PRKCE (protein kinase C epsilon) - Rat Genome Database

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Gene: PRKCE (protein kinase C epsilon) Homo sapiens
Analyze
Symbol: PRKCE
Name: protein kinase C epsilon
RGD ID: 736442
HGNC Page HGNC:9401
Description: Enables diacylglycerol-dependent serine/threonine kinase activity; enzyme activator activity; and enzyme binding activity. Involved in several processes, including positive regulation of cellular glucuronidation; positive regulation of cytokinesis; and positive regulation of epithelial cell migration. Located in several cellular components, including cytosol; endoplasmic reticulum; and intermediate filament cytoskeleton.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: MGC125656; MGC125657; nPKC-epsilon; PKCE; protein kinase C epsilon type
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38245,651,279 - 46,187,990 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl245,651,345 - 46,187,990 (+)EnsemblGRCh38hg38GRCh38
GRCh37245,878,814 - 46,415,129 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36245,732,547 - 46,268,633 (+)NCBINCBI36Build 36hg18NCBI36
Build 34245,790,693 - 46,326,779NCBI
Celera245,717,245 - 46,253,470 (+)NCBICelera
Cytogenetic Map2p21NCBI
HuRef245,617,217 - 46,153,158 (+)NCBIHuRef
CHM1_1245,810,047 - 46,345,904 (+)NCBICHM1_1
T2T-CHM13v2.0245,656,327 - 46,193,193 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(R)-adrenaline  (ISO)
(S)-nicotine  (ISO)
1,1-dichloroethene  (ISO)
1,2-dimethylhydrazine  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP,ISO)
2,2',4,4',5,5'-hexachlorobiphenyl  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (ISO)
2,2',5,5'-tetrachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,4-dibromophenyl 2,4,5-tribromophenyl ether  (EXP)
2,6-dinitrotoluene  (ISO)
2-butoxyethanol  (ISO)
3-\{1-[3-(dimethylamino)propyl]-1H-indol-3-yl\}-4-(1H-indol-3-yl)-1H-pyrrole-2,5-dione  (EXP,ISO)
4,4'-diaminodiphenylmethane  (ISO)
4,4'-sulfonyldiphenol  (EXP)
4-amino-2,6-dinitrotoluene  (ISO)
5-aza-2'-deoxycytidine  (ISO)
7,12-dimethyltetraphene  (ISO)
acetaldehyde  (EXP)
acetamide  (ISO)
acetylsalicylic acid  (EXP)
aflatoxin B1  (EXP,ISO)
Aflatoxin B2 alpha  (EXP)
all-trans-retinoic acid  (EXP)
ammonium chloride  (ISO)
amphetamine  (ISO)
arjunolic acid  (ISO)
Aroclor 1254  (EXP)
arsane  (EXP)
arsenic atom  (EXP)
arsenous acid  (ISO)
atrazine  (ISO)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP)
benzo[b]fluoranthene  (ISO)
benzo[e]pyrene  (EXP)
berberine  (ISO)
bisphenol A  (EXP,ISO)
C60 fullerene  (ISO)
cadmium atom  (ISO)
cadmium dichloride  (ISO)
calcium atom  (EXP,ISO)
calcium(0)  (EXP,ISO)
capsaicin  (EXP)
carbon nanotube  (ISO)
carvedilol  (ISO)
celecoxib  (ISO)
CGP 52608  (EXP)
CGS-21680  (ISO)
chelerythrine  (EXP,ISO)
chlorpyrifos  (ISO)
chrysene  (ISO)
cisplatin  (EXP)
clomiphene  (EXP)
clozapine  (ISO)
cobalt dichloride  (EXP,ISO)
cocaine  (ISO)
Cuprizon  (ISO)
curcumin  (EXP)
cycloheximide  (ISO)
daidzein  (ISO)
deoxycholic acid  (EXP)
deoxynivalenol  (ISO)
diarsenic trioxide  (ISO)
dibenziodolium  (EXP)
dibutyl phthalate  (ISO)
diethyl maleate  (ISO)
dioxygen  (ISO)
diuron  (EXP)
divanadium pentaoxide  (ISO)
dobutamine  (ISO)
dofetilide  (ISO)
dorsomorphin  (EXP)
doxorubicin  (EXP,ISO)
Droloxifene  (EXP)
ethanol  (ISO)
formaldehyde  (EXP)
FR900359  (EXP)
genistein  (ISO)
gingerol  (EXP)
haloperidol  (ISO)
Heptachlor epoxide  (ISO)
hexadecanoic acid  (EXP)
hydrogen peroxide  (ISO)
indometacin  (EXP)
inulin  (EXP)
isoprenaline  (ISO)
lead diacetate  (ISO)
lead(0)  (EXP,ISO)
Licochalcone A  (EXP)
lipopolysaccharide  (ISO)
lithium atom  (ISO)
lithium hydride  (ISO)
lysophosphatidylcholine  (ISO)
methamphetamine  (ISO)
methapyrilene  (EXP)
methotrexate  (ISO)
methoxychlor  (ISO)
methyl methanesulfonate  (EXP)
methylene blue  (ISO)
methylparaben  (EXP)
morin  (EXP)
myxothiazol  (ISO)
N-acetyl-L-cysteine  (ISO)
N-nitrosodiethylamine  (ISO)
nicotine  (ISO)
nimesulide  (ISO)
O-methyleugenol  (EXP)
obeticholic acid  (EXP)
ozone  (ISO)
paclitaxel  (ISO)
paracetamol  (ISO)
PCB138  (ISO)
PD123319  (ISO)
phenethyl caffeate  (ISO)
phenobarbital  (ISO)
phenylephrine  (ISO)
phorbol 12,13-dibutanoate  (ISO)
phorbol 13-acetate 12-myristate  (EXP,ISO)
picrotoxin  (ISO)
pirinixic acid  (ISO)
potassium chromate  (EXP)
pregnenolone 16alpha-carbonitrile  (ISO)
progesterone  (ISO)
propiconazole  (ISO)
prostaglandin E2  (ISO)
quercetin  (ISO)
reactive oxygen species  (EXP)
Rebamipide  (ISO)
Ro 31-8220  (ISO)
rotenone  (ISO)
S-butyl-DL-homocysteine (S,R)-sulfoximine  (ISO)
SB 431542  (EXP)
Se-methyl-L-selenocysteine  (ISO)
Se-methylselenocysteine  (ISO)
silicon dioxide  (EXP)
sodium arsenate  (ISO)
sodium cyanide  (ISO)
streptozocin  (ISO)
sunitinib  (EXP)
tamoxifen  (EXP)
tert-butyl hydroperoxide  (EXP)
tetraphene  (ISO)
thioacetamide  (ISO)
thiram  (EXP)
trichloroethene  (ISO)
trichostatin A  (EXP)
troglitazone  (EXP)
tungsten  (ISO)
tunicamycin  (ISO)
urethane  (EXP)
valproic acid  (EXP,ISO)
venlafaxine hydrochloride  (ISO)
vinclozolin  (ISO)
vincristine  (ISO)
vitamin D  (ISO)
zinc atom  (EXP)
zinc(0)  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
apoptotic process  (TAS)
cell adhesion  (IEA)
cell division  (IEA)
cell-substrate adhesion  (IEA,ISO)
cellular response to ethanol  (IEA,ISO)
cellular response to hypoxia  (IEA,ISO)
cellular response to platelet-derived growth factor stimulus  (ISO)
cellular response to prostaglandin E stimulus  (IEA,ISO)
establishment of localization in cell  (IEA,ISO)
Fc-gamma receptor signaling pathway involved in phagocytosis  (TAS)
immune system process  (IEA)
insulin secretion  (IEA,ISO)
intracellular signal transduction  (IBA,IEA,ISO)
lipopolysaccharide-mediated signaling pathway  (IEA,ISO,ISS)
locomotory exploration behavior  (IEA,ISO)
macrophage activation involved in immune response  (IEA,ISO)
MAPK cascade  (IEA,ISO)
mucus secretion  (IEA,ISO)
negative regulation of apoptotic process  (ISO)
negative regulation of mitochondrial calcium ion concentration  (ISO)
negative regulation of mitochondrial membrane potential  (ISO)
negative regulation of protein ubiquitination  (IEA)
negative regulation of release of sequestered calcium ion into cytosol  (ISO)
positive regulation of actin filament polymerization  (IEA,ISS)
positive regulation of canonical NF-kappaB signal transduction  (IEA,ISO)
positive regulation of cell-substrate adhesion  (IEA,ISO)
positive regulation of cellular glucuronidation  (IMP)
positive regulation of cytokinesis  (IMP)
positive regulation of epithelial cell migration  (IMP)
positive regulation of fibroblast migration  (IEA,ISS)
positive regulation of insulin secretion  (IEA,ISO)
positive regulation of lipid catabolic process  (IEA,ISO)
positive regulation of MAPK cascade  (IEA,ISO)
positive regulation of mucus secretion  (IEA,ISO)
positive regulation of protein localization to plasma membrane  (TAS)
positive regulation of synaptic transmission, GABAergic  (IEA,ISO)
positive regulation of wound healing  (IMP)
presynaptic modulation of chemical synaptic transmission  (ISO)
regulation of insulin secretion involved in cellular response to glucose stimulus  (IEA,ISO)
regulation of lipid metabolic process  (IEA,ISO)
regulation of peptidyl-tyrosine phosphorylation  (IEA,ISO)
regulation of primary metabolic process  (IEA)
regulation of release of sequestered calcium ion into cytosol  (IEA,ISO)
response to morphine  (IEA,ISO)
signal transduction  (IEA,TAS)
synaptic transmission, GABAergic  (IEA,ISO)
TRAM-dependent toll-like receptor 4 signaling pathway  (IEA,ISS)

Cellular Component

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. MicroRNA-143 promotes cardiac ischemia-mediated mitochondrial impairment by the inhibition of protein kinase Cepsilon. Hong H, etal., Basic Res Cardiol. 2017 Sep 8;112(6):60. doi: 10.1007/s00395-017-0649-7.
3. Protein kinase C isozymes in hypertension and hypertrophy: insight from SHHF rat hearts. Johnsen DD, etal., Mol Cell Biochem. 2005 Feb;270(1-2):63-9.
4. Protein kinase C: poised to signal. Newton AC Am J Physiol Endocrinol Metab. 2010 Mar;298(3):E395-402. Epub 2009 Nov 24.
5. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
6. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI into RGD
7. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
8. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
9. Expression of Protein Kinase C Isoforms in Pancreatic Islets and Liver of Male Goto-Kakizaki Rats, a Model of Type 2 Diabetes. Seed Ahmed M, etal., PLoS One. 2015 Sep 23;10(9):e0135781. doi: 10.1371/journal.pone.0135781. eCollection 2015.
Additional References at PubMed
PMID:1374067   PMID:1382605   PMID:1832084   PMID:1970444   PMID:2139676   PMID:2182321   PMID:3259291   PMID:7522330   PMID:7523419   PMID:7588787   PMID:7642615   PMID:7850771  
PMID:7876252   PMID:7877991   PMID:7935319   PMID:8206685   PMID:8224184   PMID:8346200   PMID:8473314   PMID:8567732   PMID:8599832   PMID:8621384   PMID:8627654   PMID:8824244  
PMID:8914829   PMID:8940095   PMID:9151826   PMID:9312127   PMID:9360998   PMID:9446795   PMID:9535877   PMID:9671211   PMID:9822674   PMID:10092595   PMID:10212259   PMID:10407019  
PMID:10417813   PMID:10438519   PMID:10491200   PMID:10536000   PMID:10641798   PMID:10679481   PMID:10801826   PMID:10843712   PMID:10848585   PMID:10862698   PMID:10945988   PMID:11044099  
PMID:11062054   PMID:11085981   PMID:11104762   PMID:11140687   PMID:11141237   PMID:11154208   PMID:11350735   PMID:11504923   PMID:11553773   PMID:11696589   PMID:11700305   PMID:11709417  
PMID:11739292   PMID:11740573   PMID:11788586   PMID:11809819   PMID:11833470   PMID:11834516   PMID:11839754   PMID:11877428   PMID:11884385   PMID:11897493   PMID:11919157   PMID:11934885  
PMID:11950841   PMID:11956211   PMID:11964154   PMID:11968018   PMID:11994357   PMID:11997513   PMID:12055197   PMID:12093536   PMID:12121973   PMID:12134071   PMID:12185081   PMID:12198125  
PMID:12205039   PMID:12223477   PMID:12372810   PMID:12372816   PMID:12385023   PMID:12477932   PMID:12482669   PMID:12505875   PMID:12505880   PMID:12536241   PMID:12628935   PMID:12640464  
PMID:12663490   PMID:12665800   PMID:12782628   PMID:12783114   PMID:12794082   PMID:12857743   PMID:12893243   PMID:12941947   PMID:12970744   PMID:12972433   PMID:14523239   PMID:14532285  
PMID:14600145   PMID:14643884   PMID:14656938   PMID:14702039   PMID:14709334   PMID:14720513   PMID:14739299   PMID:15003508   PMID:15078178   PMID:15147202   PMID:15190080   PMID:15213298  
PMID:15233804   PMID:15284224   PMID:15364951   PMID:15368451   PMID:15381704   PMID:15467757   PMID:15488737   PMID:15489334   PMID:15499829   PMID:15509588   PMID:15559761   PMID:15572354  
PMID:15627650   PMID:15632189   PMID:15689238   PMID:15691837   PMID:15695813   PMID:15698833   PMID:15718244   PMID:15784626   PMID:15809302   PMID:15815621   PMID:15827341   PMID:15894802  
PMID:15949469   PMID:15967991   PMID:16079188   PMID:16266318   PMID:16314418   PMID:16461926   PMID:16637058   PMID:16698938   PMID:16785234   PMID:16793902   PMID:16810323   PMID:16930532  
PMID:17018591   PMID:17038313   PMID:17203073   PMID:17215072   PMID:17382347   PMID:17392515   PMID:17434141   PMID:17561374   PMID:17569788   PMID:17603037   PMID:17616661   PMID:17628663  
PMID:17632570   PMID:17668322   PMID:17678893   PMID:17785460   PMID:17851107   PMID:17991733   PMID:18171914   PMID:18172602   PMID:18184679   PMID:18237277   PMID:18292183   PMID:18296444  
PMID:18317451   PMID:18319301   PMID:18398416   PMID:18408015   PMID:18436431   PMID:18458086   PMID:18462068   PMID:18556656   PMID:18577246   PMID:18604201   PMID:18663158   PMID:18844064  
PMID:18947333   PMID:18988868   PMID:19011111   PMID:19030108   PMID:19168130   PMID:19193863   PMID:19244118   PMID:19248786   PMID:19324950   PMID:19363595   PMID:19429675   PMID:19432558  
PMID:19435802   PMID:19542546   PMID:19573263   PMID:19577658   PMID:19633292   PMID:19635931   PMID:19655190   PMID:19662078   PMID:19815625   PMID:19862010   PMID:19874574   PMID:20072156  
PMID:20139978   PMID:20171211   PMID:20179209   PMID:20198332   PMID:20200978   PMID:20336759   PMID:20350291   PMID:20353823   PMID:20379614   PMID:20471435   PMID:20558438   PMID:20566643  
PMID:20677014   PMID:20732874   PMID:20936779   PMID:20965248   PMID:21041247   PMID:21081127   PMID:21124804   PMID:21236337   PMID:21277149   PMID:21283634   PMID:21411725   PMID:21423656  
PMID:21465464   PMID:21482705   PMID:21489985   PMID:21532342   PMID:21596133   PMID:21625473   PMID:21649687   PMID:21651489   PMID:21858203   PMID:21873635   PMID:21955404   PMID:21964026  
PMID:21996750   PMID:22114277   PMID:22158047   PMID:22162761   PMID:22304920   PMID:22326427   PMID:22384062   PMID:22424883   PMID:22475757   PMID:22712879   PMID:22732145   PMID:22773829  
PMID:22849349   PMID:22927445   PMID:22939624   PMID:22955280   PMID:23071564   PMID:23123196   PMID:23166209   PMID:23222517   PMID:23266964   PMID:23349801   PMID:23364795   PMID:23446634  
PMID:23457043   PMID:23524339   PMID:23562764   PMID:23564461   PMID:23589174   PMID:23612973   PMID:23708658   PMID:23824184   PMID:23824807   PMID:23934736   PMID:23967087   PMID:23977066  
PMID:23977398   PMID:24070896   PMID:24166186   PMID:24298017   PMID:24312401   PMID:24338688   PMID:24515280   PMID:24658140   PMID:24788249   PMID:24815185   PMID:24825907   PMID:24848988  
PMID:24872409   PMID:24888992   PMID:24996056   PMID:25178676   PMID:25245533   PMID:25308712   PMID:25322815   PMID:25372487   PMID:25402006   PMID:25483024   PMID:25778903   PMID:25788289  
PMID:25883219   PMID:26023164   PMID:26075907   PMID:26199377   PMID:26821209   PMID:27037060   PMID:27081176   PMID:27312950   PMID:27330081   PMID:27573736   PMID:27776404   PMID:27793751  
PMID:28004745   PMID:28056995   PMID:28223364   PMID:28286252   PMID:28402859   PMID:28476658   PMID:28492560   PMID:28591572   PMID:28611215   PMID:28765889   PMID:28934384   PMID:29038521  
PMID:29127121   PMID:29280140   PMID:29439667   PMID:29452158   PMID:29507755   PMID:29515166   PMID:29590645   PMID:30209539   PMID:30923343   PMID:31648598   PMID:31980649   PMID:32429937  
PMID:32513696   PMID:32549199   PMID:32707033   PMID:32814053   PMID:32869841   PMID:32994205   PMID:33368632   PMID:33637726   PMID:33961781   PMID:34108094   PMID:34593629   PMID:34836941  
PMID:34857952   PMID:35256949   PMID:36400183   PMID:36782184   PMID:36931259   PMID:37336366   PMID:37501577   PMID:37833790  


Genomics

Comparative Map Data
PRKCE
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38245,651,279 - 46,187,990 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl245,651,345 - 46,187,990 (+)EnsemblGRCh38hg38GRCh38
GRCh37245,878,814 - 46,415,129 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36245,732,547 - 46,268,633 (+)NCBINCBI36Build 36hg18NCBI36
Build 34245,790,693 - 46,326,779NCBI
Celera245,717,245 - 46,253,470 (+)NCBICelera
Cytogenetic Map2p21NCBI
HuRef245,617,217 - 46,153,158 (+)NCBIHuRef
CHM1_1245,810,047 - 46,345,904 (+)NCBICHM1_1
T2T-CHM13v2.0245,656,327 - 46,193,193 (+)NCBIT2T-CHM13v2.0
Prkce
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391786,472,631 - 86,965,347 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1786,475,213 - 86,965,347 (+)EnsemblGRCm39 Ensembl
GRCm381786,167,785 - 86,657,919 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1786,167,785 - 86,657,919 (+)EnsemblGRCm38mm10GRCm38
MGSCv371786,567,125 - 87,057,259 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361786,076,916 - 86,563,024 (+)NCBIMGSCv36mm8
Celera1790,540,474 - 91,038,578 (+)NCBICelera
Cytogenetic Map17E4NCBI
cM Map1756.74NCBI
Prkce
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8613,718,050 - 14,204,931 (-)NCBIGRCr8
mRatBN7.267,965,048 - 8,451,966 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl67,965,048 - 8,451,719 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx68,241,962 - 8,728,298 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.068,551,358 - 9,037,685 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.068,078,663 - 8,564,995 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.069,483,400 - 9,973,396 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl69,790,422 - 9,973,396 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.069,404,548 - 9,883,579 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.469,631,234 - 10,097,311 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.169,631,241 - 10,097,311 (+)NCBI
Celera67,696,161 - 8,179,574 (-)NCBICelera
Cytogenetic Map6q12NCBI
Prkce
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495544112,642,697 - 13,139,372 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495544112,642,703 - 13,142,396 (+)NCBIChiLan1.0ChiLan1.0
PRKCE
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21280,214,185 - 80,750,763 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12A80,218,154 - 80,754,448 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02A45,757,629 - 46,294,064 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12A46,688,109 - 47,223,421 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2A46,688,436 - 47,220,313 (+)Ensemblpanpan1.1panPan2
PRKCE
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11047,976,929 - 48,464,614 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1047,976,768 - 48,535,296 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1047,832,146 - 48,319,423 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01048,849,986 - 49,335,766 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1048,849,926 - 49,335,759 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11048,557,609 - 49,044,861 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01048,849,404 - 49,334,809 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01049,029,809 - 49,517,384 (+)NCBIUU_Cfam_GSD_1.0
Prkce
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440629234,589,765 - 35,066,607 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365086,017,551 - 6,494,427 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365086,018,374 - 6,495,216 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
PRKCE
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl394,349,889 - 94,866,306 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1394,351,277 - 94,864,549 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.23100,427,723 - 100,762,372 (-)NCBISscrofa10.2Sscrofa10.2susScr3
PRKCE
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11461,022,903 - 61,570,390 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1461,026,017 - 61,242,343 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604550,297,930 - 50,835,743 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Prkce
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462473827,118,145 - 27,627,606 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462473827,118,764 - 27,630,733 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in PRKCE
77 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_005400.3(PRKCE):c.1795G>A (p.Glu599Lys) single nucleotide variant not provided [RCV000523596] Chr2:46151104 [GRCh38]
Chr2:46378243 [GRCh37]
Chr2:2p21
pathogenic|uncertain significance
GRCh38/hg38 2p25.3-16.1(chr2:66097-55570637)x3 copy number gain See cases [RCV000052933] Chr2:66097..55570637 [GRCh38]
Chr2:66097..55797773 [GRCh37]
Chr2:56097..55651277 [NCBI36]
Chr2:2p25.3-16.1
pathogenic
GRCh38/hg38 2p21(chr2:45273296-45954468)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052632]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052632]|See cases [RCV000052632] Chr2:45273296..45954468 [GRCh38]
Chr2:45500435..46181607 [GRCh37]
Chr2:45353939..46035111 [NCBI36]
Chr2:2p21
uncertain significance
GRCh38/hg38 2p22.1-16.1(chr2:40738282-57863821)x3 copy number gain See cases [RCV000052943] Chr2:40738282..57863821 [GRCh38]
Chr2:40965422..58090956 [GRCh37]
Chr2:40818926..57944460 [NCBI36]
Chr2:2p22.1-16.1
pathogenic
NM_005400.2(PRKCE):c.348+39723C>T single nucleotide variant Lung cancer [RCV000092098] Chr2:45692171 [GRCh38]
Chr2:45919310 [GRCh37]
Chr2:2p21
uncertain significance
NM_005400.2(PRKCE):c.349-80887A>G single nucleotide variant Lung cancer [RCV000092099] Chr2:45762113 [GRCh38]
Chr2:45989252 [GRCh37]
Chr2:2p21
uncertain significance
GRCh37/hg19 2p21(chr2:45409988-45968987)x3 copy number gain See cases [RCV000515564] Chr2:45409988..45968987 [GRCh37]
Chr2:2p21
uncertain significance
GRCh38/hg38 2p21(chr2:45273355-45734463)x3 copy number gain See cases [RCV000138850] Chr2:45273355..45734463 [GRCh38]
Chr2:45500494..45961602 [GRCh37]
Chr2:45353998..45815106 [NCBI36]
Chr2:2p21
likely benign
GRCh38/hg38 2p21(chr2:46083824-46395464)x3 copy number gain See cases [RCV000138867] Chr2:46083824..46395464 [GRCh38]
Chr2:46310963..46622603 [GRCh37]
Chr2:46164467..46476107 [NCBI36]
Chr2:2p21
uncertain significance
GRCh38/hg38 2p21(chr2:45253291-45851241)x3 copy number gain See cases [RCV000140127] Chr2:45253291..45851241 [GRCh38]
Chr2:45480430..46078380 [GRCh37]
Chr2:45333934..45931884 [NCBI36]
Chr2:2p21
likely benign
GRCh38/hg38 2p21(chr2:45192069-45734384)x3 copy number gain See cases [RCV000141073] Chr2:45192069..45734384 [GRCh38]
Chr2:45419208..45961523 [GRCh37]
Chr2:45272712..45815027 [NCBI36]
Chr2:2p21
likely benign
GRCh38/hg38 2p25.1-11.2(chr2:7495123-87705899)x3 copy number gain See cases [RCV000141494] Chr2:7495123..87705899 [GRCh38]
Chr2:7635254..88005418 [GRCh37]
Chr2:7552705..87786533 [NCBI36]
Chr2:2p25.1-11.2
benign
GRCh38/hg38 2p25.3-21(chr2:236816-45983232)x3 copy number gain See cases [RCV000143682] Chr2:236816..45983232 [GRCh38]
Chr2:236816..46210371 [GRCh37]
Chr2:226816..46063875 [NCBI36]
Chr2:2p25.3-21
pathogenic
GRCh37/hg19 2p21(chr2:45412845-45976420)x3 copy number gain See cases [RCV000449035] Chr2:45412845..45976420 [GRCh37]
Chr2:2p21
uncertain significance
NC_000002.12:g.46009609_46144092dup duplication not specified [RCV001568391] Chr2:46009609..46144092 [GRCh38]
Chr2:2p21
not provided
NM_005400.3(PRKCE):c.1166C>G (p.Pro389Arg) single nucleotide variant Inborn genetic diseases [RCV003244458] Chr2:46007564 [GRCh38]
Chr2:46234703 [GRCh37]
Chr2:2p21
uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3 copy number gain not provided [RCV000752802] Chr2:14238..243048760 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
GRCh37/hg19 2p23.3-16.1(chr2:27861707-60790985)x3 copy number gain See cases [RCV000454271] Chr2:27861707..60790985 [GRCh37]
Chr2:2p23.3-16.1
pathogenic
GRCh37/hg19 2p21(chr2:45421555-45976420)x3 copy number gain See cases [RCV000446806] Chr2:45421555..45976420 [GRCh37]
Chr2:2p21
uncertain significance
GRCh37/hg19 2p21(chr2:45408934-45976420)x3 copy number gain See cases [RCV000446230] Chr2:45408934..45976420 [GRCh37]
Chr2:2p21
conflicting data from submitters
GRCh37/hg19 2p21(chr2:45899044-46739157)x3 copy number gain See cases [RCV000447020] Chr2:45899044..46739157 [GRCh37]
Chr2:2p21
uncertain significance
GRCh37/hg19 2p21(chr2:45797992-46161299)x1 copy number loss See cases [RCV000447159] Chr2:45797992..46161299 [GRCh37]
Chr2:2p21
uncertain significance
GRCh37/hg19 2p21(chr2:45408545-45976420)x3 copy number gain See cases [RCV000447191] Chr2:45408545..45976420 [GRCh37]
Chr2:2p21
uncertain significance
GRCh37/hg19 2p21(chr2:45412904-45976420)x3 copy number gain See cases [RCV000445969] Chr2:45412904..45976420 [GRCh37]
Chr2:2p21
uncertain significance
GRCh37/hg19 2p21(chr2:45408934-45975265)x3 copy number gain See cases [RCV000448551] Chr2:45408934..45975265 [GRCh37]
Chr2:2p21
uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384) copy number gain See cases [RCV000512056] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
NC_000002.11:g.38121110_47669522inv inversion Hereditary nonpolyposis colorectal neoplasms [RCV002231155] Chr2:38121110..47669522 [GRCh37]
Chr2:2p22.2-21
pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3 copy number gain See cases [RCV000511212] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
NM_005400.3(PRKCE):c.1893C>A (p.Ser631Arg) single nucleotide variant Inborn genetic diseases [RCV003266949] Chr2:46151202 [GRCh38]
Chr2:46378341 [GRCh37]
Chr2:2p21
uncertain significance
GRCh37/hg19 2p22.3-16.1(chr2:34792916-56676541)x3 copy number gain not provided [RCV000682169] Chr2:34792916..56676541 [GRCh37]
Chr2:2p22.3-16.1
pathogenic
GRCh37/hg19 2p21(chr2:45408934-45976420)x3 copy number gain not provided [RCV000682086] Chr2:45408934..45976420 [GRCh37]
Chr2:2p21
likely benign
Single allele deletion not provided [RCV000714264] Chr2:40608411..146900718 [GRCh37]
Chr2:2p22.1-q22.3
likely pathogenic
GRCh37/hg19 2p21(chr2:45919058-46045583)x3 copy number gain not provided [RCV000752935] Chr2:45919058..46045583 [GRCh37]
Chr2:2p21
benign
GRCh37/hg19 2p24.1-16.3(chr2:22665048-52850368)x3 copy number gain not provided [RCV000752875] Chr2:22665048..52850368 [GRCh37]
Chr2:2p24.1-16.3
pathogenic
GRCh37/hg19 2p21(chr2:45410658-45974136)x3 copy number gain not provided [RCV000752933] Chr2:45410658..45974136 [GRCh37]
Chr2:2p21
benign
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3 copy number gain not provided [RCV000752804] Chr2:15672..243101834 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
GRCh37/hg19 2p21(chr2:45409988-45974136)x3 copy number gain not provided [RCV000752932] Chr2:45409988..45974136 [GRCh37]
Chr2:2p21
benign
GRCh37/hg19 2p21(chr2:45409988-45968584)x3 copy number gain not provided [RCV000740415] Chr2:45409988..45968584 [GRCh37]
Chr2:2p21
benign
NM_005400.3(PRKCE):c.1104A>G (p.Ser368=) single nucleotide variant not provided [RCV000949481] Chr2:46007502 [GRCh38]
Chr2:46234641 [GRCh37]
Chr2:2p21
benign
NM_005400.3(PRKCE):c.466C>A (p.Arg156=) single nucleotide variant not provided [RCV000979234] Chr2:45976482 [GRCh38]
Chr2:46203621 [GRCh37]
Chr2:2p21
likely benign
NM_005400.3(PRKCE):c.1311G>A (p.Lys437=) single nucleotide variant not provided [RCV000951058] Chr2:46010391 [GRCh38]
Chr2:46237530 [GRCh37]
Chr2:2p21
benign
GRCh37/hg19 2p21(chr2:45412845-45976452)x3 copy number gain not provided [RCV000846066] Chr2:45412845..45976452 [GRCh37]
Chr2:2p21
uncertain significance
NM_005400.3(PRKCE):c.1365A>G (p.Thr455=) single nucleotide variant not provided [RCV000893358] Chr2:46010445 [GRCh38]
Chr2:46237584 [GRCh37]
Chr2:2p21
benign
GRCh37/hg19 2p21(chr2:45404085-45975214)x3 copy number gain not provided [RCV000846051] Chr2:45404085..45975214 [GRCh37]
Chr2:2p21
uncertain significance
NM_005400.3(PRKCE):c.1533C>G (p.Phe511Leu) single nucleotide variant See cases [RCV001198560] Chr2:46086303 [GRCh38]
Chr2:46313442 [GRCh37]
Chr2:2p21
uncertain significance
NM_005400.3(PRKCE):c.1960G>A (p.Ala654Thr) single nucleotide variant not provided [RCV000961400] Chr2:46159645 [GRCh38]
Chr2:46386784 [GRCh37]
Chr2:2p21
benign
NM_005400.3(PRKCE):c.1519C>A (p.Pro507Thr) single nucleotide variant Inborn genetic diseases [RCV002748917] Chr2:46086289 [GRCh38]
Chr2:46313428 [GRCh37]
Chr2:2p21
uncertain significance
GRCh37/hg19 2p21(chr2:46179259-47646894)x3 copy number gain not provided [RCV001005255] Chr2:46179259..47646894 [GRCh37]
Chr2:2p21
uncertain significance
GRCh37/hg19 2p21(chr2:45917633-46584622)x3 copy number gain not provided [RCV001258532] Chr2:45917633..46584622 [GRCh37]
Chr2:2p21
uncertain significance
GRCh37/hg19 2p21(chr2:45421555-45976420) copy number gain not specified [RCV002052548] Chr2:45421555..45976420 [GRCh37]
Chr2:2p21
uncertain significance
GRCh37/hg19 2p21(chr2:45899044-46739157) copy number gain not specified [RCV002052560] Chr2:45899044..46739157 [GRCh37]
Chr2:2p21
uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373) copy number gain Mosaic trisomy 2 [RCV002280628] Chr2:1..243199373 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
NC_000002.11:g.(?_38121051)_(47710088_?)dup duplication Hereditary nonpolyposis colorectal neoplasms [RCV003122260] Chr2:38121051..47710088 [GRCh37]
Chr2:2p22.2-21
uncertain significance
GRCh37/hg19 2p25.1-q13(chr2:11504318-111365996)x1 copy number loss See cases [RCV002287563] Chr2:11504318..111365996 [GRCh37]
Chr2:2p25.1-q13
pathogenic
NM_005400.3(PRKCE):c.1094A>C (p.Lys365Thr) single nucleotide variant Inborn genetic diseases [RCV002777066] Chr2:46007492 [GRCh38]
Chr2:46234631 [GRCh37]
Chr2:2p21
uncertain significance
NM_005400.3(PRKCE):c.736G>A (p.Gly246Ser) single nucleotide variant Inborn genetic diseases [RCV002751782] Chr2:45984593 [GRCh38]
Chr2:46211732 [GRCh37]
Chr2:2p21
uncertain significance
NM_005400.3(PRKCE):c.1081A>G (p.Asn361Asp) single nucleotide variant Inborn genetic diseases [RCV002844655] Chr2:46007479 [GRCh38]
Chr2:46234618 [GRCh37]
Chr2:2p21
uncertain significance
NM_005400.3(PRKCE):c.1151G>C (p.Gly384Ala) single nucleotide variant Inborn genetic diseases [RCV002782352] Chr2:46007549 [GRCh38]
Chr2:46234688 [GRCh37]
Chr2:2p21
uncertain significance
NM_005400.3(PRKCE):c.1106T>A (p.Phe369Tyr) single nucleotide variant Inborn genetic diseases [RCV002930993] Chr2:46007504 [GRCh38]
Chr2:46234643 [GRCh37]
Chr2:2p21
uncertain significance
NM_005400.3(PRKCE):c.7G>C (p.Val3Leu) single nucleotide variant Inborn genetic diseases [RCV003204331] Chr2:45652107 [GRCh38]
Chr2:45879246 [GRCh37]
Chr2:2p21
uncertain significance
NM_005400.3(PRKCE):c.1204C>T (p.Arg402Cys) single nucleotide variant Inborn genetic diseases [RCV003200044] Chr2:46007602 [GRCh38]
Chr2:46234741 [GRCh37]
Chr2:2p21
uncertain significance
NM_005400.3(PRKCE):c.1535A>G (p.Tyr512Cys) single nucleotide variant Inborn genetic diseases [RCV003347522] Chr2:46086305 [GRCh38]
Chr2:46313444 [GRCh37]
Chr2:2p21
uncertain significance
NM_005400.3(PRKCE):c.1529G>A (p.Arg510Gln) single nucleotide variant not provided [RCV003407215] Chr2:46086299 [GRCh38]
Chr2:46313438 [GRCh37]
Chr2:2p21
likely benign
NM_005400.3(PRKCE):c.966+8G>A single nucleotide variant not provided [RCV003407214] Chr2:46001554 [GRCh38]
Chr2:46228693 [GRCh37]
Chr2:2p21
benign
NM_005400.3(PRKCE):c.373_389del (p.Val125fs) deletion not provided [RCV003706320] Chr2:45843022..45843038 [GRCh38]
Chr2:46070161..46070177 [GRCh37]
Chr2:2p21
uncertain significance
miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR107hsa-miR-107OncomiRDBexternal_infoNANA22158047
MIR205hsa-miR-205-5pOncomiRDBexternal_infoNANA19244118
MIR103A1hsa-miR-103a-3pOncomiRDBexternal_infoNANA22157681
MIR31hsa-miR-31-5pMirtarbaseexternal_infoLuciferase reporter assayFunctional MTI23364795
MIR31hsa-miR-31-5pOncomiRDBexternal_infoNANA23364795

Predicted Target Of
Summary Value
Count of predictions:4029
Count of miRNA genes:1280
Interacting mature miRNAs:1659
Transcripts:ENST00000306156, ENST00000394874, ENST00000421201, ENST00000462720, ENST00000467135, ENST00000469753, ENST00000472021, ENST00000476675, ENST00000480453, ENST00000480633, ENST00000485176, ENST00000489067, ENST00000494472, ENST00000497602, ENST00000498388
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
D2S2182  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,265,669 - 46,265,906UniSTSGRCh37
Build 36246,119,173 - 46,119,410RGDNCBI36
Celera246,104,096 - 46,104,329RGD
Cytogenetic Map2p21UniSTS
HuRef246,003,793 - 46,004,026UniSTS
Marshfield Genetic Map270.31UniSTS
Marshfield Genetic Map270.31RGD
Genethon Genetic Map273.8UniSTS
TNG Radiation Hybrid Map210279.0UniSTS
deCODE Assembly Map271.94UniSTS
GeneMap99-GB4 RH Map2142.44UniSTS
Whitehead-RH Map2202.4UniSTS
Whitehead-YAC Contig Map2 UniSTS
NCBI RH Map2291.6UniSTS
D2S2378  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,258,693 - 46,258,896UniSTSGRCh37
Build 36246,112,197 - 46,112,400RGDNCBI36
Celera246,097,112 - 46,097,323RGD
Cytogenetic Map2p21UniSTS
HuRef245,996,819 - 45,997,020UniSTS
Marshfield Genetic Map270.31RGD
Marshfield Genetic Map270.31UniSTS
Genethon Genetic Map273.8UniSTS
deCODE Assembly Map271.94UniSTS
Whitehead-YAC Contig Map2 UniSTS
D2S391  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,411,503 - 46,411,648UniSTSGRCh37
GRCh37246,411,500 - 46,411,644UniSTSGRCh37
Build 36246,265,007 - 46,265,152RGDNCBI36
Celera246,249,843 - 46,249,988RGD
Celera246,249,840 - 46,249,984UniSTS
Cytogenetic Map2p21UniSTS
HuRef246,149,528 - 46,149,672UniSTS
HuRef246,149,531 - 46,149,676UniSTS
Marshfield Genetic Map270.31RGD
Genethon Genetic Map273.8UniSTS
TNG Radiation Hybrid Map210219.0UniSTS
deCODE Assembly Map272.33UniSTS
Whitehead-YAC Contig Map2 UniSTS
D2S2240  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,044,115 - 46,044,297UniSTSGRCh37
Build 36245,897,619 - 45,897,801RGDNCBI36
Celera245,882,552 - 45,882,734RGD
Cytogenetic Map2p21UniSTS
HuRef245,782,234 - 45,782,420UniSTS
Marshfield Genetic Map269.77RGD
Marshfield Genetic Map269.77UniSTS
Genethon Genetic Map273.3UniSTS
TNG Radiation Hybrid Map210395.0UniSTS
deCODE Assembly Map271.59UniSTS
WI-10633  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,219,430 - 46,219,641UniSTSGRCh37
Build 36246,072,934 - 46,073,145RGDNCBI36
Celera246,057,840 - 46,058,051RGD
Cytogenetic Map2p21UniSTS
HuRef245,957,541 - 45,957,752UniSTS
Whitehead-RH Map2205.9UniSTS
RH16512  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,252,086 - 46,252,205UniSTSGRCh37
Build 36246,105,590 - 46,105,709RGDNCBI36
Celera246,090,505 - 46,090,624RGD
Cytogenetic Map2p21UniSTS
HuRef245,990,210 - 45,990,329UniSTS
GeneMap99-GB4 RH Map2139.78UniSTS
NCBI RH Map2291.6UniSTS
SHGC-34686  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,252,081 - 46,252,205UniSTSGRCh37
Build 36246,105,585 - 46,105,709RGDNCBI36
Celera246,090,500 - 46,090,624RGD
Cytogenetic Map2p21UniSTS
HuRef245,990,205 - 45,990,329UniSTS
TNG Radiation Hybrid Map210291.0UniSTS
Stanford-G3 RH Map21905.0UniSTS
GeneMap99-GB4 RH Map2142.34UniSTS
Whitehead-RH Map2202.4UniSTS
NCBI RH Map2291.6UniSTS
GeneMap99-G3 RH Map21902.0UniSTS
WI-13380  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,414,717 - 46,414,841UniSTSGRCh37
Build 36246,268,221 - 46,268,345RGDNCBI36
Celera246,253,057 - 46,253,181RGD
Cytogenetic Map2p21UniSTS
HuRef246,152,745 - 46,152,869UniSTS
GeneMap99-GB4 RH Map2135.91UniSTS
Whitehead-RH Map2205.8UniSTS
NCBI RH Map2307.9UniSTS
RH91582  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,072,129 - 46,072,257UniSTSGRCh37
Build 36245,925,633 - 45,925,761RGDNCBI36
Celera245,910,567 - 45,910,695RGD
Cytogenetic Map2p21UniSTS
HuRef245,810,250 - 45,810,378UniSTS
GeneMap99-GB4 RH Map2142.44UniSTS
RH91418  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,265,168 - 46,265,350UniSTSGRCh37
Build 36246,118,672 - 46,118,854RGDNCBI36
Celera246,103,595 - 46,103,777RGD
Cytogenetic Map2p21UniSTS
HuRef246,003,292 - 46,003,474UniSTS
GeneMap99-GB4 RH Map2139.78UniSTS
RH98368  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,397,104 - 46,397,248UniSTSGRCh37
Build 36246,250,608 - 46,250,752RGDNCBI36
Celera246,235,444 - 46,235,588RGD
Cytogenetic Map2p21UniSTS
HuRef246,135,132 - 46,135,276UniSTS
GeneMap99-GB4 RH Map2142.44UniSTS
RH92278  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37245,900,536 - 45,900,723UniSTSGRCh37
Build 36245,754,040 - 45,754,227RGDNCBI36
Celera245,738,744 - 45,738,931RGD
Cytogenetic Map2p21UniSTS
HuRef245,638,744 - 45,638,931UniSTS
GeneMap99-GB4 RH Map2139.78UniSTS
SHGC-81643  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37245,972,647 - 45,972,945UniSTSGRCh37
Build 36245,826,151 - 45,826,449RGDNCBI36
Celera245,810,791 - 45,811,089RGD
Cytogenetic Map2p21UniSTS
HuRef245,710,864 - 45,711,162UniSTS
TNG Radiation Hybrid Map210442.0UniSTS
SHGC-84453  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,149,227 - 46,149,529UniSTSGRCh37
Build 36246,002,731 - 46,003,033RGDNCBI36
Celera245,987,629 - 45,987,931RGD
Cytogenetic Map2p21UniSTS
HuRef245,887,285 - 45,887,587UniSTS
TNG Radiation Hybrid Map210325.0UniSTS
RH119807  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,250,297 - 46,250,588UniSTSGRCh37
Build 36246,103,801 - 46,104,092RGDNCBI36
Celera246,088,718 - 46,089,009RGD
Cytogenetic Map2p21UniSTS
HuRef245,988,422 - 45,988,713UniSTS
TNG Radiation Hybrid Map210287.0UniSTS
G60078  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,219,432 - 46,219,630UniSTSGRCh37
Build 36246,072,936 - 46,073,134RGDNCBI36
Celera246,057,842 - 46,058,040RGD
Cytogenetic Map2p21UniSTS
HuRef245,957,543 - 45,957,741UniSTS
TNG Radiation Hybrid Map210305.0UniSTS
RH118474  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,040,321 - 46,040,629UniSTSGRCh37
Build 36245,893,825 - 45,894,133RGDNCBI36
Celera245,878,758 - 45,879,066RGD
Cytogenetic Map2p21UniSTS
HuRef245,778,440 - 45,778,748UniSTS
TNG Radiation Hybrid Map210399.0UniSTS
G63864  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37245,975,668 - 45,975,971UniSTSGRCh37
Build 36245,829,172 - 45,829,475RGDNCBI36
Celera245,813,812 - 45,814,115RGD
Cytogenetic Map2p21UniSTS
HuRef245,713,885 - 45,714,188UniSTS
D2S1489  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,028,383 - 46,028,978UniSTSGRCh37
Build 36245,881,887 - 45,882,482RGDNCBI36
Celera245,866,868 - 45,867,457RGD
Cytogenetic Map2p21UniSTS
HuRef245,766,611 - 45,767,206UniSTS
D2S1717E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,413,362 - 46,413,495UniSTSGRCh37
Build 36246,266,866 - 46,266,999RGDNCBI36
Celera246,251,702 - 46,251,835RGD
Cytogenetic Map2p21UniSTS
HuRef246,151,390 - 46,151,523UniSTS
D2S1953E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37245,986,922 - 45,987,008UniSTSGRCh37
Build 36245,840,426 - 45,840,512RGDNCBI36
Celera245,825,066 - 45,825,152RGD
Cytogenetic Map2p21UniSTS
HuRef245,725,136 - 45,725,222UniSTS
SHGC-107519  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,081,955 - 46,082,236UniSTSGRCh37
Build 36245,935,459 - 45,935,740RGDNCBI36
Celera245,920,391 - 45,920,672RGD
Cytogenetic Map2p21UniSTS
HuRef245,820,074 - 45,820,355UniSTS
TNG Radiation Hybrid Map210374.0UniSTS
SHGC-148352  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37245,982,641 - 45,982,985UniSTSGRCh37
Build 36245,836,145 - 45,836,489RGDNCBI36
Celera245,820,785 - 45,821,129RGD
Cytogenetic Map2p21UniSTS
HuRef245,720,855 - 45,721,199UniSTS
TNG Radiation Hybrid Map210433.0UniSTS
G20720  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,414,623 - 46,414,769UniSTSGRCh37
Build 36246,268,127 - 46,268,273RGDNCBI36
Celera246,252,963 - 46,253,109RGD
Cytogenetic Map2p21UniSTS
HuRef246,152,651 - 46,152,797UniSTS
A006D15  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,414,623 - 46,414,769UniSTSGRCh37
Build 36246,268,127 - 46,268,273RGDNCBI36
Celera246,252,963 - 46,253,109RGD
Cytogenetic Map2p21UniSTS
HuRef246,152,651 - 46,152,797UniSTS
GeneMap99-GB4 RH Map2142.44UniSTS
NCBI RH Map2291.6UniSTS
WI-19686  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,414,952 - 46,415,076UniSTSGRCh37
Build 36246,268,456 - 46,268,580RGDNCBI36
Celera246,253,293 - 46,253,417RGD
Cytogenetic Map2p21UniSTS
HuRef246,152,981 - 46,153,105UniSTS
GeneMap99-GB4 RH Map2138.36UniSTS
Whitehead-RH Map2204.0UniSTS
NCBI RH Map2291.6UniSTS
RH48314  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,387,234 - 46,387,355UniSTSGRCh37
Build 36246,240,738 - 46,240,859RGDNCBI36
Celera246,225,575 - 46,225,696RGD
Cytogenetic Map2p21UniSTS
HuRef246,125,263 - 46,125,384UniSTS
GeneMap99-GB4 RH Map2135.91UniSTS
SHGC-63514  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,414,613 - 46,414,702UniSTSGRCh37
Build 36246,268,117 - 46,268,206RGDNCBI36
Celera246,252,953 - 46,253,042RGD
Cytogenetic Map2p21UniSTS
HuRef246,152,641 - 46,152,730UniSTS
WI-10606  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,205,062 - 46,205,212UniSTSGRCh37
Build 36246,058,566 - 46,058,716RGDNCBI36
Celera246,043,475 - 46,043,625RGD
Cytogenetic Map2p21UniSTS
HuRef245,943,172 - 45,943,322UniSTS
Whitehead-RH Map2205.8UniSTS
RH68597  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,181,887 - 46,182,016UniSTSGRCh37
Build 36246,035,391 - 46,035,520RGDNCBI36
Celera246,020,305 - 46,020,434RGD
Cytogenetic Map2p21UniSTS
HuRef245,920,015 - 45,920,144UniSTS
GeneMap99-GB4 RH Map2141.05UniSTS
NCBI RH Map2291.6UniSTS
RH18396  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37246,413,301 - 46,413,403UniSTSGRCh37
Build 36246,266,805 - 46,266,907RGDNCBI36
Celera246,251,641 - 46,251,743RGD
Cytogenetic Map2p21UniSTS
HuRef246,151,329 - 46,151,431UniSTS
GeneMap99-GB4 RH Map2142.44UniSTS
NCBI RH Map2291.6UniSTS
D2S391  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map2p16UniSTS
Cytogenetic Map2p21UniSTS
Marshfield Genetic Map270.31UniSTS
Genethon Genetic Map273.8UniSTS
deCODE Assembly Map272.33UniSTS
Whitehead-YAC Contig Map2 UniSTS


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 10 3 24 15 234 16 66 16 1204 46 133 564 1 3 8 1
Low 2420 2830 1695 604 1580 444 4252 2128 2473 370 1318 1042 171 1 1201 2779 5 1
Below cutoff 2 153 6 4 134 5 37 51 44 3 7 4 3 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_005400 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005264428 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005264431 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006712050 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011532971 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011532975 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011532978 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011532980 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011532981 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011532982 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011532983 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017004486 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017004487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017004488 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017004489 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017004490 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017004491 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017004492 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024452991 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024452992 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445094 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445095 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445096 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445097 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445098 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445099 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445100 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342972 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342973 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342974 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342975 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342976 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342977 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342978 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342979 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342980 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342981 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342982 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342983 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342984 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342985 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342986 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342987 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342988 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342989 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342990 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342991 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342992 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001738846 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007078551 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008486453 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008486454 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_939695 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC017006 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC017078 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC079892 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC092600 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC115109 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK022272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK128749 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK313842 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832345 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC029576 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC051195 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC054052 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC109033 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC109034 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA424727 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471053 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU332867 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JX512458 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U51244 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X65293 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000306156   ⟹   ENSP00000306124
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl245,651,675 - 46,187,990 (+)Ensembl
RefSeq Acc Id: ENST00000394874   ⟹   ENSP00000378341
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl246,000,902 - 46,010,964 (+)Ensembl
RefSeq Acc Id: ENST00000421201   ⟹   ENSP00000394574
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl245,651,345 - 45,843,034 (+)Ensembl
RefSeq Acc Id: ENST00000462720
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl245,652,360 - 45,701,491 (+)Ensembl
RefSeq Acc Id: ENST00000467135
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl245,676,734 - 45,845,758 (+)Ensembl
RefSeq Acc Id: ENST00000469753
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl246,073,437 - 46,151,201 (+)Ensembl
RefSeq Acc Id: ENST00000472021
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl245,677,025 - 45,686,347 (+)Ensembl
RefSeq Acc Id: ENST00000476675
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl245,675,619 - 45,980,356 (+)Ensembl
RefSeq Acc Id: ENST00000480453
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl245,652,401 - 45,984,567 (+)Ensembl
RefSeq Acc Id: ENST00000480633
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl246,073,796 - 46,151,164 (+)Ensembl
RefSeq Acc Id: ENST00000485176
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl245,697,982 - 45,770,860 (+)Ensembl
RefSeq Acc Id: ENST00000489067
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl245,978,095 - 45,984,681 (+)Ensembl
RefSeq Acc Id: ENST00000494472
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl246,151,102 - 46,160,060 (+)Ensembl
RefSeq Acc Id: ENST00000497602
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl245,697,972 - 45,852,026 (+)Ensembl
RefSeq Acc Id: ENST00000498388
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl246,151,053 - 46,164,895 (+)Ensembl
RefSeq Acc Id: NM_005400   ⟹   NP_005391
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,651,675 - 46,187,990 (+)NCBI
GRCh37245,878,454 - 46,415,129 (+)NCBI
Build 36245,732,547 - 46,268,633 (+)NCBI Archive
HuRef245,617,217 - 46,153,158 (+)ENTREZGENE
CHM1_1245,810,047 - 46,345,904 (+)NCBI
T2T-CHM13v2.0245,656,718 - 46,193,193 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005264428   ⟹   XP_005264485
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,651,279 - 46,187,990 (+)NCBI
GRCh37245,878,454 - 46,415,129 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005264431   ⟹   XP_005264488
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,651,675 - 46,019,146 (+)NCBI
GRCh37245,878,454 - 46,415,129 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006712050   ⟹   XP_006712113
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38246,000,613 - 46,187,990 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011532971   ⟹   XP_011531273
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,675,723 - 46,187,990 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011532975   ⟹   XP_011531277
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,677,025 - 46,187,990 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011532978   ⟹   XP_011531280
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,697,941 - 46,187,990 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011532980   ⟹   XP_011531282
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,651,675 - 46,187,990 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011532981   ⟹   XP_011531283
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,936,719 - 46,187,990 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011532982   ⟹   XP_011531284
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,978,073 - 46,187,990 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011532983   ⟹   XP_011531285
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38246,002,858 - 46,187,990 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017004488   ⟹   XP_016859977
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,697,941 - 46,187,990 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017004490   ⟹   XP_016859979
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,675,725 - 46,187,990 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017004492   ⟹   XP_016859981
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,651,675 - 46,028,470 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047445094   ⟹   XP_047301050
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,675,723 - 46,187,990 (+)NCBI
RefSeq Acc Id: XM_047445095   ⟹   XP_047301051
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,677,025 - 46,187,990 (+)NCBI
RefSeq Acc Id: XM_047445096   ⟹   XP_047301052
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,677,025 - 46,187,990 (+)NCBI
RefSeq Acc Id: XM_047445097   ⟹   XP_047301053
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,677,140 - 46,187,990 (+)NCBI
RefSeq Acc Id: XM_047445098   ⟹   XP_047301054
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,677,025 - 46,187,990 (+)NCBI
RefSeq Acc Id: XM_047445099   ⟹   XP_047301055
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,698,033 - 46,187,990 (+)NCBI
RefSeq Acc Id: XM_047445100   ⟹   XP_047301056
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,651,279 - 46,010,517 (+)NCBI
RefSeq Acc Id: XM_054342972   ⟹   XP_054198947
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,680,774 - 46,193,193 (+)NCBI
RefSeq Acc Id: XM_054342973   ⟹   XP_054198948
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,680,774 - 46,193,193 (+)NCBI
RefSeq Acc Id: XM_054342974   ⟹   XP_054198949
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,686,362 - 46,193,193 (+)NCBI
RefSeq Acc Id: XM_054342975   ⟹   XP_054198950
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,680,774 - 46,193,193 (+)NCBI
RefSeq Acc Id: XM_054342976   ⟹   XP_054198951
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,681,846 - 46,193,193 (+)NCBI
RefSeq Acc Id: XM_054342977   ⟹   XP_054198952
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,682,191 - 46,193,193 (+)NCBI
RefSeq Acc Id: XM_054342978   ⟹   XP_054198953
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,681,846 - 46,193,193 (+)NCBI
RefSeq Acc Id: XM_054342979   ⟹   XP_054198954
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,703,072 - 46,193,193 (+)NCBI
RefSeq Acc Id: XM_054342980   ⟹   XP_054198955
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,702,980 - 46,193,193 (+)NCBI
RefSeq Acc Id: XM_054342981   ⟹   XP_054198956
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,703,072 - 46,193,193 (+)NCBI
RefSeq Acc Id: XM_054342982   ⟹   XP_054198957
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,702,980 - 46,193,193 (+)NCBI
RefSeq Acc Id: XM_054342983   ⟹   XP_054198958
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,941,725 - 46,193,193 (+)NCBI
RefSeq Acc Id: XM_054342984   ⟹   XP_054198959
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,680,776 - 46,193,193 (+)NCBI
RefSeq Acc Id: XM_054342985   ⟹   XP_054198960
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,845,105 - 46,193,193 (+)NCBI
RefSeq Acc Id: XM_054342986   ⟹   XP_054198961
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,656,718 - 46,193,193 (+)NCBI
RefSeq Acc Id: XM_054342987   ⟹   XP_054198962
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,983,027 - 46,193,193 (+)NCBI
RefSeq Acc Id: XM_054342988   ⟹   XP_054198963
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,656,718 - 46,024,470 (+)NCBI
RefSeq Acc Id: XM_054342989   ⟹   XP_054198964
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,656,718 - 46,043,699 (+)NCBI
RefSeq Acc Id: XM_054342990   ⟹   XP_054198965
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0246,005,935 - 46,193,193 (+)NCBI
RefSeq Acc Id: XM_054342991   ⟹   XP_054198966
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0246,006,910 - 46,193,193 (+)NCBI
RefSeq Acc Id: XM_054342992   ⟹   XP_054198967
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,656,327 - 46,015,843 (+)NCBI
RefSeq Acc Id: XR_007078551
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,651,675 - 46,028,470 (+)NCBI
RefSeq Acc Id: XR_008486453
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,656,718 - 46,043,699 (+)NCBI
RefSeq Acc Id: XR_008486454
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0245,656,718 - 46,043,699 (+)NCBI
RefSeq Acc Id: XR_939695
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38245,651,675 - 46,028,470 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_005391 (Get FASTA)   NCBI Sequence Viewer  
  XP_005264485 (Get FASTA)   NCBI Sequence Viewer  
  XP_005264488 (Get FASTA)   NCBI Sequence Viewer  
  XP_006712113 (Get FASTA)   NCBI Sequence Viewer  
  XP_011531273 (Get FASTA)   NCBI Sequence Viewer  
  XP_011531277 (Get FASTA)   NCBI Sequence Viewer  
  XP_011531280 (Get FASTA)   NCBI Sequence Viewer  
  XP_011531282 (Get FASTA)   NCBI Sequence Viewer  
  XP_011531283 (Get FASTA)   NCBI Sequence Viewer  
  XP_011531284 (Get FASTA)   NCBI Sequence Viewer  
  XP_011531285 (Get FASTA)   NCBI Sequence Viewer  
  XP_016859977 (Get FASTA)   NCBI Sequence Viewer  
  XP_016859979 (Get FASTA)   NCBI Sequence Viewer  
  XP_016859981 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301050 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301051 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301052 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301053 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301054 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301055 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301056 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198947 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198948 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198949 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198950 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198951 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198952 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198953 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198954 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198955 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198956 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198957 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198958 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198959 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198960 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198961 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198962 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198963 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198964 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198965 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198966 (Get FASTA)   NCBI Sequence Viewer  
  XP_054198967 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAD08855 (Get FASTA)   NCBI Sequence Viewer  
  AAI09034 (Get FASTA)   NCBI Sequence Viewer  
  AAI09035 (Get FASTA)   NCBI Sequence Viewer  
  AAX93119 (Get FASTA)   NCBI Sequence Viewer  
  AAX93253 (Get FASTA)   NCBI Sequence Viewer  
  AAY14773 (Get FASTA)   NCBI Sequence Viewer  
  ABY87556 (Get FASTA)   NCBI Sequence Viewer  
  AGC09605 (Get FASTA)   NCBI Sequence Viewer  
  BAG36574 (Get FASTA)   NCBI Sequence Viewer  
  CAA46388 (Get FASTA)   NCBI Sequence Viewer  
  EAX00257 (Get FASTA)   NCBI Sequence Viewer  
  EAX00258 (Get FASTA)   NCBI Sequence Viewer  
  EAX00259 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000306124
  ENSP00000306124.3
  ENSP00000378341.1
  ENSP00000394574.1
GenBank Protein Q02156 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_005391   ⟸   NM_005400
- UniProtKB: Q53SM5 (UniProtKB/Swiss-Prot),   Q53SL4 (UniProtKB/Swiss-Prot),   Q32MQ3 (UniProtKB/Swiss-Prot),   B0LPH7 (UniProtKB/Swiss-Prot),   Q9UE81 (UniProtKB/Swiss-Prot),   Q02156 (UniProtKB/Swiss-Prot),   L7RTI5 (UniProtKB/TrEMBL),   B2R9M7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005264488   ⟸   XM_005264431
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: XP_005264485   ⟸   XM_005264428
- Peptide Label: isoform X1
- UniProtKB: Q53SM5 (UniProtKB/Swiss-Prot),   Q53SL4 (UniProtKB/Swiss-Prot),   Q32MQ3 (UniProtKB/Swiss-Prot),   B0LPH7 (UniProtKB/Swiss-Prot),   Q9UE81 (UniProtKB/Swiss-Prot),   Q02156 (UniProtKB/Swiss-Prot),   L7RTI5 (UniProtKB/TrEMBL),   B2R9M7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006712113   ⟸   XM_006712050
- Peptide Label: isoform X8
- Sequence:
RefSeq Acc Id: XP_011531273   ⟸   XM_011532971
- Peptide Label: isoform X2
- UniProtKB: B2R9M7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011531277   ⟸   XM_011532975
- Peptide Label: isoform X2
- UniProtKB: B2R9M7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011531280   ⟸   XM_011532978
- Peptide Label: isoform X3
- UniProtKB: B2R9M7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011531282   ⟸   XM_011532980
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_011531283   ⟸   XM_011532981
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_011531284   ⟸   XM_011532982
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_011531285   ⟸   XM_011532983
- Peptide Label: isoform X9
- Sequence:
RefSeq Acc Id: XP_016859981   ⟸   XM_017004492
- Peptide Label: isoform X7
- Sequence:
RefSeq Acc Id: XP_016859979   ⟸   XM_017004490
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_016859977   ⟸   XM_017004488
- Peptide Label: isoform X3
- UniProtKB: B2R9M7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000306124   ⟸   ENST00000306156
RefSeq Acc Id: ENSP00000378341   ⟸   ENST00000394874
RefSeq Acc Id: ENSP00000394574   ⟸   ENST00000421201
RefSeq Acc Id: XP_047301056   ⟸   XM_047445100
- Peptide Label: isoform X10
RefSeq Acc Id: XP_047301050   ⟸   XM_047445094
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047301052   ⟸   XM_047445096
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047301051   ⟸   XM_047445095
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047301054   ⟸   XM_047445098
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047301053   ⟸   XM_047445097
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047301055   ⟸   XM_047445099
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054198967   ⟸   XM_054342992
- Peptide Label: isoform X10
RefSeq Acc Id: XP_054198961   ⟸   XM_054342986
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054198964   ⟸   XM_054342989
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054198963   ⟸   XM_054342988
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054198947   ⟸   XM_054342972
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054198948   ⟸   XM_054342973
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054198950   ⟸   XM_054342975
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054198959   ⟸   XM_054342984
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054198951   ⟸   XM_054342976
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054198953   ⟸   XM_054342978
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054198952   ⟸   XM_054342977
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054198949   ⟸   XM_054342974
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054198955   ⟸   XM_054342980
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054198957   ⟸   XM_054342982
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054198956   ⟸   XM_054342981
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054198954   ⟸   XM_054342979
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054198960   ⟸   XM_054342985
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054198958   ⟸   XM_054342983
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054198962   ⟸   XM_054342987
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054198965   ⟸   XM_054342990
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054198966   ⟸   XM_054342991
- Peptide Label: isoform X9
Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q02156-F1-model_v2 AlphaFold Q02156 1-737 view protein structure

Promoters
RGD ID:6860222
Promoter ID:EPDNEW_H3276
Type:initiation region
Name:PRKCE_1
Description:protein kinase C epsilon
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
GRCh38245,651,740 - 45,651,800EPDNEW
RGD ID:6797979
Promoter ID:HG_KWN:32491
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:OTTHUMT00000250751,   OTTHUMT00000258145,   OTTHUMT00000258147,   OTTHUMT00000323445
Position:
Human AssemblyChrPosition (strand)Source
Build 36245,731,161 - 45,732,707 (+)MPROMDB
RGD ID:6797980
Promoter ID:HG_KWN:32497
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3
Transcripts:OTTHUMT00000323644,   OTTHUMT00000323645
Position:
Human AssemblyChrPosition (strand)Source
Build 36246,154,041 - 46,154,541 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:9401 AgrOrtholog
COSMIC PRKCE COSMIC
Ensembl Genes ENSG00000171132 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000306156 ENTREZGENE
  ENST00000306156.8 UniProtKB/Swiss-Prot
  ENST00000394874.1 UniProtKB/TrEMBL
  ENST00000421201.1 UniProtKB/TrEMBL
Gene3D-CATH 2.60.40.150 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.30.60.20 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Transferase(Phosphotransferase) domain 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000171132 GTEx
HGNC ID HGNC:9401 ENTREZGENE
Human Proteome Map PRKCE Human Proteome Map
InterPro AGC-kinase_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  C1-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  C2_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  C2_domain_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DAG/PE-bd UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Kinase-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  nPKC_epsilon UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PE/DAG-bd UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PKC_epsilon UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Pkinase_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Prot_kin_PKC_delta UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Prot_kinase_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Protein_kinase_ATP_BS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ser/Thr_kinase_AS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:5581 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 5581 ENTREZGENE
OMIM 176975 OMIM
PANTHER C2 DOMAIN-CONTAINING PROTEIN UniProtKB/TrEMBL
  CONSERVED SERINE PROLINE-RICH PROTEIN (AFU_ORTHOLOGUE AFUA_2G01790) UniProtKB/TrEMBL
  PROTEIN KINASE C EPSILON TYPE UniProtKB/Swiss-Prot
  PROTEIN KINASE C EPSILON TYPE UniProtKB/TrEMBL
  PROTEIN KINASE C EPSILON TYPE UniProtKB/TrEMBL
  RIBOSOMAL PROTEIN S6 KINASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SERINE/THREONINE-PROTEIN KINASE UniProtKB/TrEMBL
Pfam C1_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PF00168 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Pkinase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Pkinase_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA33765 PharmGKB
PIRSF PKC_delta UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Protein_kin_C_epsilon UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PRINTS DAGPEDOMAIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE AGC_KINASE_CTER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN_KINASE_ATP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN_KINASE_DOM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN_KINASE_ST UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PS50004 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZF_DAG_PE_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZF_DAG_PE_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART S_TK_X UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  S_TKc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00109 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00239 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF49562 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF56112 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF57889 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt B0LPH7 ENTREZGENE
  B2R9M7 ENTREZGENE, UniProtKB/TrEMBL
  C9JR22_HUMAN UniProtKB/TrEMBL
  E9PBI2_HUMAN UniProtKB/TrEMBL
  KPCE_HUMAN UniProtKB/Swiss-Prot
  L7RTI5 ENTREZGENE, UniProtKB/TrEMBL
  Q02156 ENTREZGENE
  Q32MQ3 ENTREZGENE
  Q53RT0_HUMAN UniProtKB/TrEMBL
  Q53SL4 ENTREZGENE
  Q53SM5 ENTREZGENE
  Q9UE81 ENTREZGENE
UniProt Secondary B0LPH7 UniProtKB/Swiss-Prot
  Q32MQ3 UniProtKB/Swiss-Prot
  Q53SL4 UniProtKB/Swiss-Prot
  Q53SM5 UniProtKB/Swiss-Prot
  Q9UE81 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-02-02 PRKCE  protein kinase C epsilon  PRKCE  protein kinase C, epsilon  Symbol and/or name change 5135510 APPROVED