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IFNLR1

interferon lambda receptor 1

HCNC Approved Symbol
IFNLR1 (HGNC:18584)
Genomic Coordinates
1:24,154,168 - 24,187,289 (1p36.11)
Synonyms
CRF2/12, IFNLR, IL-28R1, IL28RA
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.
However, the following publication(s) suggest a possible gene disease association.
View More Disease Info
ContentsPublications
Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss.
PMID:29453195

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the IFNLR1 gene.

Frequently observed phenotypes

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

Hearing loss
 1 (50.0%)
Hearing impairment
 1 (50.0%)