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NIN

ninein

HCNC Approved Symbol
NIN (HGNC:14906)
Genomic Coordinates
14:50,719,763 - 50,831,503 (14q22.1)
Synonyms
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Seckel syndrome 7
614851AR

Diagnosed Cases

0Patient

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

Frequently observed phenotypes

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

No Results