1. Gene
  2. USP9Y - ubiquitin specific peptidase 9 Y-linked Gene

USP9Y - ubiquitin specific peptidase 9 Y-linked Gene

Homo sapiens

Also known as DFFRY; SPGFY2

Gene ID: 8287 | Gene type: protein coding

About USP9Y

Cytogenetic location: Yq11.221 Genomic coordinates (GRCh38): Y:12,701,231-12,860,839 (from NCBI)

Summary

This gene is a member of the peptidase C19 family. It encodes a protein that is similar to ubiquitin-specific proteases, which cleave the ubiquitin moiety from ubiquitin-fused precursors and ubiquitinylated proteins. [provided by RefSeq, Mar 2009]

USP9Y Products(1)

mRNA Protein Name
NM_004654.4 NP_004645.2 probable ubiquitin carboxyl-terminal hydrolase FAF-Y

USP9Y Protein Structure

UCH

UCH: Ubiquitin carboxyl-terminal hydrolase (1559 - 1955)

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  • 2555 a.a.
Protein Preferred Names Protein Names

probable ubiquitin carboxyl-terminal hydrolase FAF-Y

azoospermia factor A

Related Diseases

Diseases Alias
Spermatogenic Failure, Y-Linked, 2

SPGFY2

Spermatogenic Failure, Nonobstructive, Y-Linked

Y-Linked Spermatogenic Failure 2

Azoospermia, Nonobstructive, Y-Linked

Oligozoospermia, Nonobstructive, Y-Linked

Oligospermia, Nonobstructive, Y-Linked

Spermatogenic Arrest, Y-Linked

Nonobstructive Y-Linked Spermatogenic Failure

Spermatogenic Failure Y-Linked 2

Azoospermia Non-Obstructive Y-Linked

Non-Obstructive Azoospermia And Infertility

Oligospermia Non-Obstructive Y-Linked

Oligozoospermia Non-Obstructive Y-Linked

Spermatogenic Arrest Y-Linked

Spermatogenic Failure Nonobstructive Y-Linked

Partial Deletion Of Y

Partial Chromosome Y Deletion

Partial Deletion Of Y Chromosome Short Arm

Partial Deletion Of Chromosome Y

Partial Deletion Of The Long Arm Of The Y Chromosome

Y-Chromosome Microdeletions

Male Sterility Due To Chromosome Y Deletion

Y Chromosome Deletions

Male Infertility

Infertility, Male

Infertility Male

Male Sterility

Absolute Infertility

Spermatogenic Failure

Azoospermia

Spgf

Spermatogenic Failure, Susceptibility To

Absent Sperm

Aspermatogenesis

Infertility Due To Azoospermia

Hypospermatogenesis

Azoospermatism

Infertility
Phelan-Mcdermid Syndrome

Chromosome 22q13.3 Deletion Syndrome

22q13.3 Deletion Syndrome

Telomeric 22q13 Monosomy Syndrome

PHMDS

Deletion 22q13 Syndrome

22q13.3 Deletion

Deletion 22q13.3 Syndrome

Monosomy 22q13

Monosomy 22q13.3

22q13 Deletion Syndrome

Monosomy 22q13 Syndrome

22q13 Deletion

Chromosome Deletion

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

Orthologs Information

Species Symbol Source ID
Mus musculus USP9Y MGD MGI:1313274
Rattus norvegicus USP9Y RGD RGD:9087771