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RTN4IP1

reticulon 4 interacting protein 1

HCNC Approved Symbol
RTN4IP1 (HGNC:18647)
Genomic Coordinates
6:106,570,771 - 106,630,491 (6q21)
Synonyms
NIMP
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Optic atrophy 10 with or without ataxia, impaired intellectual development and seizures
616732AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the RTN4IP1 gene.

Frequently observed phenotypes

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

No Results