NHP2 - Gene browser

NHP2

NHP2 ribonucleoprotein

HCNC Approved Symbol: NHP2 (HGNC:14377)
Genomic Coordinates: 5:178,149,463 - 178,153,885 (5q35.3)
Synonyms: FLJ20479, NOLA2
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

0Patient

There are no patients diagnosed with a variant in the NHP2 gene.

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

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