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NLRP12

NLR family pyrin domain containing 12

HCNC Approved Symbol
NLRP12 (HGNC:22938)
Genomic Coordinates
19:53,793,584 - 53,824,403 (19q13.42)
Synonyms
RNO2, PYPAF7, Monarch1, PAN6, CLR19.3, NALP12
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 NLRP12 gene.

Frequently observed phenotypes

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

Delayed growth
 1 (33.3%)
Hiatal hernia
 1 (33.3%)
Microcephaly
 1 (33.3%)
Vomiting
 1 (33.3%)
Hearing impairment
 1 (33.3%)
NLRP12 - Gene browser | 3billion