SDCCAG8 - Gene browser

SDCCAG8

SHH signaling and ciliogenesis regulator SDCCAG8

HCNC Approved Symbol: SDCCAG8 (HGNC:10671)
Genomic Coordinates: 1:243,256,041 - 243,500,091 (1q43-q44)
Synonyms: NY-CO-8, CCCAP, SLSN7, NPHP10, BBS16
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

1Patient

In total, 1 patient was diagnosed with a variant in the SDCCAG8 gene.

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

01
Patient count

Attenuated retinal vessels: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Attenuation of retinal blood vessels: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Renal cortical necrosis: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Renal failure: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Renal insufficiency: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)