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PSMB1

proteasome 20S subunit beta 1

HCNC Approved Symbol
PSMB1 (HGNC:9537)
Genomic Coordinates
6:170,535,120 - 170,553,307 (6q27)
Synonyms
PMSB1, HC5
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Neurodevelopmental disorder with microcephaly, hypotonia, and absent language
620038AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the PSMB1 gene.

Frequently observed phenotypes

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

No Results