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SCGB3A2

secretoglobin family 3A member 2

HCNC Approved Symbol
SCGB3A2 (HGNC:18391)
Genomic Coordinates
5:147,878,711 - 147,882,191 (5q32)
Synonyms
UGRP1, LU103, PNSP1
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SCGB3A2 gene.

Frequently observed phenotypes

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

No Results
SCGB3A2 - Gene browser | 3billion