORP - Gene browser | 3billion

PRORP

PRORP

protein only RNase P catalytic subunit

HCNC Approved Symbol: PRORP (HGNC:19958)
Genomic Coordinates: 14:35,121,839 - 35,277,622 (14q13.2)
Synonyms: MRPP3, KIAA0391
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the PRORP gene.

Frequently observed phenotypes(Top 5 only)

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

01
Patient count

Developmental delay: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Sensorineural hearing impairment: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Sensorineural hearing loss: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)

Last updated: 2024-06-30

PRORP - Gene browser | 3billion