2. Gene
  3. USP9X - ubiquitin specific peptidase 9 X-linked Gene

USP9X - ubiquitin specific peptidase 9 X-linked Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as FAF; FAM; hFAM; DFFRX; MRX99; XLID99; MRXS99F

Gene ID: 8239 | Gene type: protein coding

About USP9X

Cytogenetic location: Xp11.4 Genomic coordinates (GRCh38): X:41,085,445-41,236,579 (from NCBI)

This gene has 18 transcripts (splice variants), 228 orthologues, 71 paralogues and is associated with 94 phenotypes. Ubiquitous expression in testis (RPKM 14.2), thyroid (RPKM 14.0) and 25 other tissues.

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. [provided by RefSeq, Jul 2008]

USP9X Products(4)

mRNA Protein Name
NM_001039590.3 NP_001034679.2 probable ubiquitin carboxyl-terminal hydrolase FAF-X isoform 3
NM_001039591.3 NP_001034680.2 probable ubiquitin carboxyl-terminal hydrolase FAF-X isoform 4
NM_001410748.1 NP_001397677.1 probable ubiquitin carboxyl-terminal hydrolase FAF-X isoform 5
NM_001410749.1 NP_001397678.1 probable ubiquitin carboxyl-terminal hydrolase FAF-X isoform 6

USP9X Protein Structure

UCH

UCH: Ubiquitin carboxyl-terminal hydrolase (1557 - 1953)

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  • 2400
  • 2570 a.a.
Protein Preferred Names Protein Names

probable ubiquitin carboxyl-terminal hydrolase FAF-X

Drosophila fat facets related, X-linked

USP9X Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra USP9X Q93008 MCL1 Homo sapiens Q07820
Anti Bait CoIP
20023629
Intra USP9X Q93008 SMAD4 Homo sapiens Q13485
Anti Bait CoIP
19135894
Intra USP9X Q93008 HTT Homo sapiens P42858
Y2H
17500595
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Intellectual Developmental Disorder, X-Linked 99, Syndromic, Female-Restricted

MRXS99F

Mental Retardation, X-Linked 99, Syndromic, Female-Restricted
Intellectual Developmental Disorder, X-Linked 99

XLID99

Mental Retardation, X-Linked 99

Mrx99

Mental Retardation, X-Linked, Type 99
Female-Restricted Syndromic X-Linked Intellectual Disability 99

X-Linked Female Restricted Facial Dysmorphism-Short Stature-Choanal Atresia-Intellectual Disability

Intellectual Disability, X-Linked 99, Syndromic, Female-Restricted

Female-Restricted Syndromic X-Linked Mental Retardation 99

Mrxs99f

X-Linked Facial Dysmorphism-Short Stature-Choanal Atresia-Intellectual Disability Syndrome Limited To Females
Non-Syndromic X-Linked Intellectual Disability

X-Linked Non-Syndromic Intellectual Disability

Non-Specific X-Linked Mental Retardation

X-Linked Non-Specific Intellectual Disability
Non-Syndromic X-Linked Intellectual Disability 99

Mrx99

X-Linked Mental Retardation 99
Turner Syndrome

Monosomy X

Gonadal Dysgenesis Turner Type

Ullrich-Turner Syndrome

Bonnevie-Ullrich Syndrome

Karyotype 45, X

Genital Dwarfism, Turner Type

Gonadal Dysgenesis

45,X

Turner'S Syndrome

Gonadal Dysgenesis - Turner

Monosomy X Syndrome

Xo Syndrome

Genital Dwarfism

45, X Syndrome

Bonnevie-Ulrich Syndrome

Chromosome X Monosomy X

Schereshevkii Turner Syndrome

Turner Varny Syndrome

Ts

45,X Syndrome

45,X/46,Xx Syndrome

Turners Syndrome

Gonadal Dysgenesis, 45,X

X0 Syndrome
Bardet-Biedl Syndrome

Bbs

Biedl-Bardet Syndrome
Scoliosis
Microcephaly

Microencephaly

Microcephalus

Microcephalic

Nanocephaly

Congenital Microcephaly

Brain Hypoplasia

Brain Nondevelopment

Cephalic Hypoplasia

Undeveloped Cerebrum

Undeveloped Brain

Micrencephalon

Micrencephaly
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase
Bioactive Molecules (7)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-13264 Degrasyn 99.70% Unkown
HY-111408 EOAI3402143 Inhibitor 98.95% Unkown
HY-145967 FT709 Inhibitor 99.81% Unkown
HY-149230 USP28-IN-4 Inhibitor 99.35% Unkown
HY-149229 USP28-IN-3 Inhibitor 98.26% Unkown
HY-149228 USP28-IN-2 Inhibitor / Unkown
HY-RS15570 USP9X Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Mus musculus USP9X MGD MGI:894681
Rattus norvegicus USP9X RGD RGD:1560056
Bos taurus USP9X VGNC VGNC:56957
Others USP9X NCBI