ALOX12B - Gene browser | 3billion

ALOX12B

ALOX12B

arachidonate 12-lipoxygenase, 12R type

HCNC Approved Symbol: ALOX12B (HGNC:430)
Genomic Coordinates: 17:8,072,636 - 8,087,716 (17p13.1)
Synonyms: 12R-LOX
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

6Patients

In total, 6 patients were diagnosed with a variant in the ALOX12B gene.

Frequently observed phenotypes(Top 5 only)

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

06
Patient count

Ichthyosis: 5 (83.3%)
Patient Count: 5 (83.3%)
% of total patients presenting each phenotype is shown in parentheses.
5 (83.3%)
Ichthyosis lammellaris: 2 (33.3%)
Patient Count: 2 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
2 (33.3%)
Scaly skin: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)
Congenital nonbullous ichthyosiform erythroderma: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)

Last updated: 2024-06-30

ALOX12B - Gene browser | 3billion