SSBP1 - Gene browser | 3billion

SSBP1

SSBP1

single stranded DNA binding protein 1

HCNC Approved Symbol: SSBP1 (HGNC:11317)
Genomic Coordinates: 7:141,738,321 - 141,750,488 (7q34)
Synonyms: SSBP, mtSSB
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

3Patients

In total, 3 patients were diagnosed with a variant in the SSBP1 gene.

Frequently observed phenotypes(Top 5 only)

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

03
Patient count

Optic atrophy: 2 (66.7%)
Patient Count: 2 (66.7%)
% of total patients presenting each phenotype is shown in parentheses.
2 (66.7%)
Retinal degeneration: 1 (33.3%)
Patient Count: 1 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (33.3%)
Sensorineural hearing impairment: 1 (33.3%)
Patient Count: 1 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (33.3%)

Last updated: 2024-06-30

SSBP1 - Gene browser | 3billion