USP4 (ubiquitin specific peptidase 4) - Rat Genome Database

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Gene: USP4 (ubiquitin specific peptidase 4) Homo sapiens
Analyze
Symbol: USP4
Name: ubiquitin specific peptidase 4
RGD ID: 1344173
HGNC Page HGNC:12627
Description: Enables adenosine receptor binding activity; cysteine-type deubiquitinase activity; and identical protein binding activity. Involved in several processes, including positive regulation of TORC1 signaling; protein localization to cell surface; and spliceosomal tri-snRNP complex assembly. Located in cytosol; nucleus; and plasma membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: deubiquitinating enzyme 4; LOC107986084; MGC149848; MGC149849; Sjoegren syndrome nuclear autoantigen 1 homolog; ubiquitin carboxyl-terminal esterase 4; ubiquitin carboxyl-terminal hydrolase 4; ubiquitin specific peptidase 4 (proto-oncogene); ubiquitin specific protease 4 (proto-oncogene); ubiquitin thioesterase 4; ubiquitin thiolesterase 4; ubiquitin-specific processing protease 4; ubiquitin-specific-processing protease 4; ubiquitous nuclear protein homolog; UNP; Unph
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Related Pseudogenes: LOC100421737  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38349,277,144 - 49,340,053 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl349,277,144 - 49,340,712 (-)EnsemblGRCh38hg38GRCh38
GRCh37349,314,577 - 49,377,486 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36349,289,997 - 49,352,519 (-)NCBINCBI36Build 36hg18NCBI36
Build 34349,289,997 - 49,352,519NCBI
Celera349,278,021 - 49,342,350 (-)NCBICelera
Cytogenetic Map3p21.31NCBI
HuRef349,371,896 - 49,436,532 (-)NCBIHuRef
CHM1_1349,267,379 - 49,330,367 (-)NCBICHM1_1
T2T-CHM13v2.0349,305,224 - 49,369,431 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
cytoplasm  (IDA,IEA)
cytosol  (IDA,TAS)
lysosome  (TAS)
nucleus  (IBA,IDA,IEA)
plasma membrane  (IDA)

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:7784062   PMID:8125298   PMID:8183569   PMID:9464533   PMID:9827704   PMID:11461834   PMID:11571651   PMID:11571652   PMID:12477932   PMID:12838346   PMID:15489334   PMID:16169070  
PMID:16196087   PMID:16316627   PMID:16339847   PMID:16344560   PMID:16403452   PMID:16472766   PMID:18728397   PMID:19367581   PMID:19615732   PMID:20141612   PMID:20307617   PMID:20595234  
PMID:21145461   PMID:21331078   PMID:21522127   PMID:21873635   PMID:21900206   PMID:21931648   PMID:22001210   PMID:22029577   PMID:22118674   PMID:22195557   PMID:22262844   PMID:22347420  
PMID:22626734   PMID:22706160   PMID:23022198   PMID:23105109   PMID:23128233   PMID:23313255   PMID:23388719   PMID:24270891   PMID:24412244   PMID:24798342   PMID:25082827   PMID:25404403  
PMID:25821221   PMID:25921289   PMID:26186194   PMID:26189775   PMID:26387952   PMID:26411366   PMID:26455393   PMID:26669864   PMID:26883469   PMID:27060135   PMID:27128386   PMID:27990632  
PMID:28088760   PMID:28298427   PMID:28468752   PMID:28477415   PMID:28514442   PMID:28604766   PMID:28700943   PMID:28791349   PMID:28946564   PMID:29299163   PMID:29396555   PMID:29507755  
PMID:29542252   PMID:29573006   PMID:29576527   PMID:29667299   PMID:30071870   PMID:30150323   PMID:30194441   PMID:30258100   PMID:30323974   PMID:30335615   PMID:30362572   PMID:30410068  
PMID:30514904   PMID:30862715   PMID:31091453   PMID:31219614   PMID:31330151   PMID:31586073   PMID:31748695   PMID:32235678   PMID:32308208   PMID:32410369   PMID:32549341   PMID:33038351  
PMID:33141564   PMID:33378683   PMID:33499712   PMID:33567341   PMID:33669244   PMID:33961781   PMID:34603025   PMID:34642328   PMID:34709727   PMID:34857952   PMID:35064336   PMID:35774799  
PMID:35831314   PMID:35841383   PMID:36215168   PMID:36336860   PMID:36543142   PMID:36629882   PMID:37039823   PMID:37167062   PMID:37308746   PMID:37949874   PMID:38134227   PMID:38310689  
PMID:38556105   PMID:38803224   PMID:39266638   PMID:39393052  


Genomics

Comparative Map Data
USP4
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38349,277,144 - 49,340,053 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl349,277,144 - 49,340,712 (-)EnsemblGRCh38hg38GRCh38
GRCh37349,314,577 - 49,377,486 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36349,289,997 - 49,352,519 (-)NCBINCBI36Build 36hg18NCBI36
Build 34349,289,997 - 49,352,519NCBI
Celera349,278,021 - 49,342,350 (-)NCBICelera
Cytogenetic Map3p21.31NCBI
HuRef349,371,896 - 49,436,532 (-)NCBIHuRef
CHM1_1349,267,379 - 49,330,367 (-)NCBICHM1_1
T2T-CHM13v2.0349,305,224 - 49,369,431 (-)NCBIT2T-CHM13v2.0
Usp4
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm399108,223,763 - 108,269,744 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl9108,225,052 - 108,269,744 (+)EnsemblGRCm39 Ensembl
GRCm389108,346,564 - 108,392,545 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl9108,347,853 - 108,392,545 (+)EnsemblGRCm38mm10GRCm38
MGSCv379108,250,162 - 108,294,860 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv369108,205,963 - 108,250,621 (+)NCBIMGSCv36mm8
Celera9107,957,048 - 108,001,736 (+)NCBICelera
Cytogenetic Map9F2NCBI
cM Map959.25NCBI
Usp4
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr88117,912,576 - 117,957,934 (+)NCBIGRCr8
mRatBN7.28109,035,402 - 109,079,382 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl8109,036,099 - 109,080,427 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx8114,663,178 - 114,706,678 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.08112,862,508 - 112,906,009 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.08110,705,153 - 110,748,655 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.08117,126,692 - 117,171,012 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl8117,126,692 - 117,171,012 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.08116,474,812 - 116,519,375 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Celera8108,338,833 - 108,383,118 (+)NCBICelera
Cytogenetic Map8q32NCBI
Usp4
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555321,247,110 - 1,285,121 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049555321,247,110 - 1,284,564 (-)NCBIChiLan1.0ChiLan1.0
LOC100967331
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2249,253,962 - 49,320,547 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1349,258,730 - 49,325,329 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0349,199,328 - 49,263,861 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1350,279,642 - 50,343,901 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl350,279,642 - 50,343,903 (-)Ensemblpanpan1.1panPan2
USP4
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12039,899,880 - 39,952,959 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2039,899,897 - 39,952,420 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2039,818,226 - 39,871,287 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02040,256,219 - 40,309,777 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2040,256,236 - 40,309,829 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12039,623,674 - 39,676,723 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02040,027,139 - 40,080,595 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02040,306,950 - 40,360,016 (+)NCBIUU_Cfam_GSD_1.0
Usp4
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440560264,180,540 - 64,229,266 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936529938,501 - 989,884 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936529941,042 - 989,781 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
USP4
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1331,848,851 - 31,904,243 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11331,844,780 - 31,904,418 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21335,075,799 - 35,135,425 (-)NCBISscrofa10.2Sscrofa10.2susScr3
USP4
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12210,672,920 - 10,735,374 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2210,672,388 - 10,732,104 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666041156,278,755 - 156,354,831 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Usp4
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247303,253,407 - 3,306,341 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247303,252,980 - 3,306,439 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in USP4
69 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 3p21.31-21.2(chr3:45879883-50749922)x4 copy number gain See cases [RCV000133650] Chr3:45879883..50749922 [GRCh38]
Chr3:45921375..50787353 [GRCh37]
Chr3:45896379..50762357 [NCBI36]
Chr3:3p21.31-21.2		 pathogenic
GRCh38/hg38 3p21.31(chr3:49171381-49474635)x3 copy number gain See cases [RCV000143511] Chr3:49171381..49474635 [GRCh38]
Chr3:49208814..49512068 [GRCh37]
Chr3:49183818..49487072 [NCBI36]
Chr3:3p21.31		 uncertain significance
GRCh37/hg19 3p22.2-21.31(chr3:37028313-49929220)x3 copy number gain See cases [RCV000240519] Chr3:37028313..49929220 [GRCh37]
Chr3:3p22.2-21.31		 likely pathogenic
NM_003363.4(USP4):c.212A>C (p.Asn71Thr) single nucleotide variant not specified [RCV004308217] Chr3:49335486 [GRCh38]
Chr3:49372919 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2627C>A (p.Ala876Asp) single nucleotide variant not specified [RCV004313219] Chr3:49280761 [GRCh38]
Chr3:49318194 [GRCh37]
Chr3:3p21.31		 uncertain significance
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3 copy number gain See cases [RCV000511055] Chr3:61892..197851986 [GRCh37]
Chr3:3p26.3-q29		 pathogenic
NM_003363.4(USP4):c.2479C>T (p.Arg827Cys) single nucleotide variant not specified [RCV004321858] Chr3:49284048 [GRCh38]
Chr3:49321481 [GRCh37]
Chr3:3p21.31		 uncertain significance
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986) copy number gain See cases [RCV000512358] Chr3:61892..197851986 [GRCh37]
Chr3:3p26.3-q29		 pathogenic
NM_003363.4(USP4):c.1724C>T (p.Ser575Leu) single nucleotide variant not specified [RCV004290436] Chr3:49294566 [GRCh38]
Chr3:49331999 [GRCh37]
Chr3:3p21.31		 uncertain significance
GRCh37/hg19 3p26.3-q29(chr3:61495-197838262)x3 copy number gain not provided [RCV000742138] Chr3:61495..197838262 [GRCh37]
Chr3:3p26.3-q29		 pathogenic
GRCh37/hg19 3p26.3-q29(chr3:60174-197948027)x3 copy number gain not provided [RCV000742133] Chr3:60174..197948027 [GRCh37]
Chr3:3p26.3-q29		 pathogenic
NM_003363.4(USP4):c.469A>T (p.Ser157Cys) single nucleotide variant not specified [RCV004315093] Chr3:49325737 [GRCh38]
Chr3:49363170 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2523C>T (p.Val841=) single nucleotide variant not provided [RCV000900866] Chr3:49284004 [GRCh38]
Chr3:49321437 [GRCh37]
Chr3:3p21.31		 likely benign
NM_003363.4(USP4):c.1859A>G (p.Tyr620Cys) single nucleotide variant not provided [RCV000881114] Chr3:49294431 [GRCh38]
Chr3:49331864 [GRCh37]
Chr3:3p21.31		 benign
NM_003363.4(USP4):c.5C>T (p.Ala2Val) single nucleotide variant not specified [RCV004310978] Chr3:49340020 [GRCh38]
Chr3:49377453 [GRCh37]
Chr3:3p21.31		 uncertain significance
GRCh37/hg19 3p21.31-21.1(chr3:45153770-53878616) copy number gain not provided [RCV000767704] Chr3:45153770..53878616 [GRCh37]
Chr3:3p21.31-21.1		 pathogenic
NM_003363.4(USP4):c.351C>T (p.Ile117=) single nucleotide variant not provided [RCV000922551] Chr3:49327695 [GRCh38]
Chr3:49365128 [GRCh37]
Chr3:3p21.31		 likely benign
NM_003363.4(USP4):c.1889A>G (p.Tyr630Cys) single nucleotide variant not provided [RCV000895986] Chr3:49292593 [GRCh38]
Chr3:49330026 [GRCh37]
Chr3:3p21.31		 likely benign
NM_003363.4(USP4):c.1773A>T (p.Pro591=) single nucleotide variant not provided [RCV000885581] Chr3:49294517 [GRCh38]
Chr3:49331950 [GRCh37]
Chr3:3p21.31		 likely benign
GRCh37/hg19 3p21.31(chr3:48346677-49630228)x1 copy number loss not provided [RCV001005432] Chr3:48346677..49630228 [GRCh37]
Chr3:3p21.31		 pathogenic
NM_003363.4(USP4):c.2536A>G (p.Ile846Val) single nucleotide variant not provided [RCV000953197] Chr3:49283991 [GRCh38]
Chr3:49321424 [GRCh37]
Chr3:3p21.31		 benign
NM_003363.4(USP4):c.2565C>T (p.Val855=) single nucleotide variant not provided [RCV000912004] Chr3:49280823 [GRCh38]
Chr3:49318256 [GRCh37]
Chr3:3p21.31		 likely benign
NC_000003.12:g.(?_49121216)_(49533209_?)del deletion Pierson syndrome [RCV001384888] Chr3:49158649..49570642 [GRCh37]
Chr3:3p21.31		 pathogenic
GRCh37/hg19 3p21.31-21.2(chr3:48807193-51363558)x1 copy number loss not provided [RCV001259686] Chr3:48807193..51363558 [GRCh37]
Chr3:3p21.31-21.2		 pathogenic
NC_000003.11:g.(?_48507870)_(50340407_?)del deletion Aicardi-Goutieres syndrome 1 [RCV001380369] Chr3:48507870..50340407 [GRCh37]
Chr3:3p21.31		 pathogenic
GRCh37/hg19 3p21.31(chr3:49060512-49678685) copy number gain not specified [RCV002053349] Chr3:49060512..49678685 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.1052T>G (p.Ile351Ser) single nucleotide variant not specified [RCV004328480] Chr3:49305791 [GRCh38]
Chr3:49343224 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.834G>C (p.Arg278Ser) single nucleotide variant not specified [RCV004107409] Chr3:49311516 [GRCh38]
Chr3:49348949 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.22C>T (p.Arg8Cys) single nucleotide variant not specified [RCV004198501] Chr3:49340003 [GRCh38]
Chr3:49377436 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.1558G>A (p.Glu520Lys) single nucleotide variant not specified [RCV004219373] Chr3:49298590 [GRCh38]
Chr3:49336023 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.1537G>A (p.Gly513Arg) single nucleotide variant not specified [RCV004177403] Chr3:49298611 [GRCh38]
Chr3:49336044 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.1064A>G (p.Tyr355Cys) single nucleotide variant not specified [RCV004174396] Chr3:49305779 [GRCh38]
Chr3:49343212 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.1517G>A (p.Arg506His) single nucleotide variant not specified [RCV004130168] Chr3:49298631 [GRCh38]
Chr3:49336064 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.44C>G (p.Thr15Ser) single nucleotide variant not specified [RCV004117561] Chr3:49339981 [GRCh38]
Chr3:49377414 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2602A>G (p.Ile868Val) single nucleotide variant not specified [RCV004128111] Chr3:49280786 [GRCh38]
Chr3:49318219 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2073G>T (p.Glu691Asp) single nucleotide variant not specified [RCV004082765] Chr3:49286225 [GRCh38]
Chr3:49323658 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2524G>A (p.Val842Ile) single nucleotide variant not specified [RCV004087679] Chr3:49284003 [GRCh38]
Chr3:49321436 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2775T>G (p.Asp925Glu) single nucleotide variant not specified [RCV004161309] Chr3:49278410 [GRCh38]
Chr3:49315843 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.863A>G (p.Asn288Ser) single nucleotide variant not specified [RCV004092886] Chr3:49310711 [GRCh38]
Chr3:49348144 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.299C>T (p.Ala100Val) single nucleotide variant not specified [RCV004184728] Chr3:49327747 [GRCh38]
Chr3:49365180 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.1231C>T (p.Arg411Trp) single nucleotide variant not specified [RCV004158473] Chr3:49302440 [GRCh38]
Chr3:49339873 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2704G>A (p.Val902Met) single nucleotide variant not specified [RCV004205483] Chr3:49278843 [GRCh38]
Chr3:49316276 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.1217A>G (p.His406Arg) single nucleotide variant not specified [RCV004102046] Chr3:49302454 [GRCh38]
Chr3:49339887 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.400G>A (p.Glu134Lys) single nucleotide variant not specified [RCV004077675] Chr3:49325806 [GRCh38]
Chr3:49363239 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2359A>G (p.Thr787Ala) single nucleotide variant not specified [RCV004211314] Chr3:49284497 [GRCh38]
Chr3:49321930 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.530C>T (p.Ala177Val) single nucleotide variant not specified [RCV004084765] Chr3:49324997 [GRCh38]
Chr3:49362430 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.755A>G (p.Tyr252Cys) single nucleotide variant not specified [RCV004280653] Chr3:49311595 [GRCh38]
Chr3:49349028 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.1147G>A (p.Ala383Thr) single nucleotide variant not specified [RCV004275297] Chr3:49302524 [GRCh38]
Chr3:49339957 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.70A>G (p.Met24Val) single nucleotide variant not specified [RCV004270040] Chr3:49339955 [GRCh38]
Chr3:49377388 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.1877G>C (p.Arg626Pro) single nucleotide variant not specified [RCV004248853] Chr3:49294413 [GRCh38]
Chr3:49331846 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2240G>A (p.Arg747Gln) single nucleotide variant not specified [RCV004256308] Chr3:49284880 [GRCh38]
Chr3:49322313 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2291G>C (p.Ser764Thr) single nucleotide variant not specified [RCV004255158] Chr3:49284565 [GRCh38]
Chr3:49321998 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2759A>G (p.Tyr920Cys) single nucleotide variant not specified [RCV004356054] Chr3:49278426 [GRCh38]
Chr3:49315859 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.1074C>A (p.Leu358=) single nucleotide variant not provided [RCV003433591] Chr3:49305769 [GRCh38]
Chr3:49343202 [GRCh37]
Chr3:3p21.31		 likely benign
NM_003363.4(USP4):c.173A>G (p.Asn58Ser) single nucleotide variant not specified [RCV004477415] Chr3:49335525 [GRCh38]
Chr3:49372958 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.1549G>A (p.Asp517Asn) single nucleotide variant not specified [RCV004477414] Chr3:49298599 [GRCh38]
Chr3:49336032 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2069G>A (p.Ser690Asn) single nucleotide variant not specified [RCV004477418] Chr3:49286229 [GRCh38]
Chr3:49323662 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2381A>G (p.His794Arg) single nucleotide variant not specified [RCV004477421] Chr3:49284475 [GRCh38]
Chr3:49321908 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.313C>A (p.Leu105Ile) single nucleotide variant not specified [RCV004477424] Chr3:49327733 [GRCh38]
Chr3:49365166 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.464A>G (p.His155Arg) single nucleotide variant not specified [RCV004477425] Chr3:49325742 [GRCh38]
Chr3:49363175 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.44C>T (p.Thr15Ile) single nucleotide variant not specified [RCV004688553] Chr3:49339981 [GRCh38]
Chr3:49377414 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.1984G>A (p.Glu662Lys) single nucleotide variant not specified [RCV004477416] Chr3:49286314 [GRCh38]
Chr3:49323747 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.1999C>G (p.Gln667Glu) single nucleotide variant not specified [RCV004477417] Chr3:49286299 [GRCh38]
Chr3:49323732 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2171C>G (p.Ala724Gly) single nucleotide variant not specified [RCV004477419] Chr3:49286127 [GRCh38]
Chr3:49323560 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2176G>A (p.Asp726Asn) single nucleotide variant not specified [RCV004477420] Chr3:49286122 [GRCh38]
Chr3:49323555 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2470C>T (p.His824Tyr) single nucleotide variant not specified [RCV004477422] Chr3:49284057 [GRCh38]
Chr3:49321490 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.69A>C (p.Leu23Phe) single nucleotide variant not specified [RCV004477426] Chr3:49339956 [GRCh38]
Chr3:49377389 [GRCh37]
Chr3:3p21.31		 uncertain significance
NC_000003.11:g.(?_48895920)_(49570632_?)del deletion Autosomal recessive limb-girdle muscular dystrophy type 2P [RCV004580970]|Carnitine acylcarnitine translocase deficiency [RCV004580969] Chr3:48895920..49570632 [GRCh37]
Chr3:3p21.31		 pathogenic
NM_003363.4(USP4):c.395A>T (p.Lys132Ile) single nucleotide variant not specified [RCV004680590] Chr3:49325811 [GRCh38]
Chr3:49363244 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.1928C>T (p.Pro643Leu) single nucleotide variant not specified [RCV004680591] Chr3:49292554 [GRCh38]
Chr3:49329987 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2473C>T (p.Leu825Phe) single nucleotide variant not specified [RCV004680592] Chr3:49284054 [GRCh38]
Chr3:49321487 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2747A>C (p.Tyr916Ser) single nucleotide variant not specified [RCV004680593] Chr3:49278438 [GRCh38]
Chr3:49315871 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2836A>G (p.Ser946Gly) single nucleotide variant not specified [RCV004680594] Chr3:49278349 [GRCh38]
Chr3:49315782 [GRCh37]
Chr3:3p21.31		 likely benign
NM_003363.4(USP4):c.349A>G (p.Ile117Val) single nucleotide variant not specified [RCV004680595] Chr3:49327697 [GRCh38]
Chr3:49365130 [GRCh37]
Chr3:3p21.31		 uncertain significance
NM_003363.4(USP4):c.2038A>G (p.Ser680Gly) single nucleotide variant not specified [RCV004680596] Chr3:49286260 [GRCh38]
Chr3:49323693 [GRCh37]
Chr3:3p21.31		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2713
Count of miRNA genes:950
Interacting mature miRNAs:1166
Transcripts:ENST00000265560, ENST00000351842, ENST00000415188, ENST00000416417, ENST00000431357, ENST00000461553, ENST00000462673, ENST00000464168, ENST00000475873, ENST00000483212, ENST00000485450, ENST00000486549, ENST00000488520, ENST00000491791
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
407009411GWAS658387_Hmean corpuscular hemoglobin QTL GWAS658387 (human)5e-17mean corpuscular hemoglobinmean corpuscular hemoglobin (CMO:0000290)34928275049282751Human
407297348GWAS946324_Hlymphocyte count QTL GWAS946324 (human)3e-12lymphocyte countblood lymphocyte count (CMO:0000031)34928147249281473Human
406971267GWAS620243_Hopioid use disorder QTL GWAS620243 (human)7e-11conditioned place preference behavior trait (VT:0010723)34929140049291401Human
406976323GWAS625299_Hmacrophage inflammatory protein 1b measurement QTL GWAS625299 (human)2e-18macrophage inflammatory protein 1b measurement34929564649295647Human
406943042GWAS592018_Hintelligence QTL GWAS592018 (human)2e-12intelligence34927752749277528Human
407121601GWAS770577_Hmathematical ability QTL GWAS770577 (human)6e-09mathematical ability34933311149333112Human
406998277GWAS647253_Hendometriosis, unipolar depression QTL GWAS647253 (human)3e-09endometriosis, unipolar depression34927990549279906Human
406973958GWAS622934_Hcigarettes per day measurement QTL GWAS622934 (human)7e-15cigarettes per day measurement34929733549297336Human
407280268GWAS929244_Hbody height QTL GWAS929244 (human)3e-12body height (VT:0001253)body height (CMO:0000106)34928874549288746Human
406973967GWAS622943_Hcigarettes per day measurement QTL GWAS622943 (human)9e-13cigarettes per day measurement34932632649326327Human
407119755GWAS768731_Hsmoking initiation QTL GWAS768731 (human)6e-10smoking initiation34929140049291401Human
407332754GWAS981730_Hrisk-taking behaviour QTL GWAS981730 (human)7e-10risk-taking behaviour34929879949298800Human
407335390GWAS984366_Hmean corpuscular hemoglobin QTL GWAS984366 (human)2e-26mean corpuscular hemoglobinmean corpuscular hemoglobin (CMO:0000290)34928275049282751Human
407315868GWAS964844_Hattention deficit hyperactivity disorder, autism spectrum disorder, intelligence QTL GWAS964844 (human)7e-14attention deficit hyperactivity disorder, autism spectrum disorder, intelligence34927752749277528Human
407103134GWAS752110_Hmean corpuscular hemoglobin QTL GWAS752110 (human)3e-39mean corpuscular hemoglobinmean corpuscular hemoglobin (CMO:0000290)34928275049282751Human
407294555GWAS943531_Hthioredoxin domain-containing protein 12 measurement QTL GWAS943531 (human)3e-85thioredoxin domain-containing protein 12 measurement34932508549325086Human
406965920GWAS614896_Hsmoking initiation QTL GWAS614896 (human)3e-11smoking initiation34929968749299688Human
406922787GWAS571763_Hsmoking behaviour measurement QTL GWAS571763 (human)1e-12smoking behaviour measurement34927990549279906Human
407195047GWAS844023_Hthioredoxin domain-containing protein 12 measurement QTL GWAS844023 (human)8e-55thioredoxin domain-containing protein 12 measurement34929736449297365Human
407138663GWAS787639_Hcannabis dependence QTL GWAS787639 (human)4e-14cannabis dependence34932739749327398Human
1298487BFD1_HBody fluid distribution QTL 1 (human)3.94Body fluid distributionimpedance ratio33638071262380712Human
407085926GWAS734902_Hirritability measurement QTL GWAS734902 (human)1e-09irritability measurement34929733549297336Human
407090469GWAS739445_Hobsolete_red blood cell distribution width QTL GWAS739445 (human)3e-19obsolete_red blood cell distribution widthred blood cell distribution width- standard deviation (CMO:0003232)34932435849324359Human
407414944GWAS1063920_Hhemoglobin A1 measurement QTL GWAS1063920 (human)8e-36hemoglobin A1 measurement34928459449284595Human
1298489RA4_HRheumatoid arthritis QTL 4 (human)0.0283Joint/bone inflammationrheumatoid arthritis33638071262380712Human
1643509BW293_HBody Weight QTL 293 (human)1.42Body weightBMI33638071262380712Human
406969198GWAS618174_Hcannabis dependence QTL GWAS618174 (human)7e-12cannabis dependence34929968749299688Human
406891824GWAS540800_Hthioredoxin domain-containing protein 12 measurement QTL GWAS540800 (human)2e-54thioredoxin domain-containing protein 12 measurement34930257449302575Human
407051763GWAS700739_Hsubstance-related disorder QTL GWAS700739 (human)2e-09substance-related disorder34932783649327837Human
406964467GWAS613443_Halcohol use disorder measurement QTL GWAS613443 (human)5e-12alcohol use disorder measurement34929140049291401Human
407383870GWAS1032846_Hobsolete_red blood cell distribution width QTL GWAS1032846 (human)3e-26obsolete_red blood cell distribution widthred blood cell distribution width- standard deviation (CMO:0003232)34932435849324359Human
407197810GWAS846786_Hcerebellar volume measurement QTL GWAS846786 (human)6e-10cerebellar volume measurement34930103249301033Human
406942649GWAS591625_Hhousehold income QTL GWAS591625 (human)3e-08household income34933681749336818Human
407139069GWAS788045_Hcannabis dependence QTL GWAS788045 (human)2e-12cannabis dependence34929733549297336Human
407251644GWAS900620_Hlymphocyte count QTL GWAS900620 (human)7e-12lymphocyte countblood lymphocyte count (CMO:0000031)34928147249281473Human
407386229GWAS1035205_Hobsolete_red blood cell distribution width QTL GWAS1035205 (human)2e-29obsolete_red blood cell distribution widthred blood cell distribution width- standard deviation (CMO:0003232)34932435849324359Human
2316061GLUCO194_HGlucose level QTL 194 (human)0.02Glucose level32338077449380774Human
2289308BW392_HBody weight QTL 392 (human)1.42Body weightBMI33638071262380712Human
407217851GWAS866827_Hblood protein measurement QTL GWAS866827 (human)5e-19blood protein measurementblood protein measurement (CMO:0000028)34928874549288746Human
406891902GWAS540878_HPR domain zinc finger protein 1 measurement QTL GWAS540878 (human)2e-19PR domain zinc finger protein 1 measurement34930257449302575Human

Markers in Region
SHGC-107421  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37349,323,419 - 49,323,756UniSTSGRCh37
Build 36349,298,423 - 49,298,760RGDNCBI36
Celera349,286,853 - 49,287,190RGD
Cytogenetic Map3p21.3UniSTS
HuRef349,380,736 - 49,381,073UniSTS
TNG Radiation Hybrid Map330840.0UniSTS
SHGC-57737  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37349,358,382 - 49,358,635UniSTSGRCh37
Build 36349,333,386 - 49,333,639RGDNCBI36
Celera349,322,902 - 49,323,155RGD
Cytogenetic Map3p21.3UniSTS
HuRef349,417,176 - 49,417,429UniSTS
TNG Radiation Hybrid Map330812.0UniSTS
WI-14204  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37349,354,103 - 49,354,228UniSTSGRCh37
Build 36349,329,107 - 49,329,232RGDNCBI36
Celera349,318,584 - 49,318,709RGD
Cytogenetic Map3p21.3UniSTS
HuRef349,412,861 - 49,412,986UniSTS
GeneMap99-GB4 RH Map3158.07UniSTS
Whitehead-RH Map3193.4UniSTS
USP4_8707  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37349,314,871 - 49,315,650UniSTSGRCh37
Build 36349,289,875 - 49,290,654RGDNCBI36
Celera349,278,315 - 49,279,093RGD
HuRef349,372,190 - 49,372,968UniSTS
STS-U20657  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37349,315,673 - 49,315,823UniSTSGRCh37
Build 36349,290,677 - 49,290,827RGDNCBI36
Celera349,279,116 - 49,279,266RGD
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map3p21.3UniSTS
HuRef349,372,991 - 49,373,141UniSTS
GeneMap99-GB4 RH Map3158.01UniSTS
NCBI RH Map3484.2UniSTS
RH41918  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37349,315,136 - 49,315,302UniSTSGRCh37
Build 36349,290,140 - 49,290,306RGDNCBI36
Celera349,278,580 - 49,278,746RGD
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map3p21.3UniSTS
HuRef349,372,455 - 49,372,621UniSTS
GeneMap99-GB4 RH Map3157.33UniSTS
D3S3092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37349,375,626 - 49,375,762UniSTSGRCh37
Build 36349,350,630 - 49,350,766RGDNCBI36
Celera349,340,440 - 49,340,576RGD
Cytogenetic Map3p21.3UniSTS
HuRef349,434,622 - 49,434,758UniSTS
Whitehead-RH Map3191.5UniSTS
RH45172  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37349,315,091 - 49,315,284UniSTSGRCh37
Build 36349,290,095 - 49,290,288RGDNCBI36
Celera349,278,535 - 49,278,728RGD
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map3p21.3UniSTS
HuRef349,372,410 - 49,372,603UniSTS
GeneMap99-GB4 RH Map3158.23UniSTS
SHGC-31529  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37349,315,607 - 49,315,808UniSTSGRCh37
Build 36349,290,611 - 49,290,812RGDNCBI36
Celera349,279,050 - 49,279,251RGD
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map3p21.3UniSTS
HuRef349,372,925 - 49,373,126UniSTS
TNG Radiation Hybrid Map330858.0UniSTS
Stanford-G3 RH Map32146.0UniSTS
GeneMap99-GB4 RH Map3158.34UniSTS
Whitehead-RH Map3191.4UniSTS
NCBI RH Map3484.5UniSTS
GeneMap99-G3 RH Map32044.0UniSTS
RH18550  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37349,315,065 - 49,315,258UniSTSGRCh37
Build 36349,290,069 - 49,290,262RGDNCBI36
Celera349,278,509 - 49,278,702RGD
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map3p21.3UniSTS
HuRef349,372,384 - 49,372,577UniSTS
GeneMap99-GB4 RH Map3158.12UniSTS
NCBI RH Map3484.2UniSTS
L17791  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map10p15-p14UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map11q23.1UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
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Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2439 2788 2253 4974 1726 2351 6 624 1951 465 2270 7306 6472 53 3734 1 852 1744 1617 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_030370 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001251877 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_003363 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_199443 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC121247 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF017305 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF017306 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI887410 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK127055 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK222725 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK223292 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK291795 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC068017 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC125130 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC125131 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG717217 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU632996 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471055 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068275 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA267618 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB534804 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HF584451 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U20657 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000265560   ⟹   ENSP00000265560
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl349,277,144 - 49,340,053 (-)Ensembl
Ensembl Acc Id: ENST00000351842   ⟹   ENSP00000341028
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl349,277,831 - 49,340,033 (-)Ensembl
Ensembl Acc Id: ENST00000415188   ⟹   ENSP00000408274
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl349,316,732 - 49,340,036 (-)Ensembl
Ensembl Acc Id: ENST00000416417   ⟹   ENSP00000400623
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl349,311,785 - 49,340,036 (-)Ensembl
Ensembl Acc Id: ENST00000431357   ⟹   ENSP00000399079
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl349,278,170 - 49,311,618 (-)Ensembl
Ensembl Acc Id: ENST00000461553
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl349,305,778 - 49,314,044 (-)Ensembl
Ensembl Acc Id: ENST00000462673
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl349,317,119 - 49,318,657 (-)Ensembl
Ensembl Acc Id: ENST00000464168
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl349,324,697 - 49,340,053 (-)Ensembl
Ensembl Acc Id: ENST00000475873
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl349,284,536 - 49,293,644 (-)Ensembl
Ensembl Acc Id: ENST00000483212
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl349,278,143 - 49,279,231 (-)Ensembl
Ensembl Acc Id: ENST00000485450
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl349,278,158 - 49,312,863 (-)Ensembl
Ensembl Acc Id: ENST00000486549
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl349,297,870 - 49,340,029 (-)Ensembl
Ensembl Acc Id: ENST00000488520
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl349,300,595 - 49,318,774 (-)Ensembl
Ensembl Acc Id: ENST00000491791
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl349,324,704 - 49,340,712 (-)Ensembl
RefSeq Acc Id: NM_001251877   ⟹   NP_001238806
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38349,311,785 - 49,340,053 (-)NCBI
GRCh37349,314,577 - 49,377,536 (-)NCBI
HuRef349,371,896 - 49,436,532 (-)NCBI
CHM1_1349,302,047 - 49,330,367 (-)NCBI
T2T-CHM13v2.0349,341,150 - 49,369,431 (-)NCBI
Sequence:
RefSeq Acc Id: NM_003363   ⟹   NP_003354
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38349,277,144 - 49,340,053 (-)NCBI
GRCh37349,314,577 - 49,377,536 (-)ENTREZGENE
Build 36349,289,997 - 49,352,519 (-)NCBI Archive
HuRef349,371,896 - 49,436,532 (-)ENTREZGENE
CHM1_1349,267,379 - 49,330,367 (-)NCBI
T2T-CHM13v2.0349,305,224 - 49,369,431 (-)NCBI
Sequence:
RefSeq Acc Id: NM_199443   ⟹   NP_955475
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38349,277,144 - 49,340,053 (-)NCBI
GRCh37349,314,577 - 49,377,536 (-)ENTREZGENE
Build 36349,289,997 - 49,352,519 (-)NCBI Archive
HuRef349,371,896 - 49,436,532 (-)ENTREZGENE
CHM1_1349,267,379 - 49,330,367 (-)NCBI
T2T-CHM13v2.0349,305,224 - 49,369,431 (-)NCBI
Sequence:
RefSeq Acc Id: NP_955475   ⟸   NM_199443
- Peptide Label: isoform b
- UniProtKB: Q53H56 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_003354   ⟸   NM_003363
- Peptide Label: isoform a
- UniProtKB: O43453 (UniProtKB/Swiss-Prot),   O43452 (UniProtKB/Swiss-Prot),   C9IY91 (UniProtKB/Swiss-Prot),   A8K6Y0 (UniProtKB/Swiss-Prot),   Q08AK8 (UniProtKB/Swiss-Prot),   Q13107 (UniProtKB/Swiss-Prot),   Q08AK7 (UniProtKB/TrEMBL),   Q53FJ3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001238806   ⟸   NM_001251877
- Peptide Label: isoform c
- UniProtKB: Q13107 (UniProtKB/Swiss-Prot)
- Sequence:
Ensembl Acc Id: ENSP00000408274   ⟸   ENST00000415188
Ensembl Acc Id: ENSP00000400623   ⟸   ENST00000416417
Ensembl Acc Id: ENSP00000341028   ⟸   ENST00000351842
Ensembl Acc Id: ENSP00000399079   ⟸   ENST00000431357
Ensembl Acc Id: ENSP00000265560   ⟸   ENST00000265560
Protein Domains
DUSP   Ubiquitin-like   USP

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q13107-F1-model_v2 AlphaFold Q13107 1-963 view protein structure

Promoters
RGD ID:6801920
Promoter ID:HG_KWN:45024
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid,   NB4
Transcripts:OTTHUMT00000346073
Position:
Human AssemblyChrPosition (strand)Source
Build 36349,291,626 - 49,292,126 (-)MPROMDB
RGD ID:6801940
Promoter ID:HG_KWN:45026
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:UC003CWO.1,   UC003CWP.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36349,323,711 - 49,324,211 (-)MPROMDB
RGD ID:6801921
Promoter ID:HG_KWN:45027
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000346076
Position:
Human AssemblyChrPosition (strand)Source
Build 36349,326,584 - 49,327,084 (-)MPROMDB
RGD ID:6864398
Promoter ID:EPDNEW_H5364
Type:initiation region
Name:USP4_1
Description:ubiquitin specific peptidase 4
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
GRCh38349,340,053 - 49,340,113EPDNEW
RGD ID:6801919
Promoter ID:HG_KWN:45029
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_003363,   NM_199443,   OTTHUMT00000346072,   OTTHUMT00000346077,   OTTHUMT00000346078,   OTTHUMT00000346080,   OTTHUMT00000346081
Position:
Human AssemblyChrPosition (strand)Source
Build 36349,352,521 - 49,353,272 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:12627 AgrOrtholog
COSMIC USP4 COSMIC
Ensembl Genes ENSG00000114316 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000265560 ENTREZGENE
  ENST00000265560.9 UniProtKB/Swiss-Prot
  ENST00000351842 ENTREZGENE
  ENST00000351842.8 UniProtKB/Swiss-Prot
  ENST00000415188.1 UniProtKB/TrEMBL
  ENST00000416417 ENTREZGENE
  ENST00000416417.5 UniProtKB/Swiss-Prot
  ENST00000431357.1 UniProtKB/TrEMBL
Gene3D-CATH 3.30.2230.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cysteine proteinases UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000114316 GTEx
HGNC ID HGNC:12627 ENTREZGENE
Human Proteome Map USP4 Human Proteome Map
InterPro DUSP-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Papain-like_cys_pep_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Pept_C19_DUSP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Peptidase_C19_UCH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSNA1_fam UniProtKB/TrEMBL
  Ub_carboxyl-term_hydrolase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ub_USP-typ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  USP_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  USP_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:7375 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 7375 ENTREZGENE
OMIM 603486 OMIM
PANTHER PTHR28661 UniProtKB/TrEMBL
  SJOEGREN SYNDROME NUCLEAR AUTOANTIGEN 1 UniProtKB/TrEMBL
  UBIQUITIN CARBOXYL-TERMINAL HYDROLASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  UBIQUITIN CARBOXYL-TERMINAL HYDROLASE 4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam DUSP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ubiquitin_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  UCH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA37252 PharmGKB
PROSITE DUSP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  USP_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  USP_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  USP_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART DUSP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF143791 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF54001 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A8K6Y0 ENTREZGENE
  C9IY91 ENTREZGENE
  C9JNU9_HUMAN UniProtKB/TrEMBL
  H7C189_HUMAN UniProtKB/TrEMBL
  L8EBI0_HUMAN UniProtKB/TrEMBL
  O43452 ENTREZGENE
  O43453 ENTREZGENE
  Q08AK7 ENTREZGENE, UniProtKB/TrEMBL
  Q08AK8 ENTREZGENE
  Q13107 ENTREZGENE
  Q53FJ3 ENTREZGENE, UniProtKB/TrEMBL
  Q53H56 ENTREZGENE, UniProtKB/TrEMBL
  UBP4_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary A8K6Y0 UniProtKB/Swiss-Prot
  C9IY91 UniProtKB/Swiss-Prot
  O43452 UniProtKB/Swiss-Prot
  O43453 UniProtKB/Swiss-Prot
  Q08AK8 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2021-02-25 USP4  ubiquitin specific peptidase 4  LOC107986084  Sjoegren syndrome nuclear autoantigen 1 homolog  Data merged from RGD:38657784 737654 PROVISIONAL
2016-04-12 USP4  ubiquitin specific peptidase 4  USP4  ubiquitin specific peptidase 4 (proto-oncogene)  Symbol and/or name change 5135510 APPROVED