RFXANK - Gene browser | 3billion

RFXANK

RFXANK

regulatory factor X associated ankyrin containing protein

HCNC Approved Symbol: RFXANK (HGNC:9987)
Genomic Coordinates: 19:19,192,258 - 19,201,866 (19p13.11)
Synonyms: BLS, RFX-B, ANKRA1, F14150_1, MGC138628
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 RFXANK 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

Arthritis: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Crohn disease: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Episcleritis: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Growth failure: 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

RFXANK - Gene browser | 3billion