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NOP10

NOP10 ribonucleoprotein

HCNC Approved Symbol
NOP10 (HGNC:14378)
Genomic Coordinates
15:34,341,719 - 34,343,136 (15q14)
Synonyms
NOP10P, MGC70651, NOLA3
Disease Associations
This gene is associated with the following 3 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 2
620425AR
?Dyskeratosis congenita, autosomal recessive 1
224230AR
?Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 9
620400AD

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the NOP10 gene.

Frequently observed phenotypes

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

No Results