HNF1B - Gene browser

HNF1B

HNF1 homeobox B

HCNC Approved Symbol: HNF1B (HGNC:11630)
Genomic Coordinates: 17:37,686,431 - 37,745,059 (17q12)
Synonyms: LFB3, VHNF1, HNF1beta, MODY5, HNF1β, TCF2
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

15Patients

In total, 15 patients were diagnosed with a variant in the HNF1B gene.

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

015
Patient count

Chronic kidney disease: 3 (20.0%)
Patient Count: 3 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (20.0%)
Diabetes mellitus: 3 (20.0%)
Patient Count: 3 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (20.0%)
Abnormal renal morphology: 2 (13.3%)
Patient Count: 2 (13.3%)
% of total patients presenting each phenotype is shown in parentheses.
2 (13.3%)
Kidney malformation: 2 (13.3%)
Patient Count: 2 (13.3%)
% of total patients presenting each phenotype is shown in parentheses.
2 (13.3%)
Renal cyst: 2 (13.3%)
Patient Count: 2 (13.3%)
% of total patients presenting each phenotype is shown in parentheses.
2 (13.3%)