AP2B1 (adaptor related protein complex 2 subunit beta 1) - Rat Genome Database

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Gene: AP2B1 (adaptor related protein complex 2 subunit beta 1) Homo sapiens
Analyze
Symbol: AP2B1
Name: adaptor related protein complex 2 subunit beta 1
RGD ID: 734047
HGNC Page HGNC:563
Description: Enables clathrin binding activity. Involved in clathrin-dependent endocytosis and synaptic vesicle endocytosis. Located in membrane. Part of AP-2 adaptor complex.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: adapter-related protein complex 2 beta subunit; adapter-related protein complex 2 subunit beta; adaptin, beta 2 (beta); adaptor protein complex AP-2 subunit beta; adaptor related protein complex 2 beta 1 subunit; adaptor related protein complex 2, beta 1 subunit; adaptor-related protein complex 2 subunit beta; adaptor-related protein complex 2, beta 1 subunit; ADTB2; AP-2 complex subunit beta; AP105B; AP2-BETA; beta-2-adaptin; beta-adaptin; beta2-adaptin; CLAPB1; clathrin assembly protein complex 2 beta large chain; clathrin-associated/assembly/adaptor protein, large, beta 1; DKFZp781K0743; plasma membrane adaptor HA2/AP2 adaptin beta subunit; testicular tissue protein Li 22
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Related Pseudogenes: AL136455.1   AP2B1P1  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381735,587,322 - 35,726,413 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1735,578,046 - 35,726,413 (+)EnsemblGRCh38hg38GRCh38
GRCh371733,914,341 - 34,053,432 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361730,938,395 - 31,077,549 (+)NCBINCBI36Build 36hg18NCBI36
Build 341730,938,405 - 31,077,541NCBI
Celera1730,824,398 - 30,963,574 (+)NCBICelera
Cytogenetic Map17q12NCBI
HuRef1730,099,253 - 30,238,599 (+)NCBIHuRef
CHM1_11733,978,907 - 34,118,050 (+)NCBICHM1_1
T2T-CHM13v2.01736,535,193 - 36,674,326 (+)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
1,2-dimethylhydrazine  (ISO)
1,4-dichlorobenzene  (ISO)
1-chloro-2,4-dinitrobenzene  (EXP)
17alpha-ethynylestradiol  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,4-dinitrotoluene  (ISO)
2,6-dinitrotoluene  (ISO)
2-hydroxypropanoic acid  (EXP)
4,4'-sulfonyldiphenol  (EXP,ISO)
acetylsalicylic acid  (EXP)
acrolein  (EXP)
aflatoxin B1  (EXP)
all-trans-retinoic acid  (EXP)
aristolochic acid A  (EXP)
arsenite(3-)  (EXP)
arsenous acid  (EXP)
benzo[a]pyrene  (ISO)
bisphenol A  (EXP,ISO)
bisphenol F  (ISO)
cadmium atom  (EXP)
carbon nanotube  (ISO)
CGP 52608  (EXP)
chlorpyrifos  (ISO)
clozapine  (ISO)
cocaine  (ISO)
coumarin  (EXP)
Cuprizon  (ISO)
diarsenic trioxide  (EXP)
diethylstilbestrol  (ISO)
dorsomorphin  (EXP)
ethanol  (EXP,ISO)
fluoxetine  (ISO)
folic acid  (ISO)
haloperidol  (ISO)
irinotecan  (EXP)
isotretinoin  (EXP)
ivermectin  (EXP)
lead(0)  (EXP)
methylmercury chloride  (EXP)
methylphenidate  (ISO)
N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine  (EXP)
N-nitrosodiethylamine  (ISO)
nickel atom  (EXP)
ozone  (EXP)
paracetamol  (ISO)
perfluorohexanesulfonic acid  (ISO)
perfluorooctanoic acid  (ISO)
phenobarbital  (ISO)
phenylmercury acetate  (EXP)
pirinixic acid  (ISO)
rac-lactic acid  (EXP)
resveratrol  (ISO)
SB 431542  (EXP)
testosterone  (EXP)
testosterone enanthate  (EXP)
tetrachloromethane  (ISO)
titanium dioxide  (ISO)
toluene  (ISO)
trichostatin A  (EXP)
trimellitic anhydride  (ISO)
urethane  (EXP)
valproic acid  (EXP)
venlafaxine hydrochloride  (ISO)
vinclozolin  (ISO)
zinc sulfate  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
3. Calpain hydrolysis of alpha- and beta2-adaptins decreases clathrin-dependent endocytosis and may promote neurodegeneration. Rudinskiy N, etal., J Biol Chem. 2009 May 1;284(18):12447-58. doi: 10.1074/jbc.M804740200. Epub 2009 Feb 24.
4. Synaptic vesicle endocytosis. Saheki Y and De Camilli P, Cold Spring Harb Perspect Biol. 2012 Sep 1;4(9):a005645. doi: 10.1101/cshperspect.a005645.
Additional References at PubMed
PMID:1969413   PMID:2014052   PMID:7534311   PMID:8262066   PMID:8595912   PMID:9341158   PMID:9384576   PMID:9651214   PMID:9707615   PMID:9811611   PMID:9882340   PMID:10097102  
PMID:10567358   PMID:10748223   PMID:10944104   PMID:10966473   PMID:11102472   PMID:11157096   PMID:11170396   PMID:11285224   PMID:11463741   PMID:11777907   PMID:12070169   PMID:12086608  
PMID:12121421   PMID:12221107   PMID:12419313   PMID:12429842   PMID:12429846   PMID:12477932   PMID:12577067   PMID:12732633   PMID:12900408   PMID:14530274   PMID:15020715   PMID:15489334  
PMID:15533940   PMID:15592455   PMID:15761153   PMID:15897975   PMID:15941406   PMID:16055064   PMID:16103193   PMID:16139856   PMID:16189514   PMID:16314522   PMID:16581796   PMID:16723738  
PMID:16903783   PMID:17052248   PMID:17108326   PMID:17210199   PMID:17267500   PMID:17290217   PMID:17353931   PMID:17620599   PMID:17719203   PMID:18654987   PMID:18843039   PMID:19149577  
PMID:19380743   PMID:19469909   PMID:19509056   PMID:19615732   PMID:19738201   PMID:19802344   PMID:19903820   PMID:19946888   PMID:20012524   PMID:20360068   PMID:20435073   PMID:20594957  
PMID:20603002   PMID:20936779   PMID:20965945   PMID:21118812   PMID:21145461   PMID:21499258   PMID:21762802   PMID:21873635   PMID:22103831   PMID:22139419   PMID:22323290   PMID:22360420  
PMID:22558309   PMID:22586326   PMID:22623428   PMID:22632162   PMID:22678362   PMID:22810586   PMID:22863883   PMID:23077317   PMID:23211419   PMID:23676497   PMID:23705972   PMID:23751493  
PMID:23874206   PMID:23956138   PMID:24067654   PMID:24130457   PMID:24189400   PMID:24332808   PMID:24722188   PMID:24797263   PMID:25061211   PMID:25277244   PMID:25416956   PMID:25681748  
PMID:25852190   PMID:25898166   PMID:25910212   PMID:25921289   PMID:25959826   PMID:25963833   PMID:26186194   PMID:26269175   PMID:26344197   PMID:26471122   PMID:26472760   PMID:26496610  
PMID:26638075   PMID:26673895   PMID:26680585   PMID:26831064   PMID:26950368   PMID:27107012   PMID:27107014   PMID:27173435   PMID:27248496   PMID:27545878   PMID:27684187   PMID:28190767  
PMID:28388416   PMID:28514442   PMID:28515276   PMID:28675297   PMID:28902428   PMID:28982131   PMID:29117863   PMID:29184887   PMID:29229926   PMID:29262337   PMID:29395067   PMID:29467282  
PMID:29507755   PMID:29509190   PMID:29540532   PMID:29568061   PMID:29845934   PMID:29892012   PMID:29997244   PMID:30021884   PMID:30026878   PMID:30196744   PMID:30209976   PMID:30411541  
PMID:30575818   PMID:30581152   PMID:30711629   PMID:30737378   PMID:30833792   PMID:30940648   PMID:30979931   PMID:31067453   PMID:31091453   PMID:31152661   PMID:31324722   PMID:31340145  
PMID:31462741   PMID:31586073   PMID:31671891   PMID:31871319   PMID:31980649   PMID:32041737   PMID:32176628   PMID:32296183   PMID:32460013   PMID:32665550   PMID:32707033   PMID:32780723  
PMID:32807901   PMID:33024031   PMID:33239621   PMID:33545068   PMID:33658012   PMID:33731348   PMID:33742100   PMID:33762435   PMID:33916271   PMID:33961781   PMID:34079125   PMID:34316702  
PMID:34591612   PMID:34650049   PMID:34709727   PMID:34761192   PMID:34857952   PMID:35013218   PMID:35031058   PMID:35032548   PMID:35044719   PMID:35182466   PMID:35241646   PMID:35253629  
PMID:35256949   PMID:35271311   PMID:35384245   PMID:35446349   PMID:35676659   PMID:35831314   PMID:35831895   PMID:35864588   PMID:35914814   PMID:36114006   PMID:36168627   PMID:36215168  
PMID:36244648   PMID:36398662   PMID:36490346   PMID:36517590   PMID:36526897   PMID:36574265   PMID:36604567   PMID:36736316   PMID:36901413   PMID:36912080   PMID:37071664   PMID:37232246  
PMID:37616343   PMID:37689310   PMID:37977651   PMID:38093640   PMID:38113892  


Genomics

Comparative Map Data
AP2B1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381735,587,322 - 35,726,413 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1735,578,046 - 35,726,413 (+)EnsemblGRCh38hg38GRCh38
GRCh371733,914,341 - 34,053,432 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361730,938,395 - 31,077,549 (+)NCBINCBI36Build 36hg18NCBI36
Build 341730,938,405 - 31,077,541NCBI
Celera1730,824,398 - 30,963,574 (+)NCBICelera
Cytogenetic Map17q12NCBI
HuRef1730,099,253 - 30,238,599 (+)NCBIHuRef
CHM1_11733,978,907 - 34,118,050 (+)NCBICHM1_1
T2T-CHM13v2.01736,535,193 - 36,674,326 (+)NCBIT2T-CHM13v2.0
Ap2b1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391183,189,545 - 83,295,861 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1183,189,850 - 83,295,861 (+)EnsemblGRCm39 Ensembl
GRCm381183,298,719 - 83,405,035 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1183,299,024 - 83,405,035 (+)EnsemblGRCm38mm10GRCm38
MGSCv371183,116,199 - 83,218,537 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361183,118,892 - 83,221,230 (+)NCBIMGSCv36mm8
Celera1192,894,853 - 92,999,587 (+)NCBICelera
Cytogenetic Map11CNCBI
cM Map1150.3NCBI
Ap2b1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81068,596,925 - 68,702,547 (+)NCBIGRCr8
mRatBN7.21068,099,397 - 68,205,023 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1068,099,547 - 68,205,013 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1072,723,218 - 72,825,030 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01072,228,605 - 72,330,413 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01067,692,649 - 67,794,463 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01070,516,462 - 70,621,973 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1070,520,206 - 70,621,977 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01071,035,406 - 71,067,828 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Rnor_5.01071,068,935 - 71,083,997 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41071,386,233 - 71,488,000 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11071,399,684 - 71,502,555 (+)NCBI
Celera1067,045,800 - 67,146,677 (+)NCBICelera
Cytogenetic Map10q26NCBI
Ap2b1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495548110,064,220 - 10,175,627 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495548110,061,021 - 10,175,070 (+)NCBIChiLan1.0ChiLan1.0
AP2B1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21928,750,972 - 28,892,336 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11730,632,528 - 30,769,787 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01721,070,132 - 21,208,610 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11721,363,115 - 21,501,720 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1721,363,121 - 21,501,721 (-)Ensemblpanpan1.1panPan2
AP2B1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1937,946,761 - 38,078,074 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl937,946,788 - 38,078,041 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha937,170,891 - 37,302,120 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0938,758,380 - 38,889,742 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl938,756,039 - 38,889,684 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1937,541,221 - 37,673,744 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0937,826,684 - 37,958,055 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0937,914,210 - 38,045,500 (-)NCBIUU_Cfam_GSD_1.0
Ap2b1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440560236,949,807 - 37,069,908 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493649012,233 - 127,715 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049364905,156 - 127,666 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
AP2B1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1239,800,972 - 39,932,643 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11239,803,105 - 39,940,801 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
AP2B1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11629,061,662 - 29,198,942 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1629,061,568 - 29,201,464 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666075774,355 - 913,998 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ap2b1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248753,090,656 - 3,208,593 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248753,085,518 - 3,206,930 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in AP2B1
32 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17q12(chr17:35129859-35767049)x3 copy number gain See cases [RCV000136983] Chr17:35129859..35767049 [GRCh38]
Chr17:33456878..34094068 [GRCh37]
Chr17:30480991..31118181 [NCBI36]
Chr17:17q12		 uncertain significance
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17q12(chr17:32351496-34455576)x1 copy number loss not provided [RCV000683918] Chr17:32351496..34455576 [GRCh37]
Chr17:17q12		 uncertain significance
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p11.2-q21.2(chr17:21690653-38772647)x3 copy number gain not provided [RCV000846852] Chr17:21690653..38772647 [GRCh37]
Chr17:17p11.2-q21.2		 pathogenic
NM_001030006.2(AP2B1):c.2168C>T (p.Ala723Val) single nucleotide variant not specified [RCV004331185] Chr17:35671890 [GRCh38]
Chr17:33998909 [GRCh37]
Chr17:17q12		 uncertain significance
NM_001030006.2(AP2B1):c.597G>A (p.Leu199=) single nucleotide variant not provided [RCV000953371] Chr17:35624468 [GRCh38]
Chr17:33951487 [GRCh37]
Chr17:17q12		 benign
NM_001030006.2(AP2B1):c.240G>T (p.Gln80His) single nucleotide variant not provided [RCV001249263] Chr17:35605801 [GRCh38]
Chr17:33932820 [GRCh37]
Chr17:17q12		 not provided
NC_000017.10:g.(?_33475283)_(34079869_?)dup duplication Peroxisome biogenesis disorder 3A (Zellweger) [RCV003110947] Chr17:33475283..34079869 [GRCh37]
Chr17:17q12		 uncertain significance
GRCh37/hg19 17q12(chr17:33766040-34001896)x3 copy number gain Isolated anorectal malformation [RCV002286602] Chr17:33766040..34001896 [GRCh37]
Chr17:17q12		 uncertain significance
NM_001030006.2(AP2B1):c.857C>T (p.Pro286Leu) single nucleotide variant not specified [RCV004159106] Chr17:35626761 [GRCh38]
Chr17:33953780 [GRCh37]
Chr17:17q12		 uncertain significance
NM_001030006.2(AP2B1):c.2230A>G (p.Thr744Ala) single nucleotide variant not specified [RCV004191189] Chr17:35674227 [GRCh38]
Chr17:34001246 [GRCh37]
Chr17:17q12		 uncertain significance
NM_001030006.2(AP2B1):c.1831A>C (p.Thr611Pro) single nucleotide variant not specified [RCV004111844] Chr17:35657633 [GRCh38]
Chr17:33984652 [GRCh37]
Chr17:17q12		 uncertain significance
NM_001030006.2(AP2B1):c.2143G>A (p.Gly715Ser) single nucleotide variant not specified [RCV004133169] Chr17:35671865 [GRCh38]
Chr17:33998884 [GRCh37]
Chr17:17q12		 uncertain significance
NM_001030006.2(AP2B1):c.2089C>T (p.Pro697Ser) single nucleotide variant not specified [RCV004146838] Chr17:35671811 [GRCh38]
Chr17:33998830 [GRCh37]
Chr17:17q12		 uncertain significance
NM_001030006.2(AP2B1):c.1736A>G (p.Asn579Ser) single nucleotide variant not specified [RCV004243758] Chr17:35650729 [GRCh38]
Chr17:33977748 [GRCh37]
Chr17:17q12		 uncertain significance
NM_001030006.2(AP2B1):c.2194G>A (p.Val732Ile) single nucleotide variant not specified [RCV004268253] Chr17:35674191 [GRCh38]
Chr17:34001210 [GRCh37]
Chr17:17q12		 uncertain significance
NM_001030006.2(AP2B1):c.1699A>G (p.Ile567Val) single nucleotide variant not specified [RCV004259341] Chr17:35650692 [GRCh38]
Chr17:33977711 [GRCh37]
Chr17:17q12		 uncertain significance
GRCh37/hg19 17q11.2-12(chr17:30572862-35843988) copy number loss Chromosome 17q12 deletion syndrome [RCV003319594] Chr17:30572862..35843988 [GRCh37]
Chr17:17q11.2-12		 pathogenic
NM_001030006.2(AP2B1):c.230C>G (p.Ala77Gly) single nucleotide variant not specified [RCV004351167] Chr17:35605791 [GRCh38]
Chr17:33932810 [GRCh37]
Chr17:17q12		 uncertain significance
NM_001030006.2(AP2B1):c.433G>A (p.Val145Met) single nucleotide variant not specified [RCV004362041] Chr17:35608295 [GRCh38]
Chr17:33935314 [GRCh37]
Chr17:17q12		 uncertain significance
GRCh37/hg19 17q12(chr17:33758250-34082140)x3 copy number gain not provided [RCV003485152] Chr17:33758250..34082140 [GRCh37]
Chr17:17q12		 uncertain significance
GRCh37/hg19 17q12(chr17:33769812-33983362)x3 copy number gain not provided [RCV003485153] Chr17:33769812..33983362 [GRCh37]
Chr17:17q12		 uncertain significance
NM_001030006.2(AP2B1):c.1831A>G (p.Thr611Ala) single nucleotide variant not specified [RCV004424850] Chr17:35657633 [GRCh38]
Chr17:33984652 [GRCh37]
Chr17:17q12		 uncertain significance
NM_001030006.2(AP2B1):c.1843C>G (p.Leu615Val) single nucleotide variant not specified [RCV004424851] Chr17:35657645 [GRCh38]
Chr17:33984664 [GRCh37]
Chr17:17q12		 uncertain significance
NM_001030006.2(AP2B1):c.2567A>G (p.Lys856Arg) single nucleotide variant not specified [RCV004424852] Chr17:35710261 [GRCh38]
Chr17:34037280 [GRCh37]
Chr17:17q12		 uncertain significance
NM_001030006.2(AP2B1):c.2644T>A (p.Leu882Met) single nucleotide variant not specified [RCV004424853] Chr17:35717212 [GRCh38]
Chr17:34044231 [GRCh37]
Chr17:17q12		 uncertain significance
NM_001030006.2(AP2B1):c.584A>G (p.Asn195Ser) single nucleotide variant not specified [RCV004424855] Chr17:35624455 [GRCh38]
Chr17:33951474 [GRCh37]
Chr17:17q12		 uncertain significance
NM_001030006.2(AP2B1):c.2836G>C (p.Asp946His) single nucleotide variant not specified [RCV004424854] Chr17:35723679 [GRCh38]
Chr17:34050698 [GRCh37]
Chr17:17q12		 uncertain significance
NM_001030006.2(AP2B1):c.1783A>G (p.Ile595Val) single nucleotide variant not specified [RCV004424849] Chr17:35650776 [GRCh38]
Chr17:33977795 [GRCh37]
Chr17:17q12		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4962
Count of miRNA genes:1338
Interacting mature miRNAs:1763
Transcripts:ENST00000262325, ENST00000312678, ENST00000537622, ENST00000538556, ENST00000545922, ENST00000587805, ENST00000588093, ENST00000588116, ENST00000588493, ENST00000589344, ENST00000589774, ENST00000590432, ENST00000590538, ENST00000591561, ENST00000591610, ENST00000592167, ENST00000592191, ENST00000592545, ENST00000593014
Prediction methods:Microtar, Miranda, Pita, 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
D17S1690  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371734,000,982 - 34,001,096UniSTSGRCh37
Build 361731,025,095 - 31,025,209RGDNCBI36
Celera1730,911,101 - 30,911,215RGD
Cytogenetic Map17q11.2-q12UniSTS
HuRef1730,186,123 - 30,186,237UniSTS
Whitehead-YAC Contig Map17 UniSTS
D17S2061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371734,050,854 - 34,050,948UniSTSGRCh37
Build 361731,074,967 - 31,075,061RGDNCBI36
Celera1730,960,992 - 30,961,086RGD
Cytogenetic Map17q11.2-q12UniSTS
HuRef1730,236,017 - 30,236,111UniSTS
Whitehead-YAC Contig Map17 UniSTS
WI-18136  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371733,986,987 - 33,987,112UniSTSGRCh37
Build 361731,011,100 - 31,011,225RGDNCBI36
Celera1730,897,105 - 30,897,230RGD
Cytogenetic Map17q11.2-q12UniSTS
HuRef1730,172,130 - 30,172,255UniSTS
GeneMap99-GB4 RH Map17298.0UniSTS
Whitehead-RH Map17321.7UniSTS
G59802  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371733,986,999 - 33,987,105UniSTSGRCh37
Build 361731,011,112 - 31,011,218RGDNCBI36
Celera1730,897,117 - 30,897,223RGD
Cytogenetic Map17q11.2-q12UniSTS
HuRef1730,172,142 - 30,172,248UniSTS
TNG Radiation Hybrid Map1714410.0UniSTS
G62209  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371733,975,661 - 33,975,852UniSTSGRCh37
Build 361730,999,774 - 30,999,965RGDNCBI36
Celera1730,885,772 - 30,885,968RGD
Cytogenetic Map17q11.2-q12UniSTS
HuRef1730,160,808 - 30,160,985UniSTS
RH47464  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371734,053,176 - 34,053,360UniSTSGRCh37
Build 361731,077,289 - 31,077,473RGDNCBI36
Celera1730,963,314 - 30,963,498RGD
Cytogenetic Map17q11.2-q12UniSTS
HuRef1730,238,339 - 30,238,523UniSTS
GeneMap99-GB4 RH Map17300.22UniSTS
NCBI RH Map17388.3UniSTS
SGC44707  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371734,053,242 - 34,053,368UniSTSGRCh37
Build 361731,077,355 - 31,077,481RGDNCBI36
Celera1730,963,380 - 30,963,506RGD
Cytogenetic Map17q11.2-q12UniSTS
HuRef1730,238,405 - 30,238,531UniSTS
GeneMap99-GB4 RH Map17301.75UniSTS
Whitehead-RH Map17289.0UniSTS
NCBI RH Map17352.4UniSTS
RH12574  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371734,052,227 - 34,052,364UniSTSGRCh37
Build 361731,076,340 - 31,076,477RGDNCBI36
Celera1730,962,365 - 30,962,502RGD
Cytogenetic Map17q11.2-q12UniSTS
HuRef1730,237,390 - 30,237,527UniSTS
GeneMap99-GB4 RH Map17291.21UniSTS
NCBI RH Map17398.7UniSTS
SHGC-52481  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371734,018,618 - 34,018,822UniSTSGRCh37
Build 361731,042,731 - 31,042,935RGDNCBI36
Celera1730,928,736 - 30,928,940RGD
Cytogenetic Map17q11.2-q12UniSTS
HuRef1730,203,759 - 30,203,963UniSTS
GeneMap99-G3 RH Map171863.0UniSTS
STS-W92018  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371733,986,837 - 33,987,013UniSTSGRCh37
Build 361731,010,950 - 31,011,126RGDNCBI36
Celera1730,896,955 - 30,897,131RGD
Cytogenetic Map17q11.2-q12UniSTS
HuRef1730,171,980 - 30,172,156UniSTS
GeneMap99-GB4 RH Map17295.52UniSTS
D17S1669  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371734,035,117 - 34,035,316UniSTSGRCh37
Build 361731,059,230 - 31,059,429RGDNCBI36
Celera1730,945,255 - 30,945,454RGD
Cytogenetic Map17q11.2-q12UniSTS
HuRef1730,220,283 - 30,220,482UniSTS
Whitehead-RH Map17321.7UniSTS
Whitehead-YAC Contig Map17 UniSTS
IB756  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371734,053,129 - 34,053,336UniSTSGRCh37
Build 361731,077,242 - 31,077,449RGDNCBI36
Celera1730,963,267 - 30,963,474RGD
Cytogenetic Map17q11.2-q12UniSTS
HuRef1730,238,292 - 30,238,499UniSTS
Stanford-G3 RH Map171370.0UniSTS
NCBI RH Map17386.5UniSTS
GeneMap99-G3 RH Map171871.0UniSTS
CLAPB1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X92,477,505 - 92,477,587UniSTSGRCh37
GRCh371734,036,271 - 34,037,278UniSTSGRCh37
Build 36X92,364,161 - 92,364,243RGDNCBI36
Celera1730,946,409 - 30,947,416UniSTS
CeleraX93,002,728 - 93,002,810RGD
HuRefX82,300,456 - 82,300,538UniSTS
HuRef1730,221,437 - 30,222,444UniSTS
MARC_4629-4630:966894533:1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X92,477,493 - 92,477,567UniSTSGRCh37
GRCh371734,036,291 - 34,037,290UniSTSGRCh37
Build 36X92,364,149 - 92,364,223RGDNCBI36
Celera1730,946,429 - 30,947,428UniSTS
CeleraX93,002,716 - 93,002,790RGD
HuRefX82,300,444 - 82,300,518UniSTS
HuRef1730,221,457 - 30,222,456UniSTS
SHGC-57242  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic MapXq21.32UniSTS
Cytogenetic Map17q11.2-q12UniSTS
HuRefX82,302,634 - 82,302,843UniSTS
TNG Radiation Hybrid MapX21320.0UniSTS
AP2B1-1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371733,953,804 - 33,954,458UniSTSGRCh37
Celera1730,863,924 - 30,864,580UniSTS
HuRef1730,138,965 - 30,139,620UniSTS


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 2432 2886 1620 520 1928 362 4355 2117 3701 415 1447 1607 171 1204 2788 4
Low 98 103 102 20 102 76 7 3 1 1
Below cutoff

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001030006 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001282 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005257937 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005257938 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005257941 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011524448 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011524449 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011524450 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011524451 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011524452 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011524453 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011524454 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011524455 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017024284 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017024285 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017024286 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017024287 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435508 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435509 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435510 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435511 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435512 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315283 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315284 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315285 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315286 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315287 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315288 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315289 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315290 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315291 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315292 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315293 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315294 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315295 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315296 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC004134 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC006237 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC015911 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI691147 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK289528 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK292531 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK295667 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK301522 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK304126 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY341427 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC006201 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC012150 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ421703 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX643620 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471147 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR749392 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM005335 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF456264 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF456265 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M34175 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000587805   ⟹   ENSP00000466580
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,650,650 - 35,660,120 (+)Ensembl
RefSeq Acc Id: ENST00000588093
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,587,531 - 35,601,037 (+)Ensembl
RefSeq Acc Id: ENST00000588116   ⟹   ENSP00000464966
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,624,582 - 35,657,615 (+)Ensembl
RefSeq Acc Id: ENST00000589774   ⟹   ENSP00000468183
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,578,046 - 35,608,315 (+)Ensembl
RefSeq Acc Id: ENST00000590432   ⟹   ENSP00000465357
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,587,416 - 35,605,801 (+)Ensembl
RefSeq Acc Id: ENST00000590538   ⟹   ENSP00000468813
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,587,322 - 35,608,165 (+)Ensembl
RefSeq Acc Id: ENST00000591561
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,607,837 - 35,626,720 (+)Ensembl
RefSeq Acc Id: ENST00000591610   ⟹   ENSP00000465848
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,587,322 - 35,608,292 (+)Ensembl
RefSeq Acc Id: ENST00000592167   ⟹   ENSP00000467382
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,587,566 - 35,605,766 (+)Ensembl
RefSeq Acc Id: ENST00000593014   ⟹   ENSP00000466812
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,587,738 - 35,608,260 (+)Ensembl
RefSeq Acc Id: ENST00000610402   ⟹   ENSP00000483185
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,587,322 - 35,726,413 (+)Ensembl
RefSeq Acc Id: ENST00000612035   ⟹   ENSP00000482825
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,587,322 - 35,670,898 (+)Ensembl
RefSeq Acc Id: ENST00000612116   ⟹   ENSP00000478115
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,587,452 - 35,724,091 (+)Ensembl
RefSeq Acc Id: ENST00000614600   ⟹   ENSP00000479691
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,587,367 - 35,670,898 (+)Ensembl
RefSeq Acc Id: ENST00000616681   ⟹   ENSP00000484708
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,587,314 - 35,724,086 (+)Ensembl
RefSeq Acc Id: ENST00000616784   ⟹   ENSP00000478471
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,586,899 - 35,657,791 (+)Ensembl
RefSeq Acc Id: ENST00000618940   ⟹   ENSP00000482835
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,587,515 - 35,724,086 (+)Ensembl
RefSeq Acc Id: ENST00000619183
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,621,275 - 35,670,898 (+)Ensembl
RefSeq Acc Id: ENST00000620039   ⟹   ENSP00000481246
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,587,314 - 35,724,089 (+)Ensembl
RefSeq Acc Id: ENST00000621668   ⟹   ENSP00000481704
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,587,314 - 35,670,898 (+)Ensembl
RefSeq Acc Id: ENST00000621914   ⟹   ENSP00000482315
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,587,274 - 35,726,409 (+)Ensembl
RefSeq Acc Id: ENST00000628168   ⟹   ENSP00000487324
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1735,594,031 - 35,600,985 (+)Ensembl
RefSeq Acc Id: NM_001030006   ⟹   NP_001025177
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381735,587,322 - 35,726,413 (+)NCBI
GRCh371733,913,918 - 34,053,436 (+)NCBI
Build 361730,938,395 - 31,077,549 (+)NCBI Archive
HuRef1730,099,253 - 30,238,599 (+)ENTREZGENE
CHM1_11733,978,907 - 34,118,050 (+)NCBI
T2T-CHM13v2.01736,535,242 - 36,674,326 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001282   ⟹   NP_001273
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381735,587,322 - 35,726,413 (+)NCBI
GRCh371733,913,918 - 34,053,436 (+)NCBI
Build 361730,938,395 - 31,077,549 (+)NCBI Archive
HuRef1730,099,253 - 30,238,599 (+)ENTREZGENE
CHM1_11733,978,907 - 34,118,050 (+)NCBI
T2T-CHM13v2.01736,535,242 - 36,674,326 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005257937   ⟹   XP_005257994
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381735,587,322 - 35,726,413 (+)NCBI
GRCh371733,913,918 - 34,053,436 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005257938   ⟹   XP_005257995
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381735,587,322 - 35,726,413 (+)NCBI
GRCh371733,913,918 - 34,053,436 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005257941   ⟹   XP_005257998
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381735,587,322 - 35,660,120 (+)NCBI
GRCh371733,913,918 - 34,053,436 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011524448   ⟹   XP_011522750
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381735,587,322 - 35,726,413 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011524449   ⟹   XP_011522751
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381735,587,322 - 35,726,413 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011524450   ⟹   XP_011522752
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381735,587,322 - 35,726,413 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011524451   ⟹   XP_011522753
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381735,587,322 - 35,726,413 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017024284   ⟹   XP_016879773
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381735,587,322 - 35,726,413 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017024287   ⟹   XP_016879776
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381735,587,322 - 35,660,120 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047435508   ⟹   XP_047291464
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381735,587,322 - 35,726,413 (+)NCBI
RefSeq Acc Id: XM_047435509   ⟹   XP_047291465
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381735,587,322 - 35,726,413 (+)NCBI
RefSeq Acc Id: XM_047435510   ⟹   XP_047291466
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381735,587,322 - 35,726,413 (+)NCBI
RefSeq Acc Id: XM_047435511   ⟹   XP_047291467
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381735,600,975 - 35,726,413 (+)NCBI
RefSeq Acc Id: XM_047435512   ⟹   XP_047291468
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381735,587,322 - 35,660,120 (+)NCBI
RefSeq Acc Id: XM_054315283   ⟹   XP_054171258
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01736,535,242 - 36,674,326 (+)NCBI
RefSeq Acc Id: XM_054315284   ⟹   XP_054171259
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01736,535,194 - 36,674,326 (+)NCBI
RefSeq Acc Id: XM_054315285   ⟹   XP_054171260
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01736,535,336 - 36,674,326 (+)NCBI
RefSeq Acc Id: XM_054315286   ⟹   XP_054171261
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01736,535,242 - 36,674,326 (+)NCBI
RefSeq Acc Id: XM_054315287   ⟹   XP_054171262
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01736,535,194 - 36,674,326 (+)NCBI
RefSeq Acc Id: XM_054315288   ⟹   XP_054171263
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01736,535,336 - 36,674,326 (+)NCBI
RefSeq Acc Id: XM_054315289   ⟹   XP_054171264
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01736,535,195 - 36,674,326 (+)NCBI
RefSeq Acc Id: XM_054315290   ⟹   XP_054171265
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01736,535,195 - 36,674,326 (+)NCBI
RefSeq Acc Id: XM_054315291   ⟹   XP_054171266
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01736,535,195 - 36,674,326 (+)NCBI
RefSeq Acc Id: XM_054315292   ⟹   XP_054171267
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01736,535,195 - 36,674,326 (+)NCBI
RefSeq Acc Id: XM_054315293   ⟹   XP_054171268
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01736,548,897 - 36,674,326 (+)NCBI
RefSeq Acc Id: XM_054315294   ⟹   XP_054171269
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01736,535,242 - 36,608,043 (+)NCBI
RefSeq Acc Id: XM_054315295   ⟹   XP_054171270
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01736,535,193 - 36,608,043 (+)NCBI
RefSeq Acc Id: XM_054315296   ⟹   XP_054171271
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01736,535,193 - 36,608,043 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001025177 (Get FASTA)   NCBI Sequence Viewer  
  NP_001273 (Get FASTA)   NCBI Sequence Viewer  
  XP_005257994 (Get FASTA)   NCBI Sequence Viewer  
  XP_005257995 (Get FASTA)   NCBI Sequence Viewer  
  XP_005257998 (Get FASTA)   NCBI Sequence Viewer  
  XP_011522750 (Get FASTA)   NCBI Sequence Viewer  
  XP_011522751 (Get FASTA)   NCBI Sequence Viewer  
  XP_011522752 (Get FASTA)   NCBI Sequence Viewer  
  XP_011522753 (Get FASTA)   NCBI Sequence Viewer  
  XP_016879773 (Get FASTA)   NCBI Sequence Viewer  
  XP_016879776 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291464 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291465 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291466 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291467 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291468 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171258 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171259 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171260 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171261 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171262 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171263 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171264 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171265 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171266 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171267 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171268 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171269 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171270 (Get FASTA)   NCBI Sequence Viewer  
  XP_054171271 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAA35583 (Get FASTA)   NCBI Sequence Viewer  
  AAH06201 (Get FASTA)   NCBI Sequence Viewer  
  AAH12150 (Get FASTA)   NCBI Sequence Viewer  
  AAQ20044 (Get FASTA)   NCBI Sequence Viewer  
  AEE60935 (Get FASTA)   NCBI Sequence Viewer  
  BAF82217 (Get FASTA)   NCBI Sequence Viewer  
  BAF85220 (Get FASTA)   NCBI Sequence Viewer  
  BAG58527 (Get FASTA)   NCBI Sequence Viewer  
  BAG63026 (Get FASTA)   NCBI Sequence Viewer  
  BAG65023 (Get FASTA)   NCBI Sequence Viewer  
  CAH18240 (Get FASTA)   NCBI Sequence Viewer  
  EAW80133 (Get FASTA)   NCBI Sequence Viewer  
  EAW80134 (Get FASTA)   NCBI Sequence Viewer  
  EAW80135 (Get FASTA)   NCBI Sequence Viewer  
  EAW80136 (Get FASTA)   NCBI Sequence Viewer  
  EAW80137 (Get FASTA)   NCBI Sequence Viewer  
  EAW80138 (Get FASTA)   NCBI Sequence Viewer  
  EAW80139 (Get FASTA)   NCBI Sequence Viewer  
  EAW80140 (Get FASTA)   NCBI Sequence Viewer  
  EAW80141 (Get FASTA)   NCBI Sequence Viewer  
  EAW80142 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000464966.1
  ENSP00000465357.1
  ENSP00000465848.1
  ENSP00000466580.1
  ENSP00000466812.1
  ENSP00000467382.1
  ENSP00000468183.1
  ENSP00000468813.1
  ENSP00000478115
  ENSP00000478115.1
  ENSP00000478471
  ENSP00000478471.1
  ENSP00000479691
  ENSP00000479691.1
  ENSP00000481246.1
  ENSP00000481704.1
  ENSP00000482315
  ENSP00000482315.1
  ENSP00000482825.1
  ENSP00000482835
  ENSP00000482835.1
  ENSP00000483185
  ENSP00000483185.1
  ENSP00000484708.1
  ENSP00000487324.1
GenBank Protein P63010 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_001025177   ⟸   NM_001030006
- Peptide Label: isoform a
- UniProtKB: A0A140VJE8 (UniProtKB/TrEMBL),   A8K0G3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001273   ⟸   NM_001282
- Peptide Label: isoform b
- UniProtKB: Q7Z451 (UniProtKB/Swiss-Prot),   P21851 (UniProtKB/Swiss-Prot),   A6NJP3 (UniProtKB/Swiss-Prot),   Q96J19 (UniProtKB/Swiss-Prot),   P63010 (UniProtKB/Swiss-Prot),   A8K0G3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005257998   ⟸   XM_005257941
- Peptide Label: isoform X6
- UniProtKB: A0A087WU93 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005257994   ⟸   XM_005257937
- Peptide Label: isoform X3
- UniProtKB: A0A140VJE8 (UniProtKB/TrEMBL),   A8K0G3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005257995   ⟸   XM_005257938
- Peptide Label: isoform X3
- UniProtKB: A0A140VJE8 (UniProtKB/TrEMBL),   A8K0G3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011522750   ⟸   XM_011524448
- Peptide Label: isoform X1
- UniProtKB: A8K0G3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011522753   ⟸   XM_011524451
- Peptide Label: isoform X2
- UniProtKB: A8K0G3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011522751   ⟸   XM_011524449
- Peptide Label: isoform X1
- UniProtKB: A8K0G3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011522752   ⟸   XM_011524450
- Peptide Label: isoform X1
- UniProtKB: A8K0G3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016879773   ⟸   XM_017024284
- Peptide Label: isoform X4
- UniProtKB: Q7Z451 (UniProtKB/Swiss-Prot),   P21851 (UniProtKB/Swiss-Prot),   A6NJP3 (UniProtKB/Swiss-Prot),   Q96J19 (UniProtKB/Swiss-Prot),   P63010 (UniProtKB/Swiss-Prot),   A8K0G3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016879776   ⟸   XM_017024287
- Peptide Label: isoform X6
- UniProtKB: A0A087WU93 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000481246   ⟸   ENST00000620039
RefSeq Acc Id: ENSP00000482315   ⟸   ENST00000621914
RefSeq Acc Id: ENSP00000481704   ⟸   ENST00000621668
RefSeq Acc Id: ENSP00000483185   ⟸   ENST00000610402
RefSeq Acc Id: ENSP00000478115   ⟸   ENST00000612116
RefSeq Acc Id: ENSP00000482825   ⟸   ENST00000612035
RefSeq Acc Id: ENSP00000466580   ⟸   ENST00000587805
RefSeq Acc Id: ENSP00000464966   ⟸   ENST00000588116
RefSeq Acc Id: ENSP00000487324   ⟸   ENST00000628168
RefSeq Acc Id: ENSP00000479691   ⟸   ENST00000614600
RefSeq Acc Id: ENSP00000468183   ⟸   ENST00000589774
RefSeq Acc Id: ENSP00000478471   ⟸   ENST00000616784
RefSeq Acc Id: ENSP00000484708   ⟸   ENST00000616681
RefSeq Acc Id: ENSP00000468813   ⟸   ENST00000590538
RefSeq Acc Id: ENSP00000465357   ⟸   ENST00000590432
RefSeq Acc Id: ENSP00000482835   ⟸   ENST00000618940
RefSeq Acc Id: ENSP00000465848   ⟸   ENST00000591610
RefSeq Acc Id: ENSP00000467382   ⟸   ENST00000592167
RefSeq Acc Id: ENSP00000466812   ⟸   ENST00000593014
RefSeq Acc Id: XP_047291465   ⟸   XM_047435509
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047291466   ⟸   XM_047435510
- Peptide Label: isoform X4
- UniProtKB: Q7Z451 (UniProtKB/Swiss-Prot),   P63010 (UniProtKB/Swiss-Prot),   P21851 (UniProtKB/Swiss-Prot),   A6NJP3 (UniProtKB/Swiss-Prot),   Q96J19 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047291464   ⟸   XM_047435508
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047291468   ⟸   XM_047435512
- Peptide Label: isoform X6
RefSeq Acc Id: XP_047291467   ⟸   XM_047435511
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054171271   ⟸   XM_054315296
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054171270   ⟸   XM_054315295
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054171259   ⟸   XM_054315284
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054171262   ⟸   XM_054315287
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054171265   ⟸   XM_054315290
- Peptide Label: isoform X3
- UniProtKB: A0A140VJE8 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054171267   ⟸   XM_054315292
- Peptide Label: isoform X4
- UniProtKB: Q96J19 (UniProtKB/Swiss-Prot),   Q7Z451 (UniProtKB/Swiss-Prot),   P63010 (UniProtKB/Swiss-Prot),   P21851 (UniProtKB/Swiss-Prot),   A6NJP3 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054171264   ⟸   XM_054315289
- Peptide Label: isoform X3
- UniProtKB: A0A140VJE8 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054171266   ⟸   XM_054315291
- Peptide Label: isoform X4
- UniProtKB: Q96J19 (UniProtKB/Swiss-Prot),   Q7Z451 (UniProtKB/Swiss-Prot),   P63010 (UniProtKB/Swiss-Prot),   P21851 (UniProtKB/Swiss-Prot),   A6NJP3 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054171258   ⟸   XM_054315283
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054171261   ⟸   XM_054315286
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054171269   ⟸   XM_054315294
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054171260   ⟸   XM_054315285
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054171263   ⟸   XM_054315288
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054171268   ⟸   XM_054315293
- Peptide Label: isoform X5
Protein Domains
Beta-adaptin appendage C-terminal subdomain   Clathrin adaptor alpha/beta/gamma-adaptin appendage   Clathrin/coatomer adaptor adaptin-like N-terminal

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P63010-F1-model_v2 AlphaFold P63010 1-937 view protein structure

Promoters
RGD ID:6793741
Promoter ID:HG_KWN:25791
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001030006,   NM_001282,   UC002HJS.1,   UC002HJT.1,   UC010CTV.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361730,938,331 - 30,938,832 (+)MPROMDB
RGD ID:7234649
Promoter ID:EPDNEW_H23071
Type:initiation region
Name:AP2B1_1
Description:adaptor related protein complex 2 beta 1 subunit
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H23072  EPDNEW_H23073  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381735,587,359 - 35,587,419EPDNEW
RGD ID:7234653
Promoter ID:EPDNEW_H23072
Type:initiation region
Name:AP2B1_2
Description:adaptor related protein complex 2 beta 1 subunit
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H23071  EPDNEW_H23073  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381735,587,465 - 35,587,525EPDNEW
RGD ID:7234655
Promoter ID:EPDNEW_H23073
Type:initiation region
Name:AP2B1_3
Description:adaptor related protein complex 2 beta 1 subunit
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H23071  EPDNEW_H23072  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381735,717,262 - 35,717,322EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:563 AgrOrtholog
COSMIC AP2B1 COSMIC
Ensembl Genes ENSG00000006125 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000587805.1 UniProtKB/TrEMBL
  ENST00000588116.1 UniProtKB/TrEMBL
  ENST00000589774.5 UniProtKB/TrEMBL
  ENST00000590432.5 UniProtKB/TrEMBL
  ENST00000590538.5 UniProtKB/TrEMBL
  ENST00000591610.5 UniProtKB/TrEMBL
  ENST00000592167.5 UniProtKB/TrEMBL
  ENST00000593014.3 UniProtKB/TrEMBL
  ENST00000610402 ENTREZGENE
  ENST00000610402.5 UniProtKB/Swiss-Prot
  ENST00000612035.4 UniProtKB/TrEMBL
  ENST00000612116 ENTREZGENE
  ENST00000612116.5 UniProtKB/TrEMBL
  ENST00000614600 ENTREZGENE
  ENST00000614600.4 UniProtKB/TrEMBL
  ENST00000616681.4 UniProtKB/TrEMBL
  ENST00000616784 ENTREZGENE
  ENST00000616784.4 UniProtKB/TrEMBL
  ENST00000618940 ENTREZGENE
  ENST00000618940.4 UniProtKB/Swiss-Prot
  ENST00000620039.4 UniProtKB/TrEMBL
  ENST00000621668.4 UniProtKB/TrEMBL
  ENST00000621914 ENTREZGENE
  ENST00000621914.4 UniProtKB/Swiss-Prot
  ENST00000628168.1 UniProtKB/TrEMBL
Gene3D-CATH 1.25.10.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.60.40.1150 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.30.310.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000006125 GTEx
HGNC ID HGNC:563 ENTREZGENE
Human Proteome Map AP2B1 Human Proteome Map
InterPro AP_beta UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  AP_complex_bsu_1_2_4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ARM-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ARM-type_fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Armadillo UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  B-adaptin_app_sub_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Clathrin/coatomer_adapt-like_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Clathrin_a/b/g-adaptin_app_Ig UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Clathrin_app_Ig-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Clathrin_b-adaptin_app_Ig-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Coatomer/calthrin_app_sub_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TBP_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:163 UniProtKB/Swiss-Prot
NCBI Gene 163 ENTREZGENE
OMIM 601025 OMIM
PANTHER AP-2 COMPLEX SUBUNIT BETA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR11134 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Adaptin_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Alpha_adaptinC2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  B2-adapt-app_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB AP2B1 RGD, PharmGKB
PIRSF AP_complex_beta UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART Alpha_adaptinC2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ARM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  B2-adapt-app_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF48371 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF49348 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF55711 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A087WU93 ENTREZGENE, UniProtKB/TrEMBL
  A0A087WXS3_HUMAN UniProtKB/TrEMBL
  A0A087WYD1_HUMAN UniProtKB/TrEMBL
  A0A087WZQ6_HUMAN UniProtKB/TrEMBL
  A0A087X253_HUMAN UniProtKB/TrEMBL
  A0A140VJE8 ENTREZGENE, UniProtKB/TrEMBL
  A6NJP3 ENTREZGENE
  A8K0G3 ENTREZGENE, UniProtKB/TrEMBL
  AP2B1_HUMAN UniProtKB/Swiss-Prot
  K7EJ01_HUMAN UniProtKB/TrEMBL
  K7EJX1_HUMAN UniProtKB/TrEMBL
  K7EKZ5_HUMAN UniProtKB/TrEMBL
  K7EMN7_HUMAN UniProtKB/TrEMBL
  K7EN71_HUMAN UniProtKB/TrEMBL
  K7ERB2_HUMAN UniProtKB/TrEMBL
  P21851 ENTREZGENE
  P63010 ENTREZGENE
  Q7Z451 ENTREZGENE
  Q96EL6_HUMAN UniProtKB/TrEMBL
  Q96J19 ENTREZGENE
UniProt Secondary A6NJP3 UniProtKB/Swiss-Prot
  P21851 UniProtKB/Swiss-Prot
  Q7Z451 UniProtKB/Swiss-Prot
  Q96J19 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2018-05-01 AP2B1  adaptor related protein complex 2 subunit beta 1  AP2B1  adaptor related protein complex 2 beta 1 subunit  Symbol and/or name change 5135510 APPROVED
2016-01-12 AP2B1  adaptor related protein complex 2 beta 1 subunit  AP2B1  adaptor related protein complex 2, beta 1 subunit  Symbol and/or name change 5135510 APPROVED
2015-12-22 AP2B1  adaptor related protein complex 2, beta 1 subunit  AP2B1  adaptor-related protein complex 2, beta 1 subunit  Symbol and/or name change 5135510 APPROVED