INS-IGF2 (INS-IGF2 readthrough) - Rat Genome Database

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Gene: INS-IGF2 (INS-IGF2 readthrough) Homo sapiens
Analyze
Symbol: INS-IGF2
Name: INS-IGF2 readthrough
RGD ID: 1642400
HGNC Page HGNC:33527
Description: Predicted to enable hormone activity. Predicted to be involved in insulin receptor signaling pathway. Predicted to act upstream of with a positive effect on receptor internalization. Predicted to be located in cytosol. Predicted to be active in extracellular space.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: INS-IGF2 readthrough transcript protein; INSIGF; insulin; insulin, isoform 2; insulin- insulin-like growth factor 2; insulin- insulin-like growth factor 2 read-through; insulin- insulin-like growth factor 2 read-through product
RGD Orthologs
Mouse
Rat
Squirrel
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38112,129,117 - 2,161,209 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl112,132,538 - 2,161,209 (-)EnsemblGRCh38hg38GRCh38
GRCh37112,150,347 - 2,182,439 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36112,106,926 - 2,139,015 (-)NCBINCBI36Build 36hg18NCBI36
Celera112,186,841 - 2,218,946 (-)NCBICelera
Cytogenetic Map11p15.5NCBI
HuRef111,940,864 - 1,972,702 (-)NCBIHuRef
CHM1_1112,148,968 - 2,181,387 (-)NCBICHM1_1
T2T-CHM13v2.0112,216,758 - 2,248,857 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-catechin  (ISO)
(+)-epicatechin-3-O-gallate  (ISO)
(-)-epigallocatechin 3-gallate  (ISO)
(aminooxy)acetic acid  (ISO)
(R)-adrenaline  (ISO)
(R)-carnitine  (ISO)
(R)-lipoic acid  (ISO)
(R)-noradrenaline  (ISO)
(R)-pantothenic acid  (EXP)
(R,R,R)-alpha-tocopherol  (ISO)
(S)-colchicine  (ISO)
(S)-nicotine  (ISO)
1,4-dithiothreitol  (ISO)
14-Deoxy-11,12-didehydroandrographolide  (ISO)
15-deoxy-Delta(12,14)-prostaglandin J2  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (ISO)
2,2',4,4',5,5'-hexachlorobiphenyl  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (ISO)
2,2'-Dihydroxy-4-methoxybenzophenone  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2-(4-hydroxyphenyl)ethanol  (ISO)
2-amino-2-deoxy-D-glucopyranose  (ISO)
2-arachidonoylglycerol  (ISO)
2-cyclopentyl-4-(5-phenyl-1H-pyrrolo[2,3-b]pyridin-3-yl)benzoic acid  (ISO)
2-deoxy-D-glucose  (ISO)
2-hydroxypropanoic acid  (ISO)
3',5'-cyclic AMP  (ISO)
3,3',4,4',5-pentachlorobiphenyl  (ISO)
3,3',5'-triiodo-L-thyronine  (ISO)
3,3',5'-triiodothyronine  (ISO)
3,3',5,5'-tetrabromobisphenol A  (ISO)
3,3',5-triiodo-L-thyronine  (ISO)
3,5,6-trichloro-2-pyridinol  (ISO)
3,5,6-trichloropyridine-2-one  (ISO)
3,5-diethoxycarbonyl-1,4-dihydrocollidine  (ISO)
3-aminobenzoic acid  (ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP,ISO)
3-O-methyl-D-glucose  (ISO)
4,4'-diaminodiphenylmethane  (ISO)
4,4'-sulfonyldiphenol  (ISO)
4-\{[4-(dimethylamino)phenyl]diazenyl\}phenyl-beta-lactoside  (ISO)
4-hydroxyphenyl retinamide  (ISO)
4-methyl-2-oxopentanoic acid  (ISO)
4-methylcatechol  (ISO)
4-nitrophenol  (ISO)
4-phenylbutyric acid  (EXP,ISO)
6-propyl-2-thiouracil  (ISO)
6alpha-methylprednisolone  (ISO)
7-NITROINDAZOLE  (ISO)
9-cis,11-trans-octadecadienoic acid  (ISO)
9-phenanthrol  (ISO)
AACOCF3  (ISO)
acarbose  (ISO)
acephate  (ISO)
acetate ester  (ISO)
acetylleucyl-leucyl-norleucinal  (ISO)
acrolein  (ISO)
acrylamide  (ISO)
actinomycin D  (ISO)
AICA ribonucleotide  (ISO)
aldehydo-D-glucosamine  (ISO)
aldehydo-D-glucose  (EXP,ISO)
aldehydo-D-ribose  (ISO)
all-trans-retinol  (ISO)
allopurinol  (ISO)
alloxan  (ISO)
allyl isothiocyanate  (ISO)
alpha-(methylamino)isobutyric acid  (ISO)
alpha-Zearalanol  (ISO)
AM-251  (ISO)
amino acid  (ISO)
aminophylline  (ISO)
amitrole  (ISO)
ammonium chloride  (ISO)
andrographolide  (ISO)
anthra[1,9-cd]pyrazol-6(2H)-one  (EXP)
anthranilic acid  (ISO)
apigenin  (ISO)
apocynin  (ISO)
arachidonyl-2'-chloroethylamide  (ISO)
arecoline  (ISO)
Aroclor 1254  (ISO)
arsane  (ISO)
arsenic atom  (ISO)
arsenite(3-)  (ISO)
arsenous acid  (ISO)
asiatic acid  (ISO)
astaxanthin  (ISO)
atorvastatin calcium  (ISO)
ATP  (ISO)
avobenzone  (EXP)
bafilomycin A1  (EXP)
baicalin  (ISO)
Bay-K-8644  (ISO)
benazepril  (ISO)
benzamide  (ISO)
benzamides  (ISO)
benzo[a]pyrene  (EXP,ISO)
benzoates  (ISO)
beta-D-glucosamine  (ISO)
beta-hexachlorocyclohexane  (ISO)
Betanin  (ISO)
bezafibrate  (ISO)
biotin  (EXP)
bis(2-ethylhexyl) phthalate  (EXP,ISO)
bisphenol A  (EXP,ISO)
Bisphenol A diglycidyl ether  (ISO)
boric acid  (ISO)
Bromoenol lactone  (ISO)
budesonide  (ISO)
bumetanide  (ISO)
Butylbenzyl phthalate  (EXP)
butyric acid  (ISO)
C-peptide  (ISO)
cadmium atom  (ISO)
cadmium dichloride  (ISO)
caffeine  (ISO)
calcium atom  (ISO)
calcium(0)  (ISO)
cannabidiol  (ISO)
capsaicin  (ISO)
captan  (ISO)
carbachol  (ISO)
CARBENOXOLONE  (ISO)
carbon nanotube  (ISO)
carnosine  (ISO)
celastrol  (ISO)
celecoxib  (ISO)
Chebulagic acid  (ISO)
chicoric acid  (ISO)
chlorothalonil  (ISO)
chlorpromazine  (ISO)
chlorpyrifos  (ISO)
cholesterol  (ISO)
choline  (ISO)
chromium atom  (ISO)
chromium(3+) trichloride  (ISO)
chromium(6+)  (ISO)
chrysin  (ISO)
citronellol  (ISO)
cobalt atom  (ISO)
colforsin daropate hydrochloride  (ISO)
conjugated linoleic acid  (ISO)
copper atom  (ISO)
copper(0)  (ISO)
cordycepin  (ISO)
corilagin  (ISO)
corn oil  (ISO)
cortisol  (ISO)
costunolide  (ISO)
coumarin  (ISO)
crocidolite asbestos  (EXP)
crocin-1  (ISO)
Cuprizon  (ISO)
curcumin  (ISO)
cycloheximide  (ISO)
cytochalasin B  (ISO)
D-glucitol  (ISO)
D-glucose  (EXP,ISO)
D-glyceraldehyde  (ISO)
D-ribofuranose  (ISO)
dactolisib  (ISO)
dapagliflozin  (ISO)
DDE  (ISO)
DDT  (ISO)
dehydroepiandrosterone  (ISO)
Deoxycorticosterone acetate  (ISO)
desferrioxamine B  (ISO)
dexamethasone  (EXP,ISO)
diarsenic trioxide  (ISO)
diazinon  (ISO)
diazoxide  (ISO)
dichlorvos  (ISO)
diethylstilbestrol  (ISO)
dimercaprol  (ISO)
dimethylarsinous acid  (ISO)
diosgenin  (ISO)
disodium cromoglycate  (ISO)
disodium selenite  (ISO)
dorsomorphin  (ISO)
duvoglustat  (ISO)
ebselen  (ISO)
edaravone  (ISO)
elemental selenium  (ISO)
enzyme inhibitor  (ISO)
Eremanthin  (ISO)
ethanol  (ISO)
Evodiamine  (ISO)
fenofibrate  (ISO)
ferric ammonium citrate  (EXP)
ferrostatin-1  (ISO)
fisetin  (ISO)
flunarizine  (ISO)
fluticasone  (ISO)
folic acid  (ISO)
FR900359  (ISO)
fructooligosaccharide  (ISO)
fructose  (ISO)
fulvestrant  (ISO)
furan  (ISO)
gallic acid  (ISO)
gallocatechin  (ISO)
gamma-aminobutyric acid  (ISO)
gatifloxacin  (ISO)
genistein  (ISO)
geraniol  (ISO)
gingerol  (ISO)
ginsenoside Re  (ISO)
Ginsenoside Rh4  (ISO)
gliclazide  (ISO)
glimepiride  (ISO)
glucagon  (ISO)
glucose  (EXP,ISO)
glutathione  (ISO)
glyburide  (ISO)
glyceraldehyde  (ISO)
glycerol 2-phosphate  (ISO)
glycine  (ISO)
glycogen  (ISO)
glycyrrhizinic acid  (ISO)
harmine  (ISO)
heptachlor  (ISO)
herbimycin  (ISO)
hexachlorobenzene  (ISO)
hexadecanoic acid  (EXP,ISO)
homocysteine  (ISO)
hydrogen peroxide  (ISO)
hydroxy-2-naphthalenyl-methyl phosphonic acid trisacetoxymethylester  (ISO)
hydroxytyrosol  (ISO)
imidacloprid  (ISO)
indole-3-methanol  (ISO)
indometacin  (ISO)
isoflavones  (ISO)
isoliquiritigenin  (ISO)
Isosteviol  (ISO)
ivermectin  (ISO)
kaempferol  (ISO)
L-1,4-dithiothreitol  (ISO)
L-ascorbic acid  (ISO)
L-methionine  (ISO)
lactacystin  (ISO)
lead diacetate  (ISO)
lead nitrate  (ISO)
lead(0)  (ISO)
lenalidomide  (ISO)
letrozole  (ISO)
linagliptin  (ISO)
linsidomine  (ISO)
lipoic acid  (ISO)
lipopolysaccharide  (ISO)
lithium carbonate  (ISO)
lutein  (ISO)
luteolin  (ISO)
LY294002  (ISO)
malathion  (ISO)
manganese atom  (ISO)
manganese(0)  (ISO)
mangiferin  (ISO)
manumycin A  (ISO)
melatonin  (ISO)
mercury atom  (ISO)
mercury dichloride  (ISO)
mercury(0)  (ISO)
metformin  (ISO)
methimazole  (ISO)
methoxychlor  (ISO)
methylarsonic acid  (ISO)
methylarsonite  (ISO)
methylglyoxal  (ISO)
methylmercury chloride  (ISO)
microcystin-LR  (ISO)
mitogen  (ISO)
MK-2206  (ISO)
molybdate  (ISO)
molybdenum atom  (ISO)
molybdenum trioxide  (ISO)
monensin A  (ISO)
mono(2-ethylhexyl) phthalate  (ISO)
monosodium L-glutamate  (ISO)
morin  (ISO)
myricetin  (ISO)
myrtenal  (ISO)
N-[3-(aminomethyl)benzyl]acetamidine  (ISO)
N-acetyl-L-cysteine  (ISO)
N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal  (ISO)
N-methylnicotinate  (ISO)
N-nitrosodiethylamine  (ISO)
N-nitrosodimethylamine  (ISO)
N-phosphocreatine  (ISO)
NADP zwitterion  (ISO)
NADP(+)  (ISO)
naproxen  (ISO)
naringin  (ISO)
nickel atom  (ISO)
nickel dichloride  (ISO)
nicotinamide  (ISO)
nicotine  (ISO)
nicotinic acid  (ISO)
nifedipine  (ISO)
nimesulide  (ISO)
nitric oxide  (ISO)
Nonylphenol  (ISO)
norwogonin  (ISO)
Octicizer  (ISO)
ofloxacin  (ISO)
oleanolic acid  (ISO)
oleic acid  (ISO)
orlistat  (ISO)
oxybenzone  (EXP)
ozone  (ISO)
Palbinone  (ISO)
paraquat  (ISO)
PCB138  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (ISO)
permethrin  (ISO)
phenethyl caffeate  (ISO)
phenylarsine oxide  (ISO)
phorbol 13-acetate 12-myristate  (ISO)
picolinic acid  (ISO)
pimobendan  (ISO)
pioglitazone  (EXP,ISO)
piperine  (ISO)
plumbagin  (ISO)
potassium atom  (ISO)
potassium chloride  (ISO)
potassium chromate  (ISO)
potassium cyanide  (ISO)
pravastatin  (ISO)
probenecid  (ISO)
procymidone  (ISO)
progesterone  (ISO)
psoralen  (ISO)
pterostilbene  (ISO)
pyrroloquinoline quinone  (ISO)
pyruvic acid  (ISO)
quercetin  (EXP,ISO)
quercetin 3-O-beta-D-glucofuranoside  (ISO)
quercetin 3-O-beta-D-glucopyranoside  (ISO)
quercitrin  (ISO)
quinoxyfen  (EXP,ISO)
rac-lactic acid  (ISO)
raffinose  (ISO)
raloxifene  (ISO)
Repaglinide  (ISO)
resveratrol  (ISO)
rimonabant  (ISO)
ritonavir  (ISO)
Ro 31-8220  (ISO)
royal jelly  (ISO)
Rutamarin  (ISO)
rutin  (ISO)
S-allylcysteine  (ISO)
S-butyl-DL-homocysteine (S,R)-sulfoximine  (ISO)
SB 203580  (ISO)
selenium atom  (ISO)
sertraline  (ISO)
sildenafil citrate  (ISO)
silibinin  (ISO)
sirolimus  (EXP,ISO)
sodium acetate trihydrate  (ISO)
sodium arsenite  (EXP,ISO)
sodium atom  (ISO)
sodium chloride  (ISO)
sodium fluoride  (ISO)
spironolactone  (ISO)
staurosporine  (ISO)
streptozocin  (EXP,ISO)
sucrose  (ISO)
sulfadimethoxine  (ISO)
sulforaphane  (ISO)
sulpiride  (ISO)
sumatriptan  (ISO)
superoxide  (ISO)
tacrolimus hydrate  (ISO)
taurine  (ISO)
tauroursodeoxycholic acid  (ISO)
telmisartan  (ISO)
testosterone  (ISO)
tetrachloromethane  (ISO)
thapsigargin  (EXP,ISO)
theaflavin  (ISO)
theophylline  (ISO)
thiacloprid  (ISO)
thiophanate-methyl  (ISO)
thymoquinone  (ISO)
thyroxine  (EXP)
titanium dioxide  (ISO)
tolazamide  (ISO)
tolbutamide  (ISO)
trans-rhaponticin  (ISO)
trelagliptin  (ISO)
tributylstannane  (EXP,ISO)
trichostatin A  (ISO)
triclosan  (EXP)
triflumizole  (ISO)
trimethyltin  (ISO)
triphenyl phosphate  (ISO)
tris(picolinato)chromium  (ISO)
troglitazone  (ISO)
U-73122  (ISO)
umbelliferone  (ISO)
Ursonic acid  (ISO)
valproic acid  (ISO)
vanadium atom  (ISO)
vanadium(0)  (ISO)
vildagliptin  (ISO)
vitamin E  (ISO)
Voglibose  (ISO)
warfarin  (ISO)
wogonin  (ISO)
wortmannin  (ISO)
YM-254890  (ISO)
zinc atom  (ISO)
zinc molecular entity  (ISO)
zinc(0)  (ISO)
ziram  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:2902788   PMID:7672495   PMID:7913866   PMID:8565331   PMID:10431232   PMID:10737800   PMID:11855150   PMID:15008838   PMID:15146197   PMID:16344560   PMID:16531418   PMID:17554260  
PMID:17632545   PMID:17667841   PMID:17700581   PMID:19913121   PMID:20628086   PMID:20967262   PMID:21829393   PMID:21873635   PMID:23935095   PMID:25102180   PMID:25102259   PMID:30803359  
PMID:31488892   PMID:32296183   PMID:34267199  


Genomics

Comparative Map Data
INS-IGF2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38112,129,117 - 2,161,209 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl112,132,538 - 2,161,209 (-)EnsemblGRCh38hg38GRCh38
GRCh37112,150,347 - 2,182,439 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36112,106,926 - 2,139,015 (-)NCBINCBI36Build 36hg18NCBI36
Celera112,186,841 - 2,218,946 (-)NCBICelera
Cytogenetic Map11p15.5NCBI
HuRef111,940,864 - 1,972,702 (-)NCBIHuRef
CHM1_1112,148,968 - 2,181,387 (-)NCBICHM1_1
T2T-CHM13v2.0112,216,758 - 2,248,857 (-)NCBIT2T-CHM13v2.0
Ins1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391952,252,735 - 52,253,453 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1952,252,735 - 52,253,914 (+)EnsemblGRCm39 Ensembl
GRCm381952,264,297 - 52,265,015 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1952,264,297 - 52,265,476 (+)EnsemblGRCm38mm10GRCm38
MGSCv371952,338,813 - 52,339,966 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361952,317,762 - 52,318,343 (+)NCBIMGSCv36mm8
Celera1954,451,492 - 54,452,645 (+)NCBICelera
Cytogenetic Map19D2NCBI
cM Map1946.76NCBI
Ins1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81261,186,119 - 261,186,686 (+)NCBIGRCr8
mRatBN7.21251,244,973 - 251,245,540 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1251,244,973 - 251,245,536 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1259,368,906 - 259,369,473 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01266,074,993 - 266,075,560 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01258,728,428 - 258,728,995 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01272,799,784 - 272,800,351 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1272,799,784 - 272,800,347 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01280,213,615 - 280,214,182 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41258,001,134 - 258,001,688 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11258,267,212 - 258,267,545 (+)NCBI
Celera1246,946,414 - 246,946,981 (+)NCBICelera
RH 3.4 Map11654.9RGD
Cytogenetic Map1q55NCBI
LOC120889510
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244049471,733,854 - 1,743,304 (-)NCBIHiC_Itri_2

Variants

.
Variants in INS-IGF2
264 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_000207.3(INS):c.130_144del (p.Gly44_Phe48del) deletion Neonatal insulin-dependent diabetes mellitus [RCV002464240]|not specified [RCV000517956] Chr11:2160828..2160842 [GRCh38]
Chr11:2182058..2182072 [GRCh37]
Chr11:11p15.5		 likely benign|uncertain significance
GRCh38/hg38 11p15.5-15.4(chr11:196966-4435344)x3 copy number gain See cases [RCV000050927] Chr11:196966..4435344 [GRCh38]
Chr11:196966..4456574 [GRCh37]
Chr11:186966..4413150 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
GRCh38/hg38 11p15.5-15.4(chr11:196966-3377077)x3 copy number gain See cases [RCV000050947] Chr11:196966..3377077 [GRCh38]
Chr11:196966..3398307 [GRCh37]
Chr11:186966..3354883 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
GRCh38/hg38 11p15.5-15.4(chr11:218365-3377077)x3 copy number gain See cases [RCV000053614] Chr11:218365..3377077 [GRCh38]
Chr11:218365..3398307 [GRCh37]
Chr11:208365..3354883 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
GRCh38/hg38 11p15.5-13(chr11:202758-31726224)x3 copy number gain See cases [RCV000053613] Chr11:202758..31726224 [GRCh38]
Chr11:202758..31747772 [GRCh37]
Chr11:192758..31704348 [NCBI36]
Chr11:11p15.5-13		 pathogenic
GRCh38/hg38 11p15.5-15.4(chr11:196966-3624139)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053592]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053592]|See cases [RCV000053592] Chr11:196966..3624139 [GRCh38]
Chr11:196966..3645369 [GRCh37]
Chr11:186966..3601945 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
NM_001042376.2(INS-IGF2):c.*488G>A single nucleotide variant Malignant melanoma [RCV000069292] Chr11:2146304 [GRCh38]
Chr11:2167534 [GRCh37]
Chr11:2124110 [NCBI36]
Chr11:11p15.5		 not provided
NM_000207.2(INS):c.132G>A (p.Gly44=) single nucleotide variant Malignant melanoma [RCV000069293] Chr11:2160840 [GRCh38]
Chr11:2182070 [GRCh37]
Chr11:2138646 [NCBI36]
Chr11:11p15.5		 not provided
NM_000207.3(INS):c.188-10G>A single nucleotide variant Maturity onset diabetes mellitus in young [RCV000338328]|Maturity-onset diabetes of the young type 10 [RCV001105129]|Neonatal insulin-dependent diabetes mellitus [RCV002464114]|Transient Neonatal Diabetes, Dominant/Recessive [RCV000311427]|Type 1 diabetes mellitus 2 [RCV002490797]|not provided [RCV000885544]|not specified [RCV000117278] Chr11:2160007 [GRCh38]
Chr11:2181237 [GRCh37]
Chr11:11p15.5		 benign|likely benign|uncertain significance
NM_000207.3(INS):c.143T>C (p.Phe48Ser) single nucleotide variant Hyperproinsulinemia [RCV000014307] Chr11:2160829 [GRCh38]
Chr11:2182059 [GRCh37]
Chr11:11p15.5		 pathogenic
NM_000207.3(INS):c.100C>G (p.His34Asp) single nucleotide variant Hyperproinsulinemia [RCV000014308] Chr11:2160872 [GRCh38]
Chr11:2182102 [GRCh37]
Chr11:11p15.5		 pathogenic|uncertain significance
NM_000207.3(INS):c.266G>A (p.Arg89His) single nucleotide variant Hyperproinsulinemia [RCV000014310]|INS-related condition [RCV003407328]|not provided [RCV001091846] Chr11:2159919 [GRCh38]
Chr11:2181149 [GRCh37]
Chr11:11p15.5		 pathogenic|likely pathogenic|conflicting interpretations of pathogenicity
NM_000207.3(INS):c.274G>T (p.Val92Leu) single nucleotide variant Diabetes mellitus, permanent neonatal 4 [RCV003460471]|Hyperproinsulinemia [RCV000014311] Chr11:2159911 [GRCh38]
Chr11:2181141 [GRCh37]
Chr11:11p15.5		 pathogenic|uncertain significance
NM_000207.3(INS):c.266G>T (p.Arg89Leu) single nucleotide variant Hyperproinsulinemia [RCV000014313] Chr11:2159919 [GRCh38]
Chr11:2181149 [GRCh37]
Chr11:11p15.5		 pathogenic
NM_000207.3(INS):c.266G>C (p.Arg89Pro) single nucleotide variant Hyperproinsulinemia [RCV000014315] Chr11:2159919 [GRCh38]
Chr11:2181149 [GRCh37]
Chr11:11p15.5		 pathogenic
NM_000207.3(INS):c.287G>A (p.Cys96Tyr) single nucleotide variant Diabetes mellitus, permanent neonatal 4 [RCV001089454]|Neonatal diabetes mellitus [RCV002051784]|Permanent neonatal diabetes mellitus [RCV000014319]|not provided [RCV000517445] Chr11:2159898 [GRCh38]
Chr11:2181128 [GRCh37]
Chr11:11p15.5		 pathogenic|likely pathogenic|uncertain significance|not provided
NM_000207.3(INS):c.71C>A (p.Ala24Asp) single nucleotide variant Diabetes mellitus, permanent neonatal 4 [RCV001089455]|Permanent neonatal diabetes mellitus [RCV000014320]|not provided [RCV001818156] Chr11:2160901 [GRCh38]
Chr11:2182131 [GRCh37]
Chr11:11p15.5		 pathogenic|likely risk allele|not provided
NM_000207.3(INS):c.143T>G (p.Phe48Cys) single nucleotide variant Diabetes mellitus, permanent neonatal 4 [RCV001089456]|Neonatal diabetes mellitus [RCV002051785]|Permanent neonatal diabetes mellitus [RCV000014321] Chr11:2160829 [GRCh38]
Chr11:2182059 [GRCh37]
Chr11:11p15.5		 pathogenic|likely pathogenic|likely risk allele|not provided
NM_000207.3(INS):c.16C>T (p.Arg6Cys) single nucleotide variant Maturity-onset diabetes of the young type 10 [RCV000014322] Chr11:2160956 [GRCh38]
Chr11:2182186 [GRCh37]
Chr11:11p15.5		 pathogenic|likely risk allele
NM_000207.3(INS):c.137G>A (p.Arg46Gln) single nucleotide variant Diabetes mellitus, permanent neonatal 4 [RCV003445068]|Maturity-onset diabetes of the young type 10 [RCV000014323]|not provided [RCV001851851] Chr11:2160835 [GRCh38]
Chr11:2182065 [GRCh37]
Chr11:11p15.5		 pathogenic|likely pathogenic|uncertain significance
NM_000207.3(INS):c.163C>T (p.Arg55Cys) single nucleotide variant Diabetes mellitus type 1 [RCV003445069]|Monogenic diabetes [RCV003987320]|Type 1 diabetes mellitus 2 [RCV000014324]|not provided [RCV001558886] Chr11:2160809 [GRCh38]
Chr11:2182039 [GRCh37]
Chr11:11p15.5		 pathogenic|likely pathogenic|likely risk allele
NM_000207.3(INS):c.127T>G (p.Cys43Gly) single nucleotide variant Diabetes mellitus, permanent neonatal 4 [RCV001089452]|Neonatal diabetes mellitus [RCV000030069]|Permanent neonatal diabetes mellitus [RCV000020204]|Type 2 diabetes mellitus [RCV003445080] Chr11:2160845 [GRCh38]
Chr11:2182075 [GRCh37]
Chr11:11p15.5		 pathogenic|likely pathogenic|likely risk allele|not provided
NM_000207.3(INS):c.140G>T (p.Gly47Val) single nucleotide variant Diabetes mellitus, permanent neonatal 4 [RCV003445081]|Permanent neonatal diabetes mellitus [RCV000020205] Chr11:2160832 [GRCh38]
Chr11:2182062 [GRCh37]
Chr11:11p15.5		 pathogenic|uncertain significance|not provided
NM_000207.3(INS):c.265C>T (p.Arg89Cys) single nucleotide variant Diabetes mellitus, permanent neonatal 4 [RCV001089453]|Neonatal diabetes mellitus [RCV002051790]|Permanent neonatal diabetes mellitus [RCV000020207]|not provided [RCV002513137] Chr11:2159920 [GRCh38]
Chr11:2181150 [GRCh37]
Chr11:11p15.5		 pathogenic|likely pathogenic|uncertain significance
NM_000207.3(INS):c.268G>T (p.Gly90Cys) single nucleotide variant Diabetes mellitus, permanent neonatal 4 [RCV003460486]|Permanent neonatal diabetes mellitus [RCV000020208] Chr11:2159917 [GRCh38]
Chr11:2181147 [GRCh37]
Chr11:11p15.5		 pathogenic|uncertain significance|not provided
NM_000207.3(INS):c.323A>G (p.Tyr108Cys) single nucleotide variant Diabetes mellitus, permanent neonatal 4 [RCV003389036]|Permanent neonatal diabetes mellitus [RCV000020210] Chr11:2159862 [GRCh38]
Chr11:2181092 [GRCh37]
Chr11:11p15.5		 pathogenic|likely risk allele|not provided
NM_000207.3(INS):c.94G>A (p.Gly32Ser) single nucleotide variant Diabetes mellitus, permanent neonatal 4 [RCV001089451]|Neonatal diabetes mellitus [RCV000030072]|Permanent neonatal diabetes mellitus [RCV000020212]|Type 1 diabetes mellitus 2 [RCV000117279]|not provided [RCV001775542] Chr11:2160878 [GRCh38]
Chr11:2182108 [GRCh37]
Chr11:11p15.5		 pathogenic|likely pathogenic|uncertain significance|not provided
NM_000207.3(INS):c.94G>C (p.Gly32Arg) single nucleotide variant Permanent neonatal diabetes mellitus [RCV000020213] Chr11:2160878 [GRCh38]
Chr11:2182108 [GRCh37]
Chr11:11p15.5		 pathogenic|not provided
NM_000207.3(INS):c.-9C>T single nucleotide variant Autosomal recessive DOPA responsive dystonia [RCV000266479]|Diabetes mellitus, permanent neonatal 4 [RCV003445086]|Maturity onset diabetes mellitus in young [RCV000295949]|Maturity-onset diabetes of the young type 10 [RCV001103301]|Neonatal diabetes mellitus [RCV000030068]|Transient Neonatal Diabetes, Dominant/Recessive [RCV000348477]|not provided [RCV001582500]|not specified [RCV000253792] Chr11:2160980 [GRCh38]
Chr11:2182210 [GRCh37]
Chr11:11p15.5		 benign|likely benign
NM_000207.3(INS):c.188-16C>T single nucleotide variant Neonatal diabetes mellitus [RCV000030070]|Neonatal insulin-dependent diabetes mellitus [RCV002464076]|Type 1 diabetes mellitus 2 [RCV002496459]|not provided [RCV001588831]|not specified [RCV000249140] Chr11:2160013 [GRCh38]
Chr11:2181243 [GRCh37]
Chr11:11p15.5		 benign|likely benign
NM_000207.3(INS):c.71C>T (p.Ala24Val) single nucleotide variant Neonatal diabetes mellitus [RCV000030071]|not provided [RCV001818190] Chr11:2160901 [GRCh38]
Chr11:2182131 [GRCh37]
Chr11:11p15.5		 likely pathogenic
NM_000207.3(INS):c.*59A>G single nucleotide variant Permanent neonatal diabetes mellitus [RCV000055785] Chr11:2159793 [GRCh38]
Chr11:2181023 [GRCh37]
Chr11:11p15.5		 pathogenic|not provided
NM_000207.3(INS):c.3G>A (p.Met1Ile) single nucleotide variant Diabetes mellitus, permanent neonatal 4 [RCV003445477]|Permanent neonatal diabetes mellitus [RCV000055791] Chr11:2160969 [GRCh38]
Chr11:2182199 [GRCh37]
Chr11:11p15.5		 pathogenic|uncertain significance|not provided
NM_000207.3(INS):c.3G>T (p.Met1Ile) single nucleotide variant Permanent neonatal diabetes mellitus [RCV000055792] Chr11:2160969 [GRCh38]
Chr11:2182199 [GRCh37]
Chr11:11p15.5		 pathogenic|not provided
NM_000207.3(INS):c.104T>C (p.Leu35Pro) single nucleotide variant Permanent neonatal diabetes mellitus [RCV000059608] Chr11:2160868 [GRCh38]
Chr11:2182098 [GRCh37]
Chr11:11p15.5		 not provided
NM_000207.3(INS):c.17G>A (p.Arg6His) single nucleotide variant INS-related condition [RCV003415831]|Maturity-onset diabetes of the young type 10 [RCV000059609]|not provided [RCV003556156] Chr11:2160955 [GRCh38]
Chr11:2182185 [GRCh37]
Chr11:11p15.5		 uncertain risk allele|uncertain significance|not provided
NM_000207.3(INS):c.250G>A (p.Gly84Arg) single nucleotide variant Diabetes mellitus, permanent neonatal 4 [RCV003445479]|Permanent neonatal diabetes mellitus [RCV000059611] Chr11:2159935 [GRCh38]
Chr11:2181165 [GRCh37]
Chr11:11p15.5		 uncertain significance|not provided
NM_000207.3(INS):c.287G>C (p.Cys96Ser) single nucleotide variant Permanent neonatal diabetes mellitus [RCV000059612] Chr11:2159898 [GRCh38]
Chr11:2181128 [GRCh37]
Chr11:11p15.5		 not provided
NM_000207.3(INS):c.302C>G (p.Ser101Cys) single nucleotide variant Diabetes mellitus, permanent neonatal 4 [RCV003389038]|Permanent neonatal diabetes mellitus [RCV000059613] Chr11:2159883 [GRCh38]
Chr11:2181113 [GRCh37]
Chr11:11p15.5		 likely risk allele|not provided
NM_000207.3(INS):c.308A>G (p.Tyr103Cys) single nucleotide variant Diabetes mellitus, permanent neonatal 4 [RCV003389039]|Permanent neonatal diabetes mellitus [RCV000059614]|not provided [RCV001854250] Chr11:2159877 [GRCh38]
Chr11:2181107 [GRCh37]
Chr11:11p15.5		 likely pathogenic|likely risk allele|uncertain significance|not provided
NM_000207.3(INS):c.85C>G (p.His29Asp) single nucleotide variant Diabetes mellitus, permanent neonatal 4 [RCV003445480]|Permanent neonatal diabetes mellitus [RCV000059615] Chr11:2160887 [GRCh38]
Chr11:2182117 [GRCh37]
Chr11:11p15.5		 uncertain significance|not provided
NM_000207.3(INS):c.202C>A (p.Leu68Met) single nucleotide variant INS-related condition [RCV003925020]|Type 2 diabetes mellitus [RCV003445478]|not provided [RCV000059610] Chr11:2159983 [GRCh38]
Chr11:2181213 [GRCh37]
Chr11:11p15.5		 likely benign|uncertain significance
NM_000207.2(INS):c.-366_343del deletion Permanent neonatal diabetes mellitus [RCV000055789] Chr11:2159842..2161516 [GRCh38]
Chr11:2181072..2182746 [GRCh37]
Chr11:11p15.5		 pathogenic
GRCh38/hg38 11p15.5-15.1(chr11:446754-18904742)x3 copy number gain See cases [RCV000133997] Chr11:446754..18904742 [GRCh38]
Chr11:446754..18926289 [GRCh37]
Chr11:436754..18882865 [NCBI36]
Chr11:11p15.5-15.1		 pathogenic
GRCh38/hg38 11p15.5-15.4(chr11:1975511-2888695)x3 copy number gain See cases [RCV000136112] Chr11:1975511..2888695 [GRCh38]
Chr11:1996741..2909925 [GRCh37]
Chr11:1953317..2866501 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
GRCh38/hg38 11p15.5(chr11:1975511-2138446)x3 copy number gain See cases [RCV000137018] Chr11:1975511..2138446 [GRCh38]
Chr11:1996741..2159676 [GRCh37]
Chr11:1953317..2116252 [NCBI36]
Chr11:11p15.5		 benign
GRCh38/hg38 11p15.5-15.4(chr11:1537379-3360769)x3 copy number gain See cases [RCV000136847] Chr11:1537379..3360769 [GRCh38]
Chr11:1558609..3381999 [GRCh37]
Chr11:1515185..3338575 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
GRCh38/hg38 11p15.5-15.4(chr11:1975511-3624139)x1 copy number loss See cases [RCV000137066] Chr11:1975511..3624139 [GRCh38]
Chr11:1996741..3645369 [GRCh37]
Chr11:1953317..3601945 [NCBI36]
Chr11:11p15.5-15.4		 uncertain significance
GRCh38/hg38 11p15.5(chr11:2149352-2467542)x3 copy number gain See cases [RCV000137405] Chr11:2149352..2467542 [GRCh38]
Chr11:2170582..2488772 [GRCh37]
Chr11:2127158..2445348 [NCBI36]
Chr11:11p15.5		 uncertain significance
GRCh38/hg38 11p15.5(chr11:2052381-2138446)x3 copy number gain See cases [RCV000137157] Chr11:2052381..2138446 [GRCh38]
Chr11:2073611..2159676 [GRCh37]
Chr11:2030187..2116252 [NCBI36]
Chr11:11p15.5		 uncertain significance
GRCh38/hg38 11p15.5-15.4(chr11:61793-10727969)x3 copy number gain See cases [RCV000139987] Chr11:61793..10727969 [GRCh38]
Chr11:61793..10749516 [GRCh37]
Chr11:51793..10706092 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
GRCh38/hg38 11p15.5(chr11:2127344-2159430)x3 copy number gain See cases [RCV000141243] Chr11:2127344..2159430 [GRCh38]
Chr11:2148574..2180660 [GRCh37]
Chr11:2105150..2137236 [NCBI36]
Chr11:11p15.5		 uncertain significance
NM_001127598.3(IGF2):c.82G>A (p.Gly28Arg) single nucleotide variant not specified [RCV000203020] Chr11:2140215 [GRCh38]
Chr11:2161445 [GRCh37]
Chr11:11p15.5		 uncertain significance
GRCh38/hg38 11p15.5-15.4(chr11:1132899-3213923)x1 copy number loss See cases [RCV000142464] Chr11:1132899..3213923 [GRCh38]
Chr11:1126807..3235153 [GRCh37]
Chr11:1116807..3191729 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
GRCh38/hg38 11p15.5-15.4(chr11:196855-5321874)x3 copy number gain See cases [RCV000142890] Chr11:196855..5321874 [GRCh38]
Chr11:196855..5343104 [GRCh37]
Chr11:186855..5299680 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
GRCh38/hg38 11p15.5(chr11:2106943-2565669)x3 copy number gain See cases [RCV000143587] Chr11:2106943..2565669 [GRCh38]
Chr11:2128173..2586899 [GRCh37]
Chr11:2084749..2543475 [NCBI36]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.147C>G (p.Phe49Leu) single nucleotide variant Hyperproinsulinemia [RCV000014306] Chr11:2160825 [GRCh38]
Chr11:2182055 [GRCh37]
Chr11:11p15.5		 pathogenic
NM_000207.3(INS):c.188-31G>A single nucleotide variant Diabetes mellitus, permanent neonatal 4 [RCV003445689]|Neonatal insulin-dependent diabetes mellitus [RCV002464141]|Permanent neonatal diabetes mellitus [RCV000193144]|not provided [RCV000436891] Chr11:2160028 [GRCh38]
Chr11:2181258 [GRCh37]
Chr11:11p15.5		 pathogenic|likely risk allele
NM_000207.3(INS):c.187+241G>A single nucleotide variant Diabetes mellitus, permanent neonatal 4 [RCV000258877] Chr11:2160544 [GRCh38]
Chr11:2181774 [GRCh37]
Chr11:11p15.5		 pathogenic|uncertain significance|not provided
GRCh37/hg19 11p15.5-15.4(chr11:193187-5291338)x3 copy number gain See cases [RCV000446036] Chr11:193187..5291338 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
NM_000612.6(IGF2):c.23C>A (p.Ser8Ter) single nucleotide variant Silver-Russell syndrome 3 [RCV000186560] Chr11:2135501 [GRCh38]
Chr11:2156731 [GRCh37]
Chr11:11p15.5		 pathogenic|likely pathogenic
NM_000207.3(INS):c.*9C>T single nucleotide variant Autosomal recessive DOPA responsive dystonia [RCV000402726]|Hypoinsulinemia [RCV002221215]|Maturity onset diabetes mellitus in young [RCV000344882]|Maturity-onset diabetes of the young type 10 [RCV001103214]|Transient Neonatal Diabetes, Dominant/Recessive [RCV000289877]|not provided [RCV001651115]|not specified [RCV000249051] Chr11:2159843 [GRCh38]
Chr11:2181073 [GRCh37]
Chr11:11p15.5		 association|benign|likely benign
GRCh37/hg19 11p15.5(chr11:2181002-2182229)x1 copy number loss See cases [RCV000240248] Chr11:2181002..2182229 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.187+11T>C single nucleotide variant Autosomal recessive DOPA responsive dystonia [RCV000301754]|Maturity onset diabetes mellitus in young [RCV000298547]|Maturity-onset diabetes of the young type 10 [RCV001106254]|Transient Neonatal Diabetes, Dominant/Recessive [RCV000390933]|Type 1 diabetes mellitus 2 [RCV002500856]|Type 2 diabetes mellitus [RCV002221216]|not provided [RCV001515509]|not specified [RCV000244371] Chr11:2160774 [GRCh38]
Chr11:2182004 [GRCh37]
Chr11:11p15.5		 benign|likely benign
NM_000207.3(INS):c.63A>G (p.Pro21=) single nucleotide variant Inborn genetic diseases [RCV002365256]|Maturity-onset diabetes of the young type 10 [RCV003445811]|not provided [RCV000969598]|not specified [RCV000254342] Chr11:2160909 [GRCh38]
Chr11:2182139 [GRCh37]
Chr11:11p15.5		 benign|likely benign|uncertain significance
NM_000207.3(INS):c.125T>C (p.Val42Ala) single nucleotide variant Maturity-onset diabetes of the young type 10 [RCV000240176] Chr11:2160847 [GRCh38]
Chr11:2182077 [GRCh37]
Chr11:11p15.5		 likely pathogenic|conflicting interpretations of pathogenicity
NM_000612.6(IGF2):c.518dup (p.Glu174fs) duplication not provided [RCV000520721] Chr11:2133011..2133012 [GRCh38]
Chr11:2154241..2154242 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.153A>G (p.Thr51=) single nucleotide variant Maturity-onset diabetes of the young type 10 [RCV000353376]|Transient Neonatal Diabetes, Dominant/Recessive [RCV000267973]|not specified [RCV001820896] Chr11:2160819 [GRCh38]
Chr11:2182049 [GRCh37]
Chr11:11p15.5		 likely benign|uncertain significance
NM_000207.3(INS):c.*28G>A single nucleotide variant Maturity-onset diabetes of the young type 10 [RCV000265386]|Neonatal insulin-dependent diabetes mellitus [RCV002464162]|Transient Neonatal Diabetes, Dominant/Recessive [RCV000378666] Chr11:2159824 [GRCh38]
Chr11:2181054 [GRCh37]
Chr11:11p15.5		 benign|likely benign|uncertain significance
NM_000207.3(INS):c.130G>A (p.Gly44Arg) single nucleotide variant Maturity-onset diabetes of the young type 10 [RCV000359349]|Transient Neonatal Diabetes, Dominant/Recessive [RCV000304558]|not provided [RCV001544982] Chr11:2160842 [GRCh38]
Chr11:2182072 [GRCh37]
Chr11:11p15.5		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_000207.3(INS):c.25C>T (p.Pro9Ser) single nucleotide variant INS-related condition [RCV003417983]|Maturity-onset diabetes of the young type 10 [RCV000325720]|Neonatal insulin-dependent diabetes mellitus [RCV002464166]|Transient Neonatal Diabetes, Dominant/Recessive [RCV000389656]|Type 1 diabetes mellitus 2 [RCV002467727] Chr11:2160947 [GRCh38]
Chr11:2182177 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.*42C>T single nucleotide variant Maturity-onset diabetes of the young type 10 [RCV000261205]|Neonatal insulin-dependent diabetes mellitus [RCV002464161]|Transient Neonatal Diabetes, Dominant/Recessive [RCV000316468] Chr11:2159810 [GRCh38]
Chr11:2181040 [GRCh37]
Chr11:11p15.5		 benign|uncertain significance
NM_000207.3(INS):c.*2C>T single nucleotide variant Maturity-onset diabetes of the young type 10 [RCV000380688]|Neonatal insulin-dependent diabetes mellitus [RCV002464163]|Transient Neonatal Diabetes, Dominant/Recessive [RCV000295736] Chr11:2159850 [GRCh38]
Chr11:2181080 [GRCh37]
Chr11:11p15.5		 benign|likely benign|uncertain significance
NM_000207.3(INS):c.66C>T (p.Ala22=) single nucleotide variant Maturity onset diabetes mellitus in young [RCV000264652]|Neonatal insulin-dependent diabetes mellitus [RCV002464165]|Transient Neonatal Diabetes, Dominant/Recessive [RCV000329063] Chr11:2160906 [GRCh38]
Chr11:2182136 [GRCh37]
Chr11:11p15.5		 likely benign|uncertain significance
NM_000207.3(INS):c.-18+3C>G single nucleotide variant Maturity-onset diabetes of the young type 10 [RCV000341323]|Neonatal insulin-dependent diabetes mellitus [RCV002464167]|Transient Neonatal Diabetes, Dominant/Recessive [RCV000279346] Chr11:2161165 [GRCh38]
Chr11:2182395 [GRCh37]
Chr11:11p15.5		 benign|uncertain significance
NM_000207.3(INS):c.*22A>C single nucleotide variant Autosomal recessive DOPA responsive dystonia [RCV000346143]|Diabetes mellitus type 1 [RCV003388579]|Diabetes mellitus, permanent neonatal 4 [RCV001544277]|Hyperproinsulinemia [RCV001544278]|Maturity onset diabetes mellitus in young [RCV000320451]|Maturity-onset diabetes of the young type 10 [RCV001103213]|Transient Neonatal Diabetes, Dominant/Recessive [RCV000384319]|Type 1 diabetes mellitus 2 [RCV001544276]|not provided [RCV001712011] Chr11:2159830 [GRCh38]
Chr11:2181060 [GRCh37]
Chr11:11p15.5		 benign|uncertain significance
NM_000207.3(INS):c.-18+4_-18+5insTTGC insertion Autosomal recessive DOPA responsive dystonia [RCV000353899]|Maturity onset diabetes mellitus in young [RCV000337866]|Maturity-onset diabetes of the young type 10 [RCV003463781]|Transient Neonatal Diabetes, Dominant/Recessive [RCV000401881]|not provided [RCV001660593] Chr11:2161163..2161164 [GRCh38]
Chr11:2182393..2182394 [GRCh37]
Chr11:11p15.5		 benign|likely benign|uncertain significance
NM_000207.3(INS):c.188-3C>A single nucleotide variant Maturity-onset diabetes of the young type 10 [RCV000351053]|Neonatal insulin-dependent diabetes mellitus [RCV002464164]|Transient Neonatal Diabetes, Dominant/Recessive [RCV000399757] Chr11:2160000 [GRCh38]
Chr11:2181230 [GRCh37]
Chr11:11p15.5		 likely risk allele|uncertain significance
NM_000207.3(INS):c.36G>A (p.Ala12=) single nucleotide variant Autosomal recessive DOPA responsive dystonia [RCV000361123]|Maturity onset diabetes mellitus in young [RCV000383778]|Maturity-onset diabetes of the young type 10 [RCV001108483]|Neonatal insulin-dependent diabetes mellitus [RCV002221524]|Transient Neonatal Diabetes, Dominant/Recessive [RCV000270633]|Type 1 diabetes mellitus 2 [RCV002494953]|not provided [RCV000973456] Chr11:2160936 [GRCh38]
Chr11:2182166 [GRCh37]
Chr11:11p15.5		 benign|likely benign|uncertain significance
NM_000207.3(INS):c.-17-6T>A single nucleotide variant Autosomal recessive DOPA responsive dystonia [RCV000299006]|Maturity onset diabetes mellitus in young [RCV000386638]|Maturity-onset diabetes of the young type 10 [RCV001103302]|Transient Neonatal Diabetes, Dominant/Recessive [RCV000280575]|not provided [RCV000711996] Chr11:2160994 [GRCh38]
Chr11:2182224 [GRCh37]
Chr11:11p15.5		 benign
NM_000612.6(IGF2):c.472del (p.Pro157_Leu158insTer) deletion not provided [RCV000598672] Chr11:2133058 [GRCh38]
Chr11:2154288 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.211T>C (p.Cys71Arg) single nucleotide variant not provided [RCV000731499] Chr11:2133612 [GRCh38]
Chr11:2154842 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.99C>A (p.Cys33Ter) single nucleotide variant not provided [RCV000412860] Chr11:2135425 [GRCh38]
Chr11:2156655 [GRCh37]
Chr11:11p15.5		 pathogenic
NM_000612.6(IGF2):c.97T>C (p.Cys33Arg) single nucleotide variant not provided [RCV000414320] Chr11:2135427 [GRCh38]
Chr11:2156657 [GRCh37]
Chr11:11p15.5		 likely pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:230615-6644927)x3 copy number gain See cases [RCV000449417] Chr11:230615..6644927 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
NM_000207.3(INS):c.278A>G (p.Glu93Gly) single nucleotide variant Maturity-onset diabetes of the young type 10 [RCV003446061]|Monogenic diabetes [RCV000445381] Chr11:2159907 [GRCh38]
Chr11:2181137 [GRCh37]
Chr11:11p15.5		 likely pathogenic|uncertain risk allele
NM_000612.6(IGF2):c.78C>G (p.Tyr26Ter) single nucleotide variant Silver-Russell syndrome 1 [RCV000491853]|not provided [RCV000479354] Chr11:2135446 [GRCh38]
Chr11:2156676 [GRCh37]
Chr11:11p15.5		 pathogenic
NM_000207.3(INS):c.320ACT[1] (p.Tyr108del) microsatellite Neonatal insulin-dependent diabetes mellitus [RCV002464227]|not specified [RCV000499487] Chr11:2159860..2159862 [GRCh38]
Chr11:2181090..2181092 [GRCh37]
Chr11:11p15.5		 likely benign|uncertain significance
NM_000207.3(INS):c.292A>T (p.Ser98Cys) single nucleotide variant Neonatal insulin-dependent diabetes mellitus [RCV002464226]|not specified [RCV000499676] Chr11:2159893 [GRCh38]
Chr11:2181123 [GRCh37]
Chr11:11p15.5		 uncertain risk allele|uncertain significance
NM_000207.3(INS):c.-17-70G>A single nucleotide variant Neonatal insulin-dependent diabetes mellitus [RCV002464221]|not specified [RCV000504420] Chr11:2161058 [GRCh38]
Chr11:2182288 [GRCh37]
Chr11:11p15.5		 benign|uncertain significance
NM_000207.3(INS):c.188-220C>T single nucleotide variant Neonatal insulin-dependent diabetes mellitus [RCV002464220]|not specified [RCV000502334] Chr11:2160217 [GRCh38]
Chr11:2181447 [GRCh37]
Chr11:11p15.5		 benign|likely benign
NM_000207.3(INS):c.188-96G>A single nucleotide variant Neonatal insulin-dependent diabetes mellitus [RCV002464219]|not specified [RCV000500193] Chr11:2160093 [GRCh38]
Chr11:2181323 [GRCh37]
Chr11:11p15.5		 benign|uncertain significance
NM_000207.3(INS):c.-18+21C>T single nucleotide variant Neonatal insulin-dependent diabetes mellitus [RCV002464225]|not specified [RCV000502684] Chr11:2161147 [GRCh38]
Chr11:2182377 [GRCh37]
Chr11:11p15.5		 benign|likely benign
NM_000207.3(INS):c.-39A>C single nucleotide variant Neonatal insulin-dependent diabetes mellitus [RCV002464214]|Permanent neonatal diabetes mellitus [RCV000055786] Chr11:2161189 [GRCh38]
Chr11:2182419 [GRCh37]
Chr11:11p15.5		 pathogenic|likely benign|not provided
NM_000207.2(INS):c.(?_-191)_(187_?)+1del deletion Permanent neonatal diabetes mellitus [RCV000055790] Chr11:2160784..2161341 [GRCh38]
Chr11:2182014..2182571 [GRCh37]
Chr11:11p15.5		 pathogenic|not provided
NM_000207.3(INS):c.-18+22G>A single nucleotide variant Neonatal insulin-dependent diabetes mellitus [RCV002464223]|not specified [RCV000502801] Chr11:2161146 [GRCh38]
Chr11:2182376 [GRCh37]
Chr11:11p15.5		 benign|uncertain significance
NM_000207.3(INS):c.-18+62C>T single nucleotide variant Neonatal insulin-dependent diabetes mellitus [RCV002464222]|not specified [RCV000500695] Chr11:2161106 [GRCh38]
Chr11:2182336 [GRCh37]
Chr11:11p15.5		 uncertain significance
GRCh37/hg19 11p15.5-12(chr11:230615-37698540)x3 copy number gain See cases [RCV000511561] Chr11:230615..37698540 [GRCh37]
Chr11:11p15.5-12		 pathogenic
NM_000612.6(IGF2):c.157+1_157+2insGC insertion Silver-Russell syndrome 1 [RCV000490875] Chr11:2135365..2135366 [GRCh38]
Chr11:2156595..2156596 [GRCh37]
Chr11:11p15.5		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-14.3(chr11:230615-25584362)x3 copy number gain See cases [RCV000512225] Chr11:230615..25584362 [GRCh37]
Chr11:11p15.5-14.3		 pathogenic
GRCh37/hg19 11p15.5-13(chr11:230615-31995219)x3 copy number gain See cases [RCV000512477] Chr11:230615..31995219 [GRCh37]
Chr11:11p15.5-13		 pathogenic
GRCh37/hg19 11p15.5(chr11:1690968-2277648)x3 copy number gain See cases [RCV000512345] Chr11:1690968..2277648 [GRCh37]
Chr11:11p15.5		 uncertain significance
GRCh37/hg19 11p15.5-15.1(chr11:230615-17099213)x3 copy number gain not provided [RCV000683372] Chr11:230615..17099213 [GRCh37]
Chr11:11p15.5-15.1		 pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:230615-9704511)x3 copy number gain not provided [RCV000683369] Chr11:230615..9704511 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
NM_001042376.3(INS-IGF2):c.581G>A (p.Arg194Gln) single nucleotide variant Inborn genetic diseases [RCV003183429] Chr11:2147634 [GRCh38]
Chr11:2168864 [GRCh37]
Chr11:11p15.5		 uncertain significance
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5(chr11:2101692-2150444)x1 copy number loss not provided [RCV000737384] Chr11:2101692..2150444 [GRCh37]
Chr11:11p15.5		 benign
NM_000612.6(IGF2):c.96G>C (p.Leu32=) single nucleotide variant not provided [RCV000982469] Chr11:2135428 [GRCh38]
Chr11:2156658 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.444G>A (p.Ala148=) single nucleotide variant not provided [RCV000902594] Chr11:2133086 [GRCh38]
Chr11:2154316 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.234C>G (p.Ala78=) single nucleotide variant not provided [RCV000883318] Chr11:2133589 [GRCh38]
Chr11:2154819 [GRCh37]
Chr11:11p15.5		 benign
NM_000612.6(IGF2):c.381C>T (p.Arg127=) single nucleotide variant IGF2-related condition [RCV003950615]|not provided [RCV000903609] Chr11:2133149 [GRCh38]
Chr11:2154379 [GRCh37]
Chr11:11p15.5		 benign|likely benign
NM_000612.6(IGF2):c.480T>C (p.Ala160=) single nucleotide variant IGF2-related condition [RCV003943010]|not provided [RCV000948858] Chr11:2133050 [GRCh38]
Chr11:2154280 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000207.3(INS):c.290C>G (p.Thr97Ser) single nucleotide variant Maturity-onset diabetes of the young type 10 [RCV000754809]|Neonatal insulin-dependent diabetes mellitus [RCV002464307] Chr11:2159895 [GRCh38]
Chr11:2181125 [GRCh37]
Chr11:11p15.5		 likely pathogenic|uncertain risk allele
NM_000612.6(IGF2):c.261C>T (p.Pro87=) single nucleotide variant not provided [RCV000902960] Chr11:2133562 [GRCh38]
Chr11:2154792 [GRCh37]
Chr11:11p15.5		 likely benign
NM_001127598.3(IGF2):c.97C>T (p.Gln33Ter) single nucleotide variant Inborn genetic diseases [RCV002539309]|not provided [RCV000882263] Chr11:2140200 [GRCh38]
Chr11:2161430 [GRCh37]
Chr11:11p15.5		 likely benign
NC_000011.9:g.(?_612625)_(2193840_?)dup duplication Immunodeficiency 39 [RCV001033372] Chr11:612625..2193840 [GRCh37]
Chr11:11p15.5		 uncertain significance
GRCh37/hg19 11p15.5-15.3(chr11:193146-12643136) copy number gain Silver-Russell syndrome 1 [RCV000767567] Chr11:193146..12643136 [GRCh37]
Chr11:11p15.5-15.3		 pathogenic
NM_000612.6(IGF2):c.129C>T (p.Phe43=) single nucleotide variant not provided [RCV000922798] Chr11:2135395 [GRCh38]
Chr11:2156625 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.240G>A (p.Leu80=) single nucleotide variant not provided [RCV000965162] Chr11:2133583 [GRCh38]
Chr11:2154813 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000207.3(INS):c.26C>G (p.Pro9Arg) single nucleotide variant Neonatal insulin-dependent diabetes mellitus [RCV002464311]|Permanent neonatal diabetes mellitus [RCV000768377] Chr11:2160946 [GRCh38]
Chr11:2182176 [GRCh37]
Chr11:11p15.5		 likely pathogenic|likely risk allele
NM_000612.6(IGF2):c.380G>T (p.Arg127Leu) single nucleotide variant not provided [RCV000801891] Chr11:2133150 [GRCh38]
Chr11:2154380 [GRCh37]
Chr11:11p15.5		 uncertain significance
NC_000011.9:g.(?_532616)_(2906985_?)dup duplication Neuronal ceroid lipofuscinosis [RCV001032557] Chr11:532616..2906985 [GRCh37]
Chr11:11p15.5-15.4		 uncertain significance
GRCh37/hg19 11p15.5-13(chr11:235934-33826995)x3 copy number gain not provided [RCV001006372] Chr11:235934..33826995 [GRCh37]
Chr11:11p15.5-13		 pathogenic
NM_000207.3(INS):c.286T>C (p.Cys96Arg) single nucleotide variant Diabetes mellitus [RCV001175322]|Type 1 diabetes mellitus 2 [RCV003446632] Chr11:2159899 [GRCh38]
Chr11:2181129 [GRCh37]
Chr11:11p15.5		 likely pathogenic|likely risk allele
NM_000207.3(INS):c.155C>T (p.Pro52Leu) single nucleotide variant Maturity-onset diabetes of the young type 10 [RCV001197790] Chr11:2160817 [GRCh38]
Chr11:2182047 [GRCh37]
Chr11:11p15.5		 pathogenic
NM_000612.6(IGF2):c.163C>T (p.Pro55Ser) single nucleotide variant not provided [RCV003234308] Chr11:2133660 [GRCh38]
Chr11:2154890 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.412C>G (p.Arg138Gly) single nucleotide variant not provided [RCV003106383] Chr11:2133118 [GRCh38]
Chr11:2154348 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.100G>A (p.Gly34Ser) single nucleotide variant not provided [RCV001546589]|not specified [RCV002300547] Chr11:2135424 [GRCh38]
Chr11:2156654 [GRCh37]
Chr11:11p15.5		 pathogenic|uncertain significance
NM_001042376.3(INS-IGF2):c.187+1170C>T single nucleotide variant not provided [RCV001675080] Chr11:2159615 [GRCh38]
Chr11:2180845 [GRCh37]
Chr11:11p15.5		 benign
NM_001042376.3(INS-IGF2):c.187+1219G>T single nucleotide variant not provided [RCV001679478] Chr11:2159566 [GRCh38]
Chr11:2180796 [GRCh37]
Chr11:11p15.5		 benign
NM_000612.6(IGF2):c.490C>T (p.Gln164Ter) single nucleotide variant not provided [RCV001559627] Chr11:2133040 [GRCh38]
Chr11:2154270 [GRCh37]
Chr11:11p15.5		 likely pathogenic
NM_000207.3(INS):c.67G>A (p.Ala23Thr) single nucleotide variant Diabetes mellitus type 1 [RCV003446525]|INS-IGF2-related condition [RCV003975771]|Maturity-onset diabetes of the young type 10 [RCV001107550]|Transient Neonatal Diabetes, Dominant/Recessive [RCV001108482]|Type 1 diabetes mellitus 2 [RCV002502686]|not provided [RCV000905000]|not specified [RCV003317399] Chr11:2160905 [GRCh38]
Chr11:2182135 [GRCh37]
Chr11:11p15.5		 benign|likely benign|uncertain significance
NM_001127598.3(IGF2):c.90C>T (p.Thr30=) single nucleotide variant not provided [RCV000886807] Chr11:2140207 [GRCh38]
Chr11:2161437 [GRCh37]
Chr11:11p15.5		 benign
NM_000612.6(IGF2):c.467G>A (p.Arg156His) single nucleotide variant not provided [RCV000886219] Chr11:2133063 [GRCh38]
Chr11:2154293 [GRCh37]
Chr11:11p15.5		 benign
NM_000612.6(IGF2):c.279C>T (p.Asp93=) single nucleotide variant not provided [RCV000932208] Chr11:2133544 [GRCh38]
Chr11:2154774 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000207.3(INS):c.72C>A (p.Ala24=) single nucleotide variant Inborn genetic diseases [RCV002379649]|Maturity-onset diabetes of the young type 10 [RCV001108480]|Neonatal insulin-dependent diabetes mellitus [RCV002464387]|Transient Neonatal Diabetes, Dominant/Recessive [RCV001108481]|not provided [RCV001310941] Chr11:2160900 [GRCh38]
Chr11:2182130 [GRCh37]
Chr11:11p15.5		 likely pathogenic|benign|likely benign
GRCh37/hg19 11p15.5-15.4(chr11:230616-8250724)x3 copy number gain not provided [RCV002472435] Chr11:230616..8250724 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
NM_000207.3(INS):c.153A>C (p.Thr51=) single nucleotide variant Inborn genetic diseases [RCV003164719]|Neonatal insulin-dependent diabetes mellitus [RCV002464670]|not provided [RCV003103170] Chr11:2160819 [GRCh38]
Chr11:2182049 [GRCh37]
Chr11:11p15.5		 benign|likely benign
NM_000207.3(INS):c.188-168G>C single nucleotide variant not provided [RCV001636432] Chr11:2160165 [GRCh38]
Chr11:2181395 [GRCh37]
Chr11:11p15.5		 benign
NM_000207.3(INS):c.188-111C>T single nucleotide variant not provided [RCV001621104] Chr11:2160108 [GRCh38]
Chr11:2181338 [GRCh37]
Chr11:11p15.5		 benign
NM_000207.3(INS):c.187+15C>A single nucleotide variant Maturity-onset diabetes of the young type 10 [RCV001105130]|Transient Neonatal Diabetes, Dominant/Recessive [RCV001105131] Chr11:2160770 [GRCh38]
Chr11:2182000 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.157+3A>C single nucleotide variant Silver-Russell syndrome 3 [RCV001174515] Chr11:2135364 [GRCh38]
Chr11:2156594 [GRCh37]
Chr11:11p15.5		 pathogenic
NM_000612.6(IGF2):c.110_117delinsAGGTAA (p.Leu37fs) indel Silver-Russell syndrome 3 [RCV001174513] Chr11:2135407..2135414 [GRCh38]
Chr11:2156637..2156644 [GRCh37]
Chr11:11p15.5		 pathogenic
NM_000612.6(IGF2):c.101G>A (p.Gly34Asp) single nucleotide variant Silver-Russell syndrome 3 [RCV001174514]|not provided [RCV001558444] Chr11:2135423 [GRCh38]
Chr11:2156653 [GRCh37]
Chr11:11p15.5		 pathogenic
NM_000612.6(IGF2):c.195del (p.Ile66fs) deletion Silver-Russell syndrome 3 [RCV001174516] Chr11:2133628 [GRCh38]
Chr11:2154858 [GRCh37]
Chr11:11p15.5		 pathogenic|likely pathogenic
NM_000207.3(INS):c.-18+38A>G single nucleotide variant not provided [RCV001671434] Chr11:2161130 [GRCh38]
Chr11:2182360 [GRCh37]
Chr11:11p15.5		 benign
NM_000207.3(INS):c.187+282G>A single nucleotide variant not provided [RCV001583353] Chr11:2160503 [GRCh38]
Chr11:2181733 [GRCh37]
Chr11:11p15.5		 likely benign
NM_001042376.3(INS-IGF2):c.187+1243G>A single nucleotide variant not provided [RCV001683934] Chr11:2159542 [GRCh38]
Chr11:2180772 [GRCh37]
Chr11:11p15.5		 benign
NM_000207.3(INS):c.174del (p.Glu59fs) deletion Diabetes mellitus [RCV001172535]|Neonatal insulin-dependent diabetes mellitus [RCV002464402] Chr11:2160798 [GRCh38]
Chr11:2182028 [GRCh37]
Chr11:11p15.5		 likely pathogenic
NM_001042376.3(INS-IGF2):c.337A>C (p.Thr113Pro) single nucleotide variant not provided [RCV001196443] Chr11:2149196 [GRCh38]
Chr11:2170426 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.100G>T (p.Gly34Cys) single nucleotide variant Beckwith-Wiedemann syndrome [RCV002491857]|Silver-Russell syndrome 3 [RCV001253240] Chr11:2135424 [GRCh38]
Chr11:2156654 [GRCh37]
Chr11:11p15.5		 likely pathogenic
NM_000612.6(IGF2):c.27del (p.Met9fs) deletion Silver-Russell syndrome 3 [RCV001253454] Chr11:2135497 [GRCh38]
Chr11:2156727 [GRCh37]
Chr11:11p15.5		 uncertain significance
GRCh37/hg19 11p15.5(chr11:1436158-2321134)x3 copy number gain not provided [RCV001259591] Chr11:1436158..2321134 [GRCh37]
Chr11:11p15.5		 pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:230615-4851537)x3 copy number gain See cases [RCV001263059] Chr11:230615..4851537 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
NM_000612.6(IGF2):c.520_521insC (p.Glu174fs) insertion Colorectal cancer [RCV001293830] Chr11:2133009..2133010 [GRCh38]
Chr11:2154239..2154240 [GRCh37]
Chr11:11p15.5		 pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:210300-8664358)x3 copy number gain Silver-Russell syndrome 1 [RCV001263222] Chr11:210300..8664358 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
NC_000011.9:g.(?_298501)_(4113028_?)dup duplication Early infantile epileptic encephalopathy with suppression bursts [RCV001316682] Chr11:298501..4113028 [GRCh37]
Chr11:11p15.5-15.4		 uncertain significance
NC_000011.9:g.(?_612625)_(2193840_?)dup duplication Autosomal recessive DOPA responsive dystonia [RCV001301561]|Immunodeficiency 39 [RCV001033372] Chr11:612625..2193840 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.2T>C (p.Met1Thr) single nucleotide variant not provided [RCV001366321] Chr11:2135522 [GRCh38]
Chr11:2156752 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.227G>A (p.Ser76Asn) single nucleotide variant Type 1 diabetes mellitus 2 [RCV002468238]|not provided [RCV001355710]|not specified [RCV003388002] Chr11:2159958 [GRCh38]
Chr11:2181188 [GRCh37]
Chr11:11p15.5		 likely benign|uncertain significance
GRCh37/hg19 11p15.5-15.4(chr11:10701-5080415)x2 copy number gain See cases [RCV001310286] Chr11:10701..5080415 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
NM_001127598.3(IGF2):c.162G>C (p.Gln54His) single nucleotide variant not provided [RCV001358206] Chr11:2140135 [GRCh38]
Chr11:2161365 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.227del (p.Asp76fs) deletion not provided [RCV001682665] Chr11:2133596 [GRCh38]
Chr11:2154826 [GRCh37]
Chr11:11p15.5		 likely pathogenic
NM_000207.3(INS):c.115C>T (p.Leu39Phe) single nucleotide variant Maturity-onset diabetes of the young type 10 [RCV002466269] Chr11:2160857 [GRCh38]
Chr11:2182087 [GRCh37]
Chr11:11p15.5		 likely pathogenic
NM_001007139.6(IGF2):c.-248-73= single nucleotide variant INSULIN-LIKE GROWTH FACTOR II POLYMORPHISM [RCV000015870] Chr11:2147880 [GRCh38]
Chr11:2169110 [GRCh37]
Chr11:11p15.5		 benign
NM_001127598.3(IGF2):c.34G>C (p.Ala12Pro) single nucleotide variant not provided [RCV001764851] Chr11:2140263 [GRCh38]
Chr11:2161493 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.199G>A (p.Val67Ile) single nucleotide variant Silver-Russell syndrome 3 [RCV001797006] Chr11:2133624 [GRCh38]
Chr11:2154854 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.95G>T (p.Gly32Val) single nucleotide variant not provided [RCV001817993] Chr11:2160877 [GRCh38]
Chr11:2182107 [GRCh37]
Chr11:11p15.5		 likely pathogenic
NM_000207.3(INS):c.103C>G (p.Leu35Val) single nucleotide variant not provided [RCV001818011] Chr11:2160869 [GRCh38]
Chr11:2182099 [GRCh37]
Chr11:11p15.5		 likely pathogenic
NM_000207.3(INS):c.188-97C>T single nucleotide variant not specified [RCV001819672] Chr11:2160094 [GRCh38]
Chr11:2181324 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.187+203G>A single nucleotide variant not specified [RCV001820302] Chr11:2160582 [GRCh38]
Chr11:2181812 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000207.3(INS):c.147C>T (p.Phe49=) single nucleotide variant Hyperproinsulinemia [RCV003446922]|not specified [RCV001820450] Chr11:2160825 [GRCh38]
Chr11:2182055 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.188-114G>T single nucleotide variant not specified [RCV001820595] Chr11:2160111 [GRCh38]
Chr11:2181341 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000207.3(INS):c.289A>C (p.Thr97Pro) single nucleotide variant not provided [RCV001817442] Chr11:2159896 [GRCh38]
Chr11:2181126 [GRCh37]
Chr11:11p15.5		 likely pathogenic
NM_000207.3(INS):c.-46A>G single nucleotide variant not specified [RCV001817613] Chr11:2161196 [GRCh38]
Chr11:2182426 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.187+271A>G single nucleotide variant not specified [RCV001819172] Chr11:2160514 [GRCh38]
Chr11:2181744 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.-17-74T>C single nucleotide variant not specified [RCV001819252] Chr11:2161062 [GRCh38]
Chr11:2182292 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.188-233C>T single nucleotide variant not specified [RCV001819551] Chr11:2160230 [GRCh38]
Chr11:2181460 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.188-137A>T single nucleotide variant not specified [RCV001820699] Chr11:2160134 [GRCh38]
Chr11:2181364 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.1A>G (p.Met1Val) single nucleotide variant Type 1 diabetes mellitus 2 [RCV002492128]|not provided [RCV001946765] Chr11:2160971 [GRCh38]
Chr11:2182201 [GRCh37]
Chr11:11p15.5		 pathogenic|likely pathogenic
NM_000612.6(IGF2):c.212G>A (p.Cys71Tyr) single nucleotide variant not provided [RCV001913774] Chr11:2133611 [GRCh38]
Chr11:2154841 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.293G>T (p.Ser98Ile) single nucleotide variant Neonatal diabetes mellitus [RCV002052029] Chr11:2159892 [GRCh38]
Chr11:2181122 [GRCh37]
Chr11:11p15.5		 likely pathogenic
NM_000207.3(INS):c.103C>A (p.Leu35Met) single nucleotide variant Neonatal diabetes mellitus [RCV002052033] Chr11:2160869 [GRCh38]
Chr11:2182099 [GRCh37]
Chr11:11p15.5		 likely pathogenic
NM_000612.6(IGF2):c.257C>A (p.Thr86Asn) single nucleotide variant not provided [RCV001912975] Chr11:2133566 [GRCh38]
Chr11:2154796 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.101A>C (p.His34Pro) single nucleotide variant Neonatal diabetes mellitus [RCV002052032] Chr11:2160871 [GRCh38]
Chr11:2182101 [GRCh37]
Chr11:11p15.5		 likely pathogenic
NM_000207.3(INS):c.322T>G (p.Tyr108Asp) single nucleotide variant Neonatal diabetes mellitus [RCV002052030] Chr11:2159863 [GRCh38]
Chr11:2181093 [GRCh37]
Chr11:11p15.5		 likely pathogenic
NM_000207.3(INS):c.326G>T (p.Cys109Phe) single nucleotide variant Neonatal diabetes mellitus [RCV002052031] Chr11:2159859 [GRCh38]
Chr11:2181089 [GRCh37]
Chr11:11p15.5		 likely pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:230615-5525355)x3 copy number gain not provided [RCV001825269] Chr11:230615..5525355 [GRCh37]
Chr11:11p15.5-15.4		 not provided
GRCh37/hg19 11p15.5(chr11:1719815-2321109)x3 copy number gain not provided [RCV001827983] Chr11:1719815..2321109 [GRCh37]
Chr11:11p15.5		 likely pathogenic
NM_000612.6(IGF2):c.59C>T (p.Ser20Leu) single nucleotide variant not provided [RCV001951905] Chr11:2135465 [GRCh38]
Chr11:2156695 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.245C>T (p.Thr82Met) single nucleotide variant not provided [RCV001999531] Chr11:2133578 [GRCh38]
Chr11:2154808 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.91T>G (p.Cys31Gly) single nucleotide variant not provided [RCV001864754] Chr11:2160881 [GRCh38]
Chr11:2182111 [GRCh37]
Chr11:11p15.5		 uncertain significance
NC_000011.9:g.(?_2181023)_(2182533_?)del deletion not provided [RCV001963196] Chr11:2181023..2182533 [GRCh37]
Chr11:11p15.5		 pathogenic
NC_000011.9:g.(?_2181023)_(2193087_?)del deletion Autosomal recessive DOPA responsive dystonia [RCV001972592] Chr11:2181023..2193087 [GRCh37]
Chr11:11p15.5		 pathogenic
NM_000612.6(IGF2):c.466C>T (p.Arg156Cys) single nucleotide variant Inborn genetic diseases [RCV002545884]|not provided [RCV001904487] Chr11:2133064 [GRCh38]
Chr11:2154294 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.190C>T (p.Arg64Cys) single nucleotide variant not provided [RCV001998666] Chr11:2133633 [GRCh38]
Chr11:2154863 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.307-3C>T single nucleotide variant not provided [RCV001900294] Chr11:2133226 [GRCh38]
Chr11:2154456 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.504C>T (p.His168=) single nucleotide variant not provided [RCV002129892] Chr11:2133026 [GRCh38]
Chr11:2154256 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.59C>A (p.Ser20Ter) single nucleotide variant Silver-Russell syndrome 3 [RCV002226891] Chr11:2135465 [GRCh38]
Chr11:2156695 [GRCh37]
Chr11:11p15.5		 likely pathogenic
NM_000207.3(INS):c.155C>A (p.Pro52His) single nucleotide variant Maturity-onset diabetes of the young type 10 [RCV002225237] Chr11:2160817 [GRCh38]
Chr11:2182047 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.438C>A (p.Leu146=) single nucleotide variant not provided [RCV002126713] Chr11:2133092 [GRCh38]
Chr11:2154322 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.30G>A (p.Leu10=) single nucleotide variant not provided [RCV002149812] Chr11:2135494 [GRCh38]
Chr11:2156724 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.270C>T (p.Ser90=) single nucleotide variant not provided [RCV002117652] Chr11:2133553 [GRCh38]
Chr11:2154783 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.441G>A (p.Glu147=) single nucleotide variant not provided [RCV002122753] Chr11:2133089 [GRCh38]
Chr11:2154319 [GRCh37]
Chr11:11p15.5		 benign
NM_000612.6(IGF2):c.303T>C (p.Leu101=) single nucleotide variant not provided [RCV002155588] Chr11:2133520 [GRCh38]
Chr11:2154750 [GRCh37]
Chr11:11p15.5		 likely benign
NC_000011.9:g.(?_1278740)_(2906719_?)dup duplication Autosomal recessive DOPA responsive dystonia [RCV003113999] Chr11:1278740..2906719 [GRCh37]
Chr11:11p15.5-15.4		 uncertain significance
NC_000011.9:g.(?_721044)_(3988932_?)dup duplication not provided [RCV003113442] Chr11:721044..3988932 [GRCh37]
Chr11:11p15.5-15.4		 uncertain significance
NM_000207.3(INS):c.188-5_188-4insGCGCAGTGGGGCACCTGCCACTGCGC microsatellite not provided [RCV003120429] Chr11:2160001..2160002 [GRCh38]
Chr11:2181231..2181232 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.106G>T (p.Glu36Ter) single nucleotide variant See cases [RCV003156171]|not provided [RCV003689044] Chr11:2135418 [GRCh38]
Chr11:2156648 [GRCh37]
Chr11:11p15.5		 pathogenic|likely pathogenic
NM_000207.3(INS):c.187+391C>T single nucleotide variant not specified [RCV003151541] Chr11:2160394 [GRCh38]
Chr11:2181624 [GRCh37]
Chr11:11p15.5		 likely benign
GRCh37/hg19 11p15.5-14.2(chr11:230615-26881146)x3 copy number gain See cases [RCV002286351] Chr11:230615..26881146 [GRCh37]
Chr11:11p15.5-14.2		 pathogenic
GRCh37/hg19 11p15.5(chr11:1621232-2228572) copy number gain Beckwith-Wiedemann syndrome [RCV002280763] Chr11:1621232..2228572 [GRCh37]
Chr11:11p15.5		 pathogenic
NC_000011.10:g.(499700_4999400)_(5279346_5279697)del deletion Thalassemia, gamma-delta-beta [RCV000015529] Chr11:4999400..5279346 [GRCh38]
Chr11:11p15.5-15.4		 pathogenic
NM_000612.6(IGF2):c.-6-2A>T single nucleotide variant Silver-Russell syndrome 3 [RCV002290217] Chr11:2135531 [GRCh38]
Chr11:2156761 [GRCh37]
Chr11:11p15.5		 pathogenic
NM_000207.3(INS):c.299G>A (p.Cys100Tyr) single nucleotide variant not provided [RCV003151542] Chr11:2159886 [GRCh38]
Chr11:2181116 [GRCh37]
Chr11:11p15.5		 likely pathogenic|uncertain significance
NM_001042376.3(INS-IGF2):c.584C>G (p.Pro195Arg) single nucleotide variant Inborn genetic diseases [RCV002902078] Chr11:2147631 [GRCh38]
Chr11:2168861 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.155C>G (p.Pro52Arg) single nucleotide variant Neonatal insulin-dependent diabetes mellitus [RCV002464669] Chr11:2160817 [GRCh38]
Chr11:2182047 [GRCh37]
Chr11:11p15.5		 likely pathogenic
GRCh37/hg19 11p15.5(chr11:461373-2157956)x4 copy number gain not provided [RCV002473945] Chr11:461373..2157956 [GRCh37]
Chr11:11p15.5		 pathogenic
NM_000207.3(INS):c.187+15C>T single nucleotide variant Neonatal insulin-dependent diabetes mellitus [RCV002464667] Chr11:2160770 [GRCh38]
Chr11:2182000 [GRCh37]
Chr11:11p15.5		 benign
NM_000207.3(INS):c.150C>T (p.Tyr50=) single nucleotide variant Inborn genetic diseases [RCV002390080] Chr11:2160822 [GRCh38]
Chr11:2182052 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000207.3(INS):c.212G>C (p.Gly71Ala) single nucleotide variant not provided [RCV002299561] Chr11:2159973 [GRCh38]
Chr11:2181203 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.29T>A (p.Leu10Gln) single nucleotide variant not provided [RCV002301356] Chr11:2160943 [GRCh38]
Chr11:2182173 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.518C>T (p.Pro173Leu) single nucleotide variant Inborn genetic diseases [RCV002902872] Chr11:2133012 [GRCh38]
Chr11:2154242 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.439G>A (p.Glu147Lys) single nucleotide variant not provided [RCV002614973] Chr11:2133091 [GRCh38]
Chr11:2154321 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.416G>T (p.Gly139Val) single nucleotide variant not provided [RCV002617075] Chr11:2133114 [GRCh38]
Chr11:2154344 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.386G>T (p.Gly129Val) single nucleotide variant not provided [RCV002726247] Chr11:2133144 [GRCh38]
Chr11:2154374 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.48C>G (p.Leu16=) single nucleotide variant not provided [RCV002615196] Chr11:2160924 [GRCh38]
Chr11:2182154 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.138G>T (p.Gly46=) single nucleotide variant not provided [RCV002975453] Chr11:2135386 [GRCh38]
Chr11:2156616 [GRCh37]
Chr11:11p15.5		 likely benign
NM_001042376.3(INS-IGF2):c.460C>G (p.Gln154Glu) single nucleotide variant Inborn genetic diseases [RCV002733781] Chr11:2147755 [GRCh38]
Chr11:2168985 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.503A>C (p.His168Pro) single nucleotide variant Inborn genetic diseases [RCV002974670] Chr11:2133027 [GRCh38]
Chr11:2154257 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.505G>C (p.Gly169Arg) single nucleotide variant Inborn genetic diseases [RCV002990301] Chr11:2133025 [GRCh38]
Chr11:2154255 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.21G>T (p.Lys7Asn) single nucleotide variant Inborn genetic diseases [RCV002991980]|not provided [RCV003561147] Chr11:2135503 [GRCh38]
Chr11:2156733 [GRCh37]
Chr11:11p15.5		 likely benign|uncertain significance
NM_001042376.3(INS-IGF2):c.325A>G (p.Arg109Gly) single nucleotide variant Inborn genetic diseases [RCV002859926] Chr11:2149208 [GRCh38]
Chr11:2170438 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.158-20_158-17del deletion not provided [RCV003033828] Chr11:2133682..2133685 [GRCh38]
Chr11:2154912..2154915 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.78C>T (p.Tyr26=) single nucleotide variant not provided [RCV003020758] Chr11:2135446 [GRCh38]
Chr11:2156676 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.100G>C (p.Gly34Arg) single nucleotide variant Inborn genetic diseases [RCV002692236] Chr11:2135424 [GRCh38]
Chr11:2156654 [GRCh37]
Chr11:11p15.5		 pathogenic
NM_000612.6(IGF2):c.-2C>G single nucleotide variant Inborn genetic diseases [RCV002844249] Chr11:2135525 [GRCh38]
Chr11:2156755 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.158-19T>A single nucleotide variant not provided [RCV002706066] Chr11:2133684 [GRCh38]
Chr11:2154914 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.495C>G (p.Asp165Glu) single nucleotide variant Inborn genetic diseases [RCV003008914]|not provided [RCV002999304] Chr11:2133035 [GRCh38]
Chr11:2154265 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.439G>C (p.Glu147Gln) single nucleotide variant not provided [RCV002591496] Chr11:2133091 [GRCh38]
Chr11:2154321 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.277G>A (p.Glu93Lys) single nucleotide variant not provided [RCV003079117] Chr11:2159908 [GRCh38]
Chr11:2181138 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.306G>A (p.Pro102=) single nucleotide variant not provided [RCV002736751] Chr11:2133517 [GRCh38]
Chr11:2154747 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.505G>T (p.Gly169Trp) single nucleotide variant Inborn genetic diseases [RCV002765117]|not provided [RCV003778646] Chr11:2133025 [GRCh38]
Chr11:2154255 [GRCh37]
Chr11:11p15.5		 likely benign|uncertain significance
NM_000612.6(IGF2):c.89_98del (p.Glu30fs) deletion not provided [RCV003058118] Chr11:2135426..2135435 [GRCh38]
Chr11:2156656..2156665 [GRCh37]
Chr11:11p15.5		 pathogenic
NM_000612.6(IGF2):c.285G>A (p.Ser95=) single nucleotide variant not provided [RCV002572333] Chr11:2133538 [GRCh38]
Chr11:2154768 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.99C>T (p.Cys33=) single nucleotide variant IGF2-related condition [RCV003916512]|not provided [RCV002700316] Chr11:2135425 [GRCh38]
Chr11:2156655 [GRCh37]
Chr11:11p15.5		 likely benign
NM_001042376.3(INS-IGF2):c.410G>A (p.Gly137Asp) single nucleotide variant Inborn genetic diseases [RCV002919305] Chr11:2147805 [GRCh38]
Chr11:2169035 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.207C>T (p.Gly69=) single nucleotide variant not provided [RCV002932985] Chr11:2159978 [GRCh38]
Chr11:2181208 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000207.3(INS):c.194A>G (p.Gln65Arg) single nucleotide variant not provided [RCV002663811] Chr11:2159991 [GRCh38]
Chr11:2181221 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_001042376.3(INS-IGF2):c.352G>C (p.Val118Leu) single nucleotide variant Inborn genetic diseases [RCV002792362] Chr11:2149181 [GRCh38]
Chr11:2170411 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.52G>C (p.Gly18Arg) single nucleotide variant Inborn genetic diseases [RCV002896662] Chr11:2160920 [GRCh38]
Chr11:2182150 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.144C>T (p.Arg48=) single nucleotide variant not provided [RCV002770478] Chr11:2135380 [GRCh38]
Chr11:2156610 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000207.3(INS):c.145T>C (p.Phe49Leu) single nucleotide variant Inborn genetic diseases [RCV002836176] Chr11:2160827 [GRCh38]
Chr11:2182057 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.370C>G (p.Gln124Glu) single nucleotide variant not provided [RCV003046015] Chr11:2133160 [GRCh38]
Chr11:2154390 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.20A>C (p.Lys7Thr) single nucleotide variant not provided [RCV002632007] Chr11:2135504 [GRCh38]
Chr11:2156734 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_001042376.3(INS-IGF2):c.212C>G (p.Ser71Cys) single nucleotide variant Inborn genetic diseases [RCV002807912] Chr11:2149321 [GRCh38]
Chr11:2170551 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.165C>T (p.Pro55=) single nucleotide variant not provided [RCV002581329] Chr11:2133658 [GRCh38]
Chr11:2154888 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.499G>T (p.Ala167Ser) single nucleotide variant Inborn genetic diseases [RCV002678469]|not provided [RCV003777635] Chr11:2133031 [GRCh38]
Chr11:2154261 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.421G>A (p.Val141Met) single nucleotide variant IGF2-related condition [RCV003409983]|not provided [RCV002943193] Chr11:2133109 [GRCh38]
Chr11:2154339 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.106del (p.Glu36fs) deletion Silver-Russell syndrome 3 [RCV003148454] Chr11:2135418 [GRCh38]
Chr11:2156648 [GRCh37]
Chr11:11p15.5		 likely pathogenic
NM_000612.6(IGF2):c.157+18G>C single nucleotide variant not provided [RCV002587650] Chr11:2135349 [GRCh38]
Chr11:2156579 [GRCh37]
Chr11:11p15.5		 benign
NM_000612.6(IGF2):c.157+15G>C single nucleotide variant not provided [RCV002585805] Chr11:2135352 [GRCh38]
Chr11:2156582 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000207.3(INS):c.188-11C>T single nucleotide variant not provided [RCV002586023] Chr11:2160008 [GRCh38]
Chr11:2181238 [GRCh37]
Chr11:11p15.5		 benign
NM_000612.6(IGF2):c.243_244del (p.Glu81fs) microsatellite Silver-Russell syndrome 3 [RCV003223520] Chr11:2133579..2133580 [GRCh38]
Chr11:2154809..2154810 [GRCh37]
Chr11:11p15.5		 pathogenic
NM_000612.6(IGF2):c.10C>G (p.Pro4Ala) single nucleotide variant Inborn genetic diseases [RCV003208516] Chr11:2135514 [GRCh38]
Chr11:2156744 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.357G>A (p.Trp119Ter) single nucleotide variant Silver-Russell syndrome 3 [RCV003228775] Chr11:2133173 [GRCh38]
Chr11:2154403 [GRCh37]
Chr11:11p15.5		 likely pathogenic
NM_001042376.3(INS-IGF2):c.427G>A (p.Glu143Lys) single nucleotide variant Inborn genetic diseases [RCV003345216] Chr11:2147788 [GRCh38]
Chr11:2169018 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.412C>T (p.Arg138Trp) single nucleotide variant Inborn genetic diseases [RCV003370126] Chr11:2133118 [GRCh38]
Chr11:2154348 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.232G>A (p.Ala78Thr) single nucleotide variant not specified [RCV003479820] Chr11:2133591 [GRCh38]
Chr11:2154821 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.104T>A (p.Leu35Gln) single nucleotide variant Diabetes mellitus, permanent neonatal 4 [RCV003445452] Chr11:2160868 [GRCh38]
Chr11:2182098 [GRCh37]
Chr11:11p15.5		 likely risk allele
NM_000207.3(INS):c.284G>A (p.Cys95Tyr) single nucleotide variant INS-related condition [RCV003404625] Chr11:2159901 [GRCh38]
Chr11:2181131 [GRCh37]
Chr11:11p15.5		 likely pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:192764-3362853)x3 copy number gain not provided [RCV003484828] Chr11:192764..3362853 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
NM_000612.6(IGF2):c.-6-2A>G single nucleotide variant Silver-Russell syndrome 3 [RCV003479529] Chr11:2135531 [GRCh38]
Chr11:2156761 [GRCh37]
Chr11:11p15.5		 pathogenic
NM_000612.6(IGF2):c.157+5G>A single nucleotide variant IGF2-related condition [RCV003394389] Chr11:2135362 [GRCh38]
Chr11:2156592 [GRCh37]
Chr11:11p15.5		 pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:230615-8821443)x3 copy number gain Russell-Silver syndrome [RCV003444025] Chr11:230615..8821443 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
NM_000207.3(INS):c.136C>T (p.Arg46Ter) single nucleotide variant INS-related condition [RCV003402304] Chr11:2160836 [GRCh38]
Chr11:2182066 [GRCh37]
Chr11:11p15.5		 likely pathogenic
NM_001042376.3(INS-IGF2):c.378T>G (p.Ala126=) single nucleotide variant not provided [RCV003424765] Chr11:2149155 [GRCh38]
Chr11:2170385 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000207.3(INS):c.206G>A (p.Gly69Asp) single nucleotide variant INS-related condition [RCV003410744] Chr11:2159979 [GRCh38]
Chr11:2181209 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.188-43C>T single nucleotide variant INS-related condition [RCV003402474] Chr11:2160040 [GRCh38]
Chr11:2181270 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.157+8G>C single nucleotide variant not provided [RCV003713113] Chr11:2135359 [GRCh38]
Chr11:2156589 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000207.3(INS):c.249G>A (p.Glu83=) single nucleotide variant not provided [RCV003714122] Chr11:2159936 [GRCh38]
Chr11:2181166 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.5G>A (p.Gly2Glu) single nucleotide variant not provided [RCV003849215] Chr11:2135519 [GRCh38]
Chr11:2156749 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.79C>T (p.Arg27Cys) single nucleotide variant not provided [RCV003696281] Chr11:2135445 [GRCh38]
Chr11:2156675 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.272T>C (p.Ile91Thr) single nucleotide variant not provided [RCV003696448] Chr11:2159913 [GRCh38]
Chr11:2181143 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.188-17G>A single nucleotide variant INS-related condition [RCV003956628]|not provided [RCV003877566] Chr11:2160014 [GRCh38]
Chr11:2181244 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.94C>T (p.Leu32=) single nucleotide variant not provided [RCV003829164] Chr11:2135430 [GRCh38]
Chr11:2156660 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000207.3(INS):c.316_318del (p.Glu106del) deletion not provided [RCV003544059] Chr11:2159867..2159869 [GRCh38]
Chr11:2181097..2181099 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.517C>T (p.Pro173Ser) single nucleotide variant not provided [RCV003882429] Chr11:2133013 [GRCh38]
Chr11:2154243 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.54C>T (p.Phe18=) single nucleotide variant not provided [RCV003779174] Chr11:2135470 [GRCh38]
Chr11:2156700 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.217C>T (p.Arg73Cys) single nucleotide variant not provided [RCV003573305] Chr11:2133606 [GRCh38]
Chr11:2154836 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.317A>T (p.Glu106Val) single nucleotide variant not provided [RCV003699875] Chr11:2159868 [GRCh38]
Chr11:2181098 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.305C>T (p.Pro102Leu) single nucleotide variant not provided [RCV003717061] Chr11:2133518 [GRCh38]
Chr11:2154748 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.15G>A (p.Met5Ile) single nucleotide variant not provided [RCV003814060] Chr11:2160957 [GRCh38]
Chr11:2182187 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.438C>T (p.Leu146=) single nucleotide variant not provided [RCV003724892] Chr11:2133092 [GRCh38]
Chr11:2154322 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.307-11T>G single nucleotide variant not provided [RCV003700947] Chr11:2133234 [GRCh38]
Chr11:2154464 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.318C>T (p.Pro106=) single nucleotide variant not provided [RCV003702596] Chr11:2133212 [GRCh38]
Chr11:2154442 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.145G>A (p.Gly49Ser) single nucleotide variant not provided [RCV003671201] Chr11:2135379 [GRCh38]
Chr11:2156609 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.158-20C>A single nucleotide variant not provided [RCV003814468] Chr11:2133685 [GRCh38]
Chr11:2154915 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.460C>T (p.Arg154Cys) single nucleotide variant not provided [RCV003816268] Chr11:2133070 [GRCh38]
Chr11:2154300 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.198C>T (p.Ile66=) single nucleotide variant not provided [RCV003822229] Chr11:2133625 [GRCh38]
Chr11:2154855 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.418C>T (p.His140Tyr) single nucleotide variant not provided [RCV003682273] Chr11:2133112 [GRCh38]
Chr11:2154342 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.403C>T (p.Arg135Cys) single nucleotide variant not provided [RCV003709789] Chr11:2133127 [GRCh38]
Chr11:2154357 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.321A>C (p.Arg107Ser) single nucleotide variant not provided [RCV003867389] Chr11:2133209 [GRCh38]
Chr11:2154439 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.166G>A (p.Ala56Thr) single nucleotide variant not provided [RCV003722734] Chr11:2133657 [GRCh38]
Chr11:2154887 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000612.6(IGF2):c.372G>A (p.Gln124=) single nucleotide variant not provided [RCV003711544] Chr11:2133158 [GRCh38]
Chr11:2154388 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.420C>T (p.His140=) single nucleotide variant not provided [RCV003821778] Chr11:2133110 [GRCh38]
Chr11:2154340 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.293C>T (p.Pro98Leu) single nucleotide variant not provided [RCV003730990] Chr11:2133530 [GRCh38]
Chr11:2154760 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.187+245C>T single nucleotide variant INS-related condition [RCV003912109] Chr11:2160540 [GRCh38]
Chr11:2181770 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000207.3(INS):c.224G>A (p.Gly75Asp) single nucleotide variant INS-related condition [RCV003911619] Chr11:2159961 [GRCh38]
Chr11:2181191 [GRCh37]
Chr11:11p15.5		 likely benign
NM_001127598.3(IGF2):c.39C>G (p.Pro13=) single nucleotide variant IGF2-related condition [RCV003974049] Chr11:2140258 [GRCh38]
Chr11:2161488 [GRCh37]
Chr11:11p15.5		 benign
NM_000612.6(IGF2):c.14T>A (p.Met5Lys) single nucleotide variant IGF2-related condition [RCV003919492] Chr11:2135510 [GRCh38]
Chr11:2156740 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.188-40C>T single nucleotide variant INS-related condition [RCV003969846] Chr11:2160037 [GRCh38]
Chr11:2181267 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.513C>A (p.Ala171=) single nucleotide variant not specified [RCV003988233] Chr11:2133017 [GRCh38]
Chr11:2154247 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000207.3(INS):c.6C>T (p.Ala2=) single nucleotide variant INS-IGF2-related condition [RCV003927026] Chr11:2160966 [GRCh38]
Chr11:2182196 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000207.3(INS):c.279A>G (p.Glu93=) single nucleotide variant INS-related condition [RCV003897200] Chr11:2159906 [GRCh38]
Chr11:2181136 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.521A>C (p.Glu174Ala) single nucleotide variant IGF2-related condition [RCV003982701] Chr11:2133009 [GRCh38]
Chr11:2154239 [GRCh37]
Chr11:11p15.5		 uncertain significance
NM_000207.3(INS):c.*49G>A single nucleotide variant INS-related condition [RCV003896636] Chr11:2159803 [GRCh38]
Chr11:2181033 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000207.3(INS):c.187+6C>G single nucleotide variant INS-related condition [RCV003904735] Chr11:2160779 [GRCh38]
Chr11:2182009 [GRCh37]
Chr11:11p15.5		 likely benign
NM_000612.6(IGF2):c.181C>T (p.Arg61Cys) single nucleotide variant IGF2-related condition [RCV003976354] Chr11:2133642 [GRCh38]
Chr11:2154872 [GRCh37]
Chr11:11p15.5		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1307
Count of miRNA genes:739
Interacting mature miRNAs:847
Transcripts:ENST00000356578, ENST00000397270, ENST00000476874, ENST00000481781
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

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

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

Markers in Region
A002D21  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,150,384 - 2,150,510UniSTSGRCh37
Build 36112,106,960 - 2,107,086RGDNCBI36
Celera112,186,875 - 2,187,001RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,940,906 - 1,941,032UniSTS
GeneMap99-GB4 RH Map1122.72UniSTS
NCBI RH Map1110.0UniSTS
RH75852  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,180,859 - 2,181,047UniSTSGRCh37
Build 36112,137,435 - 2,137,623RGDNCBI36
Celera112,217,366 - 2,217,554RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,971,122 - 1,971,310UniSTS
RH71336  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,174,171 - 2,174,308UniSTSGRCh37
Build 36112,130,747 - 2,130,884RGDNCBI36
Celera112,210,678 - 2,210,815RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,964,433 - 1,964,570UniSTS
G44328  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,153,571 - 2,153,745UniSTSGRCh37
Build 36112,110,147 - 2,110,321RGDNCBI36
Celera112,190,077 - 2,190,251RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,944,104 - 1,944,278UniSTS
G44339  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,182,114 - 2,182,330UniSTSGRCh37
Build 36112,138,690 - 2,138,906RGDNCBI36
Celera112,218,621 - 2,218,837RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,972,377 - 1,972,593UniSTS
D11S4734  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,170,382 - 2,170,562UniSTSGRCh37
Build 36112,126,958 - 2,127,138RGDNCBI36
Celera112,206,887 - 2,207,067RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,960,644 - 1,960,824UniSTS
GDB:179433  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,181,009 - 2,181,227UniSTSGRCh37
Build 36112,137,585 - 2,137,803RGDNCBI36
Celera112,217,516 - 2,217,734RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,971,272 - 1,971,490UniSTS
GDB:180498  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,180,933 - 2,181,153UniSTSGRCh37
Build 36112,137,509 - 2,137,729RGDNCBI36
Celera112,217,440 - 2,217,660RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,971,196 - 1,971,416UniSTS
GDB:181496  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,182,075 - 2,182,424UniSTSGRCh37
Build 36112,138,651 - 2,139,000RGDNCBI36
Celera112,218,582 - 2,218,931RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,972,338 - 1,972,687UniSTS
GDB:187027  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,153,461 - 2,153,696UniSTSGRCh37
Build 36112,110,037 - 2,110,272RGDNCBI36
Celera112,189,967 - 2,190,202RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,943,994 - 1,944,229UniSTS
GDB:197907  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,181,278 - 2,181,717UniSTSGRCh37
Build 36112,137,854 - 2,138,293RGDNCBI36
Celera112,217,785 - 2,218,224RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,971,541 - 1,971,980UniSTS
GDB:316225  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,182,617 - 2,183,430UniSTSGRCh37
Build 36112,139,193 - 2,140,006RGDNCBI36
Celera112,219,124 - 2,220,023RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,972,880 - 1,973,695UniSTS
GDB:438178  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,153,402 - 2,153,696UniSTSGRCh37
Build 36112,109,978 - 2,110,272RGDNCBI36
Celera112,189,908 - 2,190,202RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,943,935 - 1,944,229UniSTS
GDB:572840  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,153,405 - 2,153,696UniSTSGRCh37
Build 36112,109,981 - 2,110,272RGDNCBI36
Celera112,189,911 - 2,190,202RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,943,938 - 1,944,229UniSTS
IGF2  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,169,615 - 2,170,122UniSTSGRCh37
GRCh37112,152,567 - 2,153,356UniSTSGRCh37
Build 36112,126,191 - 2,126,698RGDNCBI36
Celera112,189,058 - 2,189,862UniSTS
Celera112,206,120 - 2,206,627RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,959,877 - 1,960,384UniSTS
HuRef111,943,089 - 1,943,889UniSTS
GeneMap99-GB4 RH Map1116.42UniSTS
NCBI RH Map1110.0UniSTS
STS-H87011  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,151,578 - 2,151,797UniSTSGRCh37
Build 36112,108,154 - 2,108,373RGDNCBI36
Celera112,188,069 - 2,188,288RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,942,100 - 1,942,319UniSTS
GeneMap99-GB4 RH Map1118.93UniSTS
NCBI RH Map1110.0UniSTS
PMC124986P1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,152,579 - 2,153,378UniSTSGRCh37
Build 36112,109,155 - 2,109,954RGDNCBI36
Celera112,189,070 - 2,189,884RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,943,101 - 1,943,911UniSTS
PMC151856P1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,154,415 - 2,154,823UniSTSGRCh37
Build 36112,110,991 - 2,111,399RGDNCBI36
Celera112,190,921 - 2,191,329RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,944,948 - 1,945,356UniSTS
PMC151856P2  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,153,961 - 2,154,293UniSTSGRCh37
Build 36112,110,537 - 2,110,869RGDNCBI36
Celera112,190,467 - 2,190,799RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,944,494 - 1,944,826UniSTS
PMC21842P3  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,153,466 - 2,153,696UniSTSGRCh37
Build 36112,110,042 - 2,110,272RGDNCBI36
Celera112,189,972 - 2,190,202RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,943,999 - 1,944,229UniSTS
ECD00261  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,157,224 - 2,158,142UniSTSGRCh37
Build 36112,113,800 - 2,114,718RGDNCBI36
Celera112,193,731 - 2,194,649RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,947,745 - 1,948,663UniSTS
ECD00298  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,156,257 - 2,157,173UniSTSGRCh37
Build 36112,112,833 - 2,113,749RGDNCBI36
Celera112,192,763 - 2,193,680RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,946,778 - 1,947,694UniSTS
ECD00602  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,155,340 - 2,156,238UniSTSGRCh37
Build 36112,111,916 - 2,112,814RGDNCBI36
Celera112,191,846 - 2,192,744RGD
Cytogenetic Map11p15.5UniSTS
ECD00816  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,178,167 - 2,179,056UniSTSGRCh37
Build 36112,134,743 - 2,135,632RGDNCBI36
Celera112,214,674 - 2,215,563RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,968,430 - 1,969,319UniSTS
ECD00845  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,176,262 - 2,177,150UniSTSGRCh37
Build 36112,132,838 - 2,133,726RGDNCBI36
Celera112,212,769 - 2,213,657RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,966,524 - 1,967,413UniSTS
ECD00988  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,153,402 - 2,154,284UniSTSGRCh37
Build 36112,109,978 - 2,110,860RGDNCBI36
Celera112,189,908 - 2,190,790RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,943,935 - 1,944,817UniSTS
ECD00989  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,180,053 - 2,180,935UniSTSGRCh37
Build 36112,136,629 - 2,137,511RGDNCBI36
Celera112,216,560 - 2,217,442RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,970,316 - 1,971,198UniSTS
ECD01506  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,179,088 - 2,179,951UniSTSGRCh37
Build 36112,135,664 - 2,136,527RGDNCBI36
Celera112,215,595 - 2,216,458RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,969,351 - 1,970,214UniSTS
ECD01671  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,177,201 - 2,178,058UniSTSGRCh37
Build 36112,133,777 - 2,134,634RGDNCBI36
Celera112,213,708 - 2,214,565RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,967,464 - 1,968,321UniSTS
ECD01816  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,175,359 - 2,176,211UniSTSGRCh37
Build 36112,131,935 - 2,132,787RGDNCBI36
Celera112,211,866 - 2,212,718RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,965,621 - 1,966,473UniSTS
ECD01817  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,181,008 - 2,181,860UniSTSGRCh37
Build 36112,137,584 - 2,138,436RGDNCBI36
Celera112,217,515 - 2,218,367RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,971,271 - 1,972,123UniSTS
ECD02194  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,169,406 - 2,170,244UniSTSGRCh37
Build 36112,125,982 - 2,126,820RGDNCBI36
Celera112,205,911 - 2,206,749RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,959,668 - 1,960,506UniSTS
ECD02732  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,171,990 - 2,172,809UniSTSGRCh37
Build 36112,128,566 - 2,129,385RGDNCBI36
Celera112,208,497 - 2,209,316RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,962,252 - 1,963,071UniSTS
ECD02763  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,166,711 - 2,167,529UniSTSGRCh37
Build 36112,123,287 - 2,124,105RGDNCBI36
Celera112,203,216 - 2,204,034RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,956,973 - 1,957,791UniSTS
ECD02927  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,170,293 - 2,171,105UniSTSGRCh37
Build 36112,126,869 - 2,127,681RGDNCBI36
Celera112,206,798 - 2,207,612RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,960,555 - 1,961,367UniSTS
ECD02954  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,163,166 - 2,163,977UniSTSGRCh37
Build 36112,119,742 - 2,120,553RGDNCBI36
Celera112,199,673 - 2,200,484RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,953,430 - 1,954,241UniSTS
ECD03070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,164,000 - 2,164,807UniSTSGRCh37
Build 36112,120,576 - 2,121,383RGDNCBI36
Celera112,200,507 - 2,201,314RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,954,264 - 1,955,071UniSTS
ECD03071  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,165,812 - 2,166,619UniSTSGRCh37
Build 36112,122,388 - 2,123,195RGDNCBI36
Celera112,202,317 - 2,203,124RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,956,074 - 1,956,881UniSTS
ECD03096  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,171,126 - 2,171,932UniSTSGRCh37
Build 36112,127,702 - 2,128,508RGDNCBI36
Celera112,207,633 - 2,208,439RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,961,388 - 1,962,194UniSTS
ECD03179  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,164,942 - 2,165,745UniSTSGRCh37
Build 36112,121,518 - 2,122,321RGDNCBI36
Celera112,201,449 - 2,202,250RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,955,206 - 1,956,007UniSTS
ECD03218  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,172,822 - 2,173,624UniSTSGRCh37
Build 36112,129,398 - 2,130,200RGDNCBI36
Celera112,209,329 - 2,210,131RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,963,084 - 1,963,886UniSTS
ECD03418  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,183,300 - 2,184,096UniSTSGRCh37
Build 36112,139,876 - 2,140,672RGDNCBI36
Celera112,219,893 - 2,220,689RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,973,565 - 1,974,361UniSTS
ECD03988  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,154,433 - 2,155,211UniSTSGRCh37
Build 36112,111,009 - 2,111,787RGDNCBI36
Celera112,190,939 - 2,191,717RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,944,966 - 1,945,744UniSTS
ECD04020  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,181,997 - 2,182,774UniSTSGRCh37
Build 36112,138,573 - 2,139,350RGDNCBI36
Celera112,218,504 - 2,219,281RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,972,260 - 1,973,037UniSTS
ECD04781  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,167,680 - 2,168,434UniSTSGRCh37
Build 36112,124,256 - 2,125,010RGDNCBI36
Celera112,204,185 - 2,204,939RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,957,942 - 1,958,696UniSTS
ECD05174  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,151,047 - 2,151,790UniSTSGRCh37
Build 36112,107,623 - 2,108,366RGDNCBI36
Celera112,187,538 - 2,188,281RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,941,569 - 1,942,312UniSTS
ECD05737  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,151,923 - 2,152,651UniSTSGRCh37
Build 36112,108,499 - 2,109,227RGDNCBI36
Celera112,188,414 - 2,189,142RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,942,445 - 1,943,173UniSTS
ECD06903  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,160,901 - 2,161,597UniSTSGRCh37
Build 36112,117,477 - 2,118,173RGDNCBI36
Celera112,197,408 - 2,198,104RGD
Cytogenetic Map11p15.5UniSTS
ECD07090  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,168,620 - 2,169,311UniSTSGRCh37
Build 36112,125,196 - 2,125,887RGDNCBI36
Celera112,205,125 - 2,205,816RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,958,882 - 1,959,573UniSTS
ECD07233  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,158,524 - 2,159,211UniSTSGRCh37
Build 36112,115,100 - 2,115,787RGDNCBI36
Celera112,195,031 - 2,195,718RGD
Cytogenetic Map11p15.5UniSTS
ECD07757  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,162,353 - 2,163,026UniSTSGRCh37
Build 36112,118,929 - 2,119,602RGDNCBI36
Celera112,198,860 - 2,199,533RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,952,617 - 1,953,290UniSTS
ECD08420  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,150,215 - 2,150,870UniSTSGRCh37
Build 36112,106,791 - 2,107,446RGDNCBI36
Celera112,186,706 - 2,187,361RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,940,737 - 1,941,392UniSTS
ECD11676  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,161,623 - 2,162,188UniSTSGRCh37
Build 36112,118,199 - 2,118,764RGDNCBI36
Celera112,198,130 - 2,198,695RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,951,887 - 1,952,452UniSTS
ECD18671  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,174,149 - 2,174,500UniSTSGRCh37
Build 36112,130,725 - 2,131,076RGDNCBI36
Celera112,210,656 - 2,211,007RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,964,411 - 1,964,762UniSTS
ECD19577  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,174,845 - 2,175,162UniSTSGRCh37
Build 36112,131,421 - 2,131,738RGDNCBI36
Celera112,211,352 - 2,211,669RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,965,107 - 1,965,424UniSTS
ECD21742  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,159,497 - 2,159,738UniSTSGRCh37
Build 36112,116,073 - 2,116,314RGDNCBI36
Celera112,196,004 - 2,196,245RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,949,721 - 1,949,962UniSTS
STS-S77035  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,154,008 - 2,154,221UniSTSGRCh37
Build 36112,110,584 - 2,110,797RGDNCBI36
Celera112,190,514 - 2,190,727RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,944,541 - 1,944,754UniSTS
GeneMap99-GB4 RH Map735.78UniSTS
NCBI RH Map71.7UniSTS
REN116979  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,149,982 - 2,150,209UniSTSGRCh37
Build 36112,106,558 - 2,106,785RGDNCBI36
Celera112,186,473 - 2,186,700RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,940,504 - 1,940,731UniSTS
REN116980  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,150,224 - 2,150,462UniSTSGRCh37
Build 36112,106,800 - 2,107,038RGDNCBI36
Celera112,186,715 - 2,186,953RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,940,746 - 1,940,984UniSTS
REN116981  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,150,439 - 2,150,664UniSTSGRCh37
Build 36112,107,015 - 2,107,240RGDNCBI36
Celera112,186,930 - 2,187,155RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,940,961 - 1,941,186UniSTS
REN116982  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,150,652 - 2,150,880UniSTSGRCh37
Build 36112,107,228 - 2,107,456RGDNCBI36
Celera112,187,143 - 2,187,371RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,941,174 - 1,941,402UniSTS
REN116983  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,150,859 - 2,151,118UniSTSGRCh37
Build 36112,107,435 - 2,107,694RGDNCBI36
Celera112,187,350 - 2,187,609RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,941,381 - 1,941,640UniSTS
REN116984  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,151,106 - 2,151,337UniSTSGRCh37
Build 36112,107,682 - 2,107,913RGDNCBI36
Celera112,187,597 - 2,187,828RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,941,628 - 1,941,859UniSTS
REN116985  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,151,323 - 2,151,581UniSTSGRCh37
Build 36112,107,899 - 2,108,157RGDNCBI36
Celera112,187,814 - 2,188,072RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,941,845 - 1,942,103UniSTS
REN116986  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,151,558 - 2,151,811UniSTSGRCh37
Build 36112,108,134 - 2,108,387RGDNCBI36
Celera112,188,049 - 2,188,302RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,942,080 - 1,942,333UniSTS
REN116987  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,151,904 - 2,152,131UniSTSGRCh37
Build 36112,108,480 - 2,108,707RGDNCBI36
Celera112,188,395 - 2,188,622RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,942,426 - 1,942,653UniSTS
REN116988  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,152,151 - 2,152,381UniSTSGRCh37
Build 36112,108,727 - 2,108,957RGDNCBI36
Celera112,188,642 - 2,188,872RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,942,673 - 1,942,903UniSTS
REN116989  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,152,378 - 2,152,603UniSTSGRCh37
Build 36112,108,954 - 2,109,179RGDNCBI36
Celera112,188,869 - 2,189,094RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,942,900 - 1,943,125UniSTS
REN116990  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,152,579 - 2,152,806UniSTSGRCh37
GRCh37112,152,579 - 2,152,729UniSTSGRCh37
Build 36112,109,155 - 2,109,305RGDNCBI36
Celera112,189,070 - 2,189,220RGD
Celera112,189,070 - 2,189,497UniSTS
Celera112,189,070 - 2,189,297UniSTS
Cytogenetic Map11p15.5UniSTS
HuRef111,943,101 - 1,943,251UniSTS
HuRef111,943,101 - 1,943,328UniSTS
HuRef111,943,102 - 1,943,529UniSTS
REN116991  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,153,227 - 2,153,457UniSTSGRCh37
Build 36112,109,803 - 2,110,033RGDNCBI36
Celera112,189,714 - 2,189,963RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,943,741 - 1,943,990UniSTS
REN116992  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,153,470 - 2,153,707UniSTSGRCh37
Build 36112,110,046 - 2,110,283RGDNCBI36
Celera112,189,976 - 2,190,213RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,944,003 - 1,944,240UniSTS
REN116993  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,153,683 - 2,153,954UniSTSGRCh37
Build 36112,110,259 - 2,110,530RGDNCBI36
Celera112,190,189 - 2,190,460RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,944,216 - 1,944,487UniSTS
REN116994  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,153,933 - 2,154,157UniSTSGRCh37
Build 36112,110,509 - 2,110,733RGDNCBI36
Celera112,190,439 - 2,190,663RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,944,466 - 1,944,690UniSTS
REN116995  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,154,149 - 2,154,412UniSTSGRCh37
Build 36112,110,725 - 2,110,988RGDNCBI36
Celera112,190,655 - 2,190,918RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,944,682 - 1,944,945UniSTS
REN116996  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,154,401 - 2,154,650UniSTSGRCh37
Build 36112,110,977 - 2,111,226RGDNCBI36
Celera112,190,907 - 2,191,156RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,944,934 - 1,945,183UniSTS
REN116997  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,154,631 - 2,154,858UniSTSGRCh37
Build 36112,111,207 - 2,111,434RGDNCBI36
Celera112,191,137 - 2,191,364RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,945,164 - 1,945,391UniSTS
REN116998  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,154,836 - 2,155,088UniSTSGRCh37
Build 36112,111,412 - 2,111,664RGDNCBI36
Celera112,191,342 - 2,191,594RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,945,369 - 1,945,621UniSTS
REN116999  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,155,070 - 2,155,294UniSTSGRCh37
Build 36112,111,646 - 2,111,870RGDNCBI36
Celera112,191,576 - 2,191,800RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,945,603 - 1,945,827UniSTS
REN117000  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,155,365 - 2,155,599UniSTSGRCh37
Build 36112,111,941 - 2,112,175RGDNCBI36
Celera112,191,871 - 2,192,105RGD
Cytogenetic Map11p15.5UniSTS
REN117001  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,155,575 - 2,155,819UniSTSGRCh37
Build 36112,112,151 - 2,112,395RGDNCBI36
Celera112,192,081 - 2,192,325RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,946,096 - 1,946,340UniSTS
REN117002  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,155,803 - 2,156,039UniSTSGRCh37
Build 36112,112,379 - 2,112,615RGDNCBI36
Celera112,192,309 - 2,192,545RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,946,324 - 1,946,560UniSTS
REN117003  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,156,016 - 2,156,265UniSTSGRCh37
Build 36112,112,592 - 2,112,841RGDNCBI36
Celera112,192,522 - 2,192,771RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,946,537 - 1,946,786UniSTS
REN117004  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,156,288 - 2,156,516UniSTSGRCh37
Build 36112,112,864 - 2,113,092RGDNCBI36
Celera112,192,794 - 2,193,022RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,946,809 - 1,947,037UniSTS
REN117005  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,156,495 - 2,156,735UniSTSGRCh37
Build 36112,113,071 - 2,113,311RGDNCBI36
Celera112,193,001 - 2,193,242RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,947,016 - 1,947,256UniSTS
REN117006  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,156,716 - 2,156,973UniSTSGRCh37
Build 36112,113,292 - 2,113,549RGDNCBI36
Celera112,193,223 - 2,193,480RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,947,237 - 1,947,494UniSTS
REN117007  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,156,964 - 2,157,232UniSTSGRCh37
Build 36112,113,540 - 2,113,808RGDNCBI36
Celera112,193,471 - 2,193,739RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,947,485 - 1,947,753UniSTS
REN117008  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,157,211 - 2,157,445UniSTSGRCh37
Build 36112,113,787 - 2,114,021RGDNCBI36
Celera112,193,718 - 2,193,952RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,947,732 - 1,947,966UniSTS
REN117009  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,157,431 - 2,157,664UniSTSGRCh37
Build 36112,114,007 - 2,114,240RGDNCBI36
Celera112,193,938 - 2,194,171RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,947,952 - 1,948,185UniSTS
REN117010  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,157,640 - 2,157,901UniSTSGRCh37
Build 36112,114,216 - 2,114,477RGDNCBI36
Celera112,194,147 - 2,194,408RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,948,161 - 1,948,422UniSTS
REN117011  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,157,903 - 2,158,143UniSTSGRCh37
Build 36112,114,479 - 2,114,719RGDNCBI36
Celera112,194,410 - 2,194,650RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,948,424 - 1,948,664UniSTS
REN117012  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,158,174 - 2,158,412UniSTSGRCh37
Build 36112,114,750 - 2,114,988RGDNCBI36
Celera112,194,681 - 2,194,919RGD
Cytogenetic Map11p15.5UniSTS
REN117013  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,158,406 - 2,158,661UniSTSGRCh37
Build 36112,114,982 - 2,115,237RGDNCBI36
Celera112,194,913 - 2,195,168RGD
Cytogenetic Map11p15.5UniSTS
REN117014  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,158,643 - 2,158,877UniSTSGRCh37
Build 36112,115,219 - 2,115,453RGDNCBI36
Celera112,195,150 - 2,195,384RGD
Cytogenetic Map11p15.5UniSTS
REN117015  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,158,896 - 2,159,142UniSTSGRCh37
Build 36112,115,472 - 2,115,718RGDNCBI36
Celera112,195,403 - 2,195,649RGD
Cytogenetic Map11p15.5UniSTS
REN117016  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,159,629 - 2,159,877UniSTSGRCh37
Build 36112,116,205 - 2,116,453RGDNCBI36
Celera112,196,136 - 2,196,384RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,949,853 - 1,950,101UniSTS
REN117017  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,161,319 - 2,161,554UniSTSGRCh37
Build 36112,117,895 - 2,118,130RGDNCBI36
Celera112,197,826 - 2,198,061RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,951,583 - 1,951,818UniSTS
REN117018  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,161,622 - 2,161,869UniSTSGRCh37
Build 36112,118,198 - 2,118,445RGDNCBI36
Celera112,198,129 - 2,198,376RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,951,886 - 1,952,133UniSTS
REN117019  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,162,169 - 2,162,409UniSTSGRCh37
Build 36112,118,745 - 2,118,985RGDNCBI36
Celera112,198,676 - 2,198,916RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,952,433 - 1,952,673UniSTS
REN117020  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,162,394 - 2,162,619UniSTSGRCh37
Build 36112,118,970 - 2,119,195RGDNCBI36
Celera112,198,901 - 2,199,126RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,952,658 - 1,952,883UniSTS
REN117021  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,162,596 - 2,162,831UniSTSGRCh37
Build 36112,119,172 - 2,119,407RGDNCBI36
Celera112,199,103 - 2,199,338RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,952,860 - 1,953,095UniSTS
REN117022  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,162,807 - 2,163,053UniSTSGRCh37
Build 36112,119,383 - 2,119,629RGDNCBI36
Celera112,199,314 - 2,199,560RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,953,071 - 1,953,317UniSTS
REN117023  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,163,034 - 2,163,304UniSTSGRCh37
Build 36112,119,610 - 2,119,880RGDNCBI36
Celera112,199,541 - 2,199,811RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,953,298 - 1,953,568UniSTS
REN117024  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,163,491 - 2,163,727UniSTSGRCh37
Build 36112,120,067 - 2,120,303RGDNCBI36
Celera112,199,998 - 2,200,234RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,953,755 - 1,953,991UniSTS
REN117025  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,163,703 - 2,163,927UniSTSGRCh37
Build 36112,120,279 - 2,120,503RGDNCBI36
Celera112,200,210 - 2,200,434RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,953,967 - 1,954,191UniSTS
REN117026  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,163,924 - 2,164,151UniSTSGRCh37
Build 36112,120,500 - 2,120,727RGDNCBI36
Celera112,200,431 - 2,200,658RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,954,188 - 1,954,415UniSTS
REN117027  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,164,130 - 2,164,392UniSTSGRCh37
Build 36112,120,706 - 2,120,968RGDNCBI36
Celera112,200,637 - 2,200,899RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,954,394 - 1,954,656UniSTS
REN117028  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,164,370 - 2,164,631UniSTSGRCh37
Build 36112,120,946 - 2,121,207RGDNCBI36
Celera112,200,877 - 2,201,138RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,954,634 - 1,954,895UniSTS
REN117029  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,164,620 - 2,164,864UniSTSGRCh37
Build 36112,121,196 - 2,121,440RGDNCBI36
Celera112,201,127 - 2,201,371RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,954,884 - 1,955,128UniSTS
REN117030  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,164,854 - 2,165,095UniSTSGRCh37
Build 36112,121,430 - 2,121,671RGDNCBI36
Celera112,201,361 - 2,201,602RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,955,118 - 1,955,359UniSTS
REN117031  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,165,071 - 2,165,301UniSTSGRCh37
Build 36112,121,647 - 2,121,877RGDNCBI36
Celera112,201,578 - 2,201,808RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,955,335 - 1,955,565UniSTS
REN117032  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,165,455 - 2,165,695UniSTSGRCh37
Build 36112,122,031 - 2,122,271RGDNCBI36
Celera112,201,961 - 2,202,200RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,955,718 - 1,955,957UniSTS
REN117033  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,165,704 - 2,165,945UniSTSGRCh37
Build 36112,122,280 - 2,122,521RGDNCBI36
Celera112,202,209 - 2,202,450RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,955,966 - 1,956,207UniSTS
REN117034  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,165,921 - 2,166,178UniSTSGRCh37
Build 36112,122,497 - 2,122,754RGDNCBI36
Celera112,202,426 - 2,202,683RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,956,183 - 1,956,440UniSTS
REN117035  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,166,201 - 2,166,453UniSTSGRCh37
Build 36112,122,777 - 2,123,029RGDNCBI36
Celera112,202,706 - 2,202,958RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,956,463 - 1,956,715UniSTS
REN117036  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,166,481 - 2,166,720UniSTSGRCh37
Build 36112,123,057 - 2,123,296RGDNCBI36
Celera112,202,986 - 2,203,225RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,956,743 - 1,956,982UniSTS
REN117037  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,166,718 - 2,166,943UniSTSGRCh37
Build 36112,123,294 - 2,123,519RGDNCBI36
Celera112,203,223 - 2,203,448RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,956,980 - 1,957,205UniSTS
REN117038  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,166,989 - 2,167,228UniSTSGRCh37
Build 36112,123,565 - 2,123,804RGDNCBI36
Celera112,203,494 - 2,203,733RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,957,251 - 1,957,490UniSTS
REN117039  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,167,237 - 2,167,470UniSTSGRCh37
Build 36112,123,813 - 2,124,046RGDNCBI36
Celera112,203,742 - 2,203,975RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,957,499 - 1,957,732UniSTS
REN117040  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,167,448 - 2,167,693UniSTSGRCh37
Build 36112,124,024 - 2,124,269RGDNCBI36
Celera112,203,953 - 2,204,198RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,957,710 - 1,957,955UniSTS
REN117041  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,167,670 - 2,167,920UniSTSGRCh37
Build 36112,124,246 - 2,124,496RGDNCBI36
Celera112,204,175 - 2,204,425RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,957,932 - 1,958,182UniSTS
REN117042  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,167,899 - 2,168,156UniSTSGRCh37
Build 36112,124,475 - 2,124,732RGDNCBI36
Celera112,204,404 - 2,204,661RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,958,161 - 1,958,418UniSTS
REN117043  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,168,186 - 2,168,445UniSTSGRCh37
Build 36112,124,762 - 2,125,021RGDNCBI36
Celera112,204,691 - 2,204,950RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,958,448 - 1,958,707UniSTS
REN117044  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,168,422 - 2,168,674UniSTSGRCh37
Build 36112,124,998 - 2,125,250RGDNCBI36
Celera112,204,927 - 2,205,179RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,958,684 - 1,958,936UniSTS
REN117045  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,168,657 - 2,168,908UniSTSGRCh37
Build 36112,125,233 - 2,125,484RGDNCBI36
Celera112,205,162 - 2,205,413RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,958,919 - 1,959,170UniSTS
REN117046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,168,891 - 2,169,117UniSTSGRCh37
Build 36112,125,467 - 2,125,693RGDNCBI36
Celera112,205,396 - 2,205,622RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,959,153 - 1,959,379UniSTS
REN117047  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,169,099 - 2,169,336UniSTSGRCh37
Build 36112,125,675 - 2,125,912RGDNCBI36
Celera112,205,604 - 2,205,841RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,959,361 - 1,959,598UniSTS
REN117048  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,169,316 - 2,169,541UniSTSGRCh37
Build 36112,125,892 - 2,126,117RGDNCBI36
Celera112,205,821 - 2,206,046RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,959,578 - 1,959,803UniSTS
REN117049  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,169,525 - 2,169,783UniSTSGRCh37
Build 36112,126,101 - 2,126,359RGDNCBI36
Celera112,206,030 - 2,206,288RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,959,787 - 1,960,045UniSTS
REN117050  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,169,778 - 2,170,026UniSTSGRCh37
Build 36112,126,354 - 2,126,602RGDNCBI36
Celera112,206,283 - 2,206,531RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,960,040 - 1,960,288UniSTS
REN117051  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,170,042 - 2,170,266UniSTSGRCh37
Build 36112,126,618 - 2,126,842RGDNCBI36
Celera112,206,547 - 2,206,771RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,960,304 - 1,960,528UniSTS
REN117052  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,170,311 - 2,170,561UniSTSGRCh37
Build 36112,126,887 - 2,127,137RGDNCBI36
Celera112,206,816 - 2,207,066RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,960,573 - 1,960,823UniSTS
REN117053  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,170,540 - 2,170,770UniSTSGRCh37
Build 36112,127,116 - 2,127,346RGDNCBI36
Celera112,207,045 - 2,207,275RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,960,802 - 1,961,032UniSTS
REN117054  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,170,749 - 2,171,001UniSTSGRCh37
Build 36112,127,325 - 2,127,577RGDNCBI36
Celera112,207,254 - 2,207,506RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,961,011 - 1,961,263UniSTS
REN117055  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,170,978 - 2,171,220UniSTSGRCh37
Build 36112,127,554 - 2,127,796RGDNCBI36
Celera112,207,483 - 2,207,727RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,961,240 - 1,961,482UniSTS
REN117056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,171,203 - 2,171,443UniSTSGRCh37
Build 36112,127,779 - 2,128,019RGDNCBI36
Celera112,207,710 - 2,207,950RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,961,465 - 1,961,705UniSTS
REN117057  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,171,425 - 2,171,653UniSTSGRCh37
Build 36112,128,001 - 2,128,229RGDNCBI36
Celera112,207,932 - 2,208,160RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,961,687 - 1,961,915UniSTS
REN117058  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,171,643 - 2,171,887UniSTSGRCh37
Build 36112,128,219 - 2,128,463RGDNCBI36
Celera112,208,150 - 2,208,394RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,961,905 - 1,962,149UniSTS
REN117059  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,171,902 - 2,172,136UniSTSGRCh37
Build 36112,128,478 - 2,128,712RGDNCBI36
Celera112,208,409 - 2,208,643RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,962,164 - 1,962,398UniSTS
REN117060  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,172,117 - 2,172,356UniSTSGRCh37
Build 36112,128,693 - 2,128,932RGDNCBI36
Celera112,208,624 - 2,208,863RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,962,379 - 1,962,618UniSTS
REN117061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,172,372 - 2,172,600UniSTSGRCh37
Build 36112,128,948 - 2,129,176RGDNCBI36
Celera112,208,879 - 2,209,107RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,962,634 - 1,962,862UniSTS
REN117062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,172,576 - 2,172,823UniSTSGRCh37
Build 36112,129,152 - 2,129,399RGDNCBI36
Celera112,209,083 - 2,209,330RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,962,838 - 1,963,085UniSTS
REN117063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,172,816 - 2,173,076UniSTSGRCh37
Build 36112,129,392 - 2,129,652RGDNCBI36
Celera112,209,323 - 2,209,583RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,963,078 - 1,963,338UniSTS
REN117064  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,173,053 - 2,173,304UniSTSGRCh37
Build 36112,129,629 - 2,129,880RGDNCBI36
Celera112,209,560 - 2,209,811RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,963,315 - 1,963,566UniSTS
REN117065  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,173,281 - 2,173,528UniSTSGRCh37
Build 36112,129,857 - 2,130,104RGDNCBI36
Celera112,209,788 - 2,210,035RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,963,543 - 1,963,790UniSTS
REN117066  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,173,505 - 2,173,768UniSTSGRCh37
Build 36112,130,081 - 2,130,344RGDNCBI36
Celera112,210,012 - 2,210,275RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,963,767 - 1,964,030UniSTS
REN117067  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,173,777 - 2,174,006UniSTSGRCh37
Build 36112,130,353 - 2,130,582RGDNCBI36
Celera112,210,284 - 2,210,513RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,964,039 - 1,964,268UniSTS
REN117068  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,173,986 - 2,174,218UniSTSGRCh37
Build 36112,130,562 - 2,130,794RGDNCBI36
Celera112,210,493 - 2,210,725RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,964,248 - 1,964,480UniSTS
REN117069  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,174,198 - 2,174,441UniSTSGRCh37
Build 36112,130,774 - 2,131,017RGDNCBI36
Celera112,210,705 - 2,210,948RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,964,460 - 1,964,703UniSTS
REN117070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,174,831 - 2,175,058UniSTSGRCh37
Build 36112,131,407 - 2,131,634RGDNCBI36
Celera112,211,338 - 2,211,565RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,965,093 - 1,965,320UniSTS
REN117071  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,175,075 - 2,175,303UniSTSGRCh37
Build 36112,131,651 - 2,131,879RGDNCBI36
Celera112,211,582 - 2,211,810RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,965,337 - 1,965,565UniSTS
REN117072  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,175,407 - 2,175,651UniSTSGRCh37
Build 36112,131,983 - 2,132,227RGDNCBI36
Celera112,211,914 - 2,212,158RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,965,669 - 1,965,913UniSTS
REN117073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,175,632 - 2,175,882UniSTSGRCh37
Build 36112,132,208 - 2,132,458RGDNCBI36
Celera112,212,139 - 2,212,389RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,965,894 - 1,966,144UniSTS
REN117074  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,176,237 - 2,176,483UniSTSGRCh37
Build 36112,132,813 - 2,133,059RGDNCBI36
Celera112,212,744 - 2,212,990RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,966,499 - 1,966,745UniSTS
REN117075  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,176,560 - 2,176,787UniSTSGRCh37
Build 36112,133,136 - 2,133,363RGDNCBI36
Celera112,213,067 - 2,213,294RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,966,822 - 1,967,049UniSTS
REN117076  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,176,768 - 2,177,001UniSTSGRCh37
Build 36112,133,344 - 2,133,577RGDNCBI36
Celera112,213,275 - 2,213,508RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,967,030 - 1,967,263UniSTS
REN117077  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,176,979 - 2,177,233UniSTSGRCh37
Build 36112,133,555 - 2,133,809RGDNCBI36
Celera112,213,486 - 2,213,740RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,967,241 - 1,967,496UniSTS
REN117078  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,177,214 - 2,177,479UniSTSGRCh37
Build 36112,133,790 - 2,134,055RGDNCBI36
Celera112,213,721 - 2,213,986RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,967,477 - 1,967,742UniSTS
REN117079  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,177,455 - 2,177,695UniSTSGRCh37
Build 36112,134,031 - 2,134,271RGDNCBI36
Celera112,213,962 - 2,214,202RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,967,718 - 1,967,958UniSTS
REN117080  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,177,776 - 2,178,007UniSTSGRCh37
Build 36112,134,352 - 2,134,583RGDNCBI36
Celera112,214,283 - 2,214,514RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,968,039 - 1,968,270UniSTS
REN117081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,178,011 - 2,178,254UniSTSGRCh37
Build 36112,134,587 - 2,134,830RGDNCBI36
Celera112,214,518 - 2,214,761RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,968,274 - 1,968,517UniSTS
REN117082  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,178,245 - 2,178,496UniSTSGRCh37
Build 36112,134,821 - 2,135,072RGDNCBI36
Celera112,214,752 - 2,215,003RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,968,508 - 1,968,759UniSTS
REN117083  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,178,624 - 2,178,857UniSTSGRCh37
Build 36112,135,200 - 2,135,433RGDNCBI36
Celera112,215,131 - 2,215,364RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,968,887 - 1,969,120UniSTS
REN117084  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,178,833 - 2,179,062UniSTSGRCh37
Build 36112,135,409 - 2,135,638RGDNCBI36
Celera112,215,340 - 2,215,569RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,969,096 - 1,969,325UniSTS
REN117085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,179,090 - 2,179,319UniSTSGRCh37
Build 36112,135,666 - 2,135,895RGDNCBI36
Celera112,215,597 - 2,215,826RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,969,353 - 1,969,582UniSTS
REN117086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,179,485 - 2,179,720UniSTSGRCh37
Build 36112,136,061 - 2,136,296RGDNCBI36
Celera112,215,992 - 2,216,227RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,969,748 - 1,969,983UniSTS
REN117087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,179,727 - 2,179,952UniSTSGRCh37
Build 36112,136,303 - 2,136,528RGDNCBI36
Celera112,216,234 - 2,216,459RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,969,990 - 1,970,215UniSTS
REN117088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,179,932 - 2,180,161UniSTSGRCh37
Build 36112,136,508 - 2,136,737RGDNCBI36
Celera112,216,439 - 2,216,668RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,970,195 - 1,970,424UniSTS
REN117089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,180,139 - 2,180,393UniSTSGRCh37
Build 36112,136,715 - 2,136,969RGDNCBI36
Celera112,216,646 - 2,216,900RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,970,402 - 1,970,656UniSTS
REN117090  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,180,378 - 2,180,633UniSTSGRCh37
Build 36112,136,954 - 2,137,209RGDNCBI36
Celera112,216,885 - 2,217,140RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,970,641 - 1,970,896UniSTS
REN117091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,180,681 - 2,180,933UniSTSGRCh37
Build 36112,137,257 - 2,137,509RGDNCBI36
Celera112,217,188 - 2,217,440RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,970,944 - 1,971,196UniSTS
REN117092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,180,915 - 2,181,154UniSTSGRCh37
Build 36112,137,491 - 2,137,730RGDNCBI36
Celera112,217,422 - 2,217,661RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,971,178 - 1,971,417UniSTS
REN117093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,181,135 - 2,181,390UniSTSGRCh37
Build 36112,137,711 - 2,137,966RGDNCBI36
Celera112,217,642 - 2,217,897RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,971,398 - 1,971,653UniSTS
REN117094  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,181,424 - 2,181,683UniSTSGRCh37
Build 36112,138,000 - 2,138,259RGDNCBI36
Celera112,217,931 - 2,218,190RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,971,687 - 1,971,946UniSTS
REN117095  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,181,773 - 2,182,029UniSTSGRCh37
Build 36112,138,349 - 2,138,605RGDNCBI36
Celera112,218,280 - 2,218,536RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,972,036 - 1,972,292UniSTS
REN117096  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,182,110 - 2,182,376UniSTSGRCh37
Build 36112,138,686 - 2,138,952RGDNCBI36
Celera112,218,617 - 2,218,883RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,972,373 - 1,972,639UniSTS
REN117097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,182,386 - 2,182,616UniSTSGRCh37
Build 36112,138,962 - 2,139,192RGDNCBI36
Celera112,218,893 - 2,219,123RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,972,649 - 1,972,879UniSTS
REN117100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,183,299 - 2,183,558UniSTSGRCh37
Build 36112,139,875 - 2,140,134RGDNCBI36
Celera112,219,892 - 2,220,151RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,973,564 - 1,973,823UniSTS
REN117101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,183,542 - 2,183,793UniSTSGRCh37
Build 36112,140,118 - 2,140,369RGDNCBI36
Celera112,220,135 - 2,220,386RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,973,807 - 1,974,058UniSTS
REN117102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,183,799 - 2,184,073UniSTSGRCh37
Build 36112,140,375 - 2,140,649RGDNCBI36
Celera112,220,392 - 2,220,666RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,974,064 - 1,974,338UniSTS
REN117103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,184,082 - 2,184,320UniSTSGRCh37
Build 36112,140,658 - 2,140,896RGDNCBI36
Celera112,220,675 - 2,220,913RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,974,347 - 1,974,585UniSTS
SGC35182  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,151,657 - 2,151,806UniSTSGRCh37
Build 36112,108,233 - 2,108,382RGDNCBI36
Celera112,188,148 - 2,188,297RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,942,179 - 1,942,328UniSTS
GeneMap99-GB4 RH Map1117.53UniSTS
Whitehead-RH Map1126.8UniSTS
NCBI RH Map1110.0UniSTS
WI-14149  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,150,361 - 2,150,464UniSTSGRCh37
Build 36112,106,937 - 2,107,040RGDNCBI36
Celera112,186,852 - 2,186,955RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,940,883 - 1,940,986UniSTS
GeneMap99-GB4 RH Map118.95UniSTS
Whitehead-RH Map1130.7UniSTS
PMC24644P6  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,181,089 - 2,182,063UniSTSGRCh37
Build 36112,137,665 - 2,138,639RGDNCBI36
Celera112,217,596 - 2,218,570RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,971,352 - 1,972,326UniSTS
stSG548711  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,150,250 - 2,151,894UniSTSGRCh37
Build 36112,106,826 - 2,108,470RGDNCBI36
Celera112,186,741 - 2,188,385RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,940,772 - 1,942,416UniSTS
stSG548713  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,153,228 - 2,154,934UniSTSGRCh37
Build 36112,109,804 - 2,111,510RGDNCBI36
Celera112,189,715 - 2,191,440RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,943,742 - 1,945,467UniSTS
stSG548714  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,154,924 - 2,155,105UniSTSGRCh37
Build 36112,111,500 - 2,111,681RGDNCBI36
Celera112,191,430 - 2,191,611RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,945,457 - 1,945,638UniSTS
stSG548715  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,155,131 - 2,156,480UniSTSGRCh37
Build 36112,111,707 - 2,113,056RGDNCBI36
Celera112,191,637 - 2,192,986RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,945,664 - 1,947,001UniSTS
stSG548716  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,156,560 - 2,158,225UniSTSGRCh37
Build 36112,113,136 - 2,114,801RGDNCBI36
Celera112,193,067 - 2,194,732RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,947,081 - 1,948,746UniSTS
stSG548719  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,161,385 - 2,162,844UniSTSGRCh37
Build 36112,117,961 - 2,119,420RGDNCBI36
Celera112,197,892 - 2,199,351RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,951,649 - 1,953,108UniSTS
stSG548720  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,162,831 - 2,164,476UniSTSGRCh37
Build 36112,119,407 - 2,121,052RGDNCBI36
Celera112,199,338 - 2,200,983RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,953,095 - 1,954,740UniSTS
stSG548722  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,166,056 - 2,167,340UniSTSGRCh37
Build 36112,122,632 - 2,123,916RGDNCBI36
Celera112,202,561 - 2,203,845RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,956,318 - 1,957,602UniSTS
stSG548723  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,167,340 - 2,168,708UniSTSGRCh37
Build 36112,123,916 - 2,125,284RGDNCBI36
Celera112,203,845 - 2,205,213RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,957,602 - 1,958,970UniSTS
stSG548724  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,168,778 - 2,170,122UniSTSGRCh37
Build 36112,125,354 - 2,126,698RGDNCBI36
Celera112,205,283 - 2,206,627RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,959,040 - 1,960,384UniSTS
stSG548725  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,170,103 - 2,171,436UniSTSGRCh37
Build 36112,126,679 - 2,128,012RGDNCBI36
Celera112,206,608 - 2,207,943RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,960,365 - 1,961,698UniSTS
stSG548726  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,171,534 - 2,173,140UniSTSGRCh37
Build 36112,128,110 - 2,129,716RGDNCBI36
Celera112,208,041 - 2,209,647RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,961,796 - 1,963,402UniSTS
stSG548727  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,173,121 - 2,174,437UniSTSGRCh37
Build 36112,129,697 - 2,131,013RGDNCBI36
Celera112,209,628 - 2,210,944RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,963,383 - 1,964,699UniSTS
stSG548728  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,174,434 - 2,176,165UniSTSGRCh37
Build 36112,131,010 - 2,132,741RGDNCBI36
Celera112,210,941 - 2,212,672RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,964,696 - 1,966,427UniSTS
stSG548729  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,176,146 - 2,177,639UniSTSGRCh37
Build 36112,132,722 - 2,134,215RGDNCBI36
Celera112,212,653 - 2,214,146RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,966,408 - 1,967,902UniSTS
stSG548730  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,177,618 - 2,177,867UniSTSGRCh37
Build 36112,134,194 - 2,134,443RGDNCBI36
Celera112,214,125 - 2,214,374RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,967,881 - 1,968,130UniSTS
stSG548731  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,177,926 - 2,179,207UniSTSGRCh37
Build 36112,134,502 - 2,135,783RGDNCBI36
Celera112,214,433 - 2,215,714RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,968,189 - 1,969,470UniSTS
stSG548733  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,181,102 - 2,182,635UniSTSGRCh37
Build 36112,137,678 - 2,139,211RGDNCBI36
Celera112,217,609 - 2,219,142RGD
Cytogenetic Map11p15.5UniSTS
HuRef111,971,365 - 1,972,898UniSTS
GDB:677440  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map11p15.5UniSTS
PMC123023P3  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,181,083 - 2,182,201UniSTSGRCh37
Celera112,217,590 - 2,218,708UniSTS
HuRef111,971,346 - 1,972,464UniSTS
Ins1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,181,084 - 2,182,182UniSTSGRCh37
Celera112,217,591 - 2,218,689UniSTS
HuRef111,971,347 - 1,972,445UniSTS
Ins2  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,181,103 - 2,182,189UniSTSGRCh37
Celera112,217,610 - 2,218,696UniSTS
HuRef111,971,366 - 1,972,452UniSTS
PMC21231P1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37112,181,106 - 2,182,193UniSTSGRCh37
Celera112,217,613 - 2,218,700UniSTS
HuRef111,971,369 - 1,972,456UniSTS
IGF2  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map11p15.5UniSTS
GeneMap99-GB4 RH Map1116.52UniSTS
NCBI RH Map1110.0UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component
High
Medium 82 82 82
Low 1 30 268 228 28 226 29 21 388 6 19 3 5 27
Below cutoff 349 478 561 94 160 36 888 640 2035 32 181 306 58 299 668 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_050578 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001042376 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_003512 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC130303 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC132217 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI133461 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK291594 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL568676 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW878608 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW878688 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW880662 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BE161581 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF205917 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF438519 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI042755 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ128162 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX369936 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB988622 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN338133 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA775768 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA840311 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA851509 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA858680 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ104204 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ104205 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000356578   ⟹   ENSP00000348986
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl112,132,538 - 2,161,209 (-)Ensembl
RefSeq Acc Id: ENST00000397270   ⟹   ENSP00000380440
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl112,146,626 - 2,161,209 (-)Ensembl
RefSeq Acc Id: ENST00000476874
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl112,148,934 - 2,158,336 (-)Ensembl
RefSeq Acc Id: ENST00000481781
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl112,146,623 - 2,158,391 (-)Ensembl
RefSeq Acc Id: ENST00000643349   ⟹   ENSP00000495715
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl112,131,395 - 2,149,603 (-)Ensembl
RefSeq Acc Id: NM_001042376   ⟹   NP_001035835
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,146,623 - 2,161,209 (-)NCBI
GRCh37112,150,342 - 2,182,439 (-)ENTREZGENE
Build 36112,124,432 - 2,139,015 (-)NCBI Archive
HuRef111,940,864 - 1,972,702 (-)ENTREZGENE
CHM1_1112,166,806 - 2,181,387 (-)NCBI
T2T-CHM13v2.0112,234,275 - 2,248,857 (-)NCBI
Sequence:
RefSeq Acc Id: NR_003512
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,129,117 - 2,161,209 (-)NCBI
GRCh37112,150,342 - 2,182,439 (-)ENTREZGENE
Build 36112,106,926 - 2,139,015 (-)NCBI Archive
HuRef111,940,864 - 1,972,702 (-)ENTREZGENE
CHM1_1112,148,968 - 2,181,387 (-)NCBI
T2T-CHM13v2.0112,216,758 - 2,248,857 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001035835 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein ABD93452 (Get FASTA)   NCBI Sequence Viewer  
  ABD93453 (Get FASTA)   NCBI Sequence Viewer  
  BAF84283 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000348986.4
  ENSP00000380440
  ENSP00000380440.1
  ENSP00000495715.1
GenBank Protein F8WCM5 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_001035835   ⟸   NM_001042376
- Peptide Label: precursor
- UniProtKB: Q1WM24 (UniProtKB/Swiss-Prot),   F8WCM5 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000495715   ⟸   ENST00000643349
RefSeq Acc Id: ENSP00000348986   ⟸   ENST00000356578
RefSeq Acc Id: ENSP00000380440   ⟸   ENST00000397270

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-A0A2R8Y747-F1-model_v2 AlphaFold A0A2R8Y747 1-149 view protein structure
AF-F8WCM5-F1-model_v2 AlphaFold F8WCM5 1-200 view protein structure

Promoters
RGD ID:7219329
Promoter ID:EPDNEW_H15409
Type:single initiation site
Name:INS-IGF2_3
Description:INS-IGF2 readthrough
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15410  EPDNEW_H15411  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,146,770 - 2,146,830EPDNEW
RGD ID:7219327
Promoter ID:EPDNEW_H15410
Type:initiation region
Name:INS-IGF2_2
Description:INS-IGF2 readthrough
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15409  EPDNEW_H15411  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,149,566 - 2,149,626EPDNEW
RGD ID:7219331
Promoter ID:EPDNEW_H15411
Type:initiation region
Name:INS-IGF2_1
Description:INS-IGF2 readthrough
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15410  EPDNEW_H15409  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,158,383 - 2,158,443EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:33527 AgrOrtholog
COSMIC INS-IGF2 COSMIC
Ensembl Genes ENSG00000129965 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
  ENSG00000284779 Ensembl, UniProtKB/TrEMBL
Ensembl Transcript ENST00000356578.8 UniProtKB/Swiss-Prot
  ENST00000397270 ENTREZGENE
  ENST00000397270.1 UniProtKB/Swiss-Prot
  ENST00000643349.2 UniProtKB/TrEMBL
Gene3D-CATH Insulin-like UniProtKB/Swiss-Prot
GTEx ENSG00000129965 GTEx
  ENSG00000284779 GTEx
HGNC ID HGNC:33527 ENTREZGENE
Human Proteome Map INS-IGF2 Human Proteome Map
InterPro Insulin UniProtKB/Swiss-Prot
  Insulin-like UniProtKB/Swiss-Prot
  Insulin-like_sf UniProtKB/Swiss-Prot
KEGG Report hsa:723961 UniProtKB/Swiss-Prot
NCBI Gene 723961 ENTREZGENE
PANTHER INSULIN, ISOFORM 2 UniProtKB/Swiss-Prot
  PTHR11454 UniProtKB/Swiss-Prot
Pfam Insulin UniProtKB/Swiss-Prot
PharmGKB PA162392175 PharmGKB
PRINTS INSULIN UniProtKB/Swiss-Prot
SMART IlGF UniProtKB/Swiss-Prot
Superfamily-SCOP SSF56994 UniProtKB/Swiss-Prot
UniProt A0A2R8Y747_HUMAN UniProtKB/TrEMBL
  F8WCM5 ENTREZGENE, UniProtKB/Swiss-Prot
  Q1WM24 ENTREZGENE
UniProt Secondary Q1WM24 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2011-07-27 INS-IGF2  INS-IGF2 readthrough  INS-IGF2  INS-IGF2 readthrough transcript  Symbol and/or name change 5135510 APPROVED