PSMC2 (proteasome 26S subunit, ATPase 2) - Rat Genome Database

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Gene: PSMC2 (proteasome 26S subunit, ATPase 2) Homo sapiens
Analyze
Symbol: PSMC2
Name: proteasome 26S subunit, ATPase 2
RGD ID: 732979
HGNC Page HGNC:9548
Description: Enables proteasome-activating activity. Involved in ubiquitin-dependent protein catabolic process. Located in cytoplasmic ribonucleoprotein granule and cytosol. Part of proteasome complex.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: 26S protease regulatory subunit 7; 26S proteasome AAA-ATPase subunit RPT1; 26S proteasome regulatory subunit 7; mammalian suppressor of sgv-1 of yeast; MGC3004; MSS1; Nbla10058; protease 26S subunit 7; proteasome (prosome, macropain) 26s subunit, atpase 2; proteasome (prosome, macropain) 26S subunit, ATPase, 2; proteasome 26S subunit ATPase 2; proteasome 26S subunit, ATPase, 2; putative protein product of Nbla10058; RPT1; S7; testis secretory sperm-binding protein Li 197a
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: PSMC2P1   PSMC2P2  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh387103,347,524 - 103,369,395 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7103,328,570 - 103,370,346 (+)EnsemblGRCh38hg38GRCh38
GRCh377102,987,971 - 103,009,842 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 367102,775,325 - 102,795,892 (+)NCBINCBI36Build 36hg18NCBI36
Build 347102,582,039 - 102,602,606NCBI
Celera797,795,300 - 97,815,873 (+)NCBICelera
Cytogenetic Map7q22.1NCBI
HuRef797,350,323 - 97,372,344 (+)NCBIHuRef
CHM1_17102,920,963 - 102,943,153 (+)NCBICHM1_1
T2T-CHM13v2.07104,661,962 - 104,683,844 (+)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v27102,348,337 - 102,370,208 (+)NCBI
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
(+)-schisandrin B  (ISO)
(1->4)-beta-D-glucan  (ISO)
(S)-nicotine  (ISO)
1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-hydroxy-17-methylestra-4,9,11-trien-3-one  (EXP)
1H-pyrazole  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2-amino-14,16-dimethyloctadecan-3-ol  (EXP)
2-hydroxypropanoic acid  (EXP)
2-nitrofluorene  (ISO)
3H-1,2-dithiole-3-thione  (ISO)
4,4'-diaminodiphenylmethane  (ISO)
4-(N-nitrosomethylamino)-1-(3-pyridyl)butan-1-one  (ISO)
6-propyl-2-thiouracil  (ISO)
acrylamide  (EXP)
aflatoxin B1  (ISO)
all-trans-retinoic acid  (EXP)
amitrole  (ISO)
ammonium chloride  (ISO)
arsane  (EXP)
arsenic atom  (EXP)
arsenite(3-)  (EXP)
arsenous acid  (EXP)
azoxystrobin  (ISO)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP)
beta-naphthoflavone  (EXP)
bexarotene  (ISO)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (EXP,ISO)
Bisphenol B  (EXP)
Brodifacoum  (ISO)
butyric acid  (EXP)
cadmium dichloride  (ISO)
chloropicrin  (EXP)
chlorpyrifos  (ISO)
chromium(6+)  (EXP)
copper(II) sulfate  (EXP)
cyclosporin A  (EXP)
diarsenic trioxide  (EXP)
dibutyl phthalate  (ISO)
dichlorine  (ISO)
dicrotophos  (EXP)
diethylstilbestrol  (ISO)
doxorubicin  (EXP)
ethanol  (ISO)
finasteride  (ISO)
flavonoids  (ISO)
flutamide  (ISO)
gentamycin  (ISO)
glyphosate  (ISO)
hyaluronic acid  (ISO)
hydrogen peroxide  (EXP,ISO)
hypochlorous acid  (ISO)
imidacloprid  (ISO)
ivermectin  (EXP)
ketoconazole  (EXP)
lead(0)  (EXP)
lovastatin  (ISO)
Mesaconitine  (ISO)
methapyrilene  (ISO)
methidathion  (ISO)
methimazole  (ISO)
methyl methanesulfonate  (EXP)
monocrotaline  (ISO)
monosodium L-glutamate  (ISO)
N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal  (EXP)
N-ethyl-N-nitrosourea  (ISO)
N-nitrosodimethylamine  (ISO)
nefazodone  (ISO)
nicotine  (ISO)
Nonylphenol  (ISO)
ozone  (ISO)
paracetamol  (EXP,ISO)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (ISO)
phenobarbital  (ISO)
phorbol 13-acetate 12-myristate  (ISO)
piperonyl butoxide  (ISO)
pirinixic acid  (ISO)
piroxicam  (EXP)
Propiverine  (ISO)
rac-lactic acid  (EXP)
resveratrol  (EXP)
rotenone  (ISO)
sodium arsenite  (EXP)
sulfadimethoxine  (ISO)
sulindac  (ISO)
sulindac sulfide  (EXP)
sunitinib  (EXP)
T-2 toxin  (EXP)
tamoxifen  (ISO)
tetrachloromethane  (ISO)
thiabendazole  (ISO)
trichostatin A  (EXP)
valdecoxib  (ISO)
valproic acid  (EXP,ISO)
warfarin  (ISO)
zearalenone  (ISO)

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:1377363   PMID:1602151   PMID:7711076   PMID:8500623   PMID:8811196   PMID:8889548   PMID:9079628   PMID:9295362   PMID:9464850   PMID:9473509   PMID:9811770   PMID:9846577  
PMID:10409732   PMID:10625621   PMID:10893419   PMID:11118325   PMID:11118327   PMID:11285280   PMID:11361004   PMID:11734547   PMID:12167863   PMID:12419264   PMID:12477932   PMID:12665801  
PMID:12690205   PMID:12719574   PMID:12750511   PMID:12791267   PMID:12808465   PMID:12808466   PMID:12809610   PMID:12830140   PMID:12840737   PMID:12853948   PMID:12859895   PMID:12914693  
PMID:12920286   PMID:12970176   PMID:12970355   PMID:14527406   PMID:14528300   PMID:14528301   PMID:14550573   PMID:14557625   PMID:14564014   PMID:14614829   PMID:14743216   PMID:15029244  
PMID:15231748   PMID:15340068   PMID:15489334   PMID:15610744   PMID:15782218   PMID:15831487   PMID:15953362   PMID:16130169   PMID:16169070   PMID:16189514   PMID:16210410   PMID:16236267  
PMID:16239144   PMID:16341674   PMID:16712842   PMID:16763564   PMID:17148452   PMID:17220478   PMID:17314511   PMID:17323924   PMID:17353931   PMID:17392787   PMID:17558393   PMID:17573772  
PMID:18029348   PMID:18457437   PMID:18922472   PMID:19013454   PMID:19193609   PMID:19380743   PMID:19412159   PMID:19489727   PMID:19490896   PMID:19589775   PMID:19615732   PMID:19815544  
PMID:19946888   PMID:20007692   PMID:20178748   PMID:20351748   PMID:20467437   PMID:20562859   PMID:20682791   PMID:20810900   PMID:20843792   PMID:21145461   PMID:21516116   PMID:21628461  
PMID:21630459   PMID:21726808   PMID:21733848   PMID:21767633   PMID:21873635   PMID:22078707   PMID:22119785   PMID:22268729   PMID:22275368   PMID:22586326   PMID:22623531   PMID:22645313  
PMID:22658674   PMID:22810586   PMID:22863883   PMID:22901813   PMID:22921402   PMID:22939629   PMID:22952844   PMID:23212908   PMID:23254330   PMID:23260144   PMID:23438482   PMID:23503661  
PMID:23824909   PMID:24429290   PMID:24457600   PMID:24743594   PMID:24811749   PMID:24980433   PMID:24981860   PMID:25147182   PMID:25324306   PMID:25389016   PMID:25416956   PMID:25499913  
PMID:25659154   PMID:25666615   PMID:25756610   PMID:25796446   PMID:25921289   PMID:25959826   PMID:26186194   PMID:26344197   PMID:26472760   PMID:26476452   PMID:26496610   PMID:26549023  
PMID:26618866   PMID:26748699   PMID:26831064   PMID:26885983   PMID:26972000   PMID:27107012   PMID:27114451   PMID:27371349   PMID:27428775   PMID:27462432   PMID:27542412   PMID:27591049  
PMID:27609421   PMID:27684187   PMID:27705803   PMID:27880911   PMID:27880917   PMID:27888613   PMID:28137758   PMID:28190767   PMID:28276505   PMID:28292943   PMID:28330616   PMID:28443643  
PMID:28514442   PMID:28515276   PMID:28539385   PMID:28581483   PMID:28675297   PMID:28685749   PMID:28718761   PMID:28821611   PMID:28902428   PMID:29128334   PMID:29229926   PMID:29331416  
PMID:29357390   PMID:29378950   PMID:29426014   PMID:29467282   PMID:29507755   PMID:29509190   PMID:29636472   PMID:29666234   PMID:29777862   PMID:29845934   PMID:29863498   PMID:29955894  
PMID:29979702   PMID:30033366   PMID:30110629   PMID:30217970   PMID:30257870   PMID:30352685   PMID:30425250   PMID:30442662   PMID:30455355   PMID:30462309   PMID:30463901   PMID:30619736  
PMID:30745168   PMID:30833792   PMID:31037147   PMID:31059266   PMID:31073040   PMID:31091453   PMID:31239290   PMID:31515488   PMID:31586073   PMID:31732153   PMID:31901637   PMID:31950832  
PMID:31980649   PMID:32129710   PMID:32296183   PMID:32723828   PMID:32807901   PMID:32812023   PMID:32814053   PMID:32814769   PMID:32842143   PMID:32877691   PMID:32963011   PMID:32994395  
PMID:33022573   PMID:33141564   PMID:33239621   PMID:33306668   PMID:33545068   PMID:33567341   PMID:33729478   PMID:33766124   PMID:33845483   PMID:33916271   PMID:33961781   PMID:34079125  
PMID:34244472   PMID:34294689   PMID:34373451   PMID:34499615   PMID:34597346   PMID:34711951   PMID:34728620   PMID:34732716   PMID:34761751   PMID:34979867   PMID:35032548   PMID:35140242  
PMID:35241646   PMID:35256949   PMID:35271311   PMID:35287689   PMID:35338135   PMID:35439318   PMID:35446349   PMID:35530310   PMID:35563538   PMID:35681168   PMID:35701858   PMID:35831314  
PMID:35944360   PMID:35980206   PMID:36057605   PMID:36114006   PMID:36180527   PMID:36215168   PMID:36273042   PMID:36424410   PMID:36517590   PMID:36543142   PMID:36572190   PMID:36584595  
PMID:36597993   PMID:36610398   PMID:36708875   PMID:36779763   PMID:36929488   PMID:37120454   PMID:37536630   PMID:37616343   PMID:37689310   PMID:37827155   PMID:38113892   PMID:38123344  
PMID:38280479  


Genomics

Comparative Map Data
PSMC2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh387103,347,524 - 103,369,395 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7103,328,570 - 103,370,346 (+)EnsemblGRCh38hg38GRCh38
GRCh377102,987,971 - 103,009,842 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 367102,775,325 - 102,795,892 (+)NCBINCBI36Build 36hg18NCBI36
Build 347102,582,039 - 102,602,606NCBI
Celera797,795,300 - 97,815,873 (+)NCBICelera
Cytogenetic Map7q22.1NCBI
HuRef797,350,323 - 97,372,344 (+)NCBIHuRef
CHM1_17102,920,963 - 102,943,153 (+)NCBICHM1_1
T2T-CHM13v2.07104,661,962 - 104,683,844 (+)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v27102,348,337 - 102,370,208 (+)NCBI
Psmc2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39521,990,273 - 22,008,785 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl521,990,281 - 22,008,785 (+)EnsemblGRCm39 Ensembl
GRCm38521,785,275 - 21,803,787 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl521,785,283 - 21,803,787 (+)EnsemblGRCm38mm10GRCm38
MGSCv37521,291,101 - 21,309,602 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36521,297,107 - 21,315,608 (+)NCBIMGSCv36mm8
Celera518,756,208 - 18,774,395 (+)NCBICelera
Cytogenetic Map5A3NCBI
cM Map59.97NCBI
Psmc2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8414,148,080 - 14,162,390 (-)NCBIGRCr8
mRatBN7.2413,255,850 - 13,270,160 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl413,255,856 - 13,270,185 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx418,401,118 - 18,415,400 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0414,215,883 - 14,230,158 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0412,586,755 - 12,601,037 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.049,867,132 - 9,881,383 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl49,867,101 - 9,881,484 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.049,868,269 - 9,882,520 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.448,704,100 - 8,718,351 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.148,704,099 - 8,718,351 (-)NCBI
Celera48,847,110 - 8,861,246 (-)NCBICelera
Cytogenetic Map4q11NCBI
Psmc2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554108,341,065 - 8,356,148 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554108,341,218 - 8,355,515 (+)NCBIChiLan1.0ChiLan1.0
PSMC2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v26140,201,706 - 140,227,300 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan17188,473,396 - 188,497,270 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0795,338,743 - 95,359,353 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.17108,083,019 - 108,103,595 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl7108,083,203 - 108,103,494 (+)Ensemblpanpan1.1panPan2
PSMC2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11816,845,593 - 16,859,010 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1816,845,594 - 16,858,911 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1816,488,537 - 16,501,956 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01817,136,145 - 17,149,599 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1817,136,146 - 17,149,526 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11816,900,975 - 16,914,588 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01816,839,559 - 16,853,208 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01817,107,769 - 17,121,439 (-)NCBIUU_Cfam_GSD_1.0
Psmc2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440511859,026,969 - 59,043,987 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493647920,148,632 - 20,168,130 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493647920,150,738 - 20,167,765 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
PSMC2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl9103,362,599 - 103,376,343 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.19103,362,684 - 103,376,048 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.29113,971,194 - 113,984,560 (+)NCBISscrofa10.2Sscrofa10.2susScr3
PSMC2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12172,323,691 - 72,341,647 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2172,323,803 - 72,341,488 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604231,660,968 - 31,679,446 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Psmc2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462473926,001,871 - 26,016,040 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462473926,001,871 - 26,015,633 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in PSMC2
8 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 7q22.1-31.1(chr7:101807149-112414850)x1 copy number loss See cases [RCV000050924] Chr7:101807149..112414850 [GRCh38]
Chr7:101450429..112054905 [GRCh37]
Chr7:101237149..111842141 [NCBI36]
Chr7:7q22.1-31.1
pathogenic
GRCh38/hg38 7q22.1-22.3(chr7:101525795-105432462)x3 copy number gain See cases [RCV000050705] Chr7:101525795..105432462 [GRCh38]
Chr7:101169076..105072909 [GRCh37]
Chr7:100955796..104860145 [NCBI36]
Chr7:7q22.1-22.3
pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 copy number loss See cases [RCV000052250] Chr7:53985..159282531 [GRCh38]
Chr7:53985..159075220 [GRCh37]
Chr7:149068..158767981 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7q22.1-22.3(chr7:101700341-105162893)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054156]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054156]|See cases [RCV000054156] Chr7:101700341..105162893 [GRCh38]
Chr7:101343621..104803340 [GRCh37]
Chr7:101130341..104590576 [NCBI36]
Chr7:7q22.1-22.3
pathogenic
GRCh38/hg38 7q22.1-22.3(chr7:102808199-105701108)x1 copy number loss See cases [RCV000054157] Chr7:102808199..105701108 [GRCh38]
Chr7:102448646..105341555 [GRCh37]
Chr7:102235882..105128791 [NCBI36]
Chr7:7q22.1-22.3
pathogenic
GRCh38/hg38 7q22.1(chr7:103326703-103763175)x1 copy number loss See cases [RCV000133830] Chr7:103326703..103763175 [GRCh38]
Chr7:102967150..103403622 [GRCh37]
Chr7:102754386..103190858 [NCBI36]
Chr7:7q22.1
uncertain significance
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 copy number loss See cases [RCV000135401] Chr7:54185..159282390 [GRCh38]
Chr7:54185..159075079 [GRCh37]
Chr7:149268..158767840 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3 copy number gain See cases [RCV000136717] Chr7:97419852..158923762 [GRCh38]
Chr7:97049164..158716453 [GRCh37]
Chr7:96887100..158409214 [NCBI36]
Chr7:7q21.3-36.3
pathogenic
GRCh38/hg38 7q22.1-31.31(chr7:102196924-121278641)x1 copy number loss See cases [RCV000137522] Chr7:102196924..121278641 [GRCh38]
Chr7:101912320..120918695 [GRCh37]
Chr7:101626924..120705931 [NCBI36]
Chr7:7q22.1-31.31
pathogenic
GRCh38/hg38 7q22.1(chr7:102692380-103350914)x3 copy number gain See cases [RCV000137814] Chr7:102692380..103350914 [GRCh38]
Chr7:102332827..102991361 [GRCh37]
Chr7:102120063..102778597 [NCBI36]
Chr7:7q22.1
likely benign
TMEM106B-BRAF fusion deletion Pleomorphic xanthoastrocytoma [RCV000454357] Chr7:12258147..140494267 [GRCh37]
Chr7:7p21.3-q34
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 copy number loss See cases [RCV000446044] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q22.1-36.3(chr7:98969247-159119707)x3 copy number gain See cases [RCV000447709] Chr7:98969247..159119707 [GRCh37]
Chr7:7q22.1-36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) copy number gain See cases [RCV000510686] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 copy number gain See cases [RCV000511549] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
NM_002803.4(PSMC2):c.325C>T (p.Pro109Ser) single nucleotide variant not provided [RCV003314088] Chr7:103361991 [GRCh38]
Chr7:103002438 [GRCh37]
Chr7:7q22.1
uncertain significance
GRCh37/hg19 7q22.1-22.3(chr7:102910570-105104800)x1 copy number loss not provided [RCV000682896] Chr7:102910570..105104800 [GRCh37]
Chr7:7q22.1-22.3
likely pathogenic
GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3 copy number gain not provided [RCV000682911] Chr7:98693388..159119707 [GRCh37]
Chr7:7q22.1-36.3
pathogenic
NC_000007.13:g.(20954043_21001537)_(114528369_114556605)inv inversion Childhood apraxia of speech [RCV000234948] Chr7:21001537..114528369 [GRCh37]
Chr7:7p15.3-q31.1
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 copy number gain not provided [RCV000746280] Chr7:44935..159126310 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 copy number gain not provided [RCV000746278] Chr7:10704..159122532 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 copy number gain not provided [RCV000848126] Chr7:10365..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q22.1(chr7:102333119-103158261)x3 copy number gain not provided [RCV000847426] Chr7:102333119..103158261 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_002803.4(PSMC2):c.71-1273G>T single nucleotide variant not provided [RCV001557367] Chr7:103352648 [GRCh38]
Chr7:102993095 [GRCh37]
Chr7:7q22.1
likely benign
NM_002803.4(PSMC2):c.154A>T (p.Ile52Phe) single nucleotide variant Inborn genetic diseases [RCV003261494] Chr7:103354913 [GRCh38]
Chr7:102995360 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_002803.4(PSMC2):c.71-1283C>T single nucleotide variant not provided [RCV001656809] Chr7:103352638 [GRCh38]
Chr7:102993085 [GRCh37]
Chr7:7q22.1
benign
NM_002803.4(PSMC2):c.71-1342A>G single nucleotide variant not provided [RCV001657096] Chr7:103352579 [GRCh38]
Chr7:102993026 [GRCh37]
Chr7:7q22.1
benign
Single allele complex Ring chromosome 7 [RCV002280646] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
NM_002803.4(PSMC2):c.751G>T (p.Gly251Cys) single nucleotide variant not provided [RCV001280764] Chr7:103364302 [GRCh38]
Chr7:103004749 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_002803.4(PSMC2):c.363dup (p.Val122fs) duplication not provided [RCV001752729] Chr7:103362026..103362027 [GRCh38]
Chr7:103002473..103002474 [GRCh37]
Chr7:7q22.1
uncertain significance
GRCh37/hg19 7q22.1-31.31(chr7:100676872-119156160) copy number loss not specified [RCV002053712] Chr7:100676872..119156160 [GRCh37]
Chr7:7q22.1-31.31
pathogenic
GRCh37/hg19 7q22.1-31.1(chr7:99417471-111586308) copy number loss not specified [RCV002053711] Chr7:99417471..111586308 [GRCh37]
Chr7:7q22.1-31.1
pathogenic
NC_000007.13:g.(?_102937907)_(103629803_?)del deletion Norman-Roberts syndrome [RCV001951338] Chr7:102937907..103629803 [GRCh37]
Chr7:7q22.1
pathogenic
NC_000007.13:g.(?_102937907)_(103151472_?)dup duplication Norman-Roberts syndrome [RCV001920573] Chr7:102937907..103151472 [GRCh37]
Chr7:7q22.1
uncertain significance
NC_000007.13:g.(?_102937907)_(107643330_?)dup duplication not provided [RCV003113939] Chr7:102937907..107643330 [GRCh37]
Chr7:7q22.1-31.1
uncertain significance
GRCh37/hg19 7p22.3-q36.3(chr7:56604613-96692931)x1 copy number loss See cases [RCV002287832] Chr7:56604613..96692931 [GRCh37]
Chr7:7p22.3-q36.3
uncertain significance
NM_002803.4(PSMC2):c.302T>C (p.Ile101Thr) single nucleotide variant Inborn genetic diseases [RCV002812916] Chr7:103361968 [GRCh38]
Chr7:103002415 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_002803.4(PSMC2):c.119C>G (p.Thr40Ser) single nucleotide variant Inborn genetic diseases [RCV002679630] Chr7:103354878 [GRCh38]
Chr7:102995325 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_002803.4(PSMC2):c.1192A>C (p.Arg398=) single nucleotide variant not provided [RCV003423723] Chr7:103367944 [GRCh38]
Chr7:103008391 [GRCh37]
Chr7:7q22.1
likely benign
GRCh37/hg19 7q22.1(chr7:102668567-103242665)x3 copy number gain not provided [RCV003484695] Chr7:102668567..103242665 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_002803.4(PSMC2):c.501A>G (p.Glu167=) single nucleotide variant not provided [RCV003423722] Chr7:103363349 [GRCh38]
Chr7:103003796 [GRCh37]
Chr7:7q22.1
likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:749
Count of miRNA genes:446
Interacting mature miRNAs:487
Transcripts:ENST00000292644, ENST00000425206, ENST00000435765, ENST00000457587, ENST00000460021, ENST00000544811
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.

Markers in Region
D7S2509  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377102,987,247 - 102,987,531UniSTSGRCh37
Build 367102,774,483 - 102,774,767RGDNCBI36
Celera797,794,466 - 97,794,742RGD
Cytogenetic Map7q22.1-q22.3UniSTS
Cytogenetic Map7q22.1UniSTS
HuRef797,349,607 - 97,349,883UniSTS
CRA_TCAGchr7v27102,347,613 - 102,347,897UniSTS
Marshfield Genetic Map7112.85UniSTS
Marshfield Genetic Map7112.85RGD
Genethon Genetic Map7113.4UniSTS
deCODE Assembly Map7112.22UniSTS
Whitehead-YAC Contig Map7 UniSTS
SGC32632  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377103,008,459 - 103,008,591UniSTSGRCh37
Build 367102,795,695 - 102,795,827RGDNCBI36
Celera797,815,676 - 97,815,808RGD
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map7q22.1-q22.3UniSTS
HuRef797,370,959 - 97,371,091UniSTS
CRA_TCAGchr7v27102,368,825 - 102,368,957UniSTS
GeneMap99-GB4 RH Map7522.18UniSTS
Whitehead-RH Map7491.1UniSTS
RH11504  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377103,008,370 - 103,008,515UniSTSGRCh37
Build 367102,795,606 - 102,795,751RGDNCBI36
Celera797,815,587 - 97,815,732RGD
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map7q22.1-q22.3UniSTS
HuRef797,370,870 - 97,371,015UniSTS
CRA_TCAGchr7v27102,368,736 - 102,368,881UniSTS
GeneMap99-GB4 RH Map7522.11UniSTS
RH69239  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377103,008,953 - 103,009,097UniSTSGRCh37
Build 367102,796,189 - 102,796,333RGDNCBI36
Celera797,816,170 - 97,816,314RGD
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map7q22.1-q22.3UniSTS
HuRef797,371,453 - 97,371,597UniSTS
CRA_TCAGchr7v27102,369,319 - 102,369,463UniSTS
GeneMap99-GB4 RH Map7521.67UniSTS
RH80487  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map7q22.1-q22.3UniSTS
GeneMap99-GB4 RH Map3487.31UniSTS
PSMC2  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map7q22.1-q22.3UniSTS


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 2437 2593 1718 618 1653 459 4357 2104 3564 413 1460 1612 175 1 1204 2788 6 2
Low 2 398 8 6 298 6 93 170 6 1
Below cutoff

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001204453 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_002803 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956468 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956469 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB075520 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC004668 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC093701 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298529 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298821 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK312648 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC002589 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BE269755 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM754312 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU675889 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH236947 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471070 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D11094 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM005610 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT584320 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT584848 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000292644   ⟹   ENSP00000292644
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7103,347,643 - 103,369,395 (+)Ensembl
RefSeq Acc Id: ENST00000425206   ⟹   ENSP00000393027
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7103,347,671 - 103,368,859 (+)Ensembl
RefSeq Acc Id: ENST00000435765   ⟹   ENSP00000391211
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7103,344,914 - 103,369,395 (+)Ensembl
RefSeq Acc Id: ENST00000457587   ⟹   ENSP00000401724
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7103,344,254 - 103,362,057 (+)Ensembl
RefSeq Acc Id: ENST00000460021
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7103,353,919 - 103,362,467 (+)Ensembl
RefSeq Acc Id: ENST00000676908
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7103,361,546 - 103,369,375 (+)Ensembl
RefSeq Acc Id: ENST00000677281
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7103,347,660 - 103,356,355 (+)Ensembl
RefSeq Acc Id: ENST00000677769
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7103,352,527 - 103,369,375 (+)Ensembl
RefSeq Acc Id: ENST00000677943
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7103,352,434 - 103,369,375 (+)Ensembl
RefSeq Acc Id: ENST00000678488   ⟹   ENSP00000502892
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7103,347,674 - 103,368,859 (+)Ensembl
RefSeq Acc Id: ENST00000678493   ⟹   ENSP00000502939
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7103,328,570 - 103,370,346 (+)Ensembl
RefSeq Acc Id: ENST00000678587
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7103,354,534 - 103,356,338 (+)Ensembl
RefSeq Acc Id: ENST00000679046
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7103,347,640 - 103,368,859 (+)Ensembl
RefSeq Acc Id: ENST00000679205   ⟹   ENSP00000503179
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7103,344,266 - 103,370,346 (+)Ensembl
RefSeq Acc Id: ENST00000679250   ⟹   ENSP00000503663
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7103,347,636 - 103,369,375 (+)Ensembl
RefSeq Acc Id: ENST00000679341   ⟹   ENSP00000504608
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7103,344,320 - 103,370,346 (+)Ensembl
RefSeq Acc Id: NM_001204453   ⟹   NP_001191382
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387103,347,524 - 103,362,467 (+)NCBI
GRCh377102,984,852 - 103,009,842 (+)NCBI
HuRef797,350,323 - 97,372,344 (+)ENTREZGENE
CHM1_17102,920,963 - 102,936,225 (+)NCBI
T2T-CHM13v2.07104,661,962 - 104,676,912 (+)NCBI
CRA_TCAGchr7v27102,348,337 - 102,370,208 (+)ENTREZGENE
Sequence:
RefSeq Acc Id: NM_002803   ⟹   NP_002794
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387103,347,643 - 103,369,395 (+)NCBI
GRCh377102,984,852 - 103,009,842 (+)NCBI
Build 367102,775,325 - 102,795,892 (+)NCBI Archive
HuRef797,350,323 - 97,372,344 (+)ENTREZGENE
CHM1_17102,920,963 - 102,943,153 (+)NCBI
T2T-CHM13v2.07104,662,081 - 104,683,844 (+)NCBI
CRA_TCAGchr7v27102,348,337 - 102,370,208 (+)ENTREZGENE
Sequence:
RefSeq Acc Id: NP_002794   ⟸   NM_002803
- Peptide Label: isoform 1
- UniProtKB: Q3LIA5 (UniProtKB/Swiss-Prot),   B7Z5E2 (UniProtKB/Swiss-Prot),   A4D0Q1 (UniProtKB/Swiss-Prot),   Q9UDI3 (UniProtKB/Swiss-Prot),   P35998 (UniProtKB/Swiss-Prot),   A0A140VK70 (UniProtKB/TrEMBL),   C9JX88 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001191382   ⟸   NM_001204453
- Peptide Label: isoform 2
- UniProtKB: B7Z571 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000292644   ⟸   ENST00000292644
RefSeq Acc Id: ENSP00000393027   ⟸   ENST00000425206
RefSeq Acc Id: ENSP00000401724   ⟸   ENST00000457587
RefSeq Acc Id: ENSP00000391211   ⟸   ENST00000435765
RefSeq Acc Id: ENSP00000502892   ⟸   ENST00000678488
RefSeq Acc Id: ENSP00000502939   ⟸   ENST00000678493
RefSeq Acc Id: ENSP00000504608   ⟸   ENST00000679341
RefSeq Acc Id: ENSP00000503663   ⟸   ENST00000679250
RefSeq Acc Id: ENSP00000503179   ⟸   ENST00000679205
Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P35998-F1-model_v2 AlphaFold P35998 1-433 view protein structure

Promoters
RGD ID:6806095
Promoter ID:HG_KWN:59134
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   K562
Transcripts:OTTHUMT00000347923,   OTTHUMT00000347924
Position:
Human AssemblyChrPosition (strand)Source
Build 367102,771,154 - 102,771,654 (+)MPROMDB
RGD ID:6805490
Promoter ID:HG_KWN:59135
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:ENST00000379257,   NM_001129887,   NM_014377,   OTTHUMT00000347900,   OTTHUMT00000347922,   UC003VBP.1,   UC003VBQ.1,   UC003VBR.1
Position:
Human AssemblyChrPosition (strand)Source
Build 367102,771,686 - 102,772,462 (-)MPROMDB
RGD ID:6806093
Promoter ID:HG_KWN:59136
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:NM_002803
Position:
Human AssemblyChrPosition (strand)Source
Build 367102,775,109 - 102,775,609 (+)MPROMDB
RGD ID:7211565
Promoter ID:EPDNEW_H11529
Type:initiation region
Name:PSMC2_1
Description:proteasome 26S subunit, ATPase 2
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
GRCh387103,347,643 - 103,347,703EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:9548 AgrOrtholog
COSMIC PSMC2 COSMIC
Ensembl Genes ENSG00000161057 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000292644 ENTREZGENE
  ENST00000292644.5 UniProtKB/Swiss-Prot
  ENST00000425206.6 UniProtKB/TrEMBL
  ENST00000435765.5 UniProtKB/Swiss-Prot
  ENST00000457587 ENTREZGENE
  ENST00000457587.5 UniProtKB/TrEMBL
  ENST00000678488.1 UniProtKB/TrEMBL
  ENST00000678493.1 UniProtKB/Swiss-Prot
  ENST00000679205.1 UniProtKB/Swiss-Prot
  ENST00000679250.1 UniProtKB/Swiss-Prot
  ENST00000679341.1 UniProtKB/Swiss-Prot
Gene3D-CATH 1.10.8.60 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.40.50.140 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.40.50.300 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000161057 GTEx
HGNC ID HGNC:9548 ENTREZGENE
Human Proteome Map PSMC2 Human Proteome Map
InterPro AAA+_ATPase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  AAA_lid_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ATPase_AAA_core UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ATPase_AAA_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NA-bd_OB-fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  P-loop_NTPase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PRS7-like_OB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:5701 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 5701 ENTREZGENE
OMIM 154365 OMIM
PANTHER 26S PROTEASOME REGULATORY SUBUNIT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR23073:SF13 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam AAA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  AAA_lid_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PRS7_OB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA33893 PharmGKB
PROSITE AAA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART AAA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF52540 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A140VK70 ENTREZGENE, UniProtKB/TrEMBL
  A0A7I2YQ68_HUMAN UniProtKB/TrEMBL
  A4D0Q1 ENTREZGENE
  B7Z571 ENTREZGENE, UniProtKB/TrEMBL
  B7Z5E2 ENTREZGENE
  C9JLS9_HUMAN UniProtKB/TrEMBL
  C9JX88 ENTREZGENE, UniProtKB/TrEMBL
  P35998 ENTREZGENE, UniProtKB/Swiss-Prot
  Q3LIA5 ENTREZGENE
  Q75L23_HUMAN UniProtKB/TrEMBL
  Q9UDI3 ENTREZGENE
UniProt Secondary A4D0Q1 UniProtKB/Swiss-Prot
  B7Z5E2 UniProtKB/Swiss-Prot
  Q3LIA5 UniProtKB/Swiss-Prot
  Q9UDI3 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-08-18 PSMC2  proteasome 26S subunit, ATPase 2    proteasome (prosome, macropain) 26S subunit, ATPase, 2  Symbol and/or name change 5135510 APPROVED