Gene: USP9X

Alternate names for this Gene: DFFRX|FAF|FAM|MRX99|MRXS99F

Gene Summary: This gene is a member of the peptidase C19 family and encodes a protein that is similar to ubiquitin-specific proteases. Though this gene is located on the X chromosome, it escapes X-inactivation. Mutations in this gene have been associated with Turner syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.

Gene is located in Chromosome: X

Location in Chromosome : Xp11.4

Description of this Gene: ubiquitin specific peptidase 9 X-linked

Type of Gene: protein-coding

rs1555922391 in USP9X gene and Dysmorphic features PMID 28688840 2017 Impact of clinical exomes in neurodevelopmental and neurometabolic disorders.

PMID 25763846 2015 Seizures are regulated by ubiquitin-specific peptidase 9 X-linked (USP9X), a de-ubiquitinase.

PMID 26833328 2016 De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations.

PMID 24607389 2014 Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growth.

PMID 24690944 2014 Massively parallel sequencing of patients with intellectual disability, congenital anomalies and/or autism spectrum disorders with a targeted gene panel.

rs587777317 in USP9X gene and MENTAL RETARDATION, X-LINKED 99 PMID 24607389 2014 Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growth.

rs1555922391 in USP9X gene and Muscle hypotonia PMID 24607389 2014 Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growth.

PMID 25763846 2015 Seizures are regulated by ubiquitin-specific peptidase 9 X-linked (USP9X), a de-ubiquitinase.

PMID 26833328 2016 De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations.

PMID 28688840 2017 Impact of clinical exomes in neurodevelopmental and neurometabolic disorders.

PMID 24690944 2014 Massively parallel sequencing of patients with intellectual disability, congenital anomalies and/or autism spectrum disorders with a targeted gene panel.