1. Gene
  2. USP16 - ubiquitin specific peptidase 16 Gene

USP16 - ubiquitin specific peptidase 16 Gene

Homo sapiens

Also known as UBPM; UBP-M

Gene ID: 10600 | Gene type: protein coding

About USP16

Cytogenetic location: 21q21.3 Genomic coordinates (GRCh38): 21:29,024,668-29,054,488 (from NCBI)

This gene has 6 transcripts (splice variants), 209 orthologues and 71 paralogues. Ubiquitous expression in thyroid (RPKM 20.1), testis (RPKM 16.3) and 25 other tissues.

Summary

This gene encodes a deubiquitinating Enzyme that is phosphorylated at the onset of mitosis and then dephosphorylated at the metaphase/anaphase transition. It can deubiquitinate H2A, one of two major ubiquitinated proteins of chromatin, in vitro and a mutant form of the protein was shown to block cell division. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]

USP16 Products(3)

mRNA Protein Name
NM_001001992.2 NP_001001992.1 ubiquitin carboxyl-terminal hydrolase 16 isoform b
NM_001032410.2 NP_001027582.1 ubiquitin carboxyl-terminal hydrolase 16 isoform a
NM_006447.3 NP_006438.1 ubiquitin carboxyl-terminal hydrolase 16 isoform a

USP16 Protein Structure

zf-UBP

zf-UBP: Zn-finger in ubiquitin-hydrolases and other protein (48 - 125)

UCH

UCH: Ubiquitin carboxyl-terminal hydrolase (196 - 819)

  • 0
  • 200
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  • 600
  • 823 a.a.
Protein Preferred Names Protein Names

ubiquitin carboxyl-terminal hydrolase 16

deubiquitinating enzyme 16

Related Diseases

Diseases Alias
Chronic Myelomonocytic Leukemia

Leukemia, Myelomonocytic, Chronic

Cmml

Leukemia Myelomonocytic Chronic

Cmml - [Chronic Myelomonocytic Leukaemia]

Chronic Myelomonocytic Leukaemia Without Mention Of Remission

Chronic Monocytic Leukaemia

Chronic Monocytoid Leukaemia

Down Syndrome

Trisomy 21

Complete Trisomy 21 Syndrome

Down'S Syndrome

Trisomy 21 Syndrome

Down'S Syndrome - Trisomy 21

Downs Syndrome

G Trisomy

47,Xx,+21

47,Xy,+21

Trisomy G

Down Syndrome, Susceptibility To

Chromosome 21 Trisomy

Trisomy 21 Nos

Abnormal Autosomes 21

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
Felis catus USP16 VGNC VGNC:66870
Canis familiaris USP16 VGNC VGNC:53051
Rattus norvegicus USP16 RGD RGD:1307192
Mus musculus USP16 MGD MGI:1921362
Bos taurus USP16 VGNC VGNC:52842
Macaca mulatta USP16 VGNC VGNC:78738
Others USP16 NCBI