USP10 (ubiquitin specific peptidase 10) - Rat Genome Database

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Gene: USP10 (ubiquitin specific peptidase 10) Homo sapiens
Analyze
Symbol: USP10
Name: ubiquitin specific peptidase 10
RGD ID: 1352341
HGNC Page HGNC:12608
Description: Enables several functions, including cysteine-type peptidase activity; p53 binding activity; and transmembrane transporter binding activity. Involved in several processes, including monoubiquitinated protein deubiquitination; negative regulation of canonical NF-kappaB signal transduction; and negative regulation of stress granule assembly. Located in several cellular components, including early endosome; intermediate filament cytoskeleton; and nucleoplasm. Part of protein-containing complex. Is active in cytosolic ribosome.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: deubiquitinating enzyme 10; KIAA0190; MGC2621; ubiquitin carboxyl-terminal hydrolase 10; ubiquitin specific protease 10; ubiquitin thioesterase 10; ubiquitin thiolesterase 10; ubiquitin-specific-processing protease 10; UBPO
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Related Pseudogenes: USP10P1   USP10P2   USP10P3  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381684,700,000 - 84,779,922 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1684,699,986 - 84,779,922 (+)EnsemblGRCh38hg38GRCh38
GRCh371684,733,606 - 84,813,528 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361683,291,056 - 83,371,029 (+)NCBINCBI36Build 36hg18NCBI36
Build 341683,291,084 - 83,370,670NCBI
Celera1669,035,743 - 69,115,795 (+)NCBICelera
Cytogenetic Map16q24.1NCBI
HuRef1670,486,450 - 70,566,405 (+)NCBIHuRef
CHM1_11686,145,099 - 86,225,097 (+)NCBICHM1_1
T2T-CHM13v2.01690,766,262 - 90,846,179 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
cytoplasm  (IDA,IEA)
cytosol  (IBA,IDA,IEA,TAS)
cytosolic ribosome  (IDA)
early endosome  (IBA,IDA,IEA)
endosome  (IEA)
intermediate filament cytoskeleton  (IDA)
nucleoplasm  (IDA,TAS)
nucleus  (IBA,IDA,IEA)
protein-containing complex  (IDA)

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Schizophrenia  (IAGP)
References

References - curated
# Reference Title Reference Citation
1. Long noncoding RNA H19 mediates melatonin inhibition of premature senescence of c-kit(+) cardiac progenitor cells by promoting miR-675. Cai B, etal., J Pineal Res. 2016 Aug;61(1):82-95. doi: 10.1111/jpi.12331. Epub 2016 Apr 29.
2. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8724849   PMID:9827704   PMID:11439350   PMID:12477932   PMID:12838346   PMID:14702039   PMID:15252450   PMID:15302935   PMID:15489334   PMID:16344560   PMID:16368182   PMID:16773218  
PMID:16964243   PMID:17004105   PMID:17081983   PMID:18029348   PMID:18391951   PMID:18632802   PMID:19398555   PMID:19416867   PMID:19615732   PMID:20020773   PMID:20096447   PMID:20215869  
PMID:20379614   PMID:20467437   PMID:20562859   PMID:21245042   PMID:21455491   PMID:21873635   PMID:21962518   PMID:22658674   PMID:22681889   PMID:22904170   PMID:22939629   PMID:23230274  
PMID:23279204   PMID:23287719   PMID:23383273   PMID:23775713   PMID:24009623   PMID:24163370   PMID:24169447   PMID:24255178   PMID:24270572   PMID:24270891   PMID:24332849   PMID:24768535  
PMID:24845384   PMID:24981860   PMID:24998844   PMID:25168367   PMID:25416956   PMID:25640309   PMID:25665578   PMID:25861989   PMID:25921289   PMID:26186194   PMID:26343856   PMID:26344197  
PMID:26393420   PMID:26496610   PMID:26555087   PMID:26678539   PMID:26777405   PMID:26876938   PMID:26975374   PMID:27003362   PMID:27022092   PMID:27025967   PMID:27558965   PMID:27591049  
PMID:27684187   PMID:28067227   PMID:28514442   PMID:28515276   PMID:28611215   PMID:28695742   PMID:28851806   PMID:28852924   PMID:29119051   PMID:29212181   PMID:29357390   PMID:29378906  
PMID:29395067   PMID:29576527   PMID:29581427   PMID:29698567   PMID:29802200   PMID:29803676   PMID:29891922   PMID:29892012   PMID:30056112   PMID:30067985   PMID:30107050   PMID:30209976  
PMID:30281322   PMID:30323974   PMID:30375264   PMID:30469013   PMID:30471916   PMID:30604502   PMID:30629181   PMID:30759391   PMID:30833792   PMID:30894572   PMID:30940456   PMID:30940648  
PMID:30945288   PMID:30948266   PMID:30975888   PMID:31048545   PMID:31091453   PMID:31239290   PMID:31298480   PMID:31332168   PMID:31332267   PMID:31501480   PMID:31511647   PMID:31515488  
PMID:31527615   PMID:31586073   PMID:31659108   PMID:31665637   PMID:31721429   PMID:31748695   PMID:31771591   PMID:31911859   PMID:31980649   PMID:31981475   PMID:32129945   PMID:32160526  
PMID:32217697   PMID:32296183   PMID:32302570   PMID:32382008   PMID:32416067   PMID:32423001   PMID:32640226   PMID:32694731   PMID:32780723   PMID:32807901   PMID:32814053   PMID:32905556  
PMID:33022573   PMID:33095475   PMID:33141564   PMID:33184448   PMID:33197885   PMID:33239621   PMID:33306668   PMID:33397691   PMID:33495715   PMID:33545068   PMID:33577797   PMID:33658012  
PMID:33669244   PMID:33731348   PMID:33838681   PMID:33916271   PMID:33957083   PMID:33961781   PMID:34079125   PMID:34129829   PMID:34133714   PMID:34244565   PMID:34348161   PMID:34416231  
PMID:34469731   PMID:34578187   PMID:34597346   PMID:34599966   PMID:34709727   PMID:34718347   PMID:34728620   PMID:34739333   PMID:34780058   PMID:34795231   PMID:34799561   PMID:34838592  
PMID:34901782   PMID:34914965   PMID:34967276   PMID:34983926   PMID:35007165   PMID:35013218   PMID:35156780   PMID:35163710   PMID:35211260   PMID:35256949   PMID:35271311   PMID:35271750  
PMID:35351136   PMID:35439318   PMID:35563538   PMID:35636624   PMID:35687106   PMID:35791074   PMID:35819319   PMID:35821235   PMID:35850772   PMID:35944360   PMID:35987808   PMID:36012204  
PMID:36057605   PMID:36114006   PMID:36163081   PMID:36183834   PMID:36199071   PMID:36215168   PMID:36232890   PMID:36244648   PMID:36279435   PMID:36335356   PMID:36424410   PMID:36484700  
PMID:36526897   PMID:36574265   PMID:36597993   PMID:36632454   PMID:36756718   PMID:36779763   PMID:36807568   PMID:36949071   PMID:37184153   PMID:37199168   PMID:37371055   PMID:37562219  
PMID:37717099   PMID:37786443   PMID:37827155   PMID:37860888   PMID:37863330   PMID:37873736   PMID:38280479   PMID:38317006   PMID:38456416  


Genomics

Comparative Map Data
USP10
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381684,700,000 - 84,779,922 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1684,699,986 - 84,779,922 (+)EnsemblGRCh38hg38GRCh38
GRCh371684,733,606 - 84,813,528 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361683,291,056 - 83,371,029 (+)NCBINCBI36Build 36hg18NCBI36
Build 341683,291,084 - 83,370,670NCBI
Celera1669,035,743 - 69,115,795 (+)NCBICelera
Cytogenetic Map16q24.1NCBI
HuRef1670,486,450 - 70,566,405 (+)NCBIHuRef
CHM1_11686,145,099 - 86,225,097 (+)NCBICHM1_1
T2T-CHM13v2.01690,766,262 - 90,846,179 (+)NCBIT2T-CHM13v2.0
Usp10
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm398120,637,099 - 120,684,299 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl8120,637,099 - 120,684,299 (+)EnsemblGRCm39 Ensembl
GRCm388119,910,360 - 119,957,560 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl8119,910,360 - 119,957,560 (+)EnsemblGRCm38mm10GRCm38
MGSCv378122,434,752 - 122,481,457 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv368122,796,829 - 122,843,534 (+)NCBIMGSCv36mm8
Celera8124,131,245 - 124,177,988 (+)NCBICelera
Cytogenetic Map8E1NCBI
cM Map868.61NCBI
Usp10
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81964,881,255 - 64,923,522 (+)NCBIGRCr8
mRatBN7.21947,972,858 - 48,014,900 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1947,972,611 - 48,014,897 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1954,767,502 - 54,809,229 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01955,448,244 - 55,489,969 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01957,661,267 - 57,703,079 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01952,566,274 - 52,608,820 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1952,566,607 - 52,608,817 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01963,313,910 - 63,356,424 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41950,202,951 - 50,244,677 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1947,229,671 - 47,271,396 (+)NCBICelera
Cytogenetic Map19q12NCBI
Usp10
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955541242,091 - 296,059 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955541242,182 - 296,018 (+)NCBIChiLan1.0ChiLan1.0
USP10
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21894,449,698 - 94,529,802 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan116100,366,823 - 100,446,915 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01665,367,463 - 65,447,549 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11684,719,540 - 84,787,714 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1684,712,913 - 84,787,714 (+)Ensemblpanpan1.1panPan2
USP10
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1567,736,215 - 67,774,756 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl567,736,730 - 67,809,206 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha567,750,854 - 67,823,397 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0567,968,955 - 68,042,190 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl567,968,955 - 68,042,589 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1567,984,393 - 68,056,880 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0567,819,079 - 67,892,003 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0568,234,061 - 68,306,639 (-)NCBIUU_Cfam_GSD_1.0
Usp10
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934927,554,574 - 27,618,345 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366413,307,931 - 3,350,517 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366413,308,121 - 3,350,476 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
USP10
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl63,977,231 - 4,043,533 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.163,977,235 - 4,043,539 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.264,473,366 - 4,491,966 (-)NCBISscrofa10.2Sscrofa10.2susScr3
USP10
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1570,105,653 - 70,186,512 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl570,139,470 - 70,185,884 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660475,563,590 - 5,644,539 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Usp10
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247461,554,023 - 1,617,308 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247461,553,891 - 1,616,711 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in USP10
57 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 16q23.1-24.3(chr16:78816291-90081985)x3 copy number gain See cases [RCV000050840] Chr16:78816291..90081985 [GRCh38]
Chr16:78850188..90148393 [GRCh37]
Chr16:77407689..88675894 [NCBI36]
Chr16:16q23.1-24.3		 pathogenic
GRCh38/hg38 16q23.3-24.2(chr16:83878992-87223838)x1 copy number loss See cases [RCV000051122] Chr16:83878992..87223838 [GRCh38]
Chr16:83912597..87257444 [GRCh37]
Chr16:82470098..85814945 [NCBI36]
Chr16:16q23.3-24.2		 pathogenic
GRCh38/hg38 16q22.1-24.3(chr16:70514631-90081985)x3 copy number gain See cases [RCV000052422] Chr16:70514631..90081985 [GRCh38]
Chr16:70548534..90148393 [GRCh37]
Chr16:69106035..88675894 [NCBI36]
Chr16:16q22.1-24.3		 pathogenic
GRCh38/hg38 16q21-24.3(chr16:65313395-90081985)x3 copy number gain See cases [RCV000052421] Chr16:65313395..90081985 [GRCh38]
Chr16:65347298..90148393 [GRCh37]
Chr16:63904799..88675894 [NCBI36]
Chr16:16q21-24.3		 pathogenic
GRCh38/hg38 16q23.3-24.1(chr16:84081930-85474903)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052019]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052019]|See cases [RCV000052019] Chr16:84081930..85474903 [GRCh38]
Chr16:84115535..85508509 [GRCh37]
Chr16:82673036..84066010 [NCBI36]
Chr16:16q23.3-24.1		 uncertain significance
GRCh38/hg38 16q23.1-24.3(chr16:76873569-90081985)x3 copy number gain See cases [RCV000052423] Chr16:76873569..90081985 [GRCh38]
Chr16:76907466..90148393 [GRCh37]
Chr16:75464967..88675894 [NCBI36]
Chr16:16q23.1-24.3		 pathogenic
GRCh38/hg38 16q23.3-24.3(chr16:82173150-90081985)x3 copy number gain See cases [RCV000052424] Chr16:82173150..90081985 [GRCh38]
Chr16:82206755..90148393 [GRCh37]
Chr16:80764256..88675894 [NCBI36]
Chr16:16q23.3-24.3		 pathogenic
GRCh38/hg38 16q24.1-24.3(chr16:84707538-90081985)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052425]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052425]|See cases [RCV000052425] Chr16:84707538..90081985 [GRCh38]
Chr16:84741144..90148393 [GRCh37]
Chr16:83298645..88675894 [NCBI36]
Chr16:16q24.1-24.3		 pathogenic
GRCh38/hg38 16q23.1-24.2(chr16:78704275-87819342)x1 copy number loss See cases [RCV000053359] Chr16:78704275..87819342 [GRCh38]
Chr16:78738172..87852948 [GRCh37]
Chr16:77295673..86410449 [NCBI36]
Chr16:16q23.1-24.2		 pathogenic
GRCh38/hg38 16q23.3-24.1(chr16:81753762-85714791)x1 copy number loss See cases [RCV000053360] Chr16:81753762..85714791 [GRCh38]
Chr16:81787367..85748397 [GRCh37]
Chr16:80344868..84305898 [NCBI36]
Chr16:16q23.3-24.1		 pathogenic
GRCh38/hg38 16q23.3-24.1(chr16:83016872-85087809)x1 copy number loss See cases [RCV000053361] Chr16:83016872..85087809 [GRCh38]
Chr16:83050477..85121415 [GRCh37]
Chr16:81607978..83678916 [NCBI36]
Chr16:16q23.3-24.1		 pathogenic
GRCh38/hg38 16q22.1-24.1(chr16:70414573-84908120)x1 copy number loss See cases [RCV000133814] Chr16:70414573..84908120 [GRCh38]
Chr16:70448476..84941726 [GRCh37]
Chr16:69005977..83499227 [NCBI36]
Chr16:16q22.1-24.1		 pathogenic
GRCh38/hg38 16q23.3-24.1(chr16:83399060-84908120)x1 copy number loss See cases [RCV000133929] Chr16:83399060..84908120 [GRCh38]
Chr16:83432665..84941726 [GRCh37]
Chr16:81990166..83499227 [NCBI36]
Chr16:16q23.3-24.1		 pathogenic
GRCh38/hg38 16q23.3-24.3(chr16:83988570-90081985)x3 copy number gain See cases [RCV000135659] Chr16:83988570..90081985 [GRCh38]
Chr16:84022175..90148393 [GRCh37]
Chr16:82579676..88675894 [NCBI36]
Chr16:16q23.3-24.3		 likely pathogenic
GRCh38/hg38 16q23.3-24.1(chr16:83878992-84908120)x3 copy number gain See cases [RCV000135758] Chr16:83878992..84908120 [GRCh38]
Chr16:83912597..84941726 [GRCh37]
Chr16:82470098..83499227 [NCBI36]
Chr16:16q23.3-24.1		 pathogenic|uncertain significance
GRCh38/hg38 16q23.3-24.1(chr16:83687650-86073240)x1 copy number loss See cases [RCV000136504] Chr16:83687650..86073240 [GRCh38]
Chr16:83721255..86106846 [GRCh37]
Chr16:82278756..84664347 [NCBI36]
Chr16:16q23.3-24.1		 pathogenic
GRCh38/hg38 16q23.2-24.3(chr16:80946659-90081985)x3 copy number gain See cases [RCV000136898] Chr16:80946659..90081985 [GRCh38]
Chr16:80980556..90148393 [GRCh37]
Chr16:79538057..88675894 [NCBI36]
Chr16:16q23.2-24.3		 pathogenic|likely pathogenic
GRCh38/hg38 16q22.1-24.3(chr16:70749398-90096995)x3 copy number gain See cases [RCV000137495] Chr16:70749398..90096995 [GRCh38]
Chr16:70783301..90163403 [GRCh37]
Chr16:69340802..88690904 [NCBI36]
Chr16:16q22.1-24.3		 pathogenic
GRCh38/hg38 16q23.3-24.3(chr16:83478453-89932910)x3 copy number gain See cases [RCV000137980] Chr16:83478453..89932910 [GRCh38]
Chr16:83512058..89999318 [GRCh37]
Chr16:82069559..88526819 [NCBI36]
Chr16:16q23.3-24.3		 likely pathogenic
GRCh38/hg38 16q21-24.3(chr16:65511483-90096995)x3 copy number gain See cases [RCV000139426] Chr16:65511483..90096995 [GRCh38]
Chr16:65545386..90163403 [GRCh37]
Chr16:64102887..88690904 [NCBI36]
Chr16:16q21-24.3		 pathogenic
GRCh38/hg38 16q23.1-24.3(chr16:75377981-90081992)x3 copy number gain See cases [RCV000139302] Chr16:75377981..90081992 [GRCh38]
Chr16:75411879..90148400 [GRCh37]
Chr16:73969380..88675901 [NCBI36]
Chr16:16q23.1-24.3		 pathogenic
GRCh38/hg38 16q23.2-24.3(chr16:80717291-90096662)x3 copy number gain See cases [RCV000141128] Chr16:80717291..90096662 [GRCh38]
Chr16:80751188..90163070 [GRCh37]
Chr16:79308689..88690571 [NCBI36]
Chr16:16q23.2-24.3		 pathogenic
GRCh38/hg38 16q23.1-24.3(chr16:76336203-90088654)x3 copy number gain See cases [RCV000141700] Chr16:76336203..90088654 [GRCh38]
Chr16:76370100..90155062 [GRCh37]
Chr16:74927601..88682563 [NCBI36]
Chr16:16q23.1-24.3		 pathogenic
GRCh38/hg38 16q21-24.3(chr16:64389378-90081985)x3 copy number gain See cases [RCV000142578] Chr16:64389378..90081985 [GRCh38]
Chr16:64423281..90148393 [GRCh37]
Chr16:62980782..88675894 [NCBI36]
Chr16:16q21-24.3		 pathogenic|likely pathogenic
GRCh38/hg38 16q23.2-24.3(chr16:80067315-90057871)x3 copy number gain See cases [RCV000142698] Chr16:80067315..90057871 [GRCh38]
Chr16:80101212..90124279 [GRCh37]
Chr16:78658713..88651780 [NCBI36]
Chr16:16q23.2-24.3		 pathogenic
GRCh38/hg38 16q12.2-24.3(chr16:52899183-90088654)x3 copy number gain See cases [RCV000143425] Chr16:52899183..90088654 [GRCh38]
Chr16:52933095..90155062 [GRCh37]
Chr16:51490596..88682563 [NCBI36]
Chr16:16q12.2-24.3		 pathogenic
GRCh37/hg19 16q23.1-24.3(chr16:74872514-90274440)x3 copy number gain See cases [RCV000240108] Chr16:74872514..90274440 [GRCh37]
Chr16:16q23.1-24.3		 pathogenic
t(5;16)(p15.31;q23.1) translocation not provided [RCV000203391] Chr5:1..8180513 [GRCh37]
Chr16:76935310..90354753 [GRCh37]
Chr5:5p15.33-15.31
Chr16:16q23.1-24.3		 likely pathogenic
GRCh37/hg19 16q23.3-24.1(chr16:83553094-86098013)x1 copy number loss See cases [RCV000203439] Chr16:83553094..86098013 [GRCh37]
Chr16:16q23.3-24.1		 likely pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46615804-90142285)x1 copy number loss Breast ductal adenocarcinoma [RCV000207138] Chr16:46615804..90142285 [GRCh37]
Chr16:16q11.2-24.3		 uncertain significance
GRCh37/hg19 16q22.2-24.3(chr16:72107834-90142285)x1 copy number loss Breast ductal adenocarcinoma [RCV000207182] Chr16:72107834..90142285 [GRCh37]
Chr16:16q22.2-24.3		 uncertain significance
Single allele complex Breast ductal adenocarcinoma [RCV000207314] Chr16:56368689..90141355 [GRCh37]
Chr16:16q12.2-24.3		 uncertain significance
GRCh37/hg19 16q24.1(chr16:84319435-85011988)x3 copy number gain See cases [RCV000446860] Chr16:84319435..85011988 [GRCh37]
Chr16:16q24.1		 uncertain significance
GRCh37/hg19 16q11.2-24.3(chr16:46464488-90155062)x3 copy number gain See cases [RCV000446110] Chr16:46464488..90155062 [GRCh37]
Chr16:16q11.2-24.3		 pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3 copy number gain See cases [RCV000446684] Chr16:69193..90274381 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16q24.1(chr16:84776177-85087145)x1 copy number loss See cases [RCV000510274] Chr16:84776177..85087145 [GRCh37]
Chr16:16q24.1		 likely benign
GRCh37/hg19 16p13.2-q24.3(chr16:9273328-89548493)x3 copy number gain See cases [RCV000511622] Chr16:9273328..89548493 [GRCh37]
Chr16:16p13.2-q24.3		 uncertain significance
GRCh37/hg19 16q24.1(chr16:84530234-84841354)x1 copy number loss See cases [RCV000510932] Chr16:84530234..84841354 [GRCh37]
Chr16:16q24.1		 uncertain significance
GRCh37/hg19 16q11.2-24.3(chr16:46497599-90354753)x1 copy number loss Poly (ADP-Ribose) polymerase inhibitor response [RCV000626429] Chr16:46497599..90354753 [GRCh37]
Chr16:16q11.2-24.3		 drug response
NM_005153.3(USP10):c.907G>C (p.Glu303Gln) single nucleotide variant Inborn genetic diseases [RCV003257973] Chr16:84745388 [GRCh38]
Chr16:84778994 [GRCh37]
Chr16:16q24.1		 uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062) copy number gain See cases [RCV000511296] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3 copy number gain See cases [RCV000512138] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46455960-90354753)x1 copy number loss Poly (ADP-Ribose) polymerase inhibitor response [RCV000626435] Chr16:46455960..90354753 [GRCh37]
Chr16:16q11.2-24.3		 drug response
GRCh37/hg19 16q13-24.3(chr16:57051473-89797669)x3 copy number gain See cases [RCV000512511] Chr16:57051473..89797669 [GRCh37]
Chr16:16q13-24.3		 pathogenic
GRCh37/hg19 16q23.3-24.3(chr16:83001540-90155062)x3 copy number gain See cases [RCV000512468] Chr16:83001540..90155062 [GRCh37]
Chr16:16q23.3-24.3		 likely pathogenic
GRCh37/hg19 16q23.2-24.3(chr16:79400436-90155062)x3 copy number gain not provided [RCV000683845] Chr16:79400436..90155062 [GRCh37]
Chr16:16q23.2-24.3		 pathogenic
GRCh37/hg19 16q22.2-24.3(chr16:72515938-90155062)x3 copy number gain not provided [RCV000683831] Chr16:72515938..90155062 [GRCh37]
Chr16:16q22.2-24.3		 pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90163275)x3 copy number gain not provided [RCV000738917] Chr16:88165..90163275 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90274695)x3 copy number gain not provided [RCV000738918] Chr16:88165..90274695 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:61451-90294632)x3 copy number gain not provided [RCV000738915] Chr16:61451..90294632 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
NC_000016.10:g.(?_84593050)_(85516675_?)del deletion Schizophrenia [RCV000754198] Chr16:84593050..85516675 [GRCh38]
Chr16:16q24.1		 likely pathogenic
GRCh37/hg19 16q23.3-24.1(chr16:83813294-84984350)x3 copy number gain not provided [RCV000739258] Chr16:83813294..84984350 [GRCh37]
Chr16:16q23.3-24.1		 likely benign
GRCh37/hg19 16q23.3-24.1(chr16:83330709-84866927)x1 copy number loss not provided [RCV001006830] Chr16:83330709..84866927 [GRCh37]
Chr16:16q23.3-24.1		 uncertain significance
GRCh37/hg19 16q23.3-24.3(chr16:82761333-90055381) copy number gain not provided [RCV000767619] Chr16:82761333..90055381 [GRCh37]
Chr16:16q23.3-24.3		 pathogenic
NM_005153.3(USP10):c.56A>G (p.Asn19Ser) single nucleotide variant Inborn genetic diseases [RCV003271488] Chr16:84733469 [GRCh38]
Chr16:84767075 [GRCh37]
Chr16:16q24.1		 uncertain significance
GRCh37/hg19 16q23.2-24.1(chr16:79254648-84827672)x1 copy number loss not provided [RCV000849998] Chr16:79254648..84827672 [GRCh37]
Chr16:16q23.2-24.1		 uncertain significance
GRCh37/hg19 16q24.1(chr16:84608098-85087145)x1 copy number loss not provided [RCV000847363] Chr16:84608098..85087145 [GRCh37]
Chr16:16q24.1		 uncertain significance
GRCh37/hg19 16q24.1(chr16:84785377-84899548)x3 copy number gain not provided [RCV000847090] Chr16:84785377..84899548 [GRCh37]
Chr16:16q24.1		 uncertain significance
GRCh37/hg19 16q21-24.3(chr16:61524229-90155062)x3 copy number gain not provided [RCV001249359] Chr16:61524229..90155062 [GRCh37]
Chr16:16q21-24.3		 not provided
Single allele deletion Alveolar capillary dysplasia with pulmonary venous misalignment [RCV001251455] Chr16:83931797..86285776 [GRCh37]
Chr16:16q23.3-24.1		 likely pathogenic
GRCh37/hg19 16q23.3-24.1(chr16:83866931-85276940)x3 copy number gain not provided [RCV001258657] Chr16:83866931..85276940 [GRCh37]
Chr16:16q23.3-24.1		 uncertain significance
NM_005153.3(USP10):c.332G>T (p.Gly111Val) single nucleotide variant Inborn genetic diseases [RCV003252331] Chr16:84744813 [GRCh38]
Chr16:84778419 [GRCh37]
Chr16:16q24.1		 uncertain significance
GRCh37/hg19 16q23.2-24.3(chr16:80386595-90163348)x3 copy number gain not provided [RCV001795551] Chr16:80386595..90163348 [GRCh37]
Chr16:16q23.2-24.3		 pathogenic
GRCh37/hg19 16q23.3-24.1(chr16:84134463-85705611) copy number loss not specified [RCV002052556] Chr16:84134463..85705611 [GRCh37]
Chr16:16q23.3-24.1		 uncertain significance
GRCh37/hg19 16q24.1(chr16:84319435-85011988) copy number gain not specified [RCV002052558] Chr16:84319435..85011988 [GRCh37]
Chr16:16q24.1		 uncertain significance
GRCh37/hg19 16q11.2-24.3(chr16:46503968-90155062)x3 copy number gain not provided [RCV002221458] Chr16:46503968..90155062 [GRCh37]
Chr16:16q11.2-24.3		 pathogenic
GRCh37/hg19 16q22.2-24.3(chr16:71641395-90161959)x3 copy number gain Syndromic anorectal malformation [RCV002286607] Chr16:71641395..90161959 [GRCh37]
Chr16:16q22.2-24.3		 likely pathogenic
NM_005153.3(USP10):c.932A>C (p.Asp311Ala) single nucleotide variant Inborn genetic diseases [RCV002749556] Chr16:84745413 [GRCh38]
Chr16:84779019 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.1016C>G (p.Pro339Arg) single nucleotide variant Inborn genetic diseases [RCV002817557] Chr16:84745497 [GRCh38]
Chr16:84779103 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.63C>A (p.Phe21Leu) single nucleotide variant Inborn genetic diseases [RCV002902173] Chr16:84733476 [GRCh38]
Chr16:84767082 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.245C>T (p.Thr82Ile) single nucleotide variant Inborn genetic diseases [RCV002969120] Chr16:84744726 [GRCh38]
Chr16:84778332 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.307G>T (p.Gly103Cys) single nucleotide variant Inborn genetic diseases [RCV002777642] Chr16:84744788 [GRCh38]
Chr16:84778394 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.505G>C (p.Asp169His) single nucleotide variant Inborn genetic diseases [RCV002682587] Chr16:84744986 [GRCh38]
Chr16:84778592 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.446G>A (p.Arg149His) single nucleotide variant Inborn genetic diseases [RCV002976838] Chr16:84744927 [GRCh38]
Chr16:84778533 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.473G>A (p.Gly158Glu) single nucleotide variant Inborn genetic diseases [RCV002659991] Chr16:84744954 [GRCh38]
Chr16:84778560 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.7C>T (p.Leu3Phe) single nucleotide variant Inborn genetic diseases [RCV002888853] Chr16:84700097 [GRCh38]
Chr16:84733703 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.2062C>G (p.Arg688Gly) single nucleotide variant Inborn genetic diseases [RCV002799698] Chr16:84772604 [GRCh38]
Chr16:84806210 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.1252A>C (p.Ile418Leu) single nucleotide variant Inborn genetic diseases [RCV002845774] Chr16:84758775 [GRCh38]
Chr16:84792381 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.1529T>C (p.Val510Ala) single nucleotide variant Inborn genetic diseases [RCV002952070] Chr16:84760250 [GRCh38]
Chr16:84793856 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.200C>A (p.Pro67His) single nucleotide variant Inborn genetic diseases [RCV002767752] Chr16:84744681 [GRCh38]
Chr16:84778287 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.1851G>T (p.Gln617His) single nucleotide variant Inborn genetic diseases [RCV002830351] Chr16:84768211 [GRCh38]
Chr16:84801817 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.2234C>T (p.Ala745Val) single nucleotide variant Inborn genetic diseases [RCV002804109] Chr16:84778919 [GRCh38]
Chr16:84812525 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.677G>T (p.Ser226Ile) single nucleotide variant Inborn genetic diseases [RCV002916255] Chr16:84745158 [GRCh38]
Chr16:84778764 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.2188C>G (p.Arg730Gly) single nucleotide variant Inborn genetic diseases [RCV002664438] Chr16:84775204 [GRCh38]
Chr16:84808810 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.1895A>C (p.Gln632Pro) single nucleotide variant Inborn genetic diseases [RCV002788595] Chr16:84768255 [GRCh38]
Chr16:84801861 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.320A>G (p.Glu107Gly) single nucleotide variant Inborn genetic diseases [RCV002956444] Chr16:84744801 [GRCh38]
Chr16:84778407 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.1072G>C (p.Ala358Pro) single nucleotide variant Inborn genetic diseases [RCV002645187] Chr16:84745553 [GRCh38]
Chr16:84779159 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.565G>C (p.Val189Leu) single nucleotide variant Inborn genetic diseases [RCV002744149] Chr16:84745046 [GRCh38]
Chr16:84778652 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.176T>A (p.Phe59Tyr) single nucleotide variant Inborn genetic diseases [RCV002930092] Chr16:84744657 [GRCh38]
Chr16:84778263 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.701G>A (p.Ser234Asn) single nucleotide variant Inborn genetic diseases [RCV002699537] Chr16:84745182 [GRCh38]
Chr16:84778788 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.1400G>A (p.Arg467Gln) single nucleotide variant Inborn genetic diseases [RCV002718050] Chr16:84759896 [GRCh38]
Chr16:84793502 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.1480C>T (p.Arg494Cys) single nucleotide variant Inborn genetic diseases [RCV002674258] Chr16:84760201 [GRCh38]
Chr16:84793807 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.1477A>G (p.Ile493Val) single nucleotide variant Inborn genetic diseases [RCV002792223] Chr16:84760198 [GRCh38]
Chr16:84793804 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.1156C>A (p.Pro386Thr) single nucleotide variant Inborn genetic diseases [RCV002936983] Chr16:84745637 [GRCh38]
Chr16:84779243 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.314C>G (p.Thr105Ser) single nucleotide variant Inborn genetic diseases [RCV002921594] Chr16:84744795 [GRCh38]
Chr16:84778401 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.1555G>C (p.Gly519Arg) single nucleotide variant Inborn genetic diseases [RCV002855687] Chr16:84762989 [GRCh38]
Chr16:84796595 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.998C>G (p.Thr333Ser) single nucleotide variant Inborn genetic diseases [RCV002649163] Chr16:84745479 [GRCh38]
Chr16:84779085 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.2365C>A (p.Leu789Ile) single nucleotide variant Inborn genetic diseases [RCV002674358] Chr16:84779050 [GRCh38]
Chr16:84812656 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.71C>T (p.Thr24Ile) single nucleotide variant Inborn genetic diseases [RCV002966017] Chr16:84733484 [GRCh38]
Chr16:84767090 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.1909T>G (p.Ser637Ala) single nucleotide variant Inborn genetic diseases [RCV003218048] Chr16:84768269 [GRCh38]
Chr16:84801875 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.1646G>C (p.Ser549Thr) single nucleotide variant Inborn genetic diseases [RCV003192124] Chr16:84763080 [GRCh38]
Chr16:84796686 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.367G>A (p.Ala123Thr) single nucleotide variant Inborn genetic diseases [RCV003174761] Chr16:84744848 [GRCh38]
Chr16:84778454 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.388G>A (p.Val130Met) single nucleotide variant Inborn genetic diseases [RCV003183092] Chr16:84744869 [GRCh38]
Chr16:84778475 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.2192C>G (p.Thr731Ser) single nucleotide variant Inborn genetic diseases [RCV003309441] Chr16:84775208 [GRCh38]
Chr16:84808814 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.2005A>G (p.Ile669Val) single nucleotide variant Inborn genetic diseases [RCV003263697] Chr16:84772547 [GRCh38]
Chr16:84806153 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.1211C>T (p.Thr404Ile) single nucleotide variant Inborn genetic diseases [RCV003344617] Chr16:84758734 [GRCh38]
Chr16:84792340 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.614C>A (p.Thr205Lys) single nucleotide variant Inborn genetic diseases [RCV003373946] Chr16:84745095 [GRCh38]
Chr16:84778701 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.964C>A (p.Pro322Thr) single nucleotide variant Inborn genetic diseases [RCV003350615] Chr16:84745445 [GRCh38]
Chr16:84779051 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.1649A>G (p.Asn550Ser) single nucleotide variant Inborn genetic diseases [RCV003351091] Chr16:84763083 [GRCh38]
Chr16:84796689 [GRCh37]
Chr16:16q24.1		 uncertain significance
GRCh37/hg19 16q24.1-24.2(chr16:84555718-87910245)x1 copy number loss not provided [RCV003483302] Chr16:84555718..87910245 [GRCh37]
Chr16:16q24.1-24.2		 pathogenic
GRCh37/hg19 16q24.1(chr16:84613250-84998752)x3 copy number gain not provided [RCV003485130] Chr16:84613250..84998752 [GRCh37]
Chr16:16q24.1		 uncertain significance
NM_005153.3(USP10):c.820G>A (p.Val274Ile) single nucleotide variant Inborn genetic diseases [RCV003364194] Chr16:84745301 [GRCh38]
Chr16:84778907 [GRCh37]
Chr16:16q24.1		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4190
Count of miRNA genes:1211
Interacting mature miRNAs:1519
Transcripts:ENST00000219473, ENST00000540269, ENST00000562092, ENST00000562283, ENST00000562743, ENST00000563023, ENST00000563048, ENST00000563386, ENST00000563433, ENST00000563892, ENST00000564566, ENST00000566378, ENST00000566512, ENST00000567526, ENST00000569038, ENST00000569511, ENST00000569925, ENST00000570053, ENST00000570191
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
RH79887  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371684,812,682 - 84,812,876UniSTSGRCh37
Build 361683,370,183 - 83,370,377RGDNCBI36
Celera1669,114,949 - 69,115,143RGD
Cytogenetic Map16q24.1UniSTS
HuRef1670,565,559 - 70,565,753UniSTS
USP10_1613  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371684,812,537 - 84,813,321UniSTSGRCh37
Build 361683,370,038 - 83,370,822RGDNCBI36
Celera1669,114,804 - 69,115,588RGD
HuRef1670,565,414 - 70,566,198UniSTS
HSC0DD052  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371684,813,302 - 84,813,501UniSTSGRCh37
Build 361683,370,803 - 83,371,002RGDNCBI36
Celera1669,115,569 - 69,115,768RGD
Cytogenetic Map16q24.1UniSTS
HuRef1670,566,179 - 70,566,378UniSTS
A008M09  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371684,812,034 - 84,812,154UniSTSGRCh37
Build 361683,369,535 - 83,369,655RGDNCBI36
Celera1669,114,301 - 69,114,421RGD
Cytogenetic Map16q24.1UniSTS
HuRef1670,564,911 - 70,565,031UniSTS
GeneMap99-GB4 RH Map15184.77UniSTS
D1S1423  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map10p12.1-p11.2UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map6p22.3-p21.32UniSTS
Cytogenetic Map6q22.33UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map7q11.2UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map9q12UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map18q22.1UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map10p14-p13UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map11q23-q24UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map22cen-q12.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map4q28UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map1q41-q42UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map11q24.1UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3q13UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q26UniSTS
Cytogenetic Map9p21.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic MapXq27.2UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map4q31UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map20q11.21-q11.23UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map4q31.23UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map13q33.3UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map4p15.31UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map4q24UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map10pter-q25.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map11q13.1-q13.3UniSTS
Cytogenetic Map16p13UniSTS
Cytogenetic Map15q26UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map4p15.1-p14UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map7q32.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map9p13UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map3q21-q24UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map8q24.12UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map6q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map20pter-p12UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map14q22.2UniSTS
Cytogenetic Map20p11.22-p11.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map6p22-p21UniSTS
Cytogenetic Map17q21.1-q21.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12p13.2-p12.3UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map5q22.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map4p15.3UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map10q22.3-q23.2UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map2p13.2UniSTS
Cytogenetic Map3p12.3UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map3q11.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map6p24.2UniSTS
Cytogenetic Map20q13.33UniSTS
RH91711  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map16q24.1UniSTS
GeneMap99-GB4 RH Map16470.68UniSTS
Cda0dd05  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map16q24.1UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 2416 2640 1626 533 1882 375 4357 2015 3159 387 1453 1610 174 1 1202 2788 6 2
Low 23 351 100 91 69 90 182 575 32 7 3 1 2
Below cutoff

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001272075 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_005153 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_073577 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_073578 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006721332 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011523443 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017023863 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017023864 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017023865 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017023866 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017023867 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017023868 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017023869 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047434876 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047434877 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047434878 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054314331 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054314332 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054314333 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054314334 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054314335 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054314336 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC009116 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC025280 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK055375 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK293304 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299618 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK315570 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL162049 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC000263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC064516 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX537402 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471114 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068262 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR749515 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D80012 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB077919 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GD151792 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HI179098 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MN927130 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000219473   ⟹   ENSP00000219473
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1684,700,000 - 84,779,922 (+)Ensembl
RefSeq Acc Id: ENST00000540269   ⟹   ENSP00000445589
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1684,699,995 - 84,779,922 (+)Ensembl
RefSeq Acc Id: ENST00000562092
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1684,699,995 - 84,740,312 (+)Ensembl
RefSeq Acc Id: ENST00000562283   ⟹   ENSP00000455712
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1684,700,004 - 84,744,923 (+)Ensembl
RefSeq Acc Id: ENST00000562743
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1684,699,986 - 84,745,211 (+)Ensembl
RefSeq Acc Id: ENST00000563023
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1684,733,209 - 84,744,911 (+)Ensembl
RefSeq Acc Id: ENST00000563048   ⟹   ENSP00000454902
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1684,700,004 - 84,779,015 (+)Ensembl
RefSeq Acc Id: ENST00000563386   ⟹   ENSP00000454943
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1684,700,008 - 84,744,866 (+)Ensembl
RefSeq Acc Id: ENST00000563433
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1684,759,278 - 84,764,170 (+)Ensembl
RefSeq Acc Id: ENST00000563892   ⟹   ENSP00000458089
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1684,699,995 - 84,760,236 (+)Ensembl
RefSeq Acc Id: ENST00000564566
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1684,700,002 - 84,709,322 (+)Ensembl
RefSeq Acc Id: ENST00000566378
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1684,759,836 - 84,763,013 (+)Ensembl
RefSeq Acc Id: ENST00000566512
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1684,733,138 - 84,744,780 (+)Ensembl
RefSeq Acc Id: ENST00000567526   ⟹   ENSP00000455865
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1684,768,267 - 84,778,987 (+)Ensembl
RefSeq Acc Id: ENST00000569038   ⟹   ENSP00000462762
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1684,700,029 - 84,768,270 (+)Ensembl
RefSeq Acc Id: ENST00000569511
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1684,699,995 - 84,733,061 (+)Ensembl
RefSeq Acc Id: ENST00000569925   ⟹   ENSP00000454987
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1684,768,265 - 84,779,306 (+)Ensembl
RefSeq Acc Id: ENST00000570053   ⟹   ENSP00000454751
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1684,700,040 - 84,768,275 (+)Ensembl
RefSeq Acc Id: ENST00000570191   ⟹   ENSP00000457411
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1684,700,004 - 84,779,194 (+)Ensembl
RefSeq Acc Id: NM_001272075   ⟹   NP_001259004
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381684,700,000 - 84,779,922 (+)NCBI
HuRef1670,486,450 - 70,566,405 (+)NCBI
CHM1_11686,145,099 - 86,225,097 (+)NCBI
T2T-CHM13v2.01690,766,262 - 90,846,179 (+)NCBI
Sequence:
RefSeq Acc Id: NM_005153   ⟹   NP_005144
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381684,700,000 - 84,779,922 (+)NCBI
GRCh371684,733,555 - 84,813,528 (+)ENTREZGENE
GRCh371684,733,555 - 84,813,528 (+)NCBI
Build 361683,291,056 - 83,371,029 (+)NCBI Archive
HuRef1670,486,450 - 70,566,405 (+)ENTREZGENE
CHM1_11686,145,099 - 86,225,097 (+)NCBI
T2T-CHM13v2.01690,766,262 - 90,846,179 (+)NCBI
Sequence:
RefSeq Acc Id: NR_073577
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381684,700,000 - 84,779,922 (+)NCBI
GRCh371684,733,555 - 84,813,528 (+)NCBI
HuRef1670,486,450 - 70,566,405 (+)NCBI
CHM1_11686,145,099 - 86,225,097 (+)NCBI
T2T-CHM13v2.01690,766,262 - 90,846,179 (+)NCBI
Sequence:
RefSeq Acc Id: NR_073578
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381684,700,000 - 84,779,922 (+)NCBI
GRCh371684,733,555 - 84,813,528 (+)NCBI
HuRef1670,486,450 - 70,566,405 (+)NCBI
CHM1_11686,145,099 - 86,225,097 (+)NCBI
T2T-CHM13v2.01690,766,262 - 90,846,179 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006721332   ⟹   XP_006721395
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381684,700,000 - 84,779,922 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011523443   ⟹   XP_011521745
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381684,700,000 - 84,779,922 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017023868   ⟹   XP_016879357
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381684,700,000 - 84,779,922 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047434876   ⟹   XP_047290832
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381684,700,000 - 84,779,922 (+)NCBI
RefSeq Acc Id: XM_047434877   ⟹   XP_047290833
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381684,700,000 - 84,779,922 (+)NCBI
RefSeq Acc Id: XM_047434878   ⟹   XP_047290834
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381684,700,000 - 84,779,922 (+)NCBI
RefSeq Acc Id: XM_054314331   ⟹   XP_054170306
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01690,766,262 - 90,846,179 (+)NCBI
RefSeq Acc Id: XM_054314332   ⟹   XP_054170307
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01690,766,262 - 90,846,179 (+)NCBI
RefSeq Acc Id: XM_054314333   ⟹   XP_054170308
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01690,766,262 - 90,846,179 (+)NCBI
RefSeq Acc Id: XM_054314334   ⟹   XP_054170309
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01690,766,262 - 90,846,179 (+)NCBI
RefSeq Acc Id: XM_054314335   ⟹   XP_054170310
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01690,766,262 - 90,846,179 (+)NCBI
RefSeq Acc Id: XM_054314336   ⟹   XP_054170311
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01690,766,262 - 90,846,179 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001259004 (Get FASTA)   NCBI Sequence Viewer  
  NP_005144 (Get FASTA)   NCBI Sequence Viewer  
  XP_006721395 (Get FASTA)   NCBI Sequence Viewer  
  XP_011521745 (Get FASTA)   NCBI Sequence Viewer  
  XP_016879357 (Get FASTA)   NCBI Sequence Viewer  
  XP_047290832 (Get FASTA)   NCBI Sequence Viewer  
  XP_047290833 (Get FASTA)   NCBI Sequence Viewer  
  XP_047290834 (Get FASTA)   NCBI Sequence Viewer  
  XP_054170306 (Get FASTA)   NCBI Sequence Viewer  
  XP_054170307 (Get FASTA)   NCBI Sequence Viewer  
  XP_054170308 (Get FASTA)   NCBI Sequence Viewer  
  XP_054170309 (Get FASTA)   NCBI Sequence Viewer  
  XP_054170310 (Get FASTA)   NCBI Sequence Viewer  
  XP_054170311 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH00263 (Get FASTA)   NCBI Sequence Viewer  
  AAH64516 (Get FASTA)   NCBI Sequence Viewer  
  BAA11507 (Get FASTA)   NCBI Sequence Viewer  
  BAG37945 (Get FASTA)   NCBI Sequence Viewer  
  BAG56825 (Get FASTA)   NCBI Sequence Viewer  
  BAG61546 (Get FASTA)   NCBI Sequence Viewer  
  CAB82392 (Get FASTA)   NCBI Sequence Viewer  
  CAD97644 (Get FASTA)   NCBI Sequence Viewer  
  CAH18330 (Get FASTA)   NCBI Sequence Viewer  
  CBX53857 (Get FASTA)   NCBI Sequence Viewer  
  EAW95470 (Get FASTA)   NCBI Sequence Viewer  
  EAW95471 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000219473
  ENSP00000219473.7
  ENSP00000445589.2
  ENSP00000454751.1
  ENSP00000454902.1
  ENSP00000454943.1
  ENSP00000454987.1
  ENSP00000455712.1
  ENSP00000455865.1
  ENSP00000457411
  ENSP00000457411.1
  ENSP00000458089.1
  ENSP00000462762.1
GenBank Protein Q14694 (Get FASTA)   NCBI Sequence Viewer  
  QNC49803 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_005144   ⟸   NM_005153
- Peptide Label: isoform 2
- UniProtKB: Q9BWG7 (UniProtKB/Swiss-Prot),   B4DS84 (UniProtKB/Swiss-Prot),   B2RDJ8 (UniProtKB/Swiss-Prot),   Q9NSL7 (UniProtKB/Swiss-Prot),   Q14694 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001259004   ⟸   NM_001272075
- Peptide Label: isoform 1
- UniProtKB: A0A7G6J4N4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006721395   ⟸   XM_006721332
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_011521745   ⟸   XM_011523443
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_016879357   ⟸   XM_017023868
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: ENSP00000454987   ⟸   ENST00000569925
RefSeq Acc Id: ENSP00000457411   ⟸   ENST00000570191
RefSeq Acc Id: ENSP00000454751   ⟸   ENST00000570053
RefSeq Acc Id: ENSP00000219473   ⟸   ENST00000219473
RefSeq Acc Id: ENSP00000455712   ⟸   ENST00000562283
RefSeq Acc Id: ENSP00000454902   ⟸   ENST00000563048
RefSeq Acc Id: ENSP00000454943   ⟸   ENST00000563386
RefSeq Acc Id: ENSP00000458089   ⟸   ENST00000563892
RefSeq Acc Id: ENSP00000455865   ⟸   ENST00000567526
RefSeq Acc Id: ENSP00000445589   ⟸   ENST00000540269
RefSeq Acc Id: ENSP00000462762   ⟸   ENST00000569038
RefSeq Acc Id: XP_047290833   ⟸   XM_047434877
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047290834   ⟸   XM_047434878
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047290832   ⟸   XM_047434876
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054170308   ⟸   XM_054314333
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054170309   ⟸   XM_054314334
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054170310   ⟸   XM_054314335
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054170311   ⟸   XM_054314336
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054170307   ⟸   XM_054314332
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054170306   ⟸   XM_054314331
- Peptide Label: isoform X1
Protein Domains
Ataxin-2 C-terminal   Peptidase C19 ubiquitin carboxyl-terminal hydrolase   USP

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q14694-F1-model_v2 AlphaFold Q14694 1-798 view protein structure

Promoters
RGD ID:6793587
Promoter ID:HG_KWN:24385
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000219473,   UC002FIJ.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361683,290,656 - 83,291,207 (+)MPROMDB
RGD ID:7233033
Promoter ID:EPDNEW_H22261
Type:initiation region
Name:USP10_1
Description:ubiquitin specific peptidase 10
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381684,700,004 - 84,700,064EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:12608 AgrOrtholog
COSMIC USP10 COSMIC
Ensembl Genes ENSG00000103194 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000219473 ENTREZGENE
  ENST00000219473.12 UniProtKB/Swiss-Prot
  ENST00000540269 ENTREZGENE
  ENST00000540269.6 UniProtKB/TrEMBL
  ENST00000562283.5 UniProtKB/TrEMBL
  ENST00000563048.5 UniProtKB/TrEMBL
  ENST00000563386.5 UniProtKB/TrEMBL
  ENST00000563892.5 UniProtKB/TrEMBL
  ENST00000567526.1 UniProtKB/TrEMBL
  ENST00000569038.5 UniProtKB/TrEMBL
  ENST00000569925.1 UniProtKB/TrEMBL
  ENST00000570053.1 UniProtKB/TrEMBL
  ENST00000570191 ENTREZGENE
  ENST00000570191.5 UniProtKB/Swiss-Prot
Gene3D-CATH Cysteine proteinases UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000103194 GTEx
HGNC ID HGNC:12608 ENTREZGENE
Human Proteome Map USP10 Human Proteome Map
InterPro Ataxin-2_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Papain-like_cys_pep_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Peptidase_C19_UCH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  USP_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  USP_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:9100 UniProtKB/Swiss-Prot
NCBI Gene 9100 ENTREZGENE
OMIM 609818 OMIM
PANTHER INACTIVE UBIQUITIN CARBOXYL-TERMINAL HYDROLASE 50 UniProtKB/TrEMBL
  PROTEIN GVQW1-RELATED UniProtKB/TrEMBL
  SECRETED PROTEIN UniProtKB/TrEMBL
  UBIQUITIN CARBOXYL-TERMINAL HYDROLASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  UBIQUITIN CARBOXYL-TERMINAL HYDROLASE UniProtKB/TrEMBL
  UBIQUITIN CARBOXYL-TERMINAL HYDROLASE 10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam PAM2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  UCH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA37234 PharmGKB
PROSITE USP_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  USP_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  USP_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF54001 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A7G6J4N4 ENTREZGENE, UniProtKB/TrEMBL
  B2RDJ8 ENTREZGENE
  B4DS84 ENTREZGENE
  H3BNA1_HUMAN UniProtKB/TrEMBL
  H3BNL0_HUMAN UniProtKB/TrEMBL
  H3BNP1_HUMAN UniProtKB/TrEMBL
  H3BNS8_HUMAN UniProtKB/TrEMBL
  H3BQC6_HUMAN UniProtKB/TrEMBL
  H3BQP1_HUMAN UniProtKB/TrEMBL
  H3BVF1_HUMAN UniProtKB/TrEMBL
  J3KT19_HUMAN UniProtKB/TrEMBL
  Q14694 ENTREZGENE
  Q68D90_HUMAN UniProtKB/TrEMBL
  Q6P2I0_HUMAN UniProtKB/TrEMBL
  Q9BWG7 ENTREZGENE
  Q9NSL7 ENTREZGENE
  UBP10_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary B2RDJ8 UniProtKB/Swiss-Prot
  B4DS84 UniProtKB/Swiss-Prot
  Q9BWG7 UniProtKB/Swiss-Prot
  Q9NSL7 UniProtKB/Swiss-Prot