AKT2 (AKT serine/threonine kinase 2) - Rat Genome Database

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Gene: AKT2 (AKT serine/threonine kinase 2) Homo sapiens
Analyze
Symbol: AKT2
Name: AKT serine/threonine kinase 2
RGD ID: 732407
HGNC Page HGNC:392
Description: Enables ATP binding activity; molecular function activator activity; and protein serine/threonine kinase activity. Involved in several processes, including insulin receptor signaling pathway; positive regulation of small molecule metabolic process; and regulation of transmembrane transport. Located in cytosol and nucleoplasm. Implicated in glucose metabolism disease (multiple) and reproductive organ cancer (multiple). Biomarker of colorectal cancer; high grade glioma; malignant astrocytoma; obesity; and type 2 diabetes mellitus.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: HIHGHH; Murine thymoma viral (v-akt) homolog-2; murine thymoma viral (v-akt) oncogene homolog 2; PKB beta; PKBB; PKBBETA; PRKBB; protein kinase Akt-2; protein kinase B beta; putative v-akt murine thymoma viral oncoprotein 2; rac protein kinase beta; RAC-BETA; RAC-beta serine/threonine-protein kinase; RAC-PK-beta; v-akt murine thymoma viral oncogene homolog 2
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381940,230,317 - 40,285,345 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1940,230,317 - 40,285,536 (-)EnsemblGRCh38hg38GRCh38
GRCh371940,736,224 - 40,791,252 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361945,428,064 - 45,483,105 (-)NCBINCBI36Build 36hg18NCBI36
Build 341945,431,555 - 45,483,034NCBI
Celera1937,535,771 - 37,590,707 (-)NCBICelera
Cytogenetic Map19q13.2NCBI
HuRef1937,171,156 - 37,226,119 (-)NCBIHuRef
CHM1_11940,735,896 - 40,790,984 (-)NCBICHM1_1
T2T-CHM13v2.01943,050,812 - 43,105,845 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(-)-gambogic acid  (EXP)
(1->4)-beta-D-glucan  (ISO)
(S)-nicotine  (ISO)
1,2-dichloroethane  (ISO)
1,2-dimethylhydrazine  (ISO)
1-chloro-2,4-dinitrobenzene  (EXP)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP)
17beta-hydroxy-5alpha-androstan-3-one  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (ISO)
2,2',5,5'-tetrachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2-ethoxyethanol  (ISO)
2-methoxyethanol  (ISO)
2-nitrotoluene  (ISO)
4,4'-sulfonyldiphenol  (EXP,ISO)
4-nonylphenol  (ISO)
4-phenylbutyric acid  (EXP)
4-vinylcyclohexene dioxide  (ISO)
5-fluorouracil  (EXP)
acetamide  (ISO)
acetylsalicylic acid  (EXP)
acrolein  (EXP)
acrylamide  (ISO)
afimoxifene  (EXP)
aldehydo-D-glucose  (ISO)
all-trans-retinoic acid  (ISO)
allethrin  (ISO)
alpha-pinene  (EXP)
anthra[1,9-cd]pyrazol-6(2H)-one  (ISO)
antirheumatic drug  (EXP)
arsane  (ISO)
arsenic atom  (ISO)
arsenite(3-)  (EXP)
arsenous acid  (EXP)
benzo[a]pyrene  (EXP,ISO)
Benzo[k]fluoranthene  (EXP)
berberine  (ISO)
Bergenin  (ISO)
bis(2-chloroethyl) sulfide  (ISO)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (EXP,ISO)
Bisphenol B  (EXP,ISO)
bisphenol F  (ISO)
bromochloroacetic acid  (ISO)
butanal  (EXP)
Butylbenzyl phthalate  (ISO)
butyric acid  (ISO)
C60 fullerene  (ISO)
cadmium dichloride  (ISO)
caffeine  (EXP)
cannabidiol  (EXP)
carbamazepine  (EXP)
carbon nanotube  (ISO)
carmustine  (EXP)
chlorpyrifos  (EXP)
cisplatin  (EXP)
clenbuterol  (ISO)
clozapine  (ISO)
colforsin daropate hydrochloride  (ISO)
copper atom  (EXP)
copper(0)  (EXP)
cortisol  (EXP)
crocin-1  (ISO)
Cuprizon  (ISO)
curcumin  (EXP,ISO)
D-glucose  (ISO)
decabromodiphenyl ether  (ISO)
dexamethasone  (ISO)
Di-n-octyl phthalate  (ISO)
diarsenic trioxide  (EXP)
diazinon  (ISO)
dibutyl phthalate  (ISO)
dichlorine  (ISO)
diclofenac  (EXP)
dideuterium oxide  (EXP)
dieldrin  (ISO)
diethyl phthalate  (ISO)
Diisodecyl phthalate  (ISO)
diisononyl phthalate  (ISO)
dimethoate  (EXP)
dioxygen  (EXP)
dobutamine  (ISO)
dorsomorphin  (EXP)
doxorubicin  (EXP,ISO)
epoxiconazole  (ISO)
ethanol  (ISO)
everolimus  (EXP,ISO)
finasteride  (ISO)
flutamide  (ISO)
genistein  (EXP,ISO)
glucose  (ISO)
haloperidol  (ISO)
hesperidin  (ISO)
hexachlorobenzene  (ISO)
hydralazine  (EXP)
hydrogen cyanide  (ISO)
hydroquinone  (ISO)
insulin  (EXP)
inulin  (ISO)
L-ascorbic acid  (EXP)
lead diacetate  (ISO)
lead(0)  (EXP)
losartan  (ISO)
maleic acid  (EXP)
MeIQ  (EXP)
MeIQx  (EXP)
mercury atom  (EXP)
mercury(0)  (EXP)
metformin  (ISO)
methimazole  (EXP,ISO)
methoxychlor  (ISO)
methylglyoxal  (ISO)
methylseleninic acid  (EXP)
microcystin-LR  (EXP)
MK-2206  (ISO)
N,N-diethyl-m-toluamide  (ISO)
N-[3-(aminomethyl)benzyl]acetamidine  (ISO)
N-acetyl-L-cysteine  (EXP)
N-methyl-N-nitrosourea  (ISO)
N-nitrosodiethylamine  (ISO)
N-Vinyl-2-pyrrolidone  (ISO)
nickel atom  (EXP)
nickel dichloride  (ISO)
nicotine  (ISO)
nitenpyram  (EXP)
nitrofen  (ISO)
obeticholic acid  (EXP)
oxaliplatin  (ISO)
oxidopamine  (ISO)
ozone  (EXP,ISO)
p-menthan-3-ol  (EXP)
Pachymic acid  (ISO)
paclitaxel  (EXP,ISO)
paracetamol  (ISO)
paraquat  (ISO)
PCB138  (ISO)
perfluorododecanoic acid  (ISO)
perfluoroheptanoic acid  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
perfluoroundecanoic acid  (ISO)
permethrin  (ISO)
Phellopterin  (EXP)
phenobarbital  (ISO)
PhIP  (EXP)
pirinixic acid  (ISO)
propiconazole  (ISO)
quercetin  (EXP,ISO)
resveratrol  (EXP)
SB 431542  (EXP)
silicon dioxide  (EXP)
sirolimus  (EXP)
sodium arsenite  (EXP,ISO)
sodium tungstate  (EXP)
streptozocin  (ISO)
sulindac  (EXP,ISO)
tert-butyl hydroperoxide  (EXP)
testosterone  (EXP)
thymoquinone  (ISO)
titanium dioxide  (ISO)
topotecan  (ISO)
torcetrapib  (EXP)
triciribine  (EXP)
triphenyl phosphate  (EXP)
triphenylstannane  (ISO)
Triptolide  (ISO)
tunicamycin  (EXP)
valproic acid  (EXP,ISO)
vincristine  (ISO)
xanthohumol  (EXP,ISO)
zinc atom  (ISO)
zinc(0)  (ISO)
zingerone  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
activation of GTPase activity  (ISO)
apoptotic process  (IEA)
cellular response to high light intensity  (IEA,ISO)
cellular response to hormone stimulus  (ISO)
cellular response to insulin stimulus  (IMP,ISO)
cellular response to organic cyclic compound  (ISO)
chromatin remodeling  (IEA)
fat cell differentiation  (TAS)
glucose metabolic process  (IEA,ISO)
glycogen biosynthetic process  (IEA)
insulin receptor signaling pathway  (IEA,IMP,ISO,TAS)
intracellular signal transduction  (IBA)
mammary gland epithelial cell differentiation  (TAS)
negative regulation of apoptotic process  (ISO)
negative regulation of cysteine-type endopeptidase activity involved in apoptotic process  (ISO)
negative regulation of long-chain fatty acid import across plasma membrane  (IMP)
negative regulation of RNA splicing  (ISO)
peripheral nervous system myelin maintenance  (IEA,ISO)
phosphatidylinositol 3-kinase/protein kinase B signal transduction  (ISO)
phosphorylation  (IEA)
positive regulation of adipose tissue development  (ISO)
positive regulation of cap-dependent translational initiation  (IMP)
positive regulation of cell migration  (IDA,ISO)
positive regulation of cell motility  (IMP)
positive regulation of fatty acid beta-oxidation  (IMP)
positive regulation of gene expression  (ISO)
positive regulation of glucose import  (IEA,IMP,ISO)
positive regulation of glucose metabolic process  (IMP)
positive regulation of glycogen biosynthetic process  (IMP)
positive regulation of nitric oxide biosynthetic process  (ISO)
positive regulation of peptidyl-serine phosphorylation  (ISO)
positive regulation of positive chemotaxis  (ISO)
positive regulation of protein phosphorylation  (ISO)
positive regulation of protein targeting to membrane  (IEA,ISS)
positive regulation of signal transduction  (ISO)
positive regulation of sodium ion transport  (ISO)
positive regulation of transcription by RNA polymerase II  (ISO)
protein localization to plasma membrane  (IEA,ISO)
protein modification process  (TAS)
protein phosphorylation  (IEA,ISO)
protein stabilization  (IMP)
regulation of cell cycle  (TAS)
regulation of cell migration  (TAS)
regulation of translation  (IEA)
response to hypoxia  (ISO)
response to insulin  (ISO)
response to muscle activity  (ISO)
response to nutrient levels  (ISO)
retinal rod cell apoptotic process  (IEA,ISO)
signal transduction  (TAS)

Cellular Component

Molecular Function

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

References - curated
# Reference Title Reference Citation
1. Defective signaling through Akt-2 and -3 but not Akt-1 in insulin-resistant human skeletal muscle: potential role in insulin resistance. Brozinick JT Jr, etal., Diabetes. 2003 Apr;52(4):935-41.
2. Genetic variations in a PTEN/AKT/mTOR axis and prostate cancer risk in a Chinese population. Chen J, etal., PLoS One. 2012;7(7):e40817. doi: 10.1371/journal.pone.0040817. Epub 2012 Jul 18.
3. Leptin deficiency and beta-cell dysfunction underlie type 2 diabetes in compound Akt knockout mice. Chen WS, etal., Mol Cell Biol. 2009 Jun;29(11):3151-62. Epub 2009 Mar 16.
4. PTEN-deficient tumors depend on AKT2 for maintenance and survival. Chin YR, etal., Cancer Discov. 2014 Aug;4(8):942-55. doi: 10.1158/2159-8290.CD-13-0873. Epub 2014 May 16.
5. Insulin resistance and a diabetes mellitus-like syndrome in mice lacking the protein kinase Akt2 (PKB beta). Cho H, etal., Science 2001 Jun 1;292(5522):1728-31.
6. Continuous fat oxidation in acetyl-CoA carboxylase 2 knockout mice increases total energy expenditure, reduces fat mass, and improves insulin sensitivity. Choi CS, etal., Proc Natl Acad Sci U S A. 2007 Oct 16;104(42):16480-5. Epub 2007 Oct 8.
7. Isoform-specific defects of insulin stimulation of Akt/protein kinase B (PKB) in skeletal muscle cells from type 2 diabetic patients. Cozzone D, etal., Diabetologia. 2008 Mar;51(3):512-21. Epub 2008 Jan 18.
8. A truncation mutation in TBC1D4 in a family with acanthosis nigricans and postprandial hyperinsulinemia. Dash S, etal., Proc Natl Acad Sci U S A. 2009 Jun 9;106(23):9350-5. doi: 10.1073/pnas.0900909106. Epub 2009 May 22.
9. Akt1 and akt2 play distinct roles in the initiation and metastatic phases of mammary tumor progression. Dillon RL, etal., Cancer Res. 2009 Jun 15;69(12):5057-64. Epub 2009 Jun 2.
10. The role of Akt/protein kinase B subtypes in retinal ischemic preconditioning. Dreixler JC, etal., Exp Eye Res. 2009 Mar;88(3):512-21. Epub 2008 Dec 3.
11. The evolution of phosphatidylinositol 3-kinases as regulators of growth and metabolism. Engelman JA, etal., Nat Rev Genet. 2006 Aug;7(8):606-19.
12. Gene expression profiling and functional proteomic analysis reveal perturbed kinase-mediated signaling in genetic stroke susceptibility. Fornage M, etal., Physiol Genomics. 2003 Sep 29;15(1):75-83.
13. PI3K/Akt: getting it right matters. Franke TF Oncogene. 2008 Oct 27;27(50):6473-88.
14. A family with severe insulin resistance and diabetes due to a mutation in AKT2. George S, etal., Science. 2004 May 28;304(5675):1325-8.
15. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
16. Akt mediates insulin induction of glucose uptake and up-regulation of GLUT4 gene expression in brown adipocytes. Hernandez R, etal., FEBS Lett. 2001 Apr 13;494(3):225-31.
17. Phosphoinositide 3-kinases as a common platform for multi-hormone signaling. Hirsch E, etal., J Endocrinol. 2007 Aug;194(2):243-56.
18. An activating mutation of AKT2 and human hypoglycemia. Hussain K, etal., Science. 2011 Oct 28;334(6055):474. doi: 10.1126/science.1210878. Epub 2011 Oct 6.
19. Potentiation of insulin signaling in tissues of Zucker obese rats after acute and long-term treatment with PPARgamma agonists. Jiang G, etal., Diabetes. 2002 Aug;51(8):2412-9.
20. The phosphatidylinositol 3-kinase/Akt signaling pathway modulates the endocrine differentiation of trophoblast cells. Kamei T, etal., Mol Endocrinol 2002 Jul;16(7):1469-81.
21. Inhibition of LINE-1 expression in the heart decreases ischemic damage by activation of Akt/PKB signaling. Lucchinetti E, etal., Physiol Genomics. 2006 Apr 13;25(2):314-24. Epub 2006 Jan 17.
22. Akt1 ablation inhibits, whereas Akt2 ablation accelerates, the development of mammary adenocarcinomas in mouse mammary tumor virus (MMTV)-ErbB2/neu and MMTV-polyoma middle T transgenic mice. Maroulakou IG, etal., Cancer Res. 2007 Jan 1;67(1):167-77.
23. Akt2 and Akt3 play a pivotal role in malignant gliomas. Mure H, etal., Neuro Oncol. 2010 Mar;12(3):221-32. doi: 10.1093/neuonc/nop026. Epub 2009 Dec 21.
24. Sequence mutations and amplification of PIK3CA and AKT2 genes in purified ovarian serous neoplasms. Nakayama K, etal., Cancer Biol Ther. 2006 Jul;5(7):779-85. Epub 2006 Jul 26.
25. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
26. Dwarfism, impaired skin development, skeletal muscle atrophy, delayed bone development, and impeded adipogenesis in mice lacking Akt1 and Akt2. Peng XD, etal., Genes Dev 2003 Jun 1;17(11):1352-65.
27. Satellite cell proliferation is reduced in muscles of obese Zucker rats but restored with loading. Peterson JM, etal., Am J Physiol Cell Physiol. 2008 Aug;295(2):C521-8. Epub 2008 May 28.
28. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
29. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI into RGD
30. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
31. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
32. RGD HPO Phenotype Annotation Pipeline RGD automated import pipeline for human HPO-to-gene-to-disease annotations
33. AKT proto-oncogene overexpression is an early event during sporadic colon carcinogenesis. Roy HK, etal., Carcinogenesis. 2002 Jan;23(1):201-5.
34. Knockdown of Akt isoforms by RNA silencing suppresses the growth of human prostate cancer cells in vitro and in vivo. Sasaki T, etal., Biochem Biophys Res Commun. 2010 Aug 13;399(1):79-83. doi: 10.1016/j.bbrc.2010.07.045. Epub 2010 Jul 16.
35. Janus Kinase 2 (JAK2) Dissociates Hepatosteatosis from Hepatocellular Carcinoma in Mice. Shi SY, etal., J Biol Chem. 2017 Mar 3;292(9):3789-3799. doi: 10.1074/jbc.M116.752519. Epub 2017 Jan 18.
36. Analysis of genetic variation in Akt2/PKB-beta in severe insulin resistance, lipodystrophy, type 2 diabetes, and related metabolic phenotypes. Tan K, etal., Diabetes. 2007 Mar;56(3):714-9.
37. Crosstalk between PTEN/Akt2 and TGFbeta signaling involving EGF receptor down-regulation during the tumor promotion process from the early stage in a rat two-stage hepatocarcinogenesis model. Taniai E, etal., Cancer Sci. 2009 May;100(5):813-20. Epub 2009 Mar 20.
38. Combined thiazolidinedione-metformin treatment synergistically improves insulin signalling to insulin receptor substrate-1-dependent phosphatidylinositol 3-kinase, atypical protein kinase C and protein kinase B/Akt in human diabetic muscle. Temofonte N, etal., Diabetologia. 2009 Jan;52(1):60-4. Epub 2008 Oct 30.
39. Roles of genetic variants in the PI3K and RAS/RAF pathways in susceptibility to endometrial cancer and clinical outcomes. Wang LE, etal., J Cancer Res Clin Oncol. 2012 Mar;138(3):377-85. doi: 10.1007/s00432-011-1103-0. Epub 2011 Dec 7.
40. GLUT4 translocation: the last 200 nanometers. Watson RT and Pessin JE, Cell Signal. 2007 Nov;19(11):2209-17. Epub 2007 Jun 21.
41. Pancreatic cancer: molecular pathogenesis and new therapeutic targets. Wong HH and Lemoine NR, Nat Rev Gastroenterol Hepatol. 2009 Jul;6(7):412-22. Epub 2009 Jun 9.
42. The effect Akt2 deletion on tumor development in Pten(+/-) mice. Xu PZ, etal., Oncogene. 2012 Jan 26;31(4):518-26. doi: 10.1038/onc.2011.243. Epub 2011 Jul 11.
43. Insulin action on glucose transporters through molecular switches, tracks and tethers. Zaid H, etal., Biochem J. 2008 Jul 15;413(2):201-15.
44. Reduction of Akt2 inhibits migration and invasion of glioma cells. Zhang B, etal., Int J Cancer. 2009 Aug 1;125(3):585-95.
Additional References at PubMed
PMID:1409633   PMID:1801921   PMID:3037531   PMID:8622988   PMID:8889548   PMID:9374542   PMID:9394803   PMID:9512493   PMID:9528769   PMID:9736715   PMID:10490823   PMID:10491192  
PMID:10869418   PMID:10983986   PMID:11139588   PMID:11156964   PMID:11208609   PMID:11278835   PMID:11313479   PMID:11432835   PMID:11445557   PMID:11500317   PMID:11507039   PMID:11546794  
PMID:11707444   PMID:11781143   PMID:11903042   PMID:11988487   PMID:11994280   PMID:12114503   PMID:12149249   PMID:12176337   PMID:12176997   PMID:12181350   PMID:12434148   PMID:12477932  
PMID:12480711   PMID:12482965   PMID:12517337   PMID:12517798   PMID:12524439   PMID:12545160   PMID:12733712   PMID:12791994   PMID:12808085   PMID:14500673   PMID:14504284   PMID:14612499  
PMID:14637151   PMID:14654898   PMID:14699494   PMID:14702039   PMID:14735903   PMID:14973226   PMID:15010337   PMID:15070827   PMID:15102693   PMID:15111130   PMID:15144186   PMID:15146197  
PMID:15314020   PMID:15489334   PMID:15531580   PMID:15557754   PMID:15616007   PMID:15678105   PMID:15689238   PMID:15890450   PMID:15987444   PMID:16221682   PMID:16365168   PMID:16402276  
PMID:16417406   PMID:16524887   PMID:16540465   PMID:16792529   PMID:16814735   PMID:16841089   PMID:16982699   PMID:17012749   PMID:17030088   PMID:17157319   PMID:17276404   PMID:17332325  
PMID:17349711   PMID:17372934   PMID:17482291   PMID:17535800   PMID:17576055   PMID:17577629   PMID:17804734   PMID:17825284   PMID:17895832   PMID:17908691   PMID:17914025   PMID:17942896  
PMID:18048359   PMID:18187620   PMID:18281467   PMID:18300076   PMID:18316591   PMID:18353613   PMID:18660489   PMID:18768676   PMID:18826950   PMID:18842333   PMID:18996102   PMID:19064572  
PMID:19074768   PMID:19075230   PMID:19079138   PMID:19110052   PMID:19139280   PMID:19164214   PMID:19197940   PMID:19261608   PMID:19435822   PMID:19453261   PMID:19479051   PMID:19713527  
PMID:19771908   PMID:19797172   PMID:19825827   PMID:19843246   PMID:19875456   PMID:19913121   PMID:19933843   PMID:20012528   PMID:20018949   PMID:20019835   PMID:20041213   PMID:20056178  
PMID:20056908   PMID:20059950   PMID:20102399   PMID:20109457   PMID:20116920   PMID:20133737   PMID:20186503   PMID:20301750   PMID:20354455   PMID:20398329   PMID:20409325   PMID:20447721  
PMID:20514445   PMID:20602615   PMID:20628086   PMID:20661303   PMID:20687898   PMID:20688159   PMID:20691427   PMID:20818790   PMID:20848774   PMID:20856200   PMID:21029719   PMID:21048031  
PMID:21050850   PMID:21092549   PMID:21179235   PMID:21182834   PMID:21291857   PMID:21297943   PMID:21423810   PMID:21432781   PMID:21483469   PMID:21507933   PMID:21518566   PMID:21590431  
PMID:21606541   PMID:21618512   PMID:21636708   PMID:21680733   PMID:21697490   PMID:21722267   PMID:21737686   PMID:21763505   PMID:21765914   PMID:21832049   PMID:21873635   PMID:21932427  
PMID:21979951   PMID:21988832   PMID:22031698   PMID:22107784   PMID:22158034   PMID:22261254   PMID:22480544   PMID:22556379   PMID:22748472   PMID:22778840   PMID:22809628   PMID:22904195  
PMID:22939624   PMID:22952844   PMID:23018889   PMID:23077641   PMID:23092922   PMID:23250987   PMID:23251686   PMID:23301033   PMID:23305873   PMID:23321478   PMID:23444369   PMID:23464484  
PMID:23468863   PMID:23567263   PMID:23604117   PMID:23742646   PMID:23746211   PMID:23777806   PMID:23811558   PMID:23823123   PMID:23900341   PMID:23929892   PMID:24030155   PMID:24039187  
PMID:24056770   PMID:24123662   PMID:24225433   PMID:24244375   PMID:24244431   PMID:24247267   PMID:24321521   PMID:24337067   PMID:24469921   PMID:24565443   PMID:24623414   PMID:24642468  
PMID:24656454   PMID:24658403   PMID:24699302   PMID:24769357   PMID:24797263   PMID:24819169   PMID:24946858   PMID:24970808   PMID:25025572   PMID:25059120   PMID:25104021   PMID:25134663  
PMID:25162660   PMID:25173755   PMID:25233414   PMID:25246356   PMID:25253241   PMID:25263462   PMID:25285168   PMID:25288334   PMID:25304263   PMID:25428377   PMID:25733895   PMID:25771729  
PMID:25856297   PMID:25894377   PMID:25936945   PMID:25951903   PMID:26149501   PMID:26158514   PMID:26186194   PMID:26229955   PMID:26234648   PMID:26254095   PMID:26265781   PMID:26270987  
PMID:26318486   PMID:26344197   PMID:26475619   PMID:26496610   PMID:26512921   PMID:26638075   PMID:26711268   PMID:26760575   PMID:26803515   PMID:26828791   PMID:26855332   PMID:26895380  
PMID:26953242   PMID:26971877   PMID:27067543   PMID:27105349   PMID:27166089   PMID:27189341   PMID:27545875   PMID:27563096   PMID:27663592   PMID:27871477   PMID:27878243   PMID:27906180  
PMID:28026019   PMID:28036396   PMID:28068324   PMID:28129626   PMID:28271235   PMID:28287129   PMID:28319085   PMID:28341696   PMID:28363942   PMID:28404925   PMID:28440469   PMID:28455433  
PMID:28456993   PMID:28514442   PMID:28534950   PMID:28541532   PMID:28557977   PMID:28586057   PMID:28636190   PMID:28650848   PMID:28689659   PMID:28837154   PMID:28931550   PMID:29025710  
PMID:29038421   PMID:29075783   PMID:29103612   PMID:29141982   PMID:29153407   PMID:29207197   PMID:29235817   PMID:29374601   PMID:29484395   PMID:29494643   PMID:29658179   PMID:29667444  
PMID:29782828   PMID:30071535   PMID:30536701   PMID:30541951   PMID:30598523   PMID:30628701   PMID:30877036   PMID:31091453   PMID:31252679   PMID:31496625   PMID:31598939   PMID:31671832  
PMID:31781306   PMID:31847370   PMID:31871319   PMID:31898360   PMID:31967930   PMID:31997506   PMID:32211805   PMID:32296183   PMID:32707033   PMID:32873299   PMID:32986769   PMID:33123457  
PMID:33253205   PMID:33377281   PMID:33398370   PMID:33486928   PMID:33768461   PMID:33839456   PMID:33957083   PMID:33961781   PMID:34011540   PMID:34044676   PMID:34079125   PMID:34315543  
PMID:34591612   PMID:34672954   PMID:34673243   PMID:34857952   PMID:35219877   PMID:35256949   PMID:35271311   PMID:35748872   PMID:35831314   PMID:36114006   PMID:36156852   PMID:36215168  
PMID:36217693   PMID:36229454   PMID:36409629   PMID:36640312   PMID:36719624   PMID:36736316   PMID:37567009   PMID:37827155   PMID:37879895   PMID:38113892   PMID:38244769   PMID:38396845  
PMID:38478015   PMID:38528080  


Genomics

Comparative Map Data
AKT2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381940,230,317 - 40,285,345 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1940,230,317 - 40,285,536 (-)EnsemblGRCh38hg38GRCh38
GRCh371940,736,224 - 40,791,252 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361945,428,064 - 45,483,105 (-)NCBINCBI36Build 36hg18NCBI36
Build 341945,431,555 - 45,483,034NCBI
Celera1937,535,771 - 37,590,707 (-)NCBICelera
Cytogenetic Map19q13.2NCBI
HuRef1937,171,156 - 37,226,119 (-)NCBIHuRef
CHM1_11940,735,896 - 40,790,984 (-)NCBICHM1_1
T2T-CHM13v2.01943,050,812 - 43,105,845 (-)NCBIT2T-CHM13v2.0
Akt2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39727,290,977 - 27,340,251 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl727,290,977 - 27,340,251 (+)EnsemblGRCm39 Ensembl
GRCm38727,591,552 - 27,640,826 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl727,591,552 - 27,640,826 (+)EnsemblGRCm38mm10GRCm38
MGSCv37728,376,579 - 28,424,472 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36727,314,618 - 27,348,214 (+)NCBIMGSCv36mm8
Celera722,173,505 - 22,221,607 (+)NCBICelera
Cytogenetic Map7A3NCBI
cM Map715.94NCBI
Akt2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8192,004,705 - 92,061,420 (+)NCBIGRCr8
mRatBN7.2182,877,228 - 82,933,828 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl182,883,547 - 82,933,817 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx188,296,913 - 88,335,355 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0196,784,353 - 96,822,706 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0190,052,776 - 90,091,219 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0184,400,939 - 84,451,223 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl184,411,726 - 84,450,162 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0185,617,612 - 85,667,423 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4182,686,233 - 82,726,544 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1182,764,343 - 82,804,655 (+)NCBI
Celera177,307,278 - 77,345,638 (+)NCBICelera
Cytogenetic Map1q21NCBI
Akt2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955578967,593 - 1,004,438 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955578950,258 - 1,004,438 (+)NCBIChiLan1.0ChiLan1.0
AKT2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22046,489,586 - 46,553,446 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11948,360,226 - 48,417,200 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01937,275,799 - 37,331,971 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11945,791,043 - 45,846,359 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1945,791,800 - 45,840,271 (-)Ensemblpanpan1.1panPan2
AKT2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11113,359,038 - 113,407,119 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1113,359,575 - 113,407,131 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1112,790,741 - 112,808,659 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01113,957,825 - 114,008,296 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1113,958,298 - 114,008,293 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11113,546,597 - 113,564,514 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01113,179,139 - 113,197,049 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01114,172,976 - 114,190,895 (+)NCBIUU_Cfam_GSD_1.0
Akt2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934914,224,502 - 14,265,970 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366612,652,566 - 2,694,086 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366612,652,568 - 2,694,039 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
AKT2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl648,555,795 - 48,587,919 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1648,555,785 - 48,620,472 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2644,331,695 - 44,393,119 (-)NCBISscrofa10.2Sscrofa10.2susScr3
AKT2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1634,688,585 - 34,740,458 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl634,690,462 - 34,720,781 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607312,782,360 - 12,833,428 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Akt2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_004624925273,881 - 326,984 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_004624925262,590 - 322,440 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in AKT2
163 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001626.6(AKT2):c.49G>A (p.Glu17Lys) single nucleotide variant Hypoinsulinemic hypoglycemia and body hemihypertrophy [RCV000022676] Chr19:40257052 [GRCh38]
Chr19:40762959 [GRCh37]
Chr19:19q13.2		 pathogenic
NM_001626.6(AKT2):c.821G>A (p.Arg274His) single nucleotide variant Type 2 diabetes mellitus [RCV000015016]|not provided [RCV003231106] Chr19:40237979 [GRCh38]
Chr19:40743886 [GRCh37]
Chr19:19q13.2		 pathogenic|likely pathogenic
GRCh38/hg38 19q13.12-13.2(chr19:37319377-42738688)x3 copy number gain See cases [RCV000050636] Chr19:37319377..42738688 [GRCh38]
Chr19:37810279..43242840 [GRCh37]
Chr19:42502119..47934680 [NCBI36]
Chr19:19q13.12-13.2		 pathogenic
NM_001626.6(AKT2):c.861C>A (p.Gly287=) single nucleotide variant not provided [RCV000116305] Chr19:40236356 [GRCh38]
Chr19:40742263 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.960G>A (p.Glu320=) single nucleotide variant not provided [RCV000116306] Chr19:40236257 [GRCh38]
Chr19:40742164 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.5(AKT2):c.523G>A (p.Gly175Ser) single nucleotide variant not provided [RCV000079719] Chr19:40241988 [GRCh38]
Chr19:40747895 [GRCh37]
Chr19:19q13.2		 other|not provided
GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3 copy number gain See cases [RCV000133888] Chr19:11227942..44626354 [GRCh38]
Chr19:11338618..45129651 [GRCh37]
Chr19:11199618..49821491 [NCBI36]
Chr19:19p13.2-q13.31		 pathogenic
NM_001626.6(AKT2):c.573+9C>T single nucleotide variant Type 2 diabetes mellitus [RCV000525193]|not specified [RCV000193292] Chr19:40241929 [GRCh38]
Chr19:40747836 [GRCh37]
Chr19:19q13.2		 benign|likely benign
GRCh37/hg19 19q13.12-13.2(chr19:37582250-41630908)x3 copy number gain See cases [RCV000239839] Chr19:37582250..41630908 [GRCh37]
Chr19:19q13.12-13.2		 pathogenic
NM_001626.6(AKT2):c.282C>T (p.Asp94=) single nucleotide variant Type 2 diabetes mellitus [RCV000549067] Chr19:40255163 [GRCh38]
Chr19:40761070 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.1112G>A (p.Arg371His) single nucleotide variant Non-small cell lung carcinoma [RCV000441898]|Type 2 diabetes mellitus [RCV002524689] Chr19:40235953 [GRCh38]
Chr19:40741860 [GRCh37]
Chr19:19q13.2		 likely pathogenic|uncertain significance
NM_001626.6(AKT2):c.904A>G (p.Ser302Gly) single nucleotide variant Neoplasm of the large intestine [RCV000423006] Chr19:40236313 [GRCh38]
Chr19:40742220 [GRCh37]
Chr19:19q13.2		 likely pathogenic
NM_001626.6(AKT2):c.442-8C>T single nucleotide variant Type 2 diabetes mellitus [RCV000951824]|not provided [RCV003884571]|not specified [RCV000503935] Chr19:40242077 [GRCh38]
Chr19:40747984 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.945G>A (p.Glu315=) single nucleotide variant Type 2 diabetes mellitus [RCV000554920]|Type 2 diabetes mellitus [RCV003884570]|not provided [RCV001726198]|not specified [RCV000502157] Chr19:40236272 [GRCh38]
Chr19:40742179 [GRCh37]
Chr19:19q13.2		 benign|likely benign|uncertain significance
NM_001626.6(AKT2):c.960+3G>A single nucleotide variant AKT2-related disorder [RCV003902756]|Type 2 diabetes mellitus [RCV000878195]|not provided [RCV003424053]|not specified [RCV000500423] Chr19:40236254 [GRCh38]
Chr19:40742161 [GRCh37]
Chr19:19q13.2		 benign|likely benign
NM_001626.6(AKT2):c.93C>T (p.Ser31=) single nucleotide variant Type 2 diabetes mellitus [RCV000542311]|Type 2 diabetes mellitus [RCV003884572]|not provided [RCV001529917]|not specified [RCV000500600] Chr19:40257008 [GRCh38]
Chr19:40762915 [GRCh37]
Chr19:19q13.2		 benign|likely benign
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic|uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
NM_001626.6(AKT2):c.1110G>T (p.Pro370=) single nucleotide variant Type 2 diabetes mellitus [RCV000536987]|not provided [RCV001729632] Chr19:40235955 [GRCh38]
Chr19:40741862 [GRCh37]
Chr19:19q13.2		 benign|likely benign
NM_001626.6(AKT2):c.1246G>A (p.Asp416Asn) single nucleotide variant Inborn genetic diseases [RCV000624382] Chr19:40235280 [GRCh38]
Chr19:40741187 [GRCh37]
Chr19:19q13.2		 uncertain significance
GRCh37/hg19 19q13.2(chr19:40636400-41060616)x3 copy number gain not provided [RCV000752683] Chr19:40636400..41060616 [GRCh37]
Chr19:19q13.2		 benign
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
NM_001626.6(AKT2):c.288-149T>C single nucleotide variant not provided [RCV001707126] Chr19:40242836 [GRCh38]
Chr19:40748743 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.1175+103G>A single nucleotide variant not provided [RCV001725429] Chr19:40235787 [GRCh38]
Chr19:40741694 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.288-45G>A single nucleotide variant not provided [RCV001609777] Chr19:40242732 [GRCh38]
Chr19:40748639 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.657C>T (p.Phe219=) single nucleotide variant not provided [RCV000905634] Chr19:40238956 [GRCh38]
Chr19:40744863 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.396G>A (p.Thr132=) single nucleotide variant not provided [RCV000891678] Chr19:40242579 [GRCh38]
Chr19:40748486 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.204G>A (p.Pro68=) single nucleotide variant AKT2-related disorder [RCV003948261]|Type 2 diabetes mellitus [RCV001516097]|Type 2 diabetes mellitus [RCV003884779]|not specified [RCV001817043] Chr19:40255241 [GRCh38]
Chr19:40761148 [GRCh37]
Chr19:19q13.2		 benign|likely benign|uncertain significance
NM_001626.6(AKT2):c.288-8C>T single nucleotide variant Type 2 diabetes mellitus [RCV002065741] Chr19:40242695 [GRCh38]
Chr19:40748602 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.1367-7C>T single nucleotide variant Type 2 diabetes mellitus [RCV000878007]|not specified [RCV001817049] Chr19:40233958 [GRCh38]
Chr19:40739865 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.136G>A (p.Asp46Asn) single nucleotide variant Type 2 diabetes mellitus [RCV001058890] Chr19:40256965 [GRCh38]
Chr19:40762872 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.757C>T (p.Arg253Trp) single nucleotide variant Type 2 diabetes mellitus [RCV001040025] Chr19:40238043 [GRCh38]
Chr19:40743950 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.666C>T (p.His222=) single nucleotide variant Type 2 diabetes mellitus [RCV000878599] Chr19:40238947 [GRCh38]
Chr19:40744854 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.516G>A (p.Lys172=) single nucleotide variant not provided [RCV000922706] Chr19:40241995 [GRCh38]
Chr19:40747902 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.1065C>T (p.His355=) single nucleotide variant Type 2 diabetes mellitus [RCV002066367] Chr19:40236000 [GRCh38]
Chr19:40741907 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.212A>G (p.Asn71Ser) single nucleotide variant Type 2 diabetes mellitus [RCV000964694] Chr19:40255233 [GRCh38]
Chr19:40761140 [GRCh37]
Chr19:19q13.2		 likely benign|conflicting interpretations of pathogenicity
NM_001626.6(AKT2):c.399T>G (p.Thr133=) single nucleotide variant Type 2 diabetes mellitus [RCV001398941] Chr19:40242576 [GRCh38]
Chr19:40748483 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.1110G>A (p.Pro370=) single nucleotide variant Type 2 diabetes mellitus [RCV002542103] Chr19:40235955 [GRCh38]
Chr19:40741862 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.699C>T (p.Asn233=) single nucleotide variant AKT2-related disorder [RCV003925946]|Type 2 diabetes mellitus [RCV000951627] Chr19:40238914 [GRCh38]
Chr19:40744821 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.573+8C>T single nucleotide variant Type 2 diabetes mellitus [RCV001475079] Chr19:40241930 [GRCh38]
Chr19:40747837 [GRCh37]
Chr19:19q13.2		 likely benign
GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3 copy number gain not provided [RCV000845733] Chr19:28271106..49213832 [GRCh37]
Chr19:19q11-13.33		 pathogenic
NC_000019.9:g.(?_39904727)_(42931301_?)dup duplication Diamond-Blackfan anemia [RCV003122291]|MEGF8-related Carpenter syndrome [RCV003105286]|Maple syrup urine disease [RCV003105287]|TWIST1-related craniosynostosis [RCV003105285] Chr19:39904727..42931301 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.575A>G (p.Asp192Gly) single nucleotide variant Inborn genetic diseases [RCV003273359] Chr19:40240109 [GRCh38]
Chr19:40746016 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.176-36C>T single nucleotide variant not provided [RCV001643861] Chr19:40255305 [GRCh38]
Chr19:40761212 [GRCh37]
Chr19:19q13.2		 benign
NC_000019.9:g.(?_39205089)_(40913839_?)dup duplication Type 2 diabetes mellitus [RCV003107444]|not provided [RCV003122562] Chr19:39205089..40913839 [GRCh37]
Chr19:19q13.2		 uncertain significance|no classifications from unflagged records
NM_001626.6(AKT2):c.708+115A>G single nucleotide variant not provided [RCV001619141] Chr19:40238790 [GRCh38]
Chr19:40744697 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.573+128A>C single nucleotide variant not provided [RCV001681351] Chr19:40241810 [GRCh38]
Chr19:40747717 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.573+25G>C single nucleotide variant not provided [RCV001693280] Chr19:40241913 [GRCh38]
Chr19:40747820 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.832-28A>G single nucleotide variant not provided [RCV001670999] Chr19:40236413 [GRCh38]
Chr19:40742320 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.1042C>T (p.Leu348=) single nucleotide variant not provided [RCV000975432] Chr19:40236023 [GRCh38]
Chr19:40741930 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.369G>A (p.Lys123=) single nucleotide variant not provided [RCV000980008] Chr19:40242606 [GRCh38]
Chr19:40748513 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.711G>C (p.Leu237=) single nucleotide variant Type 2 diabetes mellitus [RCV000887587]|not provided [RCV004569807] Chr19:40238089 [GRCh38]
Chr19:40743996 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.347G>C (p.Gly116Ala) single nucleotide variant Hypoinsulinemic hypoglycemia and body hemihypertrophy [RCV002466650]|Inborn genetic diseases [RCV004034780]|Type 2 diabetes mellitus [RCV001244423] Chr19:40242628 [GRCh38]
Chr19:40748535 [GRCh37]
Chr19:19q13.2		 likely benign|uncertain significance
NM_001626.6(AKT2):c.1332C>T (p.Thr444=) single nucleotide variant not provided [RCV000913319] Chr19:40235079 [GRCh38]
Chr19:40740986 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.573+312C>T single nucleotide variant not provided [RCV001678057] Chr19:40241626 [GRCh38]
Chr19:40747533 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.*58C>A single nucleotide variant not provided [RCV001594784] Chr19:40233814 [GRCh38]
Chr19:40739721 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.960+59A>G single nucleotide variant not provided [RCV001639676] Chr19:40236198 [GRCh38]
Chr19:40742105 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.287+319del deletion not provided [RCV001636528] Chr19:40254839 [GRCh38]
Chr19:40760746 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.709-164dup duplication not provided [RCV001686956] Chr19:40238253..40238254 [GRCh38]
Chr19:40744160..40744161 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.46+147A>G single nucleotide variant not provided [RCV001539624] Chr19:40265075 [GRCh38]
Chr19:40770982 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.961-13C>T single nucleotide variant Type 2 diabetes mellitus [RCV001198375]|Type 2 diabetes mellitus [RCV003770218] Chr19:40236117 [GRCh38]
Chr19:40742024 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.550C>T (p.Arg184Trp) single nucleotide variant Type 2 diabetes mellitus [RCV001233357] Chr19:40241961 [GRCh38]
Chr19:40747868 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.1363C>T (p.Arg455Cys) single nucleotide variant Type 2 diabetes mellitus [RCV001058773] Chr19:40235048 [GRCh38]
Chr19:40740955 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.526C>T (p.Arg176Cys) single nucleotide variant Type 2 diabetes mellitus [RCV001994443] Chr19:40241985 [GRCh38]
Chr19:40747892 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.282C>G (p.Asp94Glu) single nucleotide variant Type 2 diabetes mellitus [RCV001369557] Chr19:40255163 [GRCh38]
Chr19:40761070 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.1399C>T (p.Arg467Trp) single nucleotide variant Type 2 diabetes mellitus [RCV001364468]|not specified [RCV001820064] Chr19:40233919 [GRCh38]
Chr19:40739826 [GRCh37]
Chr19:19q13.2		 likely benign|uncertain significance
NM_001626.6(AKT2):c.623G>A (p.Arg208Lys) single nucleotide variant Inborn genetic diseases [RCV002547737]|Type 2 diabetes mellitus [RCV001360161] Chr19:40240061 [GRCh38]
Chr19:40745968 [GRCh37]
Chr19:19q13.2		 likely benign|uncertain significance
NM_001626.6(AKT2):c.208C>G (p.Pro70Ala) single nucleotide variant Type 2 diabetes mellitus [RCV001318264] Chr19:40255237 [GRCh38]
Chr19:40761144 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.1286A>G (p.Gln429Arg) single nucleotide variant Type 2 diabetes mellitus [RCV001317100] Chr19:40235125 [GRCh38]
Chr19:40741032 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.44G>A (p.Arg15His) single nucleotide variant Type 2 diabetes mellitus [RCV001335851]|Type 2 diabetes mellitus [RCV003770860] Chr19:40265224 [GRCh38]
Chr19:40771131 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.39C>T (p.His13=) single nucleotide variant Type 2 diabetes mellitus [RCV001499588] Chr19:40265229 [GRCh38]
Chr19:40771136 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.1023C>T (p.Tyr341=) single nucleotide variant Type 2 diabetes mellitus [RCV001393618] Chr19:40236042 [GRCh38]
Chr19:40741949 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.709-9C>T single nucleotide variant Type 2 diabetes mellitus [RCV001448639] Chr19:40238100 [GRCh38]
Chr19:40744007 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.318C>T (p.Val106=) single nucleotide variant Type 2 diabetes mellitus [RCV001444850] Chr19:40242657 [GRCh38]
Chr19:40748564 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.831+182A>G single nucleotide variant not provided [RCV001685075] Chr19:40237787 [GRCh38]
Chr19:40743694 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.831+10A>G single nucleotide variant Type 2 diabetes mellitus [RCV001455715] Chr19:40237959 [GRCh38]
Chr19:40743866 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.176-183AC[8] microsatellite not provided [RCV001654051] Chr19:40255438..40255439 [GRCh38]
Chr19:40761345..40761346 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.46+269C>T single nucleotide variant not provided [RCV001711047] Chr19:40264953 [GRCh38]
Chr19:40770860 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.708+264G>A single nucleotide variant not provided [RCV001692615] Chr19:40238641 [GRCh38]
Chr19:40744548 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.*266T>C single nucleotide variant not provided [RCV001539831] Chr19:40233606 [GRCh38]
Chr19:40739513 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.132C>T (p.Ala44=) single nucleotide variant Type 2 diabetes mellitus [RCV001486623] Chr19:40256969 [GRCh38]
Chr19:40762876 [GRCh37]
Chr19:19q13.2		 likely benign
GRCh37/hg19 19p13.11-q13.2(chr19:19546923-41313229)x3 copy number gain Specific learning disability [RCV001801194] Chr19:19546923..41313229 [GRCh37]
Chr19:19p13.11-q13.2		 pathogenic
NM_001626.6(AKT2):c.708+7C>T single nucleotide variant not specified [RCV001817521] Chr19:40238898 [GRCh38]
Chr19:40744805 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.96C>T (p.Asp32=) single nucleotide variant not specified [RCV001820254] Chr19:40257005 [GRCh38]
Chr19:40762912 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.*9C>T single nucleotide variant not specified [RCV001818062] Chr19:40233863 [GRCh38]
Chr19:40739770 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.744A>G (p.Thr248=) single nucleotide variant not specified [RCV001820480] Chr19:40238056 [GRCh38]
Chr19:40743963 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.337C>T (p.Arg113Trp) single nucleotide variant Type 2 diabetes mellitus [RCV001878194] Chr19:40242638 [GRCh38]
Chr19:40748545 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.395C>T (p.Thr132Met) single nucleotide variant Type 2 diabetes mellitus [RCV002028714] Chr19:40242580 [GRCh38]
Chr19:40748487 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.960+3G>T single nucleotide variant Inborn genetic diseases [RCV002545449]|Type 2 diabetes mellitus [RCV002035762] Chr19:40236254 [GRCh38]
Chr19:40742161 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.1036G>A (p.Gly346Ser) single nucleotide variant Type 2 diabetes mellitus [RCV002048386] Chr19:40236029 [GRCh38]
Chr19:40741936 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.268G>A (p.Val90Met) single nucleotide variant Type 2 diabetes mellitus [RCV002045984] Chr19:40255177 [GRCh38]
Chr19:40761084 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.1069C>T (p.Arg357Cys) single nucleotide variant Type 2 diabetes mellitus [RCV001997601] Chr19:40235996 [GRCh38]
Chr19:40741903 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.19A>G (p.Ile7Val) single nucleotide variant Type 2 diabetes mellitus [RCV002005776] Chr19:40265249 [GRCh38]
Chr19:40771156 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.173C>T (p.Ala58Val) single nucleotide variant Type 2 diabetes mellitus [RCV002010421] Chr19:40256928 [GRCh38]
Chr19:40762835 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.169G>A (p.Val57Ile) single nucleotide variant Type 2 diabetes mellitus [RCV002018167] Chr19:40256932 [GRCh38]
Chr19:40762839 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.427G>A (p.Ala143Thr) single nucleotide variant Type 2 diabetes mellitus [RCV001989116] Chr19:40242548 [GRCh38]
Chr19:40748455 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.1115C>T (p.Thr372Met) single nucleotide variant Type 2 diabetes mellitus [RCV001913225]|not provided [RCV003136284] Chr19:40235950 [GRCh38]
Chr19:40741857 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.126C>T (p.Pro42=) single nucleotide variant Type 2 diabetes mellitus [RCV002109693] Chr19:40256975 [GRCh38]
Chr19:40762882 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.708+9C>T single nucleotide variant Type 2 diabetes mellitus [RCV002126499] Chr19:40238896 [GRCh38]
Chr19:40744803 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.832-7C>T single nucleotide variant Type 2 diabetes mellitus [RCV002091805] Chr19:40236392 [GRCh38]
Chr19:40742299 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.822C>T (p.Arg274=) single nucleotide variant Type 2 diabetes mellitus [RCV002186980] Chr19:40237978 [GRCh38]
Chr19:40743885 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.442-20A>G single nucleotide variant Type 2 diabetes mellitus [RCV002124662] Chr19:40242089 [GRCh38]
Chr19:40747996 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.442-12T>C single nucleotide variant Type 2 diabetes mellitus [RCV002106179] Chr19:40242081 [GRCh38]
Chr19:40747988 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.1176-12G>A single nucleotide variant Type 2 diabetes mellitus [RCV002130602] Chr19:40235362 [GRCh38]
Chr19:40741269 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.1264-4G>T single nucleotide variant Type 2 diabetes mellitus [RCV002134477] Chr19:40235151 [GRCh38]
Chr19:40741058 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.1296C>T (p.Ser432=) single nucleotide variant Type 2 diabetes mellitus [RCV002169684] Chr19:40235115 [GRCh38]
Chr19:40741022 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.288-17C>T single nucleotide variant Type 2 diabetes mellitus [RCV002213897] Chr19:40242704 [GRCh38]
Chr19:40748611 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.1176-10C>G single nucleotide variant Type 2 diabetes mellitus [RCV002193094] Chr19:40235360 [GRCh38]
Chr19:40741267 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.525C>T (p.Gly175=) single nucleotide variant Type 2 diabetes mellitus [RCV002119433] Chr19:40241986 [GRCh38]
Chr19:40747893 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.288-6G>C single nucleotide variant Type 2 diabetes mellitus [RCV002200745] Chr19:40242693 [GRCh38]
Chr19:40748600 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.1176-17C>T single nucleotide variant Type 2 diabetes mellitus [RCV002141746] Chr19:40235367 [GRCh38]
Chr19:40741274 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.1366+20G>A single nucleotide variant Type 2 diabetes mellitus [RCV002122840]|not provided [RCV003408129] Chr19:40235025 [GRCh38]
Chr19:40740932 [GRCh37]
Chr19:19q13.2		 benign|likely benign
NM_001626.6(AKT2):c.708+19_708+20insGCGGCTGCCTTGGCT insertion Type 2 diabetes mellitus [RCV002139389] Chr19:40238885..40238886 [GRCh38]
Chr19:40744792..40744793 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.288-18dup duplication Type 2 diabetes mellitus [RCV002198694] Chr19:40242704..40242705 [GRCh38]
Chr19:40748611..40748612 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.1413C>G (p.Pro471=) single nucleotide variant Type 2 diabetes mellitus [RCV002103121] Chr19:40233905 [GRCh38]
Chr19:40739812 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.831+18C>T single nucleotide variant Type 2 diabetes mellitus [RCV002199403] Chr19:40237951 [GRCh38]
Chr19:40743858 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.1040G>A (p.Arg347His) single nucleotide variant Type 2 diabetes mellitus [RCV003115586] Chr19:40236025 [GRCh38]
Chr19:40741932 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.709-11T>A single nucleotide variant Type 2 diabetes mellitus [RCV003115700] Chr19:40238102 [GRCh38]
Chr19:40744009 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.984C>G (p.Gly328=) single nucleotide variant not specified [RCV002246951] Chr19:40236081 [GRCh38]
Chr19:40741988 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.1052A>G (p.Tyr351Cys) single nucleotide variant not provided [RCV002505936] Chr19:40236013 [GRCh38]
Chr19:40741920 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.709-3C>T single nucleotide variant Type 2 diabetes mellitus [RCV002908958] Chr19:40238094 [GRCh38]
Chr19:40744001 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.1032G>A (p.Met344Ile) single nucleotide variant Type 2 diabetes mellitus [RCV003014834] Chr19:40236033 [GRCh38]
Chr19:40741940 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.168C>T (p.Ser56=) single nucleotide variant Type 2 diabetes mellitus [RCV002971223] Chr19:40256933 [GRCh38]
Chr19:40762840 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.1186G>C (p.Gly396Arg) single nucleotide variant Inborn genetic diseases [RCV002704694] Chr19:40235340 [GRCh38]
Chr19:40741247 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.1068G>A (p.Glu356=) single nucleotide variant Type 2 diabetes mellitus [RCV002796771] Chr19:40235997 [GRCh38]
Chr19:40741904 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.438A>G (p.Lys146=) single nucleotide variant Type 2 diabetes mellitus [RCV002949299] Chr19:40242537 [GRCh38]
Chr19:40748444 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.508C>T (p.Arg170Trp) single nucleotide variant Inborn genetic diseases [RCV003000680] Chr19:40242003 [GRCh38]
Chr19:40747910 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.1090A>G (p.Met364Val) single nucleotide variant Type 2 diabetes mellitus [RCV002913099] Chr19:40235975 [GRCh38]
Chr19:40741882 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.430C>T (p.Arg144Trp) single nucleotide variant Type 2 diabetes mellitus [RCV003079462] Chr19:40242545 [GRCh38]
Chr19:40748452 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.641C>T (p.Ala214Val) single nucleotide variant AKT2-related disorder [RCV003403977]|Type 2 diabetes mellitus [RCV002958636] Chr19:40238972 [GRCh38]
Chr19:40744879 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.1039C>T (p.Arg347Cys) single nucleotide variant Type 2 diabetes mellitus [RCV002914748]|not provided [RCV003138401] Chr19:40236026 [GRCh38]
Chr19:40741933 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.175+13A>G single nucleotide variant Type 2 diabetes mellitus [RCV002624919] Chr19:40256913 [GRCh38]
Chr19:40762820 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.639+11C>G single nucleotide variant Type 2 diabetes mellitus [RCV003041351] Chr19:40240034 [GRCh38]
Chr19:40745941 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.574-15G>A single nucleotide variant Type 2 diabetes mellitus [RCV002918002] Chr19:40240125 [GRCh38]
Chr19:40746032 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.416C>T (p.Ala139Val) single nucleotide variant Type 2 diabetes mellitus [RCV002931823] Chr19:40242559 [GRCh38]
Chr19:40748466 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.960+20G>T single nucleotide variant Type 2 diabetes mellitus [RCV002630072] Chr19:40236237 [GRCh38]
Chr19:40742144 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.709-3C>G single nucleotide variant Type 2 diabetes mellitus [RCV002716936]|not provided [RCV003883838] Chr19:40238094 [GRCh38]
Chr19:40744001 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.961-2dup duplication Type 2 diabetes mellitus [RCV003063487] Chr19:40236105..40236106 [GRCh38]
Chr19:40742012..40742013 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.572A>G (p.Lys191Arg) single nucleotide variant Type 2 diabetes mellitus [RCV003009004] Chr19:40241939 [GRCh38]
Chr19:40747846 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.46+10C>T single nucleotide variant Type 2 diabetes mellitus [RCV002895581] Chr19:40265212 [GRCh38]
Chr19:40771119 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.1227C>T (p.Phe409=) single nucleotide variant Type 2 diabetes mellitus [RCV003051583] Chr19:40235299 [GRCh38]
Chr19:40741206 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.401A>C (p.Glu134Ala) single nucleotide variant Inborn genetic diseases [RCV002677583]|Type 2 diabetes mellitus [RCV003777617] Chr19:40242574 [GRCh38]
Chr19:40748481 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.1117C>G (p.Leu373Val) single nucleotide variant Inborn genetic diseases [RCV002656429] Chr19:40235948 [GRCh38]
Chr19:40741855 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.202C>A (p.Pro68Thr) single nucleotide variant Inborn genetic diseases [RCV003208028] Chr19:40255243 [GRCh38]
Chr19:40761150 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.831+4A>G single nucleotide variant Type 2 diabetes mellitus [RCV003778822]|not provided [RCV003141293] Chr19:40237965 [GRCh38]
Chr19:40743872 [GRCh37]
Chr19:19q13.2		 likely benign|uncertain significance
NM_001626.6(AKT2):c.574-16C>T single nucleotide variant Type 2 diabetes mellitus [RCV003791819] Chr19:40240126 [GRCh38]
Chr19:40746033 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.531C>T (p.Tyr177=) single nucleotide variant not provided [RCV003425163] Chr19:40241980 [GRCh38]
Chr19:40747887 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.1292C>T (p.Thr431Met) single nucleotide variant not provided [RCV003480319] Chr19:40235119 [GRCh38]
Chr19:40741026 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.1366+19C>T single nucleotide variant Type 2 diabetes mellitus [RCV003807689] Chr19:40235026 [GRCh38]
Chr19:40740933 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.527G>T (p.Arg176Leu) single nucleotide variant Type 2 diabetes mellitus [RCV003793990] Chr19:40241984 [GRCh38]
Chr19:40747891 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.708+8G>A single nucleotide variant AKT2-related disorder [RCV003893401]|Type 2 diabetes mellitus [RCV003782387] Chr19:40238897 [GRCh38]
Chr19:40744804 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.288-14G>T single nucleotide variant Type 2 diabetes mellitus [RCV003797430] Chr19:40242701 [GRCh38]
Chr19:40748608 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.822C>G (p.Arg274=) single nucleotide variant Type 2 diabetes mellitus [RCV003786375] Chr19:40237978 [GRCh38]
Chr19:40743885 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.283G>A (p.Glu95Lys) single nucleotide variant Type 2 diabetes mellitus [RCV003780977] Chr19:40255162 [GRCh38]
Chr19:40761069 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.380C>T (p.Pro127Leu) single nucleotide variant Type 2 diabetes mellitus [RCV003806058] Chr19:40242595 [GRCh38]
Chr19:40748502 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.387C>T (p.Asp129=) single nucleotide variant Type 2 diabetes mellitus [RCV003788513] Chr19:40242588 [GRCh38]
Chr19:40748495 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.704G>T (p.Gly235Val) single nucleotide variant Hypoinsulinemic hypoglycemia and body hemihypertrophy [RCV003883227] Chr19:40238909 [GRCh38]
Chr19:40744816 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.327C>T (p.Ser109=) single nucleotide variant Type 2 diabetes mellitus [RCV003805669] Chr19:40242648 [GRCh38]
Chr19:40748555 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.990C>T (p.Ala330=) single nucleotide variant Type 2 diabetes mellitus [RCV003796761] Chr19:40236075 [GRCh38]
Chr19:40741982 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.46+20C>T single nucleotide variant Type 2 diabetes mellitus [RCV003797077] Chr19:40265202 [GRCh38]
Chr19:40771109 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.576T>G (p.Asp192Glu) single nucleotide variant Type 2 diabetes mellitus [RCV003785972] Chr19:40240108 [GRCh38]
Chr19:40746015 [GRCh37]
Chr19:19q13.2		 uncertain significance
NM_001626.6(AKT2):c.792G>A (p.Glu264=) single nucleotide variant Type 2 diabetes mellitus [RCV003785973] Chr19:40238008 [GRCh38]
Chr19:40743915 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.1125C>T (p.Pro375=) single nucleotide variant Type 2 diabetes mellitus [RCV003792178] Chr19:40235940 [GRCh38]
Chr19:40741847 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.709-14C>T single nucleotide variant Type 2 diabetes mellitus [RCV003780521] Chr19:40238105 [GRCh38]
Chr19:40744012 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.1264-4G>A single nucleotide variant Type 2 diabetes mellitus [RCV003799748] Chr19:40235151 [GRCh38]
Chr19:40741058 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.1311G>A (p.Arg437=) single nucleotide variant Type 2 diabetes mellitus [RCV003810513] Chr19:40235100 [GRCh38]
Chr19:40741007 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.640-20C>T single nucleotide variant Type 2 diabetes mellitus [RCV003798495] Chr19:40238993 [GRCh38]
Chr19:40744900 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.582C>T (p.Val194=) single nucleotide variant Type 2 diabetes mellitus [RCV003808824] Chr19:40240102 [GRCh38]
Chr19:40746009 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.597C>T (p.Thr199=) single nucleotide variant AKT2-related disorder [RCV003949026]|Type 2 diabetes mellitus [RCV003802086] Chr19:40240087 [GRCh38]
Chr19:40745994 [GRCh37]
Chr19:19q13.2		 likely benign
GRCh37/hg19 19q11-13.2(chr19:28271146-41508851)x3 copy number gain not specified [RCV003986115] Chr19:28271146..41508851 [GRCh37]
Chr19:19q11-13.2		 pathogenic
NM_001626.6(AKT2):c.1366+106A>G single nucleotide variant not provided [RCV003992875] Chr19:40234939 [GRCh38]
Chr19:40740846 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.486C>T (p.Thr162=) single nucleotide variant AKT2-related disorder [RCV003983744] Chr19:40242025 [GRCh38]
Chr19:40747932 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.417G>A (p.Ala139=) single nucleotide variant AKT2-related disorder [RCV003964590] Chr19:40242558 [GRCh38]
Chr19:40748465 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.1281A>G (p.Lys427=) single nucleotide variant AKT2-related disorder [RCV003969489] Chr19:40235130 [GRCh38]
Chr19:40741037 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.6(AKT2):c.1367-9C>T single nucleotide variant AKT2-related disorder [RCV003921894] Chr19:40233960 [GRCh38]
Chr19:40739867 [GRCh37]
Chr19:19q13.2		 likely benign
NM_001626.5(AKT2):c.-281_-268dup duplication not provided [RCV004546385] Chr19:40285357..40285358 [GRCh38]
Chr19:40791264..40791265 [GRCh37]
Chr19:19q13.2		 benign
NM_001626.6(AKT2):c.368A>C (p.Lys123Thr) single nucleotide variant not provided [RCV004576011] Chr19:40242607 [GRCh38]
Chr19:40748514 [GRCh37]
Chr19:19q13.2		 uncertain significance
miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR184hsa-miR-184Mirtarbaseexternal_infoqRT-PCR//Luciferase reporter assay//Western blotFunctional MTI20409325
MIR184hsa-miR-184OncomiRDBexternal_infoNANA20409325
MIR708hsa-miR-708-5pMirtarbaseexternal_infoLuciferase reporter assay//qRT-PCRFunctional MTI22552290

Predicted Target Of
Summary Value
Count of predictions:15427
Count of miRNA genes:1392
Interacting mature miRNAs:1879
Transcripts:ENST00000311278, ENST00000358335, ENST00000391844, ENST00000391845, ENST00000392037, ENST00000392038, ENST00000416362, ENST00000416994, ENST00000423127, ENST00000424901, ENST00000427375, ENST00000441941, ENST00000452077, ENST00000456441, ENST00000476247, ENST00000476266, ENST00000480878, ENST00000483166, ENST00000486368, ENST00000486647, ENST00000487537, ENST00000489375, ENST00000491778, ENST00000492463, ENST00000496089, ENST00000497948, ENST00000498350, ENST00000537834, ENST00000578123, ENST00000578282, ENST00000578310, ENST00000578615, ENST00000578975, ENST00000579047, ENST00000579345, ENST00000580747, ENST00000580878, ENST00000581582, ENST00000583859, ENST00000584288, ENST00000596634, ENST00000601166
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
406910048GWAS559024_Hdiastolic blood pressure QTL GWAS559024 (human)0.0000008diastolic blood pressurediastolic blood pressure (CMO:0000005)194025454240254543Human
1559110SCL22_HSerum cholesterol level QTL 22 (human)3.590.000241Lipid levelLDL cholesterol193190759457907594Human
407031507GWAS680483_Ht-tau:beta-amyloid 1-42 ratio measurement QTL GWAS680483 (human)0.000002cerebral cortex integrity trait (VT:0010923)194027792540277926Human
407301335GWAS950311_Hlymphocyte count QTL GWAS950311 (human)8e-12lymphocyte countblood lymphocyte count (CMO:0000031)194027782140277822Human
407325681GWAS974657_Halpha fetoprotein measurement QTL GWAS974657 (human)0.000002blood alpha-fetoprotein amount (VT:0010776)194027313640273137Human
406910552GWAS559528_Hdiastolic blood pressure QTL GWAS559528 (human)2e-09diastolic blood pressurediastolic blood pressure (CMO:0000005)194025454240254543Human
407033402GWAS682378_Hcerebrospinal fluid biomarker measurement, t-tau measurement QTL GWAS682378 (human)0.0000002cerebrospinal fluid biomarker measurement, t-tau measurementcerebrospinal fluid chemistry measurement (CMO:0001241)194027792540277926Human
407225564GWAS874540_Hlymphocyte count QTL GWAS874540 (human)1e-11lymphocyte countblood lymphocyte count (CMO:0000031)194027484240274843Human
1331657COPD9_HChronic obstructive pulmonary disease QTL 9 (human)1.94Chronic airflow obstructionpost-bronchodilator FEV1193102176057021760Human
406922286GWAS571262_HDrugs used in diabetes use measurement QTL GWAS571262 (human)3e-10Drugs used in diabetes use measurement194025695340256954Human

Markers in Region
SGC30851  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371940,741,939 - 40,742,238UniSTSGRCh37
Build 361945,433,779 - 45,434,078RGDNCBI36
Celera1937,541,486 - 37,541,785RGD
Cytogenetic Map19q13.1-q13.2UniSTS
HuRef1937,176,857 - 37,177,156UniSTS
GeneMap99-GB4 RH Map19238.63UniSTS
Whitehead-RH Map19312.5UniSTS
RH11487  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371940,737,077 - 40,737,203UniSTSGRCh37
Build 361945,428,917 - 45,429,043RGDNCBI36
Celera1937,536,624 - 37,536,750RGD
Cytogenetic Map19q13.1-q13.2UniSTS
HuRef1937,172,009 - 37,172,135UniSTS
GeneMap99-GB4 RH Map19235.07UniSTS
NCBI RH Map19420.3UniSTS
D10S16   No map positions available.
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p25.1-p23UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic MapXp21.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map12p13-p12UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map4p15.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p16.3UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p22-p21.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map2q31.3UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q32-q33UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map14q23-q24.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map2p24-p21UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic MapXq25-q26UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map1q25.1-q25.2UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map4q32-q34UniSTS
Cytogenetic MapXq25-q26.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map20q11.22-q12UniSTS
Cytogenetic Map4q34.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q31.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map21q21.2UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map8q21.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map20p12UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map22q13.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map11p14UniSTS
Cytogenetic Map1p32.1UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3p13UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map8q23UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic MapXq13UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map16q12-q13UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map22qUniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic MapXp22.12-p22.11UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map8p22-p21.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map1p36.12UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map7q22-qterUniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS
D10S16  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map2q11.2-q12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map3p22UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map5q21-q22UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map1q24.1UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map4q34UniSTS
Cytogenetic Map2p22-p21UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map1p36.23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map3q26UniSTS
Cytogenetic Map12p12.1-p11.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map17qterUniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map1pter-q31.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map3p23-p21UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1p36.1-p34UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map15q24.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map3p23UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4p15.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map19qterUniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map17pUniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map2p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map3q26.2UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2432 2788 2246 4948 1725 2347 4 622 1948 464 2269 7285 6457 52 3712 848 1734 1615 174 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_012038 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001243027 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001243028 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001330511 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001626 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526620 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526622 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026470 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024451416 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024451417 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC118344 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK054771 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK055779 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK122839 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294453 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK304209 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK308006 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK308906 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK314619 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY708392 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC022779 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC032709 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC040028 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC063421 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC120994 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC120995 (Get FASTA)   NCBI Sequence Viewer