PPP2R2D (protein phosphatase 2 regulatory subunit Bdelta) - Rat Genome Database

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Gene: PPP2R2D (protein phosphatase 2 regulatory subunit Bdelta) Homo sapiens
Analyze
Symbol: PPP2R2D
Name: protein phosphatase 2 regulatory subunit Bdelta
RGD ID: 1351294
HGNC Page HGNC:23732
Description: Predicted to enable protein phosphatase regulator activity. Predicted to be involved in exit from mitosis. Predicted to be located in cytoplasm. Predicted to be part of protein phosphatase type 2A complex. Predicted to be active in cytosol.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: B55D; B55delta; MDS026; PP2A subunit B isoform B55-delta; PP2A subunit B isoform delta; PP2A subunit B isoform PR55-delta; PP2A subunit B isoform R2-delta; protein phosphatase 2, regulatory subunit B, delta isoform; serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B delta isoform
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: PPP2R2DP1  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3810131,901,008 - 131,971,533 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl10131,901,008 - 131,959,834 (+)EnsemblGRCh38hg38GRCh38
GRCh3710133,747,955 - 133,773,338 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3610133,597,950 - 133,620,044 (+)NCBINCBI36Build 36hg18NCBI36
Celera10127,392,198 - 127,414,138 (+)NCBICelera
Cytogenetic Map10q26.3NCBI
HuRef10127,299,151 - 127,320,948 (+)NCBIHuRef
CHM1_110134,029,386 - 134,051,138 (+)NCBICHM1_1
T2T-CHM13v2.010132,840,100 - 132,911,782 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
3. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:10819331   PMID:12477932   PMID:14702039   PMID:15164054   PMID:15489334   PMID:16169070   PMID:16705156   PMID:17148452   PMID:17207965   PMID:18697906   PMID:18782753   PMID:19156129  
PMID:19615732   PMID:20220139   PMID:20360068   PMID:21081666   PMID:21873635   PMID:22174317   PMID:22539979   PMID:23135275   PMID:23851495   PMID:24596207   PMID:25544563   PMID:25609649  
PMID:25756610   PMID:25816751   PMID:25963833   PMID:26186194   PMID:26344197   PMID:26496610   PMID:26618866   PMID:27173435   PMID:27432908   PMID:27557495   PMID:27880917   PMID:28330616  
PMID:28514442   PMID:28675297   PMID:29229926   PMID:29568966   PMID:30575818   PMID:31091453   PMID:31732153   PMID:31980649   PMID:32552912   PMID:32707033   PMID:32897879   PMID:33187986  
PMID:33961781   PMID:35256949   PMID:35509820   PMID:35676659   PMID:35918402   PMID:35944360   PMID:36129980   PMID:36180527   PMID:36538041   PMID:36736316   PMID:38442987  


Genomics

Comparative Map Data
PPP2R2D
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3810131,901,008 - 131,971,533 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl10131,901,008 - 131,959,834 (+)EnsemblGRCh38hg38GRCh38
GRCh3710133,747,955 - 133,773,338 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3610133,597,950 - 133,620,044 (+)NCBINCBI36Build 36hg18NCBI36
Celera10127,392,198 - 127,414,138 (+)NCBICelera
Cytogenetic Map10q26.3NCBI
HuRef10127,299,151 - 127,320,948 (+)NCBIHuRef
CHM1_110134,029,386 - 134,051,138 (+)NCBICHM1_1
T2T-CHM13v2.010132,840,100 - 132,911,782 (+)NCBIT2T-CHM13v2.0
Ppp2r2d
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm397138,448,073 - 138,484,786 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl7138,447,808 - 138,484,786 (+)EnsemblGRCm39 Ensembl
GRCm387138,846,350 - 138,883,057 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl7138,846,079 - 138,883,057 (+)EnsemblGRCm38mm10GRCm38
MGSCv377146,038,069 - 146,074,740 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv367138,684,729 - 138,721,400 (+)NCBIMGSCv36mm8
Celera7138,663,564 - 138,700,226 (+)NCBICelera
Cytogenetic Map7F4NCBI
cM Map782.95NCBI
Ppp2r2d
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81203,095,536 - 203,129,895 (+)NCBIGRCr8
mRatBN7.21193,665,918 - 193,700,277 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1193,665,855 - 193,700,274 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1202,036,415 - 202,070,486 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01209,171,502 - 209,205,573 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01201,844,985 - 201,879,055 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01211,205,903 - 211,240,216 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1211,205,903 - 211,239,888 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01218,132,463 - 218,166,450 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41198,640,771 - 198,674,758 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11198,790,763 - 198,825,066 (+)NCBI
Celera1191,357,924 - 191,391,726 (+)NCBICelera
Cytogenetic Map1q41NCBI
Ppp2r2d
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_0049554779,571,974 - 9,611,076 (+)NCBIChiLan1.0ChiLan1.0
PPP2R2D
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v28143,853,967 - 143,916,635 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan110143,859,327 - 143,921,992 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v010128,602,457 - 128,663,706 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.110132,794,414 - 132,846,602 (+)NCBIpanpan1.1PanPan1.1panPan2
PPP2R2D
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12840,008,764 - 40,030,811 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2839,987,019 - 40,030,382 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2840,045,944 - 40,093,979 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02840,626,539 - 40,674,546 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2840,624,994 - 40,671,146 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12840,111,215 - 40,159,202 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02840,098,988 - 40,147,189 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02840,498,145 - 40,546,204 (+)NCBIUU_Cfam_GSD_1.0
Ppp2r2d
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244072137,116,672 - 7,140,534 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493648618,420,764 - 18,443,485 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493648618,424,336 - 18,443,485 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
PPP2R2D
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.19124,510,800 - 124,560,872 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366604885,946,198 - 85,999,269 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ppp2r2d
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462473714,873,129 - 14,920,804 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462473714,873,129 - 14,920,886 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in PPP2R2D
21 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 10q25.2-26.3(chr10:111313099-133620674)x3 copy number gain See cases [RCV000051218] Chr10:111313099..133620674 [GRCh38]
Chr10:113072857..135434178 [GRCh37]
Chr10:113062847..135284168 [NCBI36]
Chr10:10q25.2-26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:123307835-133620674)x1 copy number loss See cases [RCV000051150] Chr10:123307835..133620674 [GRCh38]
Chr10:125067351..135434178 [GRCh37]
Chr10:125057341..135284168 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.12-26.3(chr10:120454430-133620674)x1 copy number loss See cases [RCV000051103] Chr10:120454430..133620674 [GRCh38]
Chr10:122213942..135434178 [GRCh37]
Chr10:122203932..135284168 [NCBI36]
Chr10:10q26.12-26.3		 pathogenic
GRCh38/hg38 10q26.3(chr10:131457361-133620674)x1 copy number loss See cases [RCV000050997] Chr10:131457361..133620674 [GRCh38]
Chr10:133255624..135434178 [GRCh37]
Chr10:133145614..135284168 [NCBI36]
Chr10:10q26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:122265252-133620674)x1 copy number loss See cases [RCV000051069] Chr10:122265252..133620674 [GRCh38]
Chr10:124024767..135434178 [GRCh37]
Chr10:124014757..135284168 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.3(chr10:131457361-131971639)x3 copy number gain See cases [RCV000051691] Chr10:131457361..131971639 [GRCh38]
Chr10:133255624..133785143 [GRCh37]
Chr10:133145614..133635133 [NCBI36]
Chr10:10q26.3		 uncertain significance
GRCh38/hg38 10q26.3(chr10:131914873-133613938)x1 copy number loss See cases [RCV000052643] Chr10:131914873..133613938 [GRCh38]
Chr10:133728377..135427442 [GRCh37]
Chr10:133578367..135277432 [NCBI36]
Chr10:10q26.3		 pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:126256585-133613938)x1 copy number loss See cases [RCV000052612] Chr10:126256585..133613938 [GRCh38]
Chr10:127945154..135427442 [GRCh37]
Chr10:127935144..135277432 [NCBI36]
Chr10:10q26.2-26.3		 pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:127500483-133620674)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052613]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052613]|See cases [RCV000052613] Chr10:127500483..133620674 [GRCh38]
Chr10:129298747..135434178 [GRCh37]
Chr10:129188737..135284168 [NCBI36]
Chr10:10q26.2-26.3		 pathogenic
GRCh38/hg38 10q26.3(chr10:129673966-133613938)x1 copy number loss See cases [RCV000052614] Chr10:129673966..133613938 [GRCh38]
Chr10:131472230..135427442 [GRCh37]
Chr10:131362220..135277432 [NCBI36]
Chr10:10q26.3		 pathogenic
GRCh38/hg38 10q26.3(chr10:129758596-133620674)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052615]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052615]|See cases [RCV000052615] Chr10:129758596..133620674 [GRCh38]
Chr10:131556860..135434178 [GRCh37]
Chr10:131446850..135284168 [NCBI36]
Chr10:10q26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:123580320-133558988)x1 copy number loss See cases [RCV000052611] Chr10:123580320..133558988 [GRCh38]
Chr10:125339836..135372492 [GRCh37]
Chr10:125329826..135222482 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q23.31-26.3(chr10:91048545-133620674)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053560]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053560]|See cases [RCV000053560] Chr10:91048545..133620674 [GRCh38]
Chr10:92808302..135434178 [GRCh37]
Chr10:92798282..135284168 [NCBI36]
Chr10:10q23.31-26.3		 pathogenic
GRCh38/hg38 10q24.31-26.3(chr10:100194215-132432797)x3 copy number gain See cases [RCV000053564] Chr10:100194215..132432797 [GRCh38]
Chr10:101953972..134246301 [GRCh37]
Chr10:101943962..134096291 [NCBI36]
Chr10:10q24.31-26.3		 pathogenic
GRCh38/hg38 10q25.1-26.3(chr10:106925303-133620815)x3 copy number gain See cases [RCV000053588] Chr10:106925303..133620815 [GRCh38]
Chr10:108685061..135434319 [GRCh37]
Chr10:108675051..135284309 [NCBI36]
Chr10:10q25.1-26.3		 pathogenic
GRCh38/hg38 10q26.11-26.3(chr10:117866565-133554210)x3 copy number gain See cases [RCV000053589] Chr10:117866565..133554210 [GRCh38]
Chr10:119626076..135367714 [GRCh37]
Chr10:119616066..135217704 [NCBI36]
Chr10:10q26.11-26.3		 pathogenic
NM_001291310.1(PPP2R2D):c.581C>T (p.Ser194Leu) single nucleotide variant Malignant melanoma [RCV000062014] Chr10:131947785 [GRCh38]
Chr10:133761289 [GRCh37]
Chr10:133611279 [NCBI36]
Chr10:10q26.3		 not provided
NM_001291310.1(PPP2R2D):c.587+3888G>T single nucleotide variant Lung cancer [RCV000108851] Chr10:131951679 [GRCh38]
Chr10:133765183 [GRCh37]
Chr10:10q26.3		 uncertain significance
GRCh37/hg19 10q25.2-26.3(chr10:114544537-135427143)x3 copy number gain not provided [RCV000847820] Chr10:114544537..135427143 [GRCh37]
Chr10:10q25.2-26.3		 pathogenic
GRCh38/hg38 10q26.3(chr10:131457361-131922234)x3 copy number gain See cases [RCV000133761] Chr10:131457361..131922234 [GRCh38]
Chr10:133255624..133728500 [GRCh37]
Chr10:133145614..133585728 [NCBI36]
Chr10:10q26.3		 benign
GRCh38/hg38 10q25.1-26.3(chr10:108102587-133620674)x3 copy number gain See cases [RCV000133688] Chr10:108102587..133620674 [GRCh38]
Chr10:109862345..135434178 [GRCh37]
Chr10:109852335..135284168 [NCBI36]
Chr10:10q25.1-26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:125657472-133620674)x1 copy number loss See cases [RCV000133741] Chr10:125657472..133620674 [GRCh38]
Chr10:127346041..135434178 [GRCh37]
Chr10:127336031..135284168 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:126730896-133620609)x1 copy number loss See cases [RCV000134040] Chr10:126730896..133620609 [GRCh38]
Chr10:128419465..135434113 [GRCh37]
Chr10:128409455..135284103 [NCBI36]
Chr10:10q26.2-26.3		 pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:127640489-132776585)x1 copy number loss See cases [RCV000135728] Chr10:127640489..132776585 [GRCh38]
Chr10:129438753..134590089 [GRCh37]
Chr10:129328743..134440079 [NCBI36]
Chr10:10q26.2-26.3		 pathogenic
GRCh38/hg38 10q26.3(chr10:129549258-133620674)x1 copy number loss See cases [RCV000135547] Chr10:129549258..133620674 [GRCh38]
Chr10:131347522..135434178 [GRCh37]
Chr10:131237512..135284168 [NCBI36]
Chr10:10q26.3		 pathogenic|likely benign
GRCh38/hg38 10q26.3(chr10:131761691-132178534)x3 copy number gain See cases [RCV000135558] Chr10:131761691..132178534 [GRCh38]
Chr10:133594027..133992038 [GRCh37]
Chr10:133444017..133842028 [NCBI36]
Chr10:10q26.3		 likely benign|uncertain significance
GRCh38/hg38 10q26.13-26.3(chr10:124473108-133620609)x1 copy number loss See cases [RCV000136028] Chr10:124473108..133620609 [GRCh38]
Chr10:126161677..135434113 [GRCh37]
Chr10:126151667..135284103 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.3(chr10:131457389-131922176)x3 copy number gain See cases [RCV000136036] Chr10:131457389..131922176 [GRCh38]
Chr10:133255652..133728500 [GRCh37]
Chr10:133145642..133585670 [NCBI36]
Chr10:10q26.3		 likely benign
GRCh38/hg38 10q26.3(chr10:128872419-133564028)x3 copy number gain See cases [RCV000136888] Chr10:128872419..133564028 [GRCh38]
Chr10:130670683..135377532 [GRCh37]
Chr10:130560673..135227522 [NCBI36]
Chr10:10q26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:124834858-133622588)x1 copy number loss See cases [RCV000137653] Chr10:124834858..133622588 [GRCh38]
Chr10:126523427..135436092 [GRCh37]
Chr10:126513417..135286082 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:128549913-133622588)x1 copy number loss See cases [RCV000138159] Chr10:128549913..133622588 [GRCh38]
Chr10:130348177..135436092 [GRCh37]
Chr10:130238167..135286082 [NCBI36]
Chr10:10q26.2-26.3		 pathogenic|uncertain significance
GRCh38/hg38 10q26.2-26.3(chr10:127849717-133622588)x1 copy number loss See cases [RCV000138160] Chr10:127849717..133622588 [GRCh38]
Chr10:129647981..135436092 [GRCh37]
Chr10:129537971..135286082 [NCBI36]
Chr10:10q26.2-26.3		 pathogenic|likely benign
GRCh38/hg38 10q24.31-26.3(chr10:100600492-133622588)x3 copy number gain See cases [RCV000137747] Chr10:100600492..133622588 [GRCh38]
Chr10:102360249..135436092 [GRCh37]
Chr10:102350239..135286082 [NCBI36]
Chr10:10q24.31-26.3		 pathogenic
GRCh38/hg38 10q26.3(chr10:129427520-133622588)x1 copy number loss See cases [RCV000137959] Chr10:129427520..133622588 [GRCh38]
Chr10:131225784..135436092 [GRCh37]
Chr10:131115774..135286082 [NCBI36]
Chr10:10q26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:122881207-133620609)x1 copy number loss See cases [RCV000138435] Chr10:122881207..133620609 [GRCh38]
Chr10:124640723..135434113 [GRCh37]
Chr10:124630713..135284103 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.12-26.3(chr10:120970558-133622588)x1 copy number loss See cases [RCV000139344] Chr10:120970558..133622588 [GRCh38]
Chr10:122730071..135436092 [GRCh37]
Chr10:122720061..135286082 [NCBI36]
Chr10:10q26.12-26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:125021995-133620609)x1 copy number loss See cases [RCV000139588] Chr10:125021995..133620609 [GRCh38]
Chr10:126710564..135434113 [GRCh37]
Chr10:126700554..135284103 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:125452905-133785874)x3 copy number gain See cases [RCV000141337] Chr10:125452905..133785874 [GRCh38]
Chr10:127141474..135523199 [GRCh37]
Chr10:127131464..135373189 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:127664168-133622588)x3 copy number gain See cases [RCV000140974] Chr10:127664168..133622588 [GRCh38]
Chr10:129462432..135436092 [GRCh37]
Chr10:129352422..135286082 [NCBI36]
Chr10:10q26.2-26.3		 likely pathogenic
GRCh38/hg38 10q26.11-26.3(chr10:119707856-133613639)x3 copy number gain See cases [RCV000142005] Chr10:119707856..133613639 [GRCh38]
Chr10:121467368..135427143 [GRCh37]
Chr10:121457358..135277133 [NCBI36]
Chr10:10q26.11-26.3		 pathogenic
GRCh38/hg38 10q26.3(chr10:131448228-131943718)x3 copy number gain See cases [RCV000141854] Chr10:131448228..131943718 [GRCh38]
Chr10:133246491..133757222 [GRCh37]
Chr10:133136481..133607212 [NCBI36]
Chr10:10q26.3		 likely benign|uncertain significance
GRCh38/hg38 10q26.13-26.3(chr10:121588992-133620674)x1 copy number loss See cases [RCV000142441] Chr10:121588992..133620674 [GRCh38]
Chr10:123348506..135434178 [GRCh37]
Chr10:123338496..135284168 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:121918547-133620674)x1 copy number loss See cases [RCV000142737] Chr10:121918547..133620674 [GRCh38]
Chr10:123678062..135434178 [GRCh37]
Chr10:123668052..135284168 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:127435985-133622588)x1 copy number loss See cases [RCV000143241] Chr10:127435985..133622588 [GRCh38]
Chr10:129234249..135436092 [GRCh37]
Chr10:129124239..135286082 [NCBI36]
Chr10:10q26.2-26.3		 pathogenic
GRCh38/hg38 10q26.3(chr10:131424682-133613639)x1 copy number loss See cases [RCV000143762] Chr10:131424682..133613639 [GRCh38]
Chr10:133222945..135427143 [GRCh37]
Chr10:133112935..135277133 [NCBI36]
Chr10:10q26.3		 likely pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:123986772-133613639)x1 copy number loss See cases [RCV000143623] Chr10:123986772..133613639 [GRCh38]
Chr10:125746288..135427143 [GRCh37]
Chr10:125736278..135277133 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:123576393-133613639)x1 copy number loss See cases [RCV000143544] Chr10:123576393..133613639 [GRCh38]
Chr10:125335909..135427143 [GRCh37]
Chr10:125325899..135277133 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.3(chr10:130625650-133613639)x1 copy number loss See cases [RCV000143554] Chr10:130625650..133613639 [GRCh38]
Chr10:132423914..135427143 [GRCh37]
Chr10:132313904..135277133 [NCBI36]
Chr10:10q26.3		 uncertain significance
GRCh38/hg38 10q26.3(chr10:131448252-131943718)x3 copy number gain See cases [RCV000143605] Chr10:131448252..131943718 [GRCh38]
Chr10:133246515..133757222 [GRCh37]
Chr10:133136505..133607212 [NCBI36]
Chr10:10q26.3		 uncertain significance
GRCh38/hg38 10q26.2-26.3(chr10:126794646-133613639)x1 copy number loss See cases [RCV000143615] Chr10:126794646..133613639 [GRCh38]
Chr10:128483215..135427143 [GRCh37]
Chr10:128473205..135277133 [NCBI36]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:123731209-135353867)x1 copy number loss See cases [RCV000203440] Chr10:123731209..135353867 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic|likely pathogenic
GRCh37/hg19 10q24.32-26.3(chr10:103288313-135512075)x3 copy number gain See cases [RCV000240457] Chr10:103288313..135512075 [GRCh37]
Chr10:10q24.32-26.3		 pathogenic
GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143) copy number loss Distal 10q deletion syndrome [RCV003319583] Chr10:12829206..135427143 [GRCh37]
Chr10:10p13-q26.3		 pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:122125760-135062972)x3 copy number gain See cases [RCV000449169] Chr10:122125760..135062972 [GRCh37]
Chr10:10q26.12-26.3		 likely pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:124147428-135370736)x1 copy number loss See cases [RCV000449336] Chr10:124147428..135370736 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
GRCh37/hg19 10q24.32-26.3(chr10:104633712-135427143)x3 copy number gain See cases [RCV000449386] Chr10:104633712..135427143 [GRCh37]
Chr10:10q24.32-26.3		 pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:122343861-135427143)x1 copy number loss See cases [RCV000446095] Chr10:122343861..135427143 [GRCh37]
Chr10:10q26.12-26.3		 pathogenic
GRCh37/hg19 10q24.2-26.3(chr10:100780957-135427143)x3 copy number gain See cases [RCV000446733] Chr10:100780957..135427143 [GRCh37]
Chr10:10q24.2-26.3		 pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:128465436-135427143)x1 copy number loss See cases [RCV000447132] Chr10:128465436..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.3(chr10:132468363-135367666)x1 copy number loss See cases [RCV000446777] Chr10:132468363..135367666 [GRCh37]
Chr10:10q26.3		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:93297-135378918)x3 copy number gain See cases [RCV000448750] Chr10:93297..135378918 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
GRCh37/hg19 10q26.3(chr10:133536778-133753668)x3 copy number gain See cases [RCV000448595] Chr10:133536778..133753668 [GRCh37]
Chr10:10q26.3		 likely benign
GRCh37/hg19 10q26.3(chr10:132354150-135427143)x3 copy number gain See cases [RCV000510589] Chr10:132354150..135427143 [GRCh37]
Chr10:10q26.3		 uncertain significance
GRCh37/hg19 10q26.2-26.3(chr10:129825453-135427143)x1 copy number loss See cases [RCV000511570] Chr10:129825453..135427143 [GRCh37]
Chr10:10q26.2-26.3		 likely pathogenic
GRCh37/hg19 10q26.3(chr10:133246515-133779463)x3 copy number gain See cases [RCV000511925] Chr10:133246515..133779463 [GRCh37]
Chr10:10q26.3		 uncertain significance
GRCh37/hg19 10q26.3(chr10:133246515-133784311)x3 copy number gain See cases [RCV000511470] Chr10:133246515..133784311 [GRCh37]
Chr10:10q26.3		 uncertain significance
GRCh37/hg19 10q26.2-26.3(chr10:127658004-135427143)x1 copy number loss See cases [RCV000511813] Chr10:127658004..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143) copy number gain See cases [RCV000511389] Chr10:100027..135427143 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic|uncertain significance
GRCh37/hg19 10q25.1-26.3(chr10:106003533-135427143)x3 copy number gain See cases [RCV000510813] Chr10:106003533..135427143 [GRCh37]
Chr10:10q25.1-26.3		 pathogenic
GRCh37/hg19 10q23.32-26.3(chr10:93283493-135427143)x3 copy number gain See cases [RCV000510972] Chr10:93283493..135427143 [GRCh37]
Chr10:10q23.32-26.3		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)x3 copy number gain See cases [RCV000510861] Chr10:100027..135427143 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
GRCh37/hg19 10q26.3(chr10:130693843-134772865)x1 copy number loss See cases [RCV000511280] Chr10:130693843..134772865 [GRCh37]
Chr10:10q26.3		 likely pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:129007673-135427143)x3 copy number gain See cases [RCV000512398] Chr10:129007673..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q11.21-26.3(chr10:42347406-135534747)x1 copy number loss Poly (ADP-Ribose) polymerase inhibitor response [RCV000626438] Chr10:42347406..135534747 [GRCh37]
Chr10:10q11.21-26.3		 drug response
GRCh37/hg19 10q26.3(chr10:133246491-133779463)x3 copy number gain See cases [RCV000512479] Chr10:133246491..133779463 [GRCh37]
Chr10:10q26.3		 uncertain significance
GRCh37/hg19 10q26.3(chr10:133574560-135296619)x4 copy number gain not provided [RCV000683265] Chr10:133574560..135296619 [GRCh37]
Chr10:10q26.3		 uncertain significance
GRCh37/hg19 10q26.13-26.3(chr10:127375792-135427143)x1 copy number loss not provided [RCV000683283] Chr10:127375792..135427143 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
GRCh37/hg19 10q26.11-26.3(chr10:121269222-135427143)x3 copy number gain not provided [RCV000683288] Chr10:121269222..135427143 [GRCh37]
Chr10:10q26.11-26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:125450893-135427143)x1 copy number loss not provided [RCV000683285] Chr10:125450893..135427143 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
GRCh37/hg19 10q24.33-26.3(chr10:105613040-135427143)x3 copy number gain not provided [RCV000683290] Chr10:105613040..135427143 [GRCh37]
Chr10:10q24.33-26.3		 pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:122509781-135427143)x1 copy number loss not provided [RCV000683287] Chr10:122509781..135427143 [GRCh37]
Chr10:10q26.12-26.3		 pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:123019239-135427143)x1 copy number loss not provided [RCV000683286] Chr10:123019239..135427143 [GRCh37]
Chr10:10q26.12-26.3		 pathogenic
GRCh37/hg19 10q23.33-26.3(chr10:94346520-135427143)x3 copy number gain not provided [RCV000683291] Chr10:94346520..135427143 [GRCh37]
Chr10:10q23.33-26.3		 pathogenic
GRCh37/hg19 10q26.3(chr10:131949020-135427143)x1 copy number loss not provided [RCV000683274] Chr10:131949020..135427143 [GRCh37]
Chr10:10q26.3		 pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:122443197-135477883)x1 copy number loss not provided [RCV000737305] Chr10:122443197..135477883 [GRCh37]
Chr10:10q26.12-26.3		 pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:129454892-135447971)x1 copy number loss not provided [RCV000737323] Chr10:129454892..135447971 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:98087-135477883)x3 copy number gain not provided [RCV000749465] Chr10:98087..135477883 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
GRCh37/hg19 10q26.3(chr10:133657703-133766057)x3 copy number gain not provided [RCV000749856] Chr10:133657703..133766057 [GRCh37]
Chr10:10q26.3		 benign
GRCh37/hg19 10q26.3(chr10:133733922-133973625)x1 copy number loss not provided [RCV000749857] Chr10:133733922..133973625 [GRCh37]
Chr10:10q26.3		 benign
GRCh37/hg19 10p15.3-q26.3(chr10:73232-135524321)x3 copy number gain not provided [RCV000749464] Chr10:73232..135524321 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
NM_004052.4(BNIP3):c.454A>C (p.Lys152Gln) single nucleotide variant Inborn genetic diseases [RCV003268896] Chr10:131970723 [GRCh38]
Chr10:133784227 [GRCh37]
Chr10:10q26.3		 uncertain significance
GRCh37/hg19 10q25.1-26.3(chr10:110022170-135439095) copy number gain not provided [RCV000767665] Chr10:110022170..135439095 [GRCh37]
Chr10:10q25.1-26.3		 pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:129381095-135427143)x1 copy number loss not provided [RCV001006364] Chr10:129381095..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:124988334-135427143)x3 copy number gain not provided [RCV000848791] Chr10:124988334..135427143 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
GRCh37/hg19 10q26.11-26.3(chr10:119996339-135427143)x3 copy number gain not provided [RCV001006356] Chr10:119996339..135427143 [GRCh37]
Chr10:10q26.11-26.3		 pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:129009772-135427143)x1 copy number loss not provided [RCV001006362] Chr10:129009772..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.3(chr10:133223563-133784495)x3 copy number gain not provided [RCV001259087] Chr10:133223563..133784495 [GRCh37]
Chr10:10q26.3		 likely benign
GRCh37/hg19 10q26.2-26.3(chr10:129605105-135427143)x1 copy number loss See cases [RCV002285041] Chr10:129605105..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:129031265-135427143)x1 copy number loss not provided [RCV001259085] Chr10:129031265..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:129483682-135434178) copy number loss Global developmental delay [RCV001352664] Chr10:129483682..135434178 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
Single allele deletion Distal 10q deletion syndrome [RCV001391670] Chr10:127548166..135440251 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:122785023-135457222)x1 copy number loss See cases [RCV001526488] Chr10:122785023..135457222 [GRCh37]
Chr10:10q26.12-26.3		 pathogenic
GRCh37/hg19 10q25.3-26.3(chr10:118247181-135435319)x3 copy number gain not provided [RCV001537903] Chr10:118247181..135435319 [GRCh37]
Chr10:10q25.3-26.3		 pathogenic
GRCh37/hg19 10q25.1-26.3(chr10:108455687-135427143) copy number gain not specified [RCV002052891] Chr10:108455687..135427143 [GRCh37]
Chr10:10q25.1-26.3		 pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:128465436-135427143) copy number loss not specified [RCV002052902] Chr10:128465436..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:122125760-135062972) copy number gain not specified [RCV002052894] Chr10:122125760..135062972 [GRCh37]
Chr10:10q26.12-26.3		 likely pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:129914228-135427143) copy number loss not specified [RCV002052908] Chr10:129914228..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.3(chr10:133222945-133779463)x3 copy number gain not provided [RCV001829231] Chr10:133222945..133779463 [GRCh37]
Chr10:10q26.3		 likely benign
GRCh37/hg19 10q26.12-26.3(chr10:122343861-135427143) copy number loss not specified [RCV002052895] Chr10:122343861..135427143 [GRCh37]
Chr10:10q26.12-26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:127198625-135427143)x3 copy number gain See cases [RCV002292400] Chr10:127198625..135427143 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:126914469-135427143)x1 copy number loss See cases [RCV002292397] Chr10:126914469..135427143 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:126662496-133985966)x3 copy number gain not provided [RCV002474692] Chr10:126662496..133985966 [GRCh37]
Chr10:10q26.13-26.3		 uncertain significance
GRCh37/hg19 10q26.2-26.3(chr10:130043370-135345340)x1 copy number loss not provided [RCV002473957] Chr10:130043370..135345340 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.3(chr10:132631529-135354972)x1 copy number loss not provided [RCV002475809] Chr10:132631529..135354972 [GRCh37]
Chr10:10q26.3		 uncertain significance
NM_004052.4(BNIP3):c.524T>C (p.Leu175Pro) single nucleotide variant Inborn genetic diseases [RCV002879625] Chr10:131970653 [GRCh38]
Chr10:133784157 [GRCh37]
Chr10:10q26.3		 uncertain significance
NM_004052.4(BNIP3):c.380T>C (p.Ile127Thr) single nucleotide variant Inborn genetic diseases [RCV002946492] Chr10:131970873 [GRCh38]
Chr10:133784377 [GRCh37]
Chr10:10q26.3		 uncertain significance
NM_004052.4(BNIP3):c.529A>G (p.Ile177Val) single nucleotide variant Inborn genetic diseases [RCV002761859] Chr10:131970648 [GRCh38]
Chr10:133784152 [GRCh37]
Chr10:10q26.3		 uncertain significance
NM_004052.4(BNIP3):c.299T>C (p.Ile100Thr) single nucleotide variant Inborn genetic diseases [RCV002641000] Chr10:131970954 [GRCh38]
Chr10:133784458 [GRCh37]
Chr10:10q26.3		 uncertain significance
NM_004052.4(BNIP3):c.459A>T (p.Lys153Asn) single nucleotide variant Inborn genetic diseases [RCV002921387] Chr10:131970718 [GRCh38]
Chr10:133784222 [GRCh37]
Chr10:10q26.3		 uncertain significance
GRCh37/hg19 10q26.12-26.3(chr10:122610933-135439810)x1 copy number loss not provided [RCV003222684] Chr10:122610933..135439810 [GRCh37]
Chr10:10q26.12-26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:123477898-135427143) copy number loss Distal 10q deletion syndrome [RCV003319590] Chr10:123477898..135427143 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143) copy number gain Distal trisomy 10q [RCV003319593] Chr10:11138692..135427143 [GRCh37]
Chr10:10p14-q26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:124895517-135440296)x1 copy number loss Distal 10q deletion syndrome [RCV003329543] Chr10:124895517..135440296 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
NM_004052.4(BNIP3):c.390G>T (p.Lys130Asn) single nucleotide variant Inborn genetic diseases [RCV003384980] Chr10:131970787 [GRCh38]
Chr10:133784291 [GRCh37]
Chr10:10q26.3		 uncertain significance
GRCh37/hg19 10q26.2-26.3(chr10:128289206-135427143)x1 copy number loss Distal 10q deletion syndrome [RCV003458182] Chr10:128289206..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q25.1-26.3(chr10:111378692-135427143)x3 copy number gain Distal trisomy 10q [RCV003458955] Chr10:111378692..135427143 [GRCh37]
Chr10:10q25.1-26.3		 pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:128925940-135427143)x1 copy number loss not provided [RCV003483108] Chr10:128925940..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.3(chr10:132852693-134505024)x3 copy number gain not provided [RCV003484824] Chr10:132852693..134505024 [GRCh37]
Chr10:10q26.3		 uncertain significance
GRCh37/hg19 10q26.3(chr10:133435524-135427143)x1 copy number loss not provided [RCV003483110] Chr10:133435524..135427143 [GRCh37]
Chr10:10q26.3		 uncertain significance
GRCh38/hg38 10q26.2-26.3(chr10:125976998-133427130)x1 copy number loss Duane syndrome type 1 [RCV003984306] Chr10:125976998..133427130 [GRCh38]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.3(chr10:131398569-135427143)x1 copy number loss not specified [RCV003986883] Chr10:131398569..135427143 [GRCh37]
Chr10:10q26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:125987494-135427143)x1 copy number loss not specified [RCV003986904] Chr10:125987494..135427143 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:126127397-135427143)x1 copy number loss not specified [RCV003986878] Chr10:126127397..135427143 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
GRCh37/hg19 10q23.33-26.3(chr10:95078198-135427143)x3 copy number gain not specified [RCV003986893] Chr10:95078198..135427143 [GRCh37]
Chr10:10q23.33-26.3		 pathogenic
GRCh37/hg19 10q26.3(chr10:131299771-135441274)x1 copy number loss not provided [RCV003885450] Chr10:131299771..135441274 [GRCh37]
Chr10:10q26.3		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3498
Count of miRNA genes:1037
Interacting mature miRNAs:1246
Transcripts:ENST00000422256, ENST00000455566, ENST00000470416, ENST00000472664, ENST00000482010, ENST00000490777, ENST00000517472
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

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

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

Markers in Region
STS-W67510  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710133,769,700 - 133,769,823UniSTSGRCh37
Build 3610133,619,690 - 133,619,813RGDNCBI36
Celera10127,413,784 - 127,413,907RGD
Cytogenetic Map10q26.3UniSTS
HuRef10127,320,594 - 127,320,717UniSTS
GeneMap99-GB4 RH Map10557.8UniSTS
NCBI RH Map101382.8UniSTS
WI-22094  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710133,768,670 - 133,768,925UniSTSGRCh37
Build 3610133,618,660 - 133,618,915RGDNCBI36
Celera10127,412,754 - 127,413,009RGD
Cytogenetic Map10q26.3UniSTS
HuRef10127,319,564 - 127,319,819UniSTS
GeneMap99-GB4 RH Map10557.8UniSTS
Whitehead-RH Map10666.9UniSTS
NCBI RH Map101382.8UniSTS
WI-22366  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710133,773,095 - 133,773,309UniSTSGRCh37
Build 3610133,623,085 - 133,623,299RGDNCBI36
Celera10127,417,292 - 127,417,506RGD
Cytogenetic Map10q26.3UniSTS
HuRef10127,322,255 - 127,322,469UniSTS
GeneMap99-GB4 RH Map10557.8UniSTS
Whitehead-RH Map10667.0UniSTS
NCBI RH Map101382.8UniSTS
RH80993  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710133,761,538 - 133,761,788UniSTSGRCh37
Build 3610133,611,528 - 133,611,778RGDNCBI36
Celera10127,405,873 - 127,406,123RGD
Cytogenetic Map10q26.3UniSTS
HuRef10127,312,640 - 127,312,890UniSTS
GeneMap99-GB4 RH Map10557.8UniSTS
G62056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710133,769,422 - 133,769,577UniSTSGRCh37
Build 3610133,619,412 - 133,619,567RGDNCBI36
Celera10127,413,506 - 127,413,661RGD
Cytogenetic Map10q26.3UniSTS
HuRef10127,320,316 - 127,320,471UniSTS
RH11280  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710133,773,095 - 133,773,247UniSTSGRCh37
Build 3610133,623,085 - 133,623,237RGDNCBI36
Celera10127,417,292 - 127,417,444RGD
Cytogenetic Map10q26.3UniSTS
HuRef10127,322,255 - 127,322,407UniSTS
GeneMap99-GB4 RH Map10557.8UniSTS
NCBI RH Map101382.8UniSTS


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
Medium 1803 1468 1297 138 1098 76 3403 1184 2037 285 1385 1522 74 920 2085 2
Low 629 1515 426 484 849 388 952 1009 1671 133 63 86 97 284 703 2
Below cutoff 1 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001291310 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_018461 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_033191 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006717914 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425471 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425472 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425473 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425474 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425475 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425476 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425477 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425478 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366285 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366286 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366287 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366288 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366289 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366290 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366291 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366292 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002956987 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008488228 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008488229 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB040974 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF220046 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI521071 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK000402 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK001483 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK293065 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL162274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL732395 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC047379 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC058076 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC060885 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC072402 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ023669 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471066 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FP565171 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF455295 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000455566   ⟹   ENSP00000399970
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10131,901,008 - 131,959,834 (+)Ensembl
RefSeq Acc Id: ENST00000470416   ⟹   ENSP00000485636
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10131,901,291 - 131,959,827 (+)Ensembl
RefSeq Acc Id: ENST00000472664
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10131,940,607 - 131,945,925 (+)Ensembl
RefSeq Acc Id: ENST00000482010   ⟹   ENSP00000428418
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10131,901,266 - 131,956,555 (+)Ensembl
RefSeq Acc Id: ENST00000490777
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10131,940,159 - 131,956,242 (+)Ensembl
RefSeq Acc Id: ENST00000517472
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10131,939,776 - 131,944,006 (+)Ensembl
RefSeq Acc Id: ENST00000616467   ⟹   ENSP00000481133
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10131,901,031 - 131,956,555 (+)Ensembl
RefSeq Acc Id: ENST00000649083   ⟹   ENSP00000496850
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10131,940,163 - 131,957,483 (+)Ensembl
RefSeq Acc Id: NM_001291310   ⟹   NP_001278239
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810131,901,008 - 131,959,834 (+)NCBI
CHM1_110134,029,384 - 134,054,422 (+)NCBI
T2T-CHM13v2.010132,840,100 - 132,900,087 (+)NCBI
Sequence:
RefSeq Acc Id: NM_018461   ⟹   NP_060931
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810131,901,008 - 131,959,834 (+)NCBI
GRCh3710133,747,957 - 133,770,054 (+)RGD
Build 3610133,597,950 - 133,620,044 (+)NCBI Archive
Celera10127,392,198 - 127,414,138 (+)RGD
HuRef10127,299,151 - 127,320,948 (+)RGD
CHM1_110134,029,389 - 134,054,422 (+)NCBI
T2T-CHM13v2.010132,840,100 - 132,900,087 (+)NCBI
Sequence:
RefSeq Acc Id: NR_033191
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810131,901,008 - 131,959,834 (+)NCBI
GRCh3710133,747,957 - 133,770,054 (+)RGD
Celera10127,392,198 - 127,414,138 (+)RGD
HuRef10127,299,151 - 127,320,948 (+)RGD
CHM1_110134,029,386 - 134,054,422 (+)NCBI
T2T-CHM13v2.010132,840,100 - 132,900,087 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006717914   ⟹   XP_006717977
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810131,901,008 - 131,971,533 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047425471   ⟹   XP_047281427
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810131,936,414 - 131,959,834 (+)NCBI
RefSeq Acc Id: XM_047425472   ⟹   XP_047281428
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810131,936,451 - 131,950,404 (+)NCBI
RefSeq Acc Id: XM_047425473   ⟹   XP_047281429
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810131,936,451 - 131,971,533 (+)NCBI
RefSeq Acc Id: XM_047425474   ⟹   XP_047281430
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810131,936,452 - 131,966,328 (+)NCBI
RefSeq Acc Id: XM_047425475   ⟹   XP_047281431
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810131,934,463 - 131,959,834 (+)NCBI
RefSeq Acc Id: XM_047425476   ⟹   XP_047281432
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810131,938,197 - 131,959,834 (+)NCBI
RefSeq Acc Id: XM_047425477   ⟹   XP_047281433
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810131,940,768 - 131,959,834 (+)NCBI
RefSeq Acc Id: XM_047425478   ⟹   XP_047281434
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810131,901,239 - 131,959,834 (+)NCBI
RefSeq Acc Id: XM_054366285   ⟹   XP_054222260
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010132,876,416 - 132,890,362 (+)NCBI
RefSeq Acc Id: XM_054366286   ⟹   XP_054222261
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010132,876,416 - 132,911,782 (+)NCBI
RefSeq Acc Id: XM_054366287   ⟹   XP_054222262
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010132,840,100 - 132,911,782 (+)NCBI
RefSeq Acc Id: XM_054366288   ⟹   XP_054222263
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010132,876,417 - 132,906,447 (+)NCBI
RefSeq Acc Id: XM_054366289   ⟹   XP_054222264
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010132,874,423 - 132,899,514 (+)NCBI
RefSeq Acc Id: XM_054366290   ⟹   XP_054222265
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010132,878,162 - 132,899,514 (+)NCBI
RefSeq Acc Id: XM_054366291   ⟹   XP_054222266
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010132,880,634 - 132,899,514 (+)NCBI
RefSeq Acc Id: XM_054366292   ⟹   XP_054222267
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010132,840,331 - 132,899,514 (+)NCBI
RefSeq Acc Id: XR_008488228
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010132,876,379 - 132,900,087 (+)NCBI
RefSeq Acc Id: XR_008488229
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010132,876,379 - 132,900,087 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001278239 (Get FASTA)   NCBI Sequence Viewer  
  NP_060931 (Get FASTA)   NCBI Sequence Viewer  
  XP_006717977 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281427 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281428 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281429 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281430 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281431 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281432 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281433 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281434 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222260 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222261 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222262 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222263 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222264 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222265 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222266 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222267 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAF67639 (Get FASTA)   NCBI Sequence Viewer  
  AAH47379 (Get FASTA)   NCBI Sequence Viewer  
  AAH58076 (Get FASTA)   NCBI Sequence Viewer  
  AAH72402 (Get FASTA)   NCBI Sequence Viewer  
  BAA96065 (Get FASTA)   NCBI Sequence Viewer  
  BAF85754 (Get FASTA)   NCBI Sequence Viewer  
  BAG50921 (Get FASTA)   NCBI Sequence Viewer  
  EAW49145 (Get FASTA)   NCBI Sequence Viewer  
  EAW49146 (Get FASTA)   NCBI Sequence Viewer  
  EAW49147 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000399970
  ENSP00000399970.2
  ENSP00000428418.2
  ENSP00000481133.2
  ENSP00000485636.1
  ENSP00000496850.1
GenBank Protein Q66LE6 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_060931   ⟸   NM_018461
- Peptide Label: isoform a
- UniProtKB: Q5SQJ2 (UniProtKB/Swiss-Prot),   A8KAK0 (UniProtKB/Swiss-Prot),   Q9P1Y7 (UniProtKB/Swiss-Prot),   Q66LE6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_006717977   ⟸   XM_006717914
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: NP_001278239   ⟸   NM_001291310
- Peptide Label: isoform b
- UniProtKB: Q6IN90 (UniProtKB/TrEMBL),   Q6PEG1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000496850   ⟸   ENST00000649083
RefSeq Acc Id: ENSP00000399970   ⟸   ENST00000455566
RefSeq Acc Id: ENSP00000428418   ⟸   ENST00000482010
RefSeq Acc Id: ENSP00000485636   ⟸   ENST00000470416
RefSeq Acc Id: ENSP00000481133   ⟸   ENST00000616467
RefSeq Acc Id: XP_047281434   ⟸   XM_047425478
- Peptide Label: isoform X6
- UniProtKB: Q6IN90 (UniProtKB/TrEMBL),   Q6PEG1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047281431   ⟸   XM_047425475
- Peptide Label: isoform X6
- UniProtKB: Q6IN90 (UniProtKB/TrEMBL),   Q6PEG1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047281427   ⟸   XM_047425471
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047281429   ⟸   XM_047425473
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047281428   ⟸   XM_047425472
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047281430   ⟸   XM_047425474
- Peptide Label: isoform X5
RefSeq Acc Id: XP_047281432   ⟸   XM_047425476
- Peptide Label: isoform X6
- UniProtKB: Q6IN90 (UniProtKB/TrEMBL),   Q6PEG1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047281433   ⟸   XM_047425477
- Peptide Label: isoform X6
- UniProtKB: Q6IN90 (UniProtKB/TrEMBL),   Q6PEG1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054222262   ⟸   XM_054366287
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054222267   ⟸   XM_054366292
- Peptide Label: isoform X6
- UniProtKB: Q6IN90 (UniProtKB/TrEMBL),   Q6PEG1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054222264   ⟸   XM_054366289
- Peptide Label: isoform X6
- UniProtKB: Q6IN90 (UniProtKB/TrEMBL),   Q6PEG1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054222261   ⟸   XM_054366286
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054222260   ⟸   XM_054366285
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054222263   ⟸   XM_054366288
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054222265   ⟸   XM_054366290
- Peptide Label: isoform X6
- UniProtKB: Q6IN90 (UniProtKB/TrEMBL),   Q6PEG1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054222266   ⟸   XM_054366291
- Peptide Label: isoform X6
- UniProtKB: Q6IN90 (UniProtKB/TrEMBL),   Q6PEG1 (UniProtKB/TrEMBL)

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q66LE6-F1-model_v2 AlphaFold Q66LE6 1-453 view protein structure

Promoters
RGD ID:7219013
Promoter ID:EPDNEW_H15252
Type:initiation region
Name:PPP2R2D_1
Description:protein phosphatase 2 regulatory subunit Bdelta
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
GRCh3810131,940,153 - 131,940,213EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:23732 AgrOrtholog
COSMIC PPP2R2D COSMIC
Ensembl Genes ENSG00000175470 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000455566 ENTREZGENE
  ENST00000455566.6 UniProtKB/Swiss-Prot
  ENST00000470416.5 UniProtKB/TrEMBL
  ENST00000482010.6 UniProtKB/TrEMBL
  ENST00000616467.4 UniProtKB/TrEMBL
  ENST00000649083.1 UniProtKB/TrEMBL
Gene3D-CATH 2.130.10.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000175470 GTEx
HGNC ID HGNC:23732 ENTREZGENE
Human Proteome Map PPP2R2D Human Proteome Map
InterPro PP2A_PR55 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PP2A_PR55_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD40/YVTN_repeat-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD40_repeat UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD40_repeat_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:55844 UniProtKB/Swiss-Prot
NCBI Gene 55844 ENTREZGENE
OMIM 613992 OMIM
PANTHER PTHR11871 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SERINE/THREONINE-PROTEIN PHOSPHATASE 2A 55 KDA REGULATORY SUBUNIT B DELTA ISOFORM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134899040 PharmGKB
PIRSF PP2A_PR55 UniProtKB/Swiss-Prot
PRINTS PP2APR55 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE PR55_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PR55_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART WD40 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF50978 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt 2ABD_HUMAN UniProtKB/Swiss-Prot
  A0A096LPI9_HUMAN UniProtKB/TrEMBL
  A0A0A6YYD6_HUMAN UniProtKB/TrEMBL
  A0A3B3IRK1_HUMAN UniProtKB/TrEMBL
  A8KAK0 ENTREZGENE
  H0YB06_HUMAN UniProtKB/TrEMBL
  Q5SQJ2 ENTREZGENE
  Q66LE6 ENTREZGENE
  Q6IN90 ENTREZGENE, UniProtKB/TrEMBL
  Q6PEG1 ENTREZGENE, UniProtKB/TrEMBL
  Q9P1Y7 ENTREZGENE
UniProt Secondary A8KAK0 UniProtKB/Swiss-Prot
  Q5SQJ2 UniProtKB/Swiss-Prot
  Q9P1Y7 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-05-17 PPP2R2D  protein phosphatase 2 regulatory subunit Bdelta    protein phosphatase 2 regulatory subunit B, delta  Symbol and/or name change 5135510 APPROVED
2015-11-24 PPP2R2D  protein phosphatase 2 regulatory subunit B, delta    protein phosphatase 2, regulatory subunit B, delta  Symbol and/or name change 5135510 APPROVED
2011-07-27 PPP2R2D  protein phosphatase 2, regulatory subunit B, delta  PPP2R2D  protein phosphatase 2, regulatory subunit B, delta isoform  Symbol and/or name change 5135510 APPROVED