PEG3 (paternally expressed 3) - Rat Genome Database

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Gene: PEG3 (paternally expressed 3) Homo sapiens
Analyze
Symbol: PEG3
Name: paternally expressed 3
RGD ID: 1322359
HGNC Page HGNC:8826
Description: Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within negative regulation of transcription by RNA polymerase II and positive regulation of transcription by RNA polymerase II. Predicted to be located in cytoplasm. Predicted to be part of autophagosome. Predicted to be active in nucleus.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: DKFZp781A095; KIAA0287; Kruppel-type zinc finger protein; paternally expressed gene 3; paternally-expressed gene 3 protein; PW1; zinc finger and SCAN domain-containing protein 24; ZKSCAN22; ZNF904; ZSCAN24
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
GRCh381956,810,082 - 56,840,726 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1956,810,077 - 56,840,728 (-)EnsemblGRCh38hg38GRCh38
GRCh371957,321,450 - 57,352,094 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361962,015,615 - 62,043,876 (-)NCBINCBI36Build 36hg18NCBI36
Build 341962,015,614 - 62,043,876NCBI
Celera1954,363,548 - 54,394,181 (-)NCBICelera
Cytogenetic Map19q13.43NCBI
HuRef1953,630,947 - 53,661,577 (-)NCBIHuRef
CHM1_11957,315,016 - 57,345,647 (-)NCBICHM1_1
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(1->4)-beta-D-glucan  (ISO)
1,2-dimethylhydrazine  (ISO)
17beta-estradiol  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (ISO)
2,3',4,4',5-Pentachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
3,3',5,5'-tetrabromobisphenol A  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
4,4'-sulfonyldiphenol  (ISO)
4-hydroxyphenyl retinamide  (ISO)
acetazolamide  (ISO)
aflatoxin B1  (EXP,ISO)
all-trans-retinoic acid  (ISO)
antirheumatic drug  (EXP)
benzo[a]pyrene  (EXP)
benzo[a]pyrene diol epoxide I  (EXP)
bisphenol A  (EXP,ISO)
bisphenol F  (ISO)
cadmium atom  (EXP,ISO)
cadmium dichloride  (EXP,ISO)
caffeine  (EXP)
CGP 52608  (EXP)
chlorpyrifos  (ISO)
cyclosporin A  (EXP,ISO)
dicrotophos  (EXP)
doxorubicin  (EXP)
endosulfan  (ISO)
ethanol  (ISO)
folic acid  (ISO)
formaldehyde  (EXP)
FR900359  (EXP)
gentamycin  (ISO)
glufosinate  (ISO)
glyphosate  (ISO)
Heptachlor epoxide  (ISO)
hydroquinone  (EXP)
inulin  (ISO)
isoprenaline  (ISO)
lead(0)  (EXP)
leflunomide  (EXP)
methoxychlor  (ISO)
methylseleninic acid  (EXP)
mono(2-ethylhexyl) phthalate  (ISO)
N-methyl-4-phenylpyridinium  (ISO)
N-nitrosodiethylamine  (ISO)
nickel atom  (EXP)
ozone  (ISO)
paracetamol  (ISO)
PD 0325901  (EXP)
perfluorohexanesulfonic acid  (ISO)
perfluorononanoic acid  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (EXP,ISO)
phenobarbital  (ISO)
pirinixic acid  (ISO)
resveratrol  (EXP)
rifampicin  (EXP)
rotenone  (ISO)
sodium arsenate  (ISO)
sodium fluoride  (ISO)
tetrachloromethane  (ISO)
thapsigargin  (ISO)
titanium dioxide  (ISO)
trichloroethene  (ISO)
tris(2-butoxyethyl) phosphate  (EXP)
tunicamycin  (EXP)
valproic acid  (EXP,ISO)
vinclozolin  (ISO)
zinc atom  (EXP)
zinc dichloride  (EXP)
zinc(0)  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
autophagosome  (ISO,ISS)
cytoplasm  (IEA)
nucleus  (IBA,IEA,ISS)

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:9149948   PMID:9500555   PMID:10681424   PMID:10708526   PMID:11181995   PMID:11260267   PMID:11331620   PMID:11746496   PMID:11943780   PMID:12477932   PMID:15174051   PMID:15489334  
PMID:16023706   PMID:16713569   PMID:18029348   PMID:18286529   PMID:19367087   PMID:19397955   PMID:19834535   PMID:20064927   PMID:21873635   PMID:23151531   PMID:23414517   PMID:23418553  
PMID:23798385   PMID:23936039   PMID:24120702   PMID:25751651   PMID:26838788   PMID:27075691   PMID:27104590   PMID:28027390   PMID:28174297   PMID:28798237   PMID:28852087   PMID:29080840  
PMID:29229926   PMID:31420931   PMID:32729618   PMID:33023834   PMID:34192708   PMID:35914814   PMID:35944360   PMID:36244648   PMID:37001595  


Genomics

Comparative Map Data
PEG3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381956,810,082 - 56,840,726 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1956,810,077 - 56,840,728 (-)EnsemblGRCh38hg38GRCh38
GRCh371957,321,450 - 57,352,094 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361962,015,615 - 62,043,876 (-)NCBINCBI36Build 36hg18NCBI36
Build 341962,015,614 - 62,043,876NCBI
Celera1954,363,548 - 54,394,181 (-)NCBICelera
Cytogenetic Map19q13.43NCBI
HuRef1953,630,947 - 53,661,577 (-)NCBIHuRef
CHM1_11957,315,016 - 57,345,647 (-)NCBICHM1_1
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBIT2T-CHM13v2.0
Peg3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3976,706,891 - 6,733,443 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl76,706,891 - 6,733,430 (-)EnsemblGRCm39 Ensembl
GRCm3876,703,892 - 6,730,462 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl76,703,892 - 6,730,431 (-)EnsemblGRCm38mm10GRCm38
MGSCv3776,658,671 - 6,683,130 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3676,310,046 - 6,334,505 (-)NCBIMGSCv36mm8
Celera76,434,503 - 6,458,962 (-)NCBICelera
Cytogenetic Map7A1NCBI
cM Map73.89NCBI
Peg3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8176,130,965 - 76,157,774 (+)NCBIGRCr8
mRatBN7.2167,097,874 - 67,124,692 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl167,097,904 - 67,124,671 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx172,449,234 - 72,476,014 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0181,086,304 - 81,113,084 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0174,280,635 - 74,307,415 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0170,210,810 - 70,237,450 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl170,222,964 - 70,237,443 (+)EnsemblRnor6.0rn6Rnor6.0
RGSC_v3.4165,513,912 - 65,526,040 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera164,850,188 - 64,876,970 (+)NCBICelera
Cytogenetic Map1q12NCBI
Peg3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_00495556785,913 - 96,236 (+)NCBIChiLan1.0ChiLan1.0
LOC100987733
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22063,057,542 - 63,127,394 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11964,845,656 - 64,915,499 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01953,830,193 - 53,860,760 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11962,624,109 - 62,654,698 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1962,588,511 - 62,654,661 (-)Ensemblpanpan1.1panPan2
PEG3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11101,091,161 - 101,123,552 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1101,098,669 - 101,121,032 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1101,293,080 - 101,325,474 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01101,742,068 - 101,774,234 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1101,742,090 - 101,774,245 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11101,412,707 - 101,445,138 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01101,098,745 - 101,131,169 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01101,854,582 - 101,887,018 (+)NCBIUU_Cfam_GSD_1.0
Peg3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024409349872,878 - 903,119 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936882577,395 - 591,042 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936882577,424 - 607,691 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
PEG3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl661,285,456 - 61,292,885 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1661,281,931 - 61,307,788 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2656,618,090 - 56,643,389 (-)NCBISscrofa10.2Sscrofa10.2susScr3
Pig Cytomap6q11-q22NCBI
PEG3
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1649,284,174 - 49,300,162 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl649,284,064 - 49,313,455 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660452,300,183 - 2,329,639 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Peg3
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248321,210,070 - 1,223,456 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248321,194,472 - 1,223,382 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in PEG3
105 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19q13.33-13.43(chr19:50191219-58535818)x3 copy number gain See cases [RCV000050883] Chr19:50191219..58535818 [GRCh38]
Chr19:50694476..59047185 [GRCh37]
Chr19:55386288..63738997 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3 copy number gain See cases [RCV000052925] Chr19:49907832..58557889 [GRCh38]
Chr19:50411089..59069256 [GRCh37]
Chr19:55102901..63761068 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:51141518-58539965)x3 copy number gain See cases [RCV000052926] Chr19:51141518..58539965 [GRCh38]
Chr19:51644775..59051332 [GRCh37]
Chr19:56336587..63743144 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh38/hg38 19q13.43(chr19:56363208-58581203)x3 copy number gain See cases [RCV000052927] Chr19:56363208..58581203 [GRCh38]
Chr19:56874577..59092570 [GRCh37]
Chr19:61566389..63784382 [NCBI36]
Chr19:19q13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3 copy number gain See cases [RCV000052914] Chr19:47908540..58539965 [GRCh38]
Chr19:48411797..59051332 [GRCh37]
Chr19:53103609..63743144 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3 copy number gain See cases [RCV000052915] Chr19:47929575..58572206 [GRCh38]
Chr19:48432832..59083573 [GRCh37]
Chr19:53124644..63775385 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
NM_006210.2(PEG3):c.3333C>T (p.Asp1111=) single nucleotide variant Malignant melanoma [RCV000072399] Chr19:56815109 [GRCh38]
Chr19:57326477 [GRCh37]
Chr19:62018289 [NCBI36]
Chr19:19q13.43		 not provided
NM_006210.2(PEG3):c.702C>T (p.Leu234=) single nucleotide variant Malignant melanoma [RCV000072400] Chr19:56818670 [GRCh38]
Chr19:57330038 [GRCh37]
Chr19:62021850 [NCBI36]
Chr19:19q13.43		 not provided
NM_006210.2(PEG3):c.203G>A (p.Arg68Gln) single nucleotide variant Malignant melanoma [RCV000072401] Chr19:56824453 [GRCh38]
Chr19:57335821 [GRCh37]
Chr19:62027633 [NCBI36]
Chr19:19q13.43		 not provided
NM_006210.2(PEG3):c.2162C>T (p.Ser721Phe) single nucleotide variant Malignant melanoma [RCV000063652] Chr19:56816280 [GRCh38]
Chr19:57327648 [GRCh37]
Chr19:62019460 [NCBI36]
Chr19:19q13.43		 not provided
NM_006210.2(PEG3):c.985G>A (p.Gly329Arg) single nucleotide variant Malignant melanoma [RCV000063653] Chr19:56817457 [GRCh38]
Chr19:57328825 [GRCh37]
Chr19:62020637 [NCBI36]
Chr19:19q13.43		 not provided
GRCh38/hg38 19q13.41-13.43(chr19:52612432-58581203)x3 copy number gain See cases [RCV000134174] Chr19:52612432..58581203 [GRCh38]
Chr19:53115685..59092570 [GRCh37]
Chr19:57807497..63784382 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52955056-58581203)x3 copy number gain See cases [RCV000134139] Chr19:52955056..58581203 [GRCh38]
Chr19:53458309..59092570 [GRCh37]
Chr19:58150121..63784382 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh38/hg38 19q13.42-13.43(chr19:55550939-57031576)x1 copy number loss See cases [RCV000135287] Chr19:55550939..57031576 [GRCh38]
Chr19:56062305..57542944 [GRCh37]
Chr19:60754117..62234756 [NCBI36]
Chr19:19q13.42-13.43		 likely pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3 copy number gain See cases [RCV000135843] Chr19:50152520..58581203 [GRCh38]
Chr19:50655777..59092570 [GRCh37]
Chr19:55347589..63784382 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.42-13.43(chr19:55048514-56972458)x3 copy number gain See cases [RCV000138139] Chr19:55048514..56972458 [GRCh38]
Chr19:55595687..57483826 [GRCh37]
Chr19:60251694..62175638 [NCBI36]
Chr19:19q13.42-13.43		 likely pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52143873-58445521)x3 copy number gain See cases [RCV000142008] Chr19:52143873..58445521 [GRCh38]
Chr19:52647126..58956888 [GRCh37]
Chr19:57338938..63648700 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh38/hg38 19q13.43(chr19:56353449-58445521)x3 copy number gain See cases [RCV000141900] Chr19:56353449..58445521 [GRCh38]
Chr19:56864818..58956888 [GRCh37]
Chr19:61556630..63648700 [NCBI36]
Chr19:19q13.43		 uncertain significance
GRCh38/hg38 19q13.42-13.43(chr19:55037146-56982033)x3 copy number gain See cases [RCV000142245] Chr19:55037146..56982033 [GRCh38]
Chr19:55548514..57493401 [GRCh37]
Chr19:60240326..62185213 [NCBI36]
Chr19:19q13.42-13.43		 uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:56200298-57654005)x1 copy number loss Breast ductal adenocarcinoma [RCV000207313] Chr19:56200298..57654005 [GRCh37]
Chr19:19q13.42-13.43		 uncertain significance
chr19:56133299..57648277 complex variant complex Breast ductal adenocarcinoma [RCV000207023] Chr19:56133299..57648277 [GRCh37]
Chr19:19q13.42-13.43		 uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3 copy number gain See cases [RCV000445925] Chr19:50489390..59095359 [GRCh37]
Chr19:19q13.33-13.43		 pathogenic
GRCh37/hg19 19q13.42-13.43(chr19:54344821-58956888)x3 copy number gain See cases [RCV000448186] Chr19:54344821..58956888 [GRCh37]
Chr19:19q13.42-13.43		 pathogenic
GRCh37/hg19 19q13.42-13.43(chr19:55549385-57489784)x3 copy number gain See cases [RCV000510290] Chr19:55549385..57489784 [GRCh37]
Chr19:19q13.42-13.43		 uncertain significance
NM_006210.3(PEG3):c.3548G>T (p.Arg1183Ile) single nucleotide variant Inborn genetic diseases [RCV003287579] Chr19:56814894 [GRCh38]
Chr19:57326262 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_001387356.1(ZIM2):c.202C>T (p.Arg68Trp) single nucleotide variant Inborn genetic diseases [RCV003249506] Chr19:56821743 [GRCh38]
Chr19:57333111 [GRCh37]
Chr19:19q13.43		 uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:55844155-57408007)x3 copy number gain See cases [RCV000511123] Chr19:55844155..57408007 [GRCh37]
Chr19:19q13.42-13.43		 uncertain significance
GRCh37/hg19 19q13.43(chr19:56706500-58956888)x3 copy number gain See cases [RCV000512396] Chr19:56706500..58956888 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.2666G>A (p.Arg889His) single nucleotide variant Inborn genetic diseases [RCV003256505] Chr19:56815776 [GRCh38]
Chr19:57327144 [GRCh37]
Chr19:19q13.43		 likely benign
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic|uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19q13.43(chr19:56565455-57401997)x1 copy number loss not provided [RCV000684087] Chr19:56565455..57401997 [GRCh37]
Chr19:19q13.43		 uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:54196216-58759679)x3 copy number gain not provided [RCV000684095] Chr19:54196216..58759679 [GRCh37]
Chr19:19q13.42-13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19q13.33-13.43(chr19:50740074-59097160)x3 copy number gain not provided [RCV000740208] Chr19:50740074..59097160 [GRCh37]
Chr19:19q13.33-13.43		 pathogenic
NM_006210.3(PEG3):c.4265C>G (p.Ala1422Gly) single nucleotide variant not provided [RCV000958463] Chr19:56814177 [GRCh38]
Chr19:57325545 [GRCh37]
Chr19:19q13.43		 likely benign
NM_001387356.1(ZIM2):c.487C>G (p.Arg163Gly) single nucleotide variant PEG3-related condition [RCV003936177]|not provided [RCV000973798] Chr19:56817749 [GRCh38]
Chr19:57329117 [GRCh37]
Chr19:19q13.43		 likely benign
NM_006210.3(PEG3):c.4206_4226dup (p.1398EVEAAEP[4]) duplication not provided [RCV000903354] Chr19:56814215..56814216 [GRCh38]
Chr19:57325583..57325584 [GRCh37]
Chr19:19q13.43		 likely benign
NM_006210.3(PEG3):c.4506A>T (p.Glu1502Asp) single nucleotide variant not provided [RCV000969328] Chr19:56813936 [GRCh38]
Chr19:57325304 [GRCh37]
Chr19:19q13.43		 benign|likely benign
NM_006210.3(PEG3):c.1597G>T (p.Val533Leu) single nucleotide variant not provided [RCV000971133] Chr19:56816845 [GRCh38]
Chr19:57328213 [GRCh37]
Chr19:19q13.43		 benign
NM_001387356.1(ZIM2):c.17-4T>G single nucleotide variant not provided [RCV000883860] Chr19:56823683 [GRCh38]
Chr19:57335051 [GRCh37]
Chr19:19q13.43		 benign
NM_006210.3(PEG3):c.1787A>G (p.His596Arg) single nucleotide variant not provided [RCV000972958] Chr19:56816655 [GRCh38]
Chr19:57328023 [GRCh37]
Chr19:19q13.43		 benign
NM_006210.3(PEG3):c.2092T>G (p.Ser698Ala) single nucleotide variant not provided [RCV000971132] Chr19:56816350 [GRCh38]
Chr19:57327718 [GRCh37]
Chr19:19q13.43		 benign
NM_001387356.1(ZIM2):c.253G>A (p.Glu85Lys) single nucleotide variant not provided [RCV000966622] Chr19:56821692 [GRCh38]
Chr19:57333060 [GRCh37]
Chr19:19q13.43		 benign
NM_006210.3(PEG3):c.2883A>G (p.Thr961=) single nucleotide variant not provided [RCV000965462] Chr19:56815559 [GRCh38]
Chr19:57326927 [GRCh37]
Chr19:19q13.43		 benign
NM_006210.3(PEG3):c.3831C>T (p.Thr1277=) single nucleotide variant not provided [RCV000949849] Chr19:56814611 [GRCh38]
Chr19:57325979 [GRCh37]
Chr19:19q13.43		 benign
NM_006210.3(PEG3):c.2378T>C (p.Val793Ala) single nucleotide variant not provided [RCV000969329] Chr19:56816064 [GRCh38]
Chr19:57327432 [GRCh37]
Chr19:19q13.43		 benign
NM_006210.3(PEG3):c.4089A>G (p.Ala1363=) single nucleotide variant not provided [RCV000926471] Chr19:56814353 [GRCh38]
Chr19:57325721 [GRCh37]
Chr19:19q13.43		 likely benign
NM_001387356.1(ZIM2):c.49G>A (p.Asp17Asn) single nucleotide variant not provided [RCV000882273] Chr19:56823647 [GRCh38]
Chr19:57335015 [GRCh37]
Chr19:19q13.43		 likely benign
NM_006210.3(PEG3):c.225G>A (p.Leu75=) single nucleotide variant not provided [RCV000964391] Chr19:56824431 [GRCh38]
Chr19:57335799 [GRCh37]
Chr19:19q13.43		 benign
NM_001387356.1(ZIM2):c.155G>A (p.Arg52Gln) single nucleotide variant not provided [RCV000880042] Chr19:56822788 [GRCh38]
Chr19:57334156 [GRCh37]
Chr19:19q13.43		 likely benign
NM_006210.3(PEG3):c.4167C>T (p.Gly1389=) single nucleotide variant not provided [RCV000904757] Chr19:56814275 [GRCh38]
Chr19:57325643 [GRCh37]
Chr19:19q13.43		 benign
NM_006210.3(PEG3):c.202C>T (p.Arg68Ter) single nucleotide variant not provided [RCV000897170] Chr19:56824454 [GRCh38]
Chr19:57335822 [GRCh37]
Chr19:19q13.43		 likely benign
NM_006210.3(PEG3):c.4367C>T (p.Ala1456Val) single nucleotide variant not provided [RCV000948011] Chr19:56814075 [GRCh38]
Chr19:57325443 [GRCh37]
Chr19:19q13.43		 benign
NM_006210.3(PEG3):c.933C>T (p.His311=) single nucleotide variant not provided [RCV000948012] Chr19:56817509 [GRCh38]
Chr19:57328877 [GRCh37]
Chr19:19q13.43		 benign
NM_006210.3(PEG3):c.333G>A (p.Pro111=) single nucleotide variant not provided [RCV000892204] Chr19:56824323 [GRCh38]
Chr19:57335691 [GRCh37]
Chr19:19q13.43		 likely benign
NM_006210.3(PEG3):c.3724G>A (p.Glu1242Lys) single nucleotide variant Inborn genetic diseases [RCV003292547] Chr19:56814718 [GRCh38]
Chr19:57326086 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.4083T>C (p.Asp1361=) single nucleotide variant not provided [RCV000910575] Chr19:56814359 [GRCh38]
Chr19:57325727 [GRCh37]
Chr19:19q13.43		 benign|likely benign
NM_001387356.1(ZIM2):c.348C>A (p.His116Gln) single nucleotide variant PEG3-related condition [RCV003932927]|not provided [RCV000907873] Chr19:56818649 [GRCh38]
Chr19:57330017 [GRCh37]
Chr19:19q13.43		 likely benign
NM_006210.3(PEG3):c.3870T>A (p.Ser1290=) single nucleotide variant not provided [RCV000885345] Chr19:56814572 [GRCh38]
Chr19:57325940 [GRCh37]
Chr19:19q13.43		 likely benign
NM_006210.3(PEG3):c.3933C>T (p.Tyr1311=) single nucleotide variant not provided [RCV000885837] Chr19:56814509 [GRCh38]
Chr19:57325877 [GRCh37]
Chr19:19q13.43		 benign
NM_006210.3(PEG3):c.2515G>C (p.Val839Leu) single nucleotide variant not provided [RCV000964080] Chr19:56815927 [GRCh38]
Chr19:57327295 [GRCh37]
Chr19:19q13.43		 benign
NM_001387356.1(ZIM2):c.101T>C (p.Phe34Ser) single nucleotide variant not provided [RCV000898774] Chr19:56823595 [GRCh38]
Chr19:57334963 [GRCh37]
Chr19:19q13.43		 likely benign
NM_006210.3(PEG3):c.2390G>T (p.Ser797Ile) single nucleotide variant not provided [RCV000955045] Chr19:56816052 [GRCh38]
Chr19:57327420 [GRCh37]
Chr19:19q13.43		 benign
NM_006210.3(PEG3):c.2790T>C (p.Arg930=) single nucleotide variant not provided [RCV000889169] Chr19:56815652 [GRCh38]
Chr19:57327020 [GRCh37]
Chr19:19q13.43		 benign
NM_006210.3(PEG3):c.4701C>T (p.Asp1567=) single nucleotide variant not provided [RCV000889287] Chr19:56813741 [GRCh38]
Chr19:57325109 [GRCh37]
Chr19:19q13.43		 benign
NM_006210.3(PEG3):c.1871A>G (p.Glu624Gly) single nucleotide variant not provided [RCV000889288] Chr19:56816571 [GRCh38]
Chr19:57327939 [GRCh37]
Chr19:19q13.43		 benign
NM_006210.3(PEG3):c.2201G>A (p.Ser734Asn) single nucleotide variant Inborn genetic diseases [RCV003294998] Chr19:56816241 [GRCh38]
Chr19:57327609 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.1529G>A (p.Cys510Tyr) single nucleotide variant not provided [RCV001355115] Chr19:56816913 [GRCh38]
Chr19:57328281 [GRCh37]
Chr19:19q13.43		 uncertain significance
GRCh37/hg19 19q13.43(chr19:57136208-57478257) copy number gain not specified [RCV002052692] Chr19:57136208..57478257 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.3058G>A (p.Ala1020Thr) single nucleotide variant not provided [RCV002263196] Chr19:56815384 [GRCh38]
Chr19:57326752 [GRCh37]
Chr19:19q13.43		 likely benign
NM_006210.3(PEG3):c.1333A>G (p.Ile445Val) single nucleotide variant Inborn genetic diseases [RCV002681998] Chr19:56817109 [GRCh38]
Chr19:57328477 [GRCh37]
Chr19:19q13.43		 likely benign
NM_006210.3(PEG3):c.3005A>G (p.Tyr1002Cys) single nucleotide variant Inborn genetic diseases [RCV002749891] Chr19:56815437 [GRCh38]
Chr19:57326805 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.3440C>T (p.Thr1147Ile) single nucleotide variant Inborn genetic diseases [RCV002945814] Chr19:56815002 [GRCh38]
Chr19:57326370 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.1886G>A (p.Cys629Tyr) single nucleotide variant Inborn genetic diseases [RCV002945361] Chr19:56816556 [GRCh38]
Chr19:57327924 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.2330C>T (p.Ser777Phe) single nucleotide variant Inborn genetic diseases [RCV002749971] Chr19:56816112 [GRCh38]
Chr19:57327480 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.4080A>T (p.Glu1360Asp) single nucleotide variant Inborn genetic diseases [RCV002973528] Chr19:56814362 [GRCh38]
Chr19:57325730 [GRCh37]
Chr19:19q13.43		 likely benign
NM_006210.3(PEG3):c.4738G>A (p.Ala1580Thr) single nucleotide variant Inborn genetic diseases [RCV002689393] Chr19:56813704 [GRCh38]
Chr19:57325072 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.3059C>T (p.Ala1020Val) single nucleotide variant Inborn genetic diseases [RCV002901710] Chr19:56815383 [GRCh38]
Chr19:57326751 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.4438G>A (p.Asp1480Asn) single nucleotide variant Inborn genetic diseases [RCV002973508] Chr19:56814004 [GRCh38]
Chr19:57325372 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.1810C>T (p.Arg604Cys) single nucleotide variant Inborn genetic diseases [RCV002992153] Chr19:56816632 [GRCh38]
Chr19:57328000 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.3325T>A (p.Cys1109Ser) single nucleotide variant Inborn genetic diseases [RCV002860998] Chr19:56815117 [GRCh38]
Chr19:57326485 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.1009C>T (p.Arg337Trp) single nucleotide variant Inborn genetic diseases [RCV002969721] Chr19:56817433 [GRCh38]
Chr19:57328801 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.1804C>T (p.Arg602Cys) single nucleotide variant Inborn genetic diseases [RCV002818563] Chr19:56816638 [GRCh38]
Chr19:57328006 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.3872T>C (p.Phe1291Ser) single nucleotide variant Inborn genetic diseases [RCV002732459] Chr19:56814570 [GRCh38]
Chr19:57325938 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.304C>G (p.Leu102Val) single nucleotide variant Inborn genetic diseases [RCV002728910] Chr19:56824352 [GRCh38]
Chr19:57335720 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.1138A>G (p.Thr380Ala) single nucleotide variant Inborn genetic diseases [RCV002901914] Chr19:56817304 [GRCh38]
Chr19:57328672 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.4634A>G (p.Tyr1545Cys) single nucleotide variant Inborn genetic diseases [RCV002973920] Chr19:56813808 [GRCh38]
Chr19:57325176 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.4460T>C (p.Ile1487Thr) single nucleotide variant Inborn genetic diseases [RCV002868384] Chr19:56813982 [GRCh38]
Chr19:57325350 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.2939A>G (p.His980Arg) single nucleotide variant Inborn genetic diseases [RCV002759833] Chr19:56815503 [GRCh38]
Chr19:57326871 [GRCh37]
Chr19:19q13.43		 likely benign
NM_006210.3(PEG3):c.1811G>A (p.Arg604His) single nucleotide variant Inborn genetic diseases [RCV002998266] Chr19:56816631 [GRCh38]
Chr19:57327999 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.1862A>G (p.Tyr621Cys) single nucleotide variant Inborn genetic diseases [RCV002821078] Chr19:56816580 [GRCh38]
Chr19:57327948 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_001387356.1(ZIM2):c.46G>A (p.Asp16Asn) single nucleotide variant Inborn genetic diseases [RCV002738808] Chr19:56823650 [GRCh38]
Chr19:57335018 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.2761G>A (p.Glu921Lys) single nucleotide variant Inborn genetic diseases [RCV002738522] Chr19:56815681 [GRCh38]
Chr19:57327049 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.4298T>C (p.Ile1433Thr) single nucleotide variant Inborn genetic diseases [RCV002869480] Chr19:56814144 [GRCh38]
Chr19:57325512 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.1280G>A (p.Ser427Asn) single nucleotide variant Inborn genetic diseases [RCV002850091] Chr19:56817162 [GRCh38]
Chr19:57328530 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.977C>G (p.Ser326Cys) single nucleotide variant Inborn genetic diseases [RCV002713561] Chr19:56817465 [GRCh38]
Chr19:57328833 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.23C>T (p.Ser8Phe) single nucleotide variant Inborn genetic diseases [RCV002699182] Chr19:56824633 [GRCh38]
Chr19:57336001 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.4748A>G (p.Gln1583Arg) single nucleotide variant Inborn genetic diseases [RCV002802401] Chr19:56813694 [GRCh38]
Chr19:57325062 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.2870T>C (p.Phe957Ser) single nucleotide variant Inborn genetic diseases [RCV002893155] Chr19:56815572 [GRCh38]
Chr19:57326940 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.2749A>C (p.Lys917Gln) single nucleotide variant Inborn genetic diseases [RCV002709752] Chr19:56815693 [GRCh38]
Chr19:57327061 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.221G>C (p.Trp74Ser) single nucleotide variant Inborn genetic diseases [RCV002893746] Chr19:56824435 [GRCh38]
Chr19:57335803 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.4301G>A (p.Gly1434Glu) single nucleotide variant Inborn genetic diseases [RCV002955521] Chr19:56814141 [GRCh38]
Chr19:57325509 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.3707A>G (p.His1236Arg) single nucleotide variant Inborn genetic diseases [RCV002743386] Chr19:56814735 [GRCh38]
Chr19:57326103 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.1971C>G (p.Asn657Lys) single nucleotide variant Inborn genetic diseases [RCV002935590] Chr19:56816471 [GRCh38]
Chr19:57327839 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.3410G>T (p.Ser1137Ile) single nucleotide variant Inborn genetic diseases [RCV002812560] Chr19:56815032 [GRCh38]
Chr19:57326400 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.1799G>A (p.Arg600His) single nucleotide variant Inborn genetic diseases [RCV002669211] Chr19:56816643 [GRCh38]
Chr19:57328011 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.3625C>T (p.Arg1209Trp) single nucleotide variant Inborn genetic diseases [RCV002878108] Chr19:56814817 [GRCh38]
Chr19:57326185 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_001387356.1(ZIM2):c.437C>T (p.Thr146Met) single nucleotide variant Inborn genetic diseases [RCV002989037] Chr19:56817799 [GRCh38]
Chr19:57329167 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.3680G>A (p.Cys1227Tyr) single nucleotide variant Inborn genetic diseases [RCV002878109] Chr19:56814762 [GRCh38]
Chr19:57326130 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.1741C>T (p.His581Tyr) single nucleotide variant Inborn genetic diseases [RCV002703292] Chr19:56816701 [GRCh38]
Chr19:57328069 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.325A>G (p.Lys109Glu) single nucleotide variant Inborn genetic diseases [RCV002941703] Chr19:56824331 [GRCh38]
Chr19:57335699 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.3217A>G (p.Thr1073Ala) single nucleotide variant Inborn genetic diseases [RCV002919968] Chr19:56815225 [GRCh38]
Chr19:57326593 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.1758T>A (p.Phe586Leu) single nucleotide variant Inborn genetic diseases [RCV002878107] Chr19:56816684 [GRCh38]
Chr19:57328052 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.890A>C (p.Lys297Thr) single nucleotide variant Inborn genetic diseases [RCV002944817] Chr19:56817552 [GRCh38]
Chr19:57328920 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.3349G>A (p.Val1117Met) single nucleotide variant Inborn genetic diseases [RCV002679141] Chr19:56815093 [GRCh38]
Chr19:57326461 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.1805G>A (p.Arg602His) single nucleotide variant Inborn genetic diseases [RCV002944368] Chr19:56816637 [GRCh38]
Chr19:57328005 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.3713C>G (p.Ser1238Cys) single nucleotide variant Inborn genetic diseases [RCV002722486] Chr19:56814729 [GRCh38]
Chr19:57326097 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.2456G>A (p.Arg819His) single nucleotide variant Inborn genetic diseases [RCV003280691] Chr19:56815986 [GRCh38]
Chr19:57327354 [GRCh37]
Chr19:19q13.43		 likely benign
NM_006210.3(PEG3):c.992C>A (p.Ala331Glu) single nucleotide variant Inborn genetic diseases [RCV003203910] Chr19:56817450 [GRCh38]
Chr19:57328818 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.1132A>C (p.Asn378His) single nucleotide variant Inborn genetic diseases [RCV003211388] Chr19:56817310 [GRCh38]
Chr19:57328678 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.3279C>A (p.Asp1093Glu) single nucleotide variant Inborn genetic diseases [RCV003199776] Chr19:56815163 [GRCh38]
Chr19:57326531 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.4676C>G (p.Ala1559Gly) single nucleotide variant Inborn genetic diseases [RCV003258335] Chr19:56813766 [GRCh38]
Chr19:57325134 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.1108G>T (p.Ala370Ser) single nucleotide variant Inborn genetic diseases [RCV003183683] Chr19:56817334 [GRCh38]
Chr19:57328702 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.1010G>A (p.Arg337Gln) single nucleotide variant Inborn genetic diseases [RCV003357553] Chr19:56817432 [GRCh38]
Chr19:57328800 [GRCh37]
Chr19:19q13.43		 likely benign
NM_006210.3(PEG3):c.148C>G (p.Arg50Gly) single nucleotide variant Inborn genetic diseases [RCV003359580] Chr19:56824508 [GRCh38]
Chr19:57335876 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.4624T>C (p.Cys1542Arg) single nucleotide variant Inborn genetic diseases [RCV003385674] Chr19:56813818 [GRCh38]
Chr19:57325186 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.2607T>A (p.Asn869Lys) single nucleotide variant Inborn genetic diseases [RCV003364326] Chr19:56815835 [GRCh38]
Chr19:57327203 [GRCh37]
Chr19:19q13.43		 uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3 copy number gain not provided [RCV003485200] Chr19:49625130..57647352 [GRCh37]
Chr19:19q13.33-13.43		 likely pathogenic
GRCh37/hg19 19q13.43(chr19:56949121-57419586)x3 copy number gain not provided [RCV003485202] Chr19:56949121..57419586 [GRCh37]
Chr19:19q13.43		 uncertain significance
NM_006210.3(PEG3):c.1813G>A (p.Gly605Arg) single nucleotide variant not provided [RCV003457050] Chr19:56816629 [GRCh38]
Chr19:57327997 [GRCh37]
Chr19:19q13.43		 benign
NM_006210.3(PEG3):c.3310G>A (p.Asp1104Asn) single nucleotide variant PEG3-related condition [RCV003954169]|not provided [RCV003425454] Chr19:56815132 [GRCh38]
Chr19:57326500 [GRCh37]
Chr19:19q13.43		 likely benign
NM_006210.3(PEG3):c.4068AGA[6] (p.Glu1360_Asp1361insGlu) microsatellite not provided [RCV003407140] Chr19:56814359..56814360 [GRCh38]
Chr19:57325727..57325728 [GRCh37]
Chr19:19q13.43		 likely benign
GRCh37/hg19 19q13.42-13.43(chr19:56080158-57672397)x1 copy number loss not specified [RCV003986104] Chr19:56080158..57672397 [GRCh37]
Chr19:19q13.42-13.43		 uncertain significance
NM_006210.3(PEG3):c.4213GAAGTGGAGGCTGCTGAGCCA[1] (p.1398EVEAAEP[2]) microsatellite PEG3-related condition [RCV003972145] Chr19:56814188..56814208 [GRCh38]
Chr19:57325556..57325576 [GRCh37]
Chr19:19q13.43		 likely benign
NM_006210.3(PEG3):c.4450G>A (p.Gly1484Ser) single nucleotide variant PEG3-related condition [RCV003969757] Chr19:56813992 [GRCh38]
Chr19:57325360 [GRCh37]
Chr19:19q13.43		 likely benign
NM_006210.3(PEG3):c.3130G>A (p.Glu1044Lys) single nucleotide variant PEG3-related condition [RCV003941814] Chr19:56815312 [GRCh38]
Chr19:57326680 [GRCh37]
Chr19:19q13.43		 likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3512
Count of miRNA genes:995
Interacting mature miRNAs:1189
Transcripts:ENST00000326441, ENST00000423103, ENST00000593695, ENST00000594389, ENST00000594706, ENST00000596261, ENST00000598410, ENST00000599534, ENST00000599565, ENST00000599577, ENST00000600833
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
SHGC-32171  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371957,323,516 - 57,323,644UniSTSGRCh37
Build 361962,015,328 - 62,015,456RGDNCBI36
Celera1954,365,619 - 54,365,747RGD
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map19q13.4UniSTS
HuRef1953,633,019 - 53,633,147UniSTS
TNG Radiation Hybrid Map1922405.0UniSTS
Stanford-G3 RH Map192856.0UniSTS
Whitehead-RH Map19370.0UniSTS
NCBI RH Map19596.6UniSTS
GeneMap99-G3 RH Map192867.0UniSTS
STS-W93046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371957,323,905 - 57,324,056UniSTSGRCh37
Build 361962,015,717 - 62,015,868RGDNCBI36
Celera1954,366,008 - 54,366,159RGD
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map19q13.4UniSTS
GeneMap99-GB4 RH Map19284.08UniSTS
D19S699E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371957,325,121 - 57,325,220UniSTSGRCh37
Build 361962,016,933 - 62,017,032RGDNCBI36
Celera1954,367,224 - 54,367,323RGD
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map19q13.4UniSTS
HuRef1953,634,624 - 53,634,723UniSTS
RH18153  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371957,323,516 - 57,323,785UniSTSGRCh37
Build 361962,015,328 - 62,015,597RGDNCBI36
Celera1954,365,619 - 54,365,888RGD
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map19q13.4UniSTS
HuRef1953,633,019 - 53,633,288UniSTS
SGC34114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371957,321,495 - 57,321,619UniSTSGRCh37
Build 361962,013,307 - 62,013,431RGDNCBI36
Celera1954,363,598 - 54,363,722RGD
Cytogenetic Map19q13.4UniSTS
HuRef1953,630,997 - 53,631,121UniSTS
GeneMap99-GB4 RH Map19289.56UniSTS
Whitehead-RH Map19365.4UniSTS
NCBI RH Map19600.0UniSTS
RH17474  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371957,321,511 - 57,321,718UniSTSGRCh37
Build 361962,013,323 - 62,013,530RGDNCBI36
Celera1954,363,614 - 54,363,821RGD
Cytogenetic Map19q13.4UniSTS
HuRef1953,631,013 - 53,631,220UniSTS
GeneMap99-GB4 RH Map19284.01UniSTS
RH66112  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.4UniSTS
GeneMap99-GB4 RH Map19290.76UniSTS
PEG3  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371957,328,153 - 57,328,397UniSTSGRCh37
Celera1954,370,256 - 54,370,500UniSTS
HuRef1953,637,656 - 53,637,900UniSTS
WI-22317  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371957,321,518 - 57,322,645UniSTSGRCh37
Celera1954,363,621 - 54,364,748UniSTS
Cytogenetic Map19q13.4UniSTS
HuRef1953,631,020 - 53,632,148UniSTS
GeneMap99-GB4 RH Map19285.82UniSTS
Whitehead-RH Map19368.5UniSTS
NCBI RH Map19586.5UniSTS


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 adipose tissue appendage entire extraembryonic component
High 1
Medium 285 94 658 37 10 33 133 47 2781 31 805 103 4 15 114 4
Low 1913 2086 991 521 544 363 3548 1672 888 275 490 1264 158 1189 2274
Below cutoff 119 729 53 50 899 50 444 452 9 72 63 81 1 400

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_012989 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001146184 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001146185 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001146187 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369717 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369718 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369719 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369720 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369721 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369722 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369723 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369724 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369725 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369726 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369727 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369728 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369729 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369730 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369731 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369732 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369733 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369734 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369735 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369736 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369737 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369738 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369739 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_006210 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_161475 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_161476 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB003039 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB006625 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC006115 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF208967 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF208968 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF208969 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF208970 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH010107 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI089069 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK295679 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK307476 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC037330 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC052616 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC136268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC150272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471135 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR933682 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HF583851 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U90336 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000326441   ⟹   ENSP00000326581
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1956,810,082 - 56,840,726 (-)Ensembl
RefSeq Acc Id: ENST00000593695   ⟹   ENSP00000472402
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1956,813,675 - 56,840,696 (-)Ensembl
RefSeq Acc Id: ENST00000594389   ⟹   ENSP00000469144
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1956,824,546 - 56,840,709 (-)Ensembl
RefSeq Acc Id: ENST00000598410   ⟹   ENSP00000473190
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1956,813,148 - 56,840,726 (-)Ensembl
RefSeq Acc Id: ENST00000599534   ⟹   ENSP00000472395
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1956,813,678 - 56,825,006 (-)Ensembl
RefSeq Acc Id: ENST00000599565
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1956,810,091 - 56,811,283 (-)Ensembl
RefSeq Acc Id: ENST00000599577   ⟹   ENSP00000469486
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1956,813,678 - 56,840,696 (-)Ensembl
RefSeq Acc Id: ENST00000600833   ⟹   ENSP00000470467
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1956,816,790 - 56,824,648 (-)Ensembl
RefSeq Acc Id: ENST00000647621   ⟹   ENSP00000496853
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1956,812,819 - 56,840,726 (-)Ensembl
RefSeq Acc Id: ENST00000647852   ⟹   ENSP00000497332
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1956,814,388 - 56,833,747 (-)Ensembl
RefSeq Acc Id: ENST00000648694   ⟹   ENSP00000496914
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1956,810,077 - 56,840,726 (-)Ensembl
RefSeq Acc Id: ENST00000649233   ⟹   ENSP00000498047
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1956,810,102 - 56,840,728 (-)Ensembl
RefSeq Acc Id: ENST00000649428   ⟹   ENSP00000498138
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1956,810,187 - 56,837,818 (-)Ensembl
RefSeq Acc Id: ENST00000649680   ⟹   ENSP00000497512
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1956,810,121 - 56,840,726 (-)Ensembl
RefSeq Acc Id: ENST00000649735   ⟹   ENSP00000497800
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1956,812,158 - 56,840,661 (-)Ensembl
RefSeq Acc Id: ENST00000649876   ⟹   ENSP00000496867
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1956,810,121 - 56,840,726 (-)Ensembl
RefSeq Acc Id: ENST00000650102   ⟹   ENSP00000497466
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1956,811,081 - 56,840,726 (-)Ensembl
RefSeq Acc Id: ENST00000650632   ⟹   ENSP00000497971
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1956,810,918 - 56,840,726 (-)Ensembl
RefSeq Acc Id: NM_001146184   ⟹   NP_001139656
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
GRCh371957,285,730 - 57,352,121 (-)NCBI
HuRef1953,630,947 - 53,661,577 (-)ENTREZGENE
CHM1_11957,315,016 - 57,345,647 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001146185   ⟹   NP_001139657
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
GRCh371957,285,730 - 57,352,121 (-)NCBI
HuRef1953,630,947 - 53,661,577 (-)ENTREZGENE
CHM1_11957,315,016 - 57,345,647 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001146187   ⟹   NP_001139659
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
GRCh371957,285,730 - 57,352,121 (-)NCBI
HuRef1953,630,947 - 53,661,577 (-)ENTREZGENE
CHM1_11957,315,016 - 57,345,647 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369717   ⟹   NP_001356646
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369718   ⟹   NP_001356647
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369719   ⟹   NP_001356648
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369720   ⟹   NP_001356649
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369721   ⟹   NP_001356650
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369722   ⟹   NP_001356651
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369723   ⟹   NP_001356652
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369724   ⟹   NP_001356653
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369725   ⟹   NP_001356654
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369726   ⟹   NP_001356655
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369727   ⟹   NP_001356656
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369728   ⟹   NP_001356657
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369729   ⟹   NP_001356658
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369730   ⟹   NP_001356659
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369731   ⟹   NP_001356660
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369732   ⟹   NP_001356661
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369733   ⟹   NP_001356662
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,837,808 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,932,876 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369734   ⟹   NP_001356663
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369735   ⟹   NP_001356664
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369736   ⟹   NP_001356665
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369737   ⟹   NP_001356666
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369738   ⟹   NP_001356667
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369739   ⟹   NP_001356668
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NM_006210   ⟹   NP_006201
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,810,082 - 56,840,726 (-)NCBI
GRCh371957,285,730 - 57,352,121 (-)NCBI
Build 361962,015,615 - 62,043,876 (-)NCBI Archive
HuRef1953,630,947 - 53,661,577 (-)ENTREZGENE
CHM1_11957,315,016 - 57,345,647 (-)NCBI
T2T-CHM13v2.01959,905,167 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NR_161475
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,831,018 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,926,103 - 59,935,794 (-)NCBI
Sequence:
RefSeq Acc Id: NR_161476
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,831,018 - 56,840,726 (-)NCBI
T2T-CHM13v2.01959,926,103 - 59,935,794 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001139656 (Get FASTA)   NCBI Sequence Viewer  
  NP_001139657 (Get FASTA)   NCBI Sequence Viewer  
  NP_001139659 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356646 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356647 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356648 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356649 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356650 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356651 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356652 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356653 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356654 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356655 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356656 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356657 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356658 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356659 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356660 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356661 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356662 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356663 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356664 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356665 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356666 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356667 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356668 (Get FASTA)   NCBI Sequence Viewer  
  NP_006201 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAB50011 (Get FASTA)   NCBI Sequence Viewer  
  AAC83176 (Get FASTA)   NCBI Sequence Viewer  
  AAG35739 (Get FASTA)   NCBI Sequence Viewer  
  AAG35740 (Get FASTA)   NCBI Sequence Viewer  
  AAG35741 (Get FASTA)   NCBI Sequence Viewer  
  AAG35742 (Get FASTA)   NCBI Sequence Viewer  
  AAG42324 (Get FASTA)   NCBI Sequence Viewer  
  AAG42325 (Get FASTA)   NCBI Sequence Viewer  
  AAH52616 (Get FASTA)   NCBI Sequence Viewer  
  AAI36269 (Get FASTA)   NCBI Sequence Viewer  
  AAI50273 (Get FASTA)   NCBI Sequence Viewer  
  BAA22956 (Get FASTA)   NCBI Sequence Viewer  
  BAB85588 (Get FASTA)   NCBI Sequence Viewer  
  BAG58536 (Get FASTA)   NCBI Sequence Viewer  
  CAI45975 (Get FASTA)   NCBI Sequence Viewer  
  CCQ43348 (Get FASTA)   NCBI Sequence Viewer  
  EAW72474 (Get FASTA)   NCBI Sequence Viewer  
  EAW72476 (Get FASTA)   NCBI Sequence Viewer  
  EAW72477 (Get FASTA)   NCBI Sequence Viewer  
  EAW72478 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000326581
  ENSP00000326581.7
  ENSP00000469144.1
  ENSP00000469486
  ENSP00000469486.1
  ENSP00000470467.2
  ENSP00000472395.1
  ENSP00000472402
  ENSP00000472402.1
  ENSP00000473190
  ENSP00000473190.1
  ENSP00000496853
  ENSP00000496853.1
  ENSP00000496867
  ENSP00000496867.1
  ENSP00000496914
  ENSP00000496914.1
  ENSP00000497332
  ENSP00000497332.1
  ENSP00000497466
  ENSP00000497466.1
  ENSP00000497512
  ENSP00000497512.1
  ENSP00000497800.1
  ENSP00000497971
  ENSP00000497971.1
  ENSP00000498047
  ENSP00000498047.1
  ENSP00000498138
  ENSP00000498138.1
GenBank Protein Q9GZU2 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_001139657   ⟸   NM_001146185
- Peptide Label: isoform 2
- UniProtKB: B9EG68 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001139659   ⟸   NM_001146187
- Peptide Label: isoform 3
- UniProtKB: B9EG68 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001139656   ⟸   NM_001146184
- Peptide Label: isoform 1
- UniProtKB: Q8TF75 (UniProtKB/Swiss-Prot),   Q7Z7H7 (UniProtKB/Swiss-Prot),   Q5H9P9 (UniProtKB/Swiss-Prot),   P78418 (UniProtKB/Swiss-Prot),   C9JP50 (UniProtKB/Swiss-Prot),   B4DIM4 (UniProtKB/Swiss-Prot),   A7E2B8 (UniProtKB/Swiss-Prot),   Q9GZY2 (UniProtKB/Swiss-Prot),   Q9GZU2 (UniProtKB/Swiss-Prot),   Q96Q96 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_006201   ⟸   NM_006210
- Peptide Label: isoform 1
- UniProtKB: Q8TF75 (UniProtKB/Swiss-Prot),   Q7Z7H7 (UniProtKB/Swiss-Prot),   Q5H9P9 (UniProtKB/Swiss-Prot),   P78418 (UniProtKB/Swiss-Prot),   C9JP50 (UniProtKB/Swiss-Prot),   B4DIM4 (UniProtKB/Swiss-Prot),   A7E2B8 (UniProtKB/Swiss-Prot),   Q9GZY2 (UniProtKB/Swiss-Prot),   Q9GZU2 (UniProtKB/Swiss-Prot),   Q96Q96 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001356654   ⟸   NM_001369725
- Peptide Label: isoform 3
- UniProtKB: B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356650   ⟸   NM_001369721
- Peptide Label: isoform 3
- UniProtKB: B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356646   ⟸   NM_001369717
- Peptide Label: isoform 4
- UniProtKB: Q96Q96 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356666   ⟸   NM_001369737
- Peptide Label: isoform 6
- UniProtKB: A0A3B3IRU6 (UniProtKB/TrEMBL),   B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356651   ⟸   NM_001369722
- Peptide Label: isoform 3
- UniProtKB: B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356661   ⟸   NM_001369732
- Peptide Label: isoform 3
- UniProtKB: B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356649   ⟸   NM_001369720
- Peptide Label: isoform 3
- UniProtKB: B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356664   ⟸   NM_001369735
- Peptide Label: isoform 6
- UniProtKB: A0A3B3IRU6 (UniProtKB/TrEMBL),   B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356665   ⟸   NM_001369736
- Peptide Label: isoform 6
- UniProtKB: A0A3B3IRU6 (UniProtKB/TrEMBL),   B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356663   ⟸   NM_001369734
- Peptide Label: isoform 6
- UniProtKB: A0A3B3IRU6 (UniProtKB/TrEMBL),   B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356668   ⟸   NM_001369739
- Peptide Label: isoform 3
- UniProtKB: B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356656   ⟸   NM_001369727
- Peptide Label: isoform 3
- UniProtKB: B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356658   ⟸   NM_001369729
- Peptide Label: isoform 3
- UniProtKB: B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356648   ⟸   NM_001369719
- Peptide Label: isoform 5
- UniProtKB: Q96Q96 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356647   ⟸   NM_001369718
- Peptide Label: isoform 4
- UniProtKB: Q96Q96 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356652   ⟸   NM_001369723
- Peptide Label: isoform 3
- UniProtKB: B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356657   ⟸   NM_001369728
- Peptide Label: isoform 3
- UniProtKB: B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356659   ⟸   NM_001369730
- Peptide Label: isoform 3
- UniProtKB: B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356667   ⟸   NM_001369738
- Peptide Label: isoform 6
- UniProtKB: A0A3B3IRU6 (UniProtKB/TrEMBL),   B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356660   ⟸   NM_001369731
- Peptide Label: isoform 3
- UniProtKB: B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356655   ⟸   NM_001369726
- Peptide Label: isoform 3
- UniProtKB: B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356653   ⟸   NM_001369724
- Peptide Label: isoform 3
- UniProtKB: B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001356662   ⟸   NM_001369733
- Peptide Label: isoform 3
- UniProtKB: B9EG68 (UniProtKB/TrEMBL)
RefSeq Acc Id: ENSP00000496914   ⟸   ENST00000648694
RefSeq Acc Id: ENSP00000498138   ⟸   ENST00000649428
RefSeq Acc Id: ENSP00000498047   ⟸   ENST00000649233
RefSeq Acc Id: ENSP00000496867   ⟸   ENST00000649876
RefSeq Acc Id: ENSP00000497800   ⟸   ENST00000649735
RefSeq Acc Id: ENSP00000497512   ⟸   ENST00000649680
RefSeq Acc Id: ENSP00000473190   ⟸   ENST00000598410
RefSeq Acc Id: ENSP00000472395   ⟸   ENST00000599534
RefSeq Acc Id: ENSP00000469486   ⟸   ENST00000599577
RefSeq Acc Id: ENSP00000497466   ⟸   ENST00000650102
RefSeq Acc Id: ENSP00000497971   ⟸   ENST00000650632
RefSeq Acc Id: ENSP00000470467   ⟸   ENST00000600833
RefSeq Acc Id: ENSP00000326581   ⟸   ENST00000326441
RefSeq Acc Id: ENSP00000472402   ⟸   ENST00000593695
RefSeq Acc Id: ENSP00000469144   ⟸   ENST00000594389
RefSeq Acc Id: ENSP00000496853   ⟸   ENST00000647621
RefSeq Acc Id: ENSP00000497332   ⟸   ENST00000647852
Protein Domains
C2H2-type   SCAN box

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9GZU2-F1-model_v2 AlphaFold Q9GZU2 1-1588 view protein structure

Promoters
RGD ID:13205851
Promoter ID:EPDNEW_H26506
Type:initiation region
Name:PEG3_6
Description:paternally expressed 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26507  EPDNEW_H26508  EPDNEW_H26509  EPDNEW_H26510  EPDNEW_H26511  EPDNEW_H26512  EPDNEW_H26514  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,812,516 - 56,812,576EPDNEW
RGD ID:13205853
Promoter ID:EPDNEW_H26507
Type:initiation region
Name:PEG3_2
Description:paternally expressed 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26506  EPDNEW_H26508  EPDNEW_H26509  EPDNEW_H26510  EPDNEW_H26511  EPDNEW_H26512  EPDNEW_H26514  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,812,817 - 56,812,877EPDNEW
RGD ID:13205855
Promoter ID:EPDNEW_H26508
Type:initiation region
Name:PEG3_4
Description:paternally expressed 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26506  EPDNEW_H26507  EPDNEW_H26509  EPDNEW_H26510  EPDNEW_H26511  EPDNEW_H26512  EPDNEW_H26514  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,814,356 - 56,814,416EPDNEW
RGD ID:13205857
Promoter ID:EPDNEW_H26509
Type:initiation region
Name:PEG3_3
Description:paternally expressed 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26506  EPDNEW_H26507  EPDNEW_H26508  EPDNEW_H26510  EPDNEW_H26511  EPDNEW_H26512  EPDNEW_H26514  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,816,721 - 56,816,781EPDNEW
RGD ID:13205859
Promoter ID:EPDNEW_H26510
Type:initiation region
Name:PEG3_8
Description:paternally expressed 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26506  EPDNEW_H26507  EPDNEW_H26508  EPDNEW_H26509  EPDNEW_H26511  EPDNEW_H26512  EPDNEW_H26514  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,836,049 - 56,836,109EPDNEW
RGD ID:13205861
Promoter ID:EPDNEW_H26511
Type:initiation region
Name:PEG3_7
Description:paternally expressed 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26506  EPDNEW_H26507  EPDNEW_H26508  EPDNEW_H26509  EPDNEW_H26510  EPDNEW_H26512  EPDNEW_H26514  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,837,815 - 56,837,875EPDNEW
RGD ID:13205863
Promoter ID:EPDNEW_H26512
Type:initiation region
Name:PEG3_5
Description:paternally expressed 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26506  EPDNEW_H26507  EPDNEW_H26508  EPDNEW_H26509  EPDNEW_H26510  EPDNEW_H26511  EPDNEW_H26514  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,838,069 - 56,838,129EPDNEW
RGD ID:13205869
Promoter ID:EPDNEW_H26514
Type:initiation region
Name:PEG3_1
Description:paternally expressed 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26506  EPDNEW_H26507  EPDNEW_H26508  EPDNEW_H26509  EPDNEW_H26510  EPDNEW_H26511  EPDNEW_H26512  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381956,840,726 - 56,840,786EPDNEW
RGD ID:6795812
Promoter ID:HG_KWN:31141
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:ENST00000292074,   NM_001146184,   NM_001146185,   NM_001146187,   NM_001146326,   NM_001146327,   NM_006210,   NM_015363,   NR_024059,   UC002QNR.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361962,043,631 - 62,044,131 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:8826 AgrOrtholog
COSMIC PEG3 COSMIC
Ensembl Genes ENSG00000198300 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000326441 ENTREZGENE
  ENST00000326441.15 UniProtKB/Swiss-Prot
  ENST00000593695 ENTREZGENE
  ENST00000593695.5 UniProtKB/Swiss-Prot
  ENST00000594389.1 UniProtKB/TrEMBL
  ENST00000598410 ENTREZGENE
  ENST00000598410.5 UniProtKB/Swiss-Prot
  ENST00000599534.5 UniProtKB/Swiss-Prot
  ENST00000599577 ENTREZGENE
  ENST00000599577.5 UniProtKB/Swiss-Prot
  ENST00000600833.2 UniProtKB/TrEMBL
  ENST00000647621 ENTREZGENE
  ENST00000647621.1 UniProtKB/TrEMBL
  ENST00000647852 ENTREZGENE
  ENST00000647852.1 UniProtKB/TrEMBL
  ENST00000648694 ENTREZGENE
  ENST00000648694.1 UniProtKB/Swiss-Prot
  ENST00000649233 ENTREZGENE
  ENST00000649233.1 UniProtKB/Swiss-Prot
  ENST00000649428 ENTREZGENE
  ENST00000649428.1 UniProtKB/Swiss-Prot
  ENST00000649680 ENTREZGENE
  ENST00000649680.1 UniProtKB/Swiss-Prot
  ENST00000649735.1 UniProtKB/TrEMBL
  ENST00000649876 ENTREZGENE
  ENST00000649876.1 UniProtKB/Swiss-Prot
  ENST00000650102 ENTREZGENE
  ENST00000650102.1 UniProtKB/Swiss-Prot
  ENST00000650632 ENTREZGENE
  ENST00000650632.1 UniProtKB/Swiss-Prot
Gene3D-CATH 1.10.4020.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Classic Zinc Finger UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000198300 GTEx
HGNC ID HGNC:8826 ENTREZGENE
Human Proteome Map PEG3 Human Proteome Map
InterPro SCAN_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SCAN_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_type UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:5178 UniProtKB/Swiss-Prot
NCBI Gene 5178 ENTREZGENE
OMIM 601483 OMIM
PANTHER CHROMATIN-LINKED ADAPTOR FOR MSL PROTEINS, ISOFORM B-RELATED UniProtKB/Swiss-Prot
  FI01424P-RELATED UniProtKB/TrEMBL
  IP01015P-RELATED UniProtKB/TrEMBL
  PATERNALLY-EXPRESSED GENE 3 PROTEIN UniProtKB/TrEMBL
  PROTEIN ZBED8-RELATED UniProtKB/TrEMBL
  SCAN DOMAIN-CONTAINING PROTEIN 3 UniProtKB/TrEMBL
  ZINC FINGER AND SCAN DOMAIN-CONTAINING UniProtKB/TrEMBL
  ZINC FINGER PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC FINGER PROTEIN 141-RELATED UniProtKB/TrEMBL
Pfam SCAN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA33171 PharmGKB
PROSITE SCAN_BOX UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC_FINGER_C2H2_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC_FINGER_C2H2_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART SCAN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZnF_C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP Retrovirus capsid dimerization domain-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF57667 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A3B3IRU6 ENTREZGENE, UniProtKB/TrEMBL
  A0A3B3ISL2_HUMAN UniProtKB/TrEMBL
  A0A3B3ITJ6_HUMAN UniProtKB/TrEMBL
  A7E2B8 ENTREZGENE
  B4DIM4 ENTREZGENE
  B9EG68 ENTREZGENE, UniProtKB/TrEMBL
  C9JP50 ENTREZGENE
  L8EAH8_HUMAN UniProtKB/TrEMBL
  M0QXG1_HUMAN UniProtKB/TrEMBL
  M0QZD4_HUMAN UniProtKB/TrEMBL
  P78418 ENTREZGENE
  PEG3_HUMAN UniProtKB/Swiss-Prot
  Q5H9P9 ENTREZGENE
  Q7Z7H7 ENTREZGENE
  Q8TF75 ENTREZGENE
  Q96Q96 ENTREZGENE, UniProtKB/TrEMBL
  Q9GZU2 ENTREZGENE
  Q9GZY2 ENTREZGENE
UniProt Secondary A7E2B8 UniProtKB/Swiss-Prot
  B4DIM4 UniProtKB/Swiss-Prot
  C9JP50 UniProtKB/Swiss-Prot
  P78418 UniProtKB/Swiss-Prot
  Q5H9P9 UniProtKB/Swiss-Prot
  Q7Z7H7 UniProtKB/Swiss-Prot
  Q8TF75 UniProtKB/Swiss-Prot
  Q9GZY2 UniProtKB/Swiss-Prot