INSR - Gene browser | 3billion

INSR

INSR

insulin receptor

HCNC Approved Symbol: INSR (HGNC:6091)
Genomic Coordinates: 19:7,112,265 - 7,294,414 (19p13.2)
Synonyms: CD220
Disease Associations: This gene is associated with the following 4 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the INSR gene.

Frequently observed phenotypes(Top 5 only)

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

02
Patient count

Acanthosis nigricans: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Hypoglycemic seizures: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Mental impairment: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)

Last updated: 2024-06-30

INSR - Gene browser | 3billion