RFX7 - Gene browser | 3billion

RFX7

RFX7

regulatory factor X7

HCNC Approved Symbol: RFX7 (HGNC:25777)
Genomic Coordinates: 15:56,087,280 - 56,245,082 (15q21.3)
Synonyms: FLJ12994, RFXDC2
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 RFX7 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

Autism spectrum disorder: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Global developmental delay: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
No language: 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

RFX7 - Gene browser | 3billion