IGF2 (insulin like growth factor 2) - Rat Genome Database
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Gene: IGF2 (insulin like growth factor 2) Homo sapiens
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Symbol: IGF2
Name: insulin like growth factor 2
RGD ID: 737149
HGNC Page HGNC
Description: Exhibits signaling receptor binding activity. Involved in positive regulation of activated T cell proliferation; positive regulation of mitotic nuclear division; and positive regulation of signal transduction. Predicted to localize to extracellular space. Implicated in Silver-Russell syndrome; choriocarcinoma; hepatocellular carcinoma; and rheumatoid arthritis. Biomarker of several diseases, including Lewy body dementia; acquired immunodeficiency syndrome; arthritis (multiple); inflammatory bowel disease (multiple); and neurodegenerative disease (multiple).
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: C11orf43; FLJ22066; FLJ44734; GRDF; IGF-II; INSIGF; insulin-like growth factor 2 (somatomedin A); insulin-like growth factor II; insulin-like growth factor type 2; PP9974; preptin; putative insulin-like growth factor II associated protein; somatomedin A; somatomedin-A; SRS3; T3M-11-derived growth factor
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl112,129,112 - 2,141,238 (-)EnsemblGRCh38hg38GRCh38
GRCh38112,129,117 - 2,149,566 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37112,150,342 - 2,170,833 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36112,106,923 - 2,127,409 (-)NCBINCBI36hg18NCBI36
Build 34112,110,531 - 2,116,578NCBI
Celera112,186,838 - 2,207,338 (-)NCBI
Cytogenetic Map11p15.5NCBI
HuRef111,940,869 - 1,961,095 (-)NCBIHuRef
CHM1_1112,148,968 - 2,169,786 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View
acquired immunodeficiency syndrome  (IEP)
adrenocortical carcinoma  (EXP)
Alcoholic Liver Diseases  (ISO)
alcoholic neuropathy  (ISO)
Alzheimer's disease  (EXP,IEP,ISO)
anemia  (EXP)
Animal Mammary Neoplasms  (ISO)
atherosclerosis  (EXP)
autistic disorder  (EXP)
Beckwith-Wiedemann syndrome  (EXP)
bone development disease  (EXP)
brain infarction  (ISO)
Brain Injuries  (ISO)
breast cancer  (IEP)
choriocarcinoma  (IDA)
Chronic Hepatitis C  (IAGP)
cognitive disorder  (EXP)
Colonic Neoplasms  (EXP)
Colorectal Neoplasms  (EXP)
congenital diaphragmatic hernia  (ISO)
congenital disorder of glycosylation Ia  (IEP)
Diabetic Nephropathies  (IDA,ISO)
Diaphragmatic Hernia  (EXP)
Embryo Loss  (ISO)
Ependymomas  (IEP)
Experimental Diabetes Mellitus  (IDA,ISO)
Experimental Liver Neoplasms  (ISO)
Fetal Growth Retardation  (EXP,ISO)
Gastrointestinal Diseases  (IEP)
Growth Disorders  (EXP)
Hepatic Echinococcosis  (IEP)
hepatoblastoma  (EXP)
hepatocellular carcinoma  (EXP,IAGP,ISO)
hypoglycemia  (EXP)
Hypoxia-Ischemia, Brain  (IEP)
immunodeficiency 39  (IAGP)
inflammatory bowel disease  (IEP,ISO)
Lewy body dementia  (EXP,IEP)
liver cirrhosis  (IEP)
Liver Neoplasms  (EXP)
Lung Injury  (ISO)
Memory Disorders  (EXP,ISO)
meningitis  (IEP)
Metabolic Syndrome  (ISO)
multiple sclerosis  (IEP)
multiple system atrophy  (IEP)
Neoplasm Metastasis  (ISO)
nephroblastoma  (EXP)
Nerve Degeneration  (EXP)
neuronal ceroid lipofuscinosis  (IAGP)
obesity  (EXP)
osteoarthritis  (IEP)
osteoporosis  (ISO)
Parkinson's disease  (EXP,IEP)
placenta disease  (EXP)
polyhydramnios  (EXP)
Postmenopausal Osteoporosis  (IDA)
pre-malignant neoplasm  (EXP)
Radiation Injuries, Experimental  (ISO)
rhabdomyosarcoma  (EXP)
rheumatoid arthritis  (IAGP,IEP)
Silver-Russell syndrome  (EXP,IAGP)
Silver-Russell Syndrome 3  (IAGP)
Spontaneous Abortions  (EXP)
type 1 diabetes mellitus  (ISO)
type 1 diabetes mellitus 2  (ISS)
type 2 diabetes mellitus  (ISO)
ulcerative colitis  (IEP)
ventricular septal defect  (IEP)

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(-)-epigallocatechin 3-gallate  (EXP)
(S)-nicotine  (ISO)
1-naphthyl isothiocyanate  (ISO)
17alpha-ethynylestradiol  (EXP,ISO)
17beta-estradiol  (EXP)
2,2',4,4'-Tetrabromodiphenyl ether  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2-acetamidofluorene  (ISO)
2-ethoxyethanol  (ISO)
2-methoxyethanol  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP)
3-methylcholanthrene  (ISO)
4,4'-diaminodiphenylmethane  (ISO)
4,4'-sulfonyldiphenol  (EXP,ISO)
4-hydroxyphenyl retinamide  (ISO)
5-aza-2'-deoxycytidine  (EXP)
7,12-dimethyltetraphene  (ISO)
acetylsalicylic acid  (EXP)
aflatoxin B1  (EXP)
all-trans-4-oxoretinoic acid  (EXP)
all-trans-retinoic acid  (EXP,ISO)
alpha-naphthoflavone  (ISO)
aluminium sulfate (anhydrous)  (EXP)
aluminium trifluoride  (EXP)
ammonium chloride  (ISO)
antirheumatic drug  (EXP)
arsenous acid  (EXP)
benzimidazoles  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP)
benzo[b]fluoranthene  (EXP)
benzylpenicillin  (EXP)
bexarotene  (ISO)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (EXP,ISO)
bisphenol F  (ISO)
bortezomib  (EXP)
budesonide  (ISO)
buta-1,3-diene  (ISO)
butanal  (EXP)
cadmium atom  (EXP,ISO)
calciol  (ISO)
calcium atom  (ISO)
calcium(0)  (ISO)
capsaicin  (ISO)
carbon nanotube  (EXP)
carbonyl sulfide  (ISO)
carmustine  (EXP)
choline  (ISO)
chromium atom  (ISO)
cisplatin  (EXP)
cobalt atom  (ISO)
cobalt dichloride  (EXP)
cocaine  (ISO)
corticosterone  (ISO)
cortisol  (EXP)
crocidolite asbestos  (EXP)
CU-O LINKAGE  (EXP)
curcumin  (EXP)
dantrolene  (EXP)
DDE  (ISO)
DDT  (ISO)
dexamethasone  (EXP,ISO)
diarsenic trioxide  (EXP)
diazinon  (ISO)
dibenz[a,h]anthracene  (EXP)
dibutyl phthalate  (ISO)
dichloroacetic acid  (ISO)
dicrotophos  (EXP)
diethylstilbestrol  (ISO)
dioxygen  (EXP)
doxorubicin  (EXP)
estrone  (EXP)
ethanol  (ISO)
ethylene glycol bis(2-aminoethyl)tetraacetic acid  (EXP)
fenvalerate  (ISO)
fluoxetine  (ISO)
folic acid  (EXP,ISO)
fonofos  (EXP)
fulvestrant  (ISO)
furan  (ISO)
genistein  (ISO)
glycidol  (ISO)
gold atom  (EXP)
gold(0)  (EXP)
hexadecanoic acid  (EXP)
hydrogen peroxide  (ISO)
indometacin  (EXP)
L-methionine  (ISO)
lanthanum atom  (ISO)
lead diacetate  (EXP,ISO)
lead nitrate  (ISO)
lead(0)  (EXP)
lead(2+)  (EXP)
lipopolysaccharide  (ISO)
LY294002  (EXP,ISO)
manganese(II) chloride  (EXP)
metformin  (EXP)
monosodium L-glutamate  (ISO)
N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal  (EXP)
N-nitrosodiethylamine  (ISO)
N-nitrosodimethylamine  (ISO)
nickel atom  (EXP)
nickel dichloride  (ISO)
nickel subsulfide  (ISO)
nicotine  (ISO)
nifedipine  (EXP)
nitrofen  (ISO)
ochratoxin A  (EXP)
oxaliplatin  (ISO)
panobinostat  (EXP)
paracetamol  (EXP)
paraquat  (ISO)
parathion  (EXP)
pentanal  (EXP)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (EXP)
phenylarsine oxide  (ISO)
phenylmercury acetate  (EXP)
phenytoin  (ISO)
phthalic acid  (EXP)
progesterone  (EXP)
propanal  (EXP)
propiconazole  (ISO)
quercetin  (EXP)
raloxifene  (ISO)
resveratrol  (EXP)
rotenone  (ISO)
SB 203580  (EXP)
serpentine asbestos  (EXP)
silicon dioxide  (EXP)
sodium arsenite  (EXP,ISO)
sunitinib  (EXP)
tamoxifen  (EXP,ISO)
temozolomide  (EXP)
terbufos  (EXP)
testosterone  (EXP)
tetrachloromethane  (EXP,ISO)
tetramethrin  (ISO)
tipifarnib  (ISO)
topotecan  (ISO)
trichloroacetic acid  (ISO)
trichostatin A  (EXP)
triclosan  (EXP)
trimellitic anhydride  (ISO)
triphenyl phosphate  (ISO)
urethane  (ISO)
valproic acid  (EXP,ISO)
vinclozolin  (ISO)
vinyl carbamate  (ISO)
vorinostat  (EXP)
wortmannin  (EXP)
zinc atom  (EXP)
zinc(0)  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
animal organ morphogenesis  (IEA,ISO)
cellular protein metabolic process  (TAS)
cellular response to mechanical stimulus  (ISO)
embryonic placenta development  (ISS)
embryonic placenta morphogenesis  (ISS)
exocrine pancreas development  (IEA,ISO)
female pregnancy  (ISO)
glucose metabolic process  (IEA)
in utero embryonic development  (ISS)
insulin receptor signaling pathway  (TAS)
insulin receptor signaling pathway via phosphatidylinositol 3-kinase  (ISS)
memory  (ISO)
multicellular organism development  (TAS)
negative regulation of muscle cell differentiation  (ISS)
negative regulation of natural killer cell mediated cytotoxicity  (ISO)
negative regulation of transcription by RNA polymerase II  (ISS)
osteoblast differentiation  (IEA,ISO)
platelet degranulation  (TAS)
positive regulation of activated T cell proliferation  (IBA,IDA)
positive regulation of angiogenesis  (ISO)
positive regulation of blood vessel endothelial cell migration  (ISO)
positive regulation of catalytic activity  (ISS)
positive regulation of cell division  (IEA)
positive regulation of cell population proliferation  (IC,IDA)
positive regulation of glycogen (starch) synthase activity  (IBA,ISS)
positive regulation of glycogen biosynthetic process  (ISS)
positive regulation of insulin receptor signaling pathway  (IBA,IDA)
positive regulation of MAPK cascade  (IBA,IDA)
positive regulation of mitotic nuclear division  (IDA)
positive regulation of multicellular organism growth  (IEA,ISO)
positive regulation of organ growth  (IEA)
positive regulation of peptidyl-tyrosine phosphorylation  (IBA,ISS)
positive regulation of protein kinase B signaling  (IDA)
positive regulation of protein phosphorylation  (ISS)
positive regulation of protein serine/threonine kinase activity  (IEA)
positive regulation of skeletal muscle tissue growth  (IEA)
positive regulation of steroid hormone biosynthetic process  (ISO)
positive regulation of transcription by RNA polymerase II  (IBA,ISO)
positive regulation of vascular endothelial cell proliferation  (IBA)
regulation of gene expression by genetic imprinting  (TAS)
regulation of histone modification  (ISS)
regulation of muscle cell differentiation  (IBA,ISS)
regulation of transcription, DNA-templated  (NAS)
response to drug  (ISO)
response to estradiol  (ISO)
response to ethanol  (ISO)
response to nicotine  (ISO)
response to nutrient levels  (ISO)
response to organic cyclic compound  (ISO)
response to radiation  (ISO)
skeletal system development  (TAS)
spongiotrophoblast cell proliferation  (IEA)
striated muscle cell differentiation  (IEA,ISO)
wound healing  (ISO)

Cellular Component

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

Human Phenotype
Abnormal external genitalia  (IAGP)
Abnormal foot morphology  (IAGP)
Abnormality of cardiovascular system morphology  (IAGP)
Abnormality of the cardiovascular system  (IAGP)
Abnormality of the dentition  (IAGP)
Abnormality of the ureter  (IAGP)
Accelerated skeletal maturation  (IAGP)
Adrenocortical carcinoma  (IAGP)
Adrenocortical cytomegaly  (IAGP)
Ambiguous genitalia  (IAGP)
Asthma  (IAGP)
Asymmetric growth  (IAGP)
Asymmetry of the thorax  (IAGP)
Attention deficit hyperactivity disorder  (IAGP)
Autosomal dominant inheritance  (IAGP)
Bifid scrotum  (IAGP)
Blue sclerae  (IAGP)
Cafe-au-lait spot  (IAGP)
Cardiomegaly  (IAGP)
Cardiomyopathy  (IAGP)
Cleft palate  (IAGP)
Clinodactyly of the 5th finger  (IAGP)
Coarse facial features  (IAGP)
Congenital posterior urethral valve  (IAGP)
Craniofacial disproportion  (IAGP)
Craniopharyngioma  (IAGP)
Cryptorchidism  (IAGP)
Dandy-Walker malformation  (IAGP)
Decreased body weight  (IAGP)
Decreased fetal movement  (IAGP)
Decreased response to growth hormone stimuation test  (IAGP)
Delayed closure of the anterior fontanelle  (IAGP)
Delayed cranial suture closure  (IAGP)
Delayed skeletal maturation  (IAGP)
Delayed speech and language development  (IAGP)
Dental crowding  (IAGP)
Diastasis recti  (IAGP)
Downturned corners of mouth  (IAGP)
Dysmenorrhea  (IAGP)
Ectrodactyly  (IAGP)
Enlarged kidney  (IAGP)
Facial asymmetry  (IAGP)
Failure to thrive  (IAGP)
Fasting hypoglycemia  (IAGP)
Feeding difficulties in infancy  (IAGP)
Finger clinodactyly  (IAGP)
Frontal bossing  (IAGP)
Generalized hypotonia  (IAGP)
Global developmental delay  (IAGP)
Gonadoblastoma  (IAGP)
Hemihypertrophy  (IAGP)
Hepatoblastoma  (IAGP)
Hepatocellular carcinoma  (IAGP)
Hepatomegaly  (IAGP)
Heterogeneous  (IAGP)
High palate  (IAGP)
Hyperhidrosis  (IAGP)
Hypoglycemia  (IAGP)
Hypoplastic fingernail  (IAGP)
Hypospadias  (IAGP)
Hypothyroidism  (IAGP)
Impaired pain sensation  (IAGP)
Increased body mass index  (IAGP)
Infantile muscular hypotonia  (IAGP)
Inguinal hernia  (IAGP)
Intellectual disability  (IAGP)
Intellectual disability, mild  (IAGP)
Intrauterine growth retardation  (IAGP)
Large fontanelles  (IAGP)
Low-set ears  (IAGP)
Lower limb asymmetry  (IAGP)
Macroglossia  (IAGP)
Melanocytic nevus  (IAGP)
Micrognathia  (IAGP)
Microphallus  (IAGP)
Midface retrusion  (IAGP)
Motor delay  (IAGP)
Myelomeningocele  (IAGP)
Neonatal hypoglycemia  (IAGP)
Nephroblastoma  (IAGP)
Nephrocalcinosis  (IAGP)
Nephrolithiasis  (IAGP)
Nevus flammeus  (IAGP)
Oligohydramnios  (IAGP)
Omphalocele  (IAGP)
Overgrowth  (IAGP)
Overgrowth of external genitalia  (IAGP)
Pancreatic hyperplasia  (IAGP)
Patent ductus arteriosus  (IAGP)
Polydactyly  (IAGP)
Posterior helix pit  (IAGP)
Postnatal growth retardation  (IAGP)
Prominent forehead  (IAGP)
Prominent metopic ridge  (IAGP)
Prominent occiput  (IAGP)
Proptosis  (IAGP)
Protruding ear  (IAGP)
Relative macrocephaly  (IAGP)
Renal cortical cysts  (IAGP)
Retrognathia  (IAGP)
Scoliosis  (IAGP)
Seizure  (IAGP)
Severe intrauterine growth retardation  (IAGP)
Short 5th finger  (IAGP)
Short chin  (IAGP)
Short distal phalanx of the 5th finger  (IAGP)
Short middle phalanx of the 5th finger  (IAGP)
Short stature  (IAGP)
Small for gestational age  (IAGP)
Small placenta  (IAGP)
Somatic mutation  (IAGP)
Specific learning disability  (IAGP)
Sporadic  (IAGP)
Syndactyly  (IAGP)
Testicular seminoma  (IAGP)
Triangular face  (IAGP)
Umbilical hernia  (IAGP)
Upper limb asymmetry  (IAGP)
Urethral valve  (IAGP)
Vesicoureteral reflux  (IAGP)
X-linked recessive inheritance  (IAGP)
References

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Additional References at PubMed
PMID:658418   PMID:1282023   PMID:1486331   PMID:1569071   PMID:1656956   PMID:1684848   PMID:1714916   PMID:1730789   PMID:1733942   PMID:1845984   PMID:2450353   PMID:2465304  
PMID:2722836   PMID:2967174   PMID:3002851   PMID:3167054   PMID:3476948   PMID:3569524   PMID:3652904   PMID:3653397   PMID:3683205   PMID:3881277   PMID:6189745   PMID:6382021  
PMID:6382022   PMID:7527339   PMID:7680905   PMID:7683646   PMID:7730145   PMID:7797478   PMID:8298652   PMID:8385745   PMID:8424751   PMID:8547330   PMID:8589713   PMID:8781553  
PMID:8889548   PMID:8939990   PMID:8968759   PMID:9144427   PMID:9446566   PMID:9497324   PMID:9722589   PMID:9722981   PMID:9972281   PMID:10084601   PMID:10336724   PMID:10342887  
PMID:10407151   PMID:10512690   PMID:10611375   PMID:10731720   PMID:10810289   PMID:10884343   PMID:11049980   PMID:11500939   PMID:11522816   PMID:11600567   PMID:11749962   PMID:11793026  
PMID:11811790   PMID:11849996   PMID:11889182   PMID:11903044   PMID:11937266   PMID:11969341   PMID:12005306   PMID:12006706   PMID:12032304   PMID:12075589   PMID:12125963   PMID:12127559  
PMID:12138094   PMID:12243757   PMID:12270940   PMID:12388463   PMID:12446294   PMID:12477932   PMID:12519841   PMID:12532445   PMID:12548223   PMID:12558805   PMID:12575534   PMID:12579496  
PMID:12586351   PMID:12605037   PMID:12610512   PMID:12637750   PMID:12700030   PMID:12702581   PMID:12719950   PMID:12727212   PMID:12732844   PMID:12765950   PMID:12782403   PMID:12804776  
PMID:12881524   PMID:13679437   PMID:14614750   PMID:14645199   PMID:14645508   PMID:14695992   PMID:14710345   PMID:14718574   PMID:14749262   PMID:14749349   PMID:14764950   PMID:14996863  
PMID:15003992   PMID:15140223   PMID:15146197   PMID:15163116   PMID:15181035   PMID:15191555   PMID:15205474   PMID:15217931   PMID:15298990   PMID:15342556   PMID:15355996   PMID:15359740  
PMID:15471867   PMID:15489334   PMID:15498874   PMID:15528386   PMID:15621215   PMID:15642732   PMID:15645136   PMID:15694994   PMID:15701574   PMID:15706404   PMID:15731405   PMID:15769738  
PMID:15797461   PMID:15799974   PMID:15809062   PMID:15935984   PMID:15954927   PMID:15956340   PMID:15970649   PMID:15987847   PMID:16018936   PMID:16037384   PMID:16040806   PMID:16102992  
PMID:16115888   PMID:16166779   PMID:16247461   PMID:16251897   PMID:16303743   PMID:16330588   PMID:16344560   PMID:16344718   PMID:16489075   PMID:16518847   PMID:16525660   PMID:16531418  
PMID:16603642   PMID:16612114   PMID:16716263   PMID:16857788   PMID:16868148   PMID:16888814   PMID:16926156   PMID:16935391   PMID:17029194   PMID:17072986   PMID:17285535   PMID:17289909  
PMID:17294726   PMID:17310846   PMID:17325026   PMID:17339271   PMID:17341887   PMID:17360667   PMID:17369847   PMID:17407457   PMID:17440932   PMID:17475626   PMID:17488802   PMID:17554260  
PMID:17560154   PMID:17569086   PMID:17591929   PMID:17620336   PMID:17632545   PMID:17635080   PMID:17639583   PMID:17640993   PMID:17667841   PMID:17700581   PMID:17786320   PMID:17919721  
PMID:17972051   PMID:18006818   PMID:18022169   PMID:18035699   PMID:18046459   PMID:18085551   PMID:18159214   PMID:18199734   PMID:18245780   PMID:18259111   PMID:18287964   PMID:18297687  
PMID:18308616   PMID:18349294   PMID:18350600   PMID:18358696   PMID:18372285   PMID:18428028   PMID:18464243   PMID:18467708   PMID:18481170   PMID:18520331   PMID:18524796   PMID:18537183  
PMID:18541649   PMID:18562769   PMID:18573128   PMID:18604514   PMID:18607558   PMID:18611974   PMID:18616667   PMID:18619647   PMID:18636124   PMID:18676680   PMID:18701505   PMID:18728168  
PMID:18772331   PMID:18786438   PMID:18788888   PMID:18794369   PMID:18803353   PMID:18832656   PMID:18931647   PMID:18955703   PMID:18980977   PMID:19034281   PMID:19064563   PMID:19064572  
PMID:19066168   PMID:19121847   PMID:19124506   PMID:19127217   PMID:19170196   PMID:19208780   PMID:19218281   PMID:19242102   PMID:19259766   PMID:19276395   PMID:19293570   PMID:19317253  
PMID:19333718   PMID:19336370   PMID:19365888   PMID:19367319   PMID:19390492   PMID:19407853   PMID:19417744   PMID:19421925   PMID:19427670   PMID:19453261   PMID:19499149   PMID:19502451  
PMID:19513555   PMID:19546867   PMID:19549920   PMID:19560381   PMID:19584898   PMID:19586133   PMID:19588890   PMID:19598235   PMID:19625176   PMID:19672298   PMID:19689072   PMID:19692168  
PMID:19713175   PMID:19724140   PMID:19737423   PMID:19749460   PMID:19767753   PMID:19769965   PMID:19786462   PMID:19843644   PMID:19876004   PMID:19913121   PMID:19919531   PMID:19924280  
PMID:19938957   PMID:19948975   PMID:19950580   PMID:19953105   PMID:19956766   PMID:19956846   PMID:19957330   PMID:19962924   PMID:20007505   PMID:20010889   PMID:20027339   PMID:20042264  
PMID:20057340   PMID:20089431   PMID:20119675   PMID:20157191   PMID:20206398   PMID:20301471   PMID:20301499   PMID:20301534   PMID:20301568   PMID:20338046   PMID:20364576   PMID:20388800  
PMID:20403354   PMID:20403997   PMID:20416304   PMID:20418667   PMID:20422427   PMID:20427254   PMID:20443017   PMID:20452482   PMID:20453000   PMID:20468064   PMID:20472480   PMID:20479215  
PMID:20483645   PMID:20484977   PMID:20540659   PMID:20564319   PMID:20592487   PMID:20628086   PMID:20634197   PMID:20637510   PMID:20639793   PMID:20651370   PMID:20661447   PMID:20673868  
PMID:20709701   PMID:20734064   PMID:20842449   PMID:20861572   PMID:20884247   PMID:20929508   PMID:20937833   PMID:20945273   PMID:21078522   PMID:21109978   PMID:21164426   PMID:21251749  
PMID:21268128   PMID:21278389   PMID:21282187   PMID:21380782   PMID:21410323   PMID:21432864   PMID:21506705   PMID:21535266   PMID:21536749   PMID:21548981   PMID:21576258   PMID:21613208  
PMID:21636975   PMID:21668571   PMID:21672538   PMID:21704210   PMID:21708937   PMID:21733157   PMID:21744995   PMID:21757716   PMID:21761181   PMID:21798010   PMID:21805044   PMID:21823995  
PMID:21829393   PMID:21852217   PMID:21873635   PMID:21880216   PMID:21889930   PMID:21900206   PMID:21926269   PMID:22042095   PMID:22069105   PMID:22082268   PMID:22098246   PMID:22121898  
PMID:22140443   PMID:22188815   PMID:22189999   PMID:22242132   PMID:22245250   PMID:22248018   PMID:22253814   PMID:22253890   PMID:22309801   PMID:22341586   PMID:22347413   PMID:22372631  
PMID:22377707   PMID:22392079   PMID:22395465   PMID:22399759   PMID:22434232   PMID:22447362   PMID:22479380   PMID:22486985   PMID:22527168   PMID:22565227   PMID:22571677   PMID:22630333  
PMID:22646060   PMID:22662119   PMID:22666415   PMID:22679513   PMID:22684773   PMID:22770937   PMID:22800756   PMID:22879348   PMID:22893718   PMID:22902352   PMID:22907587   PMID:22926517  
PMID:22982059   PMID:22994732   PMID:23023303   PMID:23028800   PMID:23035551   PMID:23039012   PMID:23047069   PMID:23079385   PMID:23079386   PMID:23118352   PMID:23151531   PMID:23166326  
PMID:23171475   PMID:23207153   PMID:23227253   PMID:23257688   PMID:23299523   PMID:23319492   PMID:23363476   PMID:23376485   PMID:23388414   PMID:23410103   PMID:23479510   PMID:23485847  
PMID:23497056   PMID:23530192   PMID:23539881   PMID:23558990   PMID:23593202   PMID:23620526   PMID:23623986   PMID:23677070   PMID:23690138   PMID:23714241   PMID:23724145   PMID:23725790  
PMID:23750643   PMID:23757053   PMID:23775149   PMID:23840540   PMID:23840686   PMID:23844573   PMID:23890452   PMID:23936387   PMID:23943562   PMID:23962719   PMID:24081183   PMID:24112161  
PMID:24178245   PMID:24182837   PMID:24184209   PMID:24266751   PMID:24318096   PMID:24349121   PMID:24380854   PMID:24407433   PMID:24451943   PMID:24454871   PMID:24469060   PMID:24498411  
PMID:24558376   PMID:24599933   PMID:24656929   PMID:24706416   PMID:24711554   PMID:24725430   PMID:24732467   PMID:24804818   PMID:24846856   PMID:24883437   PMID:24886724   PMID:24904527  
PMID:24915949   PMID:24916376   PMID:24932685   PMID:24956249   PMID:24972507   PMID:24986528   PMID:25001656   PMID:25066218   PMID:25068994   PMID:25086101   PMID:25089899   PMID:25090267  
PMID:25110432   PMID:25171170   PMID:25200291   PMID:25277046   PMID:25292066   PMID:25293351   PMID:25395389   PMID:25416956   PMID:25423083   PMID:25435370   PMID:25458127   PMID:25503665  
PMID:25556430   PMID:25639378   PMID:25670080   PMID:25719943   PMID:25739014   PMID:25740666   PMID:25743702   PMID:25771989   PMID:25874233   PMID:25890304   PMID:25918994   PMID:25931278  
PMID:25971976   PMID:25987019   PMID:25993872   PMID:26015264   PMID:26056743   PMID:26056800   PMID:26063187   PMID:26063585   PMID:26066673   PMID:26068014   PMID:26116569   PMID:26118397  
PMID:26154720   PMID:26333472   PMID:26336825   PMID:26397886   PMID:26400872   PMID:26407907   PMID:26475334   PMID:26496499   PMID:26676988   PMID:26677828   PMID:26751131   PMID:26760116  
PMID:26840070   PMID:26976474   PMID:26984550   PMID:27023171   PMID:27180807   PMID:27185872   PMID:27275535   PMID:27326759   PMID:27337954   PMID:27366946   PMID:27466488   PMID:27486970  
PMID:27510031   PMID:27535174   PMID:27535712   PMID:27535767   PMID:27546618   PMID:27548502   PMID:27582487   PMID:27612309   PMID:27614046   PMID:27621468   PMID:27650505   PMID:27667266  
PMID:27687727   PMID:27701793   PMID:27768959   PMID:27780718   PMID:27797252   PMID:27869826   PMID:27874091   PMID:27895308   PMID:28081695   PMID:28186102   PMID:28295307   PMID:28324020  
PMID:28389567   PMID:28460554   PMID:28514442   PMID:28534511   PMID:28611215   PMID:28629288   PMID:28653763   PMID:28681154   PMID:28729397   PMID:28753127   PMID:28778973   PMID:28829218  
PMID:28838971   PMID:28871451   PMID:28873464   PMID:29017567   PMID:29017633   PMID:29039467   PMID:29107196   PMID:29115555   PMID:29134283   PMID:29157910   PMID:29207103   PMID:29239100  
PMID:29277274   PMID:29328418   PMID:29335842   PMID:29374985   PMID:29413895   PMID:29414792   PMID:29562959   PMID:29604392   PMID:29608283   PMID:29716918   PMID:29758070   PMID:29889555  
PMID:29951828   PMID:29970663   PMID:30044176   PMID:30073757   PMID:30082314   PMID:30176105   PMID:30202859   PMID:30226576   PMID:30231881   PMID:30244832   PMID:30270743   PMID:30277114  
PMID:30382470   PMID:30423304   PMID:30672383   PMID:30672430   PMID:30680773   PMID:30686519   PMID:30714617   PMID:30745181   PMID:30745570   PMID:30949792   PMID:31053723   PMID:31114986  
PMID:31182144   PMID:31194812   PMID:31210310   PMID:31270394   PMID:31291686   PMID:31298373   PMID:31366504   PMID:31370882   PMID:31378849   PMID:31391242   PMID:31542774   PMID:31544945  
PMID:31591438   PMID:31841752   PMID:31914674   PMID:31922228   PMID:31926240   PMID:31941753   PMID:32070145   PMID:32150081   PMID:32161368   PMID:32191705   PMID:32296183   PMID:32352694  
PMID:32399056   PMID:32427884   PMID:32987099   PMID:33293585  


Genomics

Comparative Map Data
IGF2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl112,129,112 - 2,141,238 (-)EnsemblGRCh38hg38GRCh38
GRCh38112,129,117 - 2,149,566 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37112,150,342 - 2,170,833 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36112,106,923 - 2,127,409 (-)NCBINCBI36hg18NCBI36
Build 34112,110,531 - 2,116,578NCBI
Celera112,186,838 - 2,207,338 (-)NCBI
Cytogenetic Map11p15.5NCBI
HuRef111,940,869 - 1,961,095 (-)NCBIHuRef
CHM1_1112,148,968 - 2,169,786 (-)NCBICHM1_1
Igf2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm397142,204,505 - 142,220,566 (-)NCBIGRCm39mm39
GRCm39 Ensembl7142,204,503 - 142,220,553 (-)Ensembl
GRCm387142,650,768 - 142,666,816 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl7142,650,766 - 142,666,816 (-)EnsemblGRCm38mm10GRCm38
MGSCv377149,836,673 - 149,846,940 (-)NCBIGRCm37mm9NCBIm37
MGSCv367142,460,158 - 142,468,879 (-)NCBImm8
Celera7142,407,105 - 142,417,364 (-)NCBICelera
Cytogenetic Map7F5NCBI
cM Map787.99NCBI
Igf2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21197,814,409 - 197,831,802 (-)NCBI
Rnor_6.0 Ensembl1215,828,102 - 215,846,911 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.01215,828,102 - 215,839,081 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01222,722,921 - 222,733,868 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41202,906,624 - 202,915,231 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11203,094,689 - 203,103,297 (-)NCBI
Celera1195,432,460 - 195,442,561 (-)NCBICelera
Cytogenetic Map1q41NCBI
Igf2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495542213,880,471 - 13,888,566 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495542213,880,525 - 13,907,963 (-)NCBIChiLan1.0ChiLan1.0
IGF2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1112,202,764 - 2,228,890 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl112,202,743 - 2,228,890 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0112,170,190 - 2,199,442 (-)NCBIMhudiblu_PPA_v0panPan3
IGF2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11846,294,036 - 46,311,982 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1846,294,019 - 46,311,982 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1844,906,773 - 44,921,790 (-)NCBI
ROS_Cfam_1.01846,973,499 - 46,991,455 (-)NCBI
UMICH_Zoey_3.11846,425,198 - 46,440,216 (-)NCBI
UNSW_CanFamBas_1.01846,005,530 - 46,020,544 (-)NCBI
UU_Cfam_GSD_1.01846,751,952 - 46,766,988 (-)NCBI
Igf2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_ltri_2NW_0244049471,719,158 - 1,727,419 (-)NCBI
SpeTri2.0NW_004936816972,902 - 981,232 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
IGF2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.121,469,183 - 1,496,417 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Pig Cytomap2pNCBI
IGF2
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.111,937,414 - 1,951,238 (-)NCBI
ChlSab1.1 Ensembl11,936,830 - 1,945,388 (-)Ensembl
Igf2
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462476714,969,977 - 14,997,577 (-)NCBI

Position Markers
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
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
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: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: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
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
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
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
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
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
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 - 2,152,729UniSTSGRCh37
GRCh37112,152,579 - 2,152,806UniSTSGRCh37
Build 36112,109,155 - 2,109,305RGDNCBI36
Celera112,189,070 - 2,189,497UniSTS
Celera112,189,070 - 2,189,220RGD
Celera112,189,070 - 2,189,297UniSTS
Cytogenetic Map11p15.5UniSTS
HuRef111,943,102 - 1,943,529UniSTS
HuRef111,943,101 - 1,943,328UniSTS
HuRef111,943,101 - 1,943,251UniSTS
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
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
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
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
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
D8S2278  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3p25.3-p24.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map10q11UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map12q21.31UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic MapXp22.1UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map4q34.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map2p23.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map12p12.3UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map14q22UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map4q31UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map15q15-q21.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map12q14.3-q15UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map21q21.1UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1p13-p12UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map10q21.1UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map14q31UniSTS
GDB:677440  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map11p15.5UniSTS
IGF2  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map11p15.5UniSTS
GeneMap99-GB4 RH Map1116.52UniSTS
NCBI RH Map1110.0UniSTS

miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR125B1hsa-miR-125b-5pMirtarbaseexternal_infoLuciferase reporter assay//Northern blot//Western Functional MTI21200031
MIRLET7A2hsa-let-7a-5pMirtarbaseexternal_infoLuciferase reporter assayFunctional MTI17974952
MIR125B2hsa-miR-125b-5pMirtarbaseexternal_infoLuciferase reporter assay//Northern blot//Western Functional MTI21200031
MIR615hsa-miR-615-5pMirtarbaseexternal_infoLuciferase reporter assayFunctional MTI22819824
MIR615hsa-miR-615-5pOncomiRDBexternal_infoNANA22819824
MIRLET7A1hsa-let-7a-5pMirtarbaseexternal_infoLuciferase reporter assayFunctional MTI17974952
MIR150hsa-miR-150-5pMirtarbaseexternal_infoLuciferase reporter assayNon-Functional MTI21200031

Predicted Target Of
Summary Value
Count of predictions:9376
Count of miRNA genes:938
Interacting mature miRNAs:1172
Transcripts:ENST00000300632, ENST00000381389, ENST00000381392, ENST00000381395, ENST00000381406, ENST00000416167, ENST00000418738, ENST00000434045
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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


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 visual system adipose tissue appendage entire extraembryonic component
High 17 34 32 32 2 4 6 10 35 8 1 1
Medium 1575 1938 1346 427 190 355 2930 1893 1003 149 1036 840 78 1198 2139 3
Low 771 601 319 151 679 61 1369 275 2612 206 336 652 94 1 6 647 1
Below cutoff 48 442 19 10 490 14 42 18 81 47 38 80 2 1 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_008849 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NG_050578 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_000612 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001007139 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001127598 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001291861 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001291862 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA040827 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC132217 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF318382 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF517226 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH002704 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH005228 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK025719 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074614 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK126688 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK313938 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY971350 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC000531 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC011786 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC042127 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC053318 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC073756 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BE270173 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM667567 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP233290 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ014465 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT007013 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471158 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN277570 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA641853 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ104203 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU326141 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU622024 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FB571441 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GM741469 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM481219 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM481220 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  J03242 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M17426 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M17863 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M29645 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  S51971 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  S77035 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X00910 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X03425 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X03426 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X03427 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X03562 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X06159 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X06160 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X06161 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X06259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X06260 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X07868 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X53038 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X56539 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X56540 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Y13633 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000381389   ⟹   ENSP00000370796
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl112,132,673 - 2,141,016 (-)Ensembl
RefSeq Acc Id: ENST00000381392   ⟹   ENSP00000370799
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl112,132,640 - 2,137,287 (-)Ensembl
RefSeq Acc Id: ENST00000381395   ⟹   ENSP00000370802
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl112,129,112 - 2,137,290 (-)Ensembl
RefSeq Acc Id: ENST00000381406   ⟹   ENSP00000370813
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl112,129,112 - 2,138,974 (-)Ensembl
RefSeq Acc Id: ENST00000416167   ⟹   ENSP00000414497
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl112,129,117 - 2,139,389 (-)Ensembl
RefSeq Acc Id: ENST00000418738   ⟹   ENSP00000402047
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl112,132,716 - 2,137,305 (-)Ensembl
RefSeq Acc Id: ENST00000434045   ⟹   ENSP00000391826
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl112,132,500 - 2,141,238 (-)Ensembl
RefSeq Acc Id: NM_000612   ⟹   NP_000603
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,129,117 - 2,139,389 (-)NCBI
GRCh37112,150,346 - 2,179,611 (-)NCBI
Build 36112,106,923 - 2,116,780 (-)NCBI Archive
HuRef111,940,869 - 1,961,095 (-)ENTREZGENE
CHM1_1112,148,968 - 2,158,828 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001007139   ⟹   NP_001007140
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,129,117 - 2,149,566 (-)NCBI
GRCh38112,129,112 - 2,149,603 (-)NCBI
GRCh37112,150,346 - 2,179,611 (-)NCBI
Build 36112,106,923 - 2,127,409 (-)NCBI Archive
HuRef111,940,869 - 1,961,095 (-)ENTREZGENE
CHM1_1112,148,968 - 2,169,786 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001127598   ⟹   NP_001121070
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,129,117 - 2,140,943 (-)NCBI
GRCh37112,150,346 - 2,179,611 (-)NCBI
HuRef111,940,869 - 1,961,095 (-)ENTREZGENE
CHM1_1112,148,968 - 2,161,307 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001291861   ⟹   NP_001278790
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,129,117 - 2,137,288 (-)NCBI
CHM1_1112,148,968 - 2,157,142 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001291862   ⟹   NP_001278791
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,129,117 - 2,140,943 (-)NCBI
CHM1_1112,148,968 - 2,161,307 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_000603 (Get FASTA)   NCBI Sequence Viewer  
  NP_001007140 (Get FASTA)   NCBI Sequence Viewer  
  NP_001121070 (Get FASTA)   NCBI Sequence Viewer  
  NP_001278790 (Get FASTA)   NCBI Sequence Viewer  
  NP_001278791 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAA52443 (Get FASTA)   NCBI Sequence Viewer  
  AAA52536 (Get FASTA)   NCBI Sequence Viewer  
  AAA52544 (Get FASTA)   NCBI Sequence Viewer  
  AAA52545 (Get FASTA)   NCBI Sequence Viewer  
  AAA60088 (Get FASTA)   NCBI Sequence Viewer  
  AAB34155 (Get FASTA)   NCBI Sequence Viewer  
  AAD14908 (Get FASTA)   NCBI Sequence Viewer  
  AAH00531 (Get FASTA)   NCBI Sequence Viewer  
  AAL55889 (Get FASTA)   NCBI Sequence Viewer  
  AAM51825 (Get FASTA)   NCBI Sequence Viewer  
  AAP35659 (Get FASTA)   NCBI Sequence Viewer  
  AAY40360 (Get FASTA)   NCBI Sequence Viewer  
  ABD93451 (Get FASTA)   NCBI Sequence Viewer  
  ACC95538 (Get FASTA)   NCBI Sequence Viewer  
  ADO21454 (Get FASTA)   NCBI Sequence Viewer  
  ADO21455 (Get FASTA)   NCBI Sequence Viewer  
  BAG36657 (Get FASTA)   NCBI Sequence Viewer  
  BAG54360 (Get FASTA)   NCBI Sequence Viewer  
  CAA25426 (Get FASTA)   NCBI Sequence Viewer  
  CAA27155 (Get FASTA)   NCBI Sequence Viewer  
  CAA27156 (Get FASTA)   NCBI Sequence Viewer  
  CAA27157 (Get FASTA)   NCBI Sequence Viewer  
  CAA27249 (Get FASTA)   NCBI Sequence Viewer  
  CAA29516 (Get FASTA)   NCBI Sequence Viewer  
  CAA29517 (Get FASTA)   NCBI Sequence Viewer  
  CAA29518 (Get FASTA)   NCBI Sequence Viewer  
  CAA30717 (Get FASTA)   NCBI Sequence Viewer  
  CAR95138 (Get FASTA)   NCBI Sequence Viewer  
  CAV31678 (Get FASTA)   NCBI Sequence Viewer  
  EAX02485 (Get FASTA)   NCBI Sequence Viewer  
  P01344 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_001007140   ⟸   NM_001007139
- Peptide Label: isoform 1 preproprotein
- UniProtKB: P01344 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001121070   ⟸   NM_001127598
- Peptide Label: isoform 2
- UniProtKB: P01344 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_000603   ⟸   NM_000612
- Peptide Label: isoform 1 preproprotein
- UniProtKB: P01344 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001278791   ⟸   NM_001291862
- Peptide Label: isoform 1 preproprotein
- UniProtKB: P01344 (UniProtKB/Swiss-Prot),   E3UN46 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001278790   ⟸   NM_001291861
- Peptide Label: isoform 1 preproprotein
- UniProtKB: P01344 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000414497   ⟸   ENST00000416167
RefSeq Acc Id: ENSP00000402047   ⟸   ENST00000418738
RefSeq Acc Id: ENSP00000391826   ⟸   ENST00000434045
RefSeq Acc Id: ENSP00000370796   ⟸   ENST00000381389
RefSeq Acc Id: ENSP00000370802   ⟸   ENST00000381395
RefSeq Acc Id: ENSP00000370799   ⟸   ENST00000381392
RefSeq Acc Id: ENSP00000370813   ⟸   ENST00000381406
Protein Domains
IlGF

Promoters
RGD ID:6850060
Promoter ID:EP28009
Type:single initiation site
Name:HS_IGF2_4
Description:Insulin-like growth factor II, IGF2 gene.
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Notes:homology_group=Homology group 155; Mammalian insulin-like growth factor 2 E3/E4.
Alternative Promoters:alternative promoter #4 of 4; 5' exon 4; site 1.; see alsoEP17071  EP28010  EP17072  
Tissues & Cell Lines:fetus, adult, nonhepatic tissue
Experiment Methods:Nuclease protection; experiments performed with closely related; gene; Primer extension; experiments performed with closely related; gene
Position:
Human AssemblyChrPosition (strand)Source
Build 36112,115,093 - 2,115,153EPD
RGD ID:6850056
Promoter ID:EP17072
Type:single initiation site
Name:HS_IGF2_3
Description:Insulin-like growth factor II, IGF2 gene.
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Notes:homology_group=Homology group 137; Mammalian insulin-like growth factor 2 E2/E3.
Alternative Promoters:alternative promoter #3 of 4; 5' exon 3; site 1.; see alsoEP17071  EP28010  EP28009  
Tissues & Cell Lines:fetus, adult, nonhepatic tissue
Experiment Methods:Sequencing of a full-length cDNA
Position:
Human AssemblyChrPosition (strand)Source
Build 36112,117,199 - 2,117,259EPD
RGD ID:6850052
Promoter ID:EP28010
Type:initiation region
Name:HS_IGF2_2
Description:Insulin-like growth factor II, IGF2 gene.
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:alternative promoter #2 of 4; 5' exon 2; site 1.; see alsoEP17071  EP17072  EP28009  
Tissues & Cell Lines:fetus, liver
Experiment Methods:Primer extension
Position:
Human AssemblyChrPosition (strand)Source
Build 36112,119,052 - 2,119,112EPD
RGD ID:7219305
Promoter ID:EPDNEW_H15398
Type:initiation region
Name:IGF2_10
Description:insulin like growth factor 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15399  EPDNEW_H15400  EPDNEW_H15401  EPDNEW_H15402  EPDNEW_H15404  EPDNEW_H15403  EPDNEW_H15406  EPDNEW_H15405  EPDNEW_H15408  EPDNEW_H15407  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,129,576 - 2,129,636EPDNEW
RGD ID:7219307
Promoter ID:EPDNEW_H15399
Type:initiation region
Name:IGF2_3
Description:insulin like growth factor 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15398  EPDNEW_H15400  EPDNEW_H15401  EPDNEW_H15402  EPDNEW_H15404  EPDNEW_H15403  EPDNEW_H15406  EPDNEW_H15405  EPDNEW_H15408  EPDNEW_H15407  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,130,576 - 2,130,636EPDNEW
RGD ID:7219309
Promoter ID:EPDNEW_H15400
Type:initiation region
Name:IGF2_8
Description:insulin like growth factor 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15398  EPDNEW_H15399  EPDNEW_H15401  EPDNEW_H15402  EPDNEW_H15404  EPDNEW_H15403  EPDNEW_H15406  EPDNEW_H15405  EPDNEW_H15408  EPDNEW_H15407  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,130,770 - 2,130,830EPDNEW
RGD ID:7219311
Promoter ID:EPDNEW_H15401
Type:initiation region
Name:IGF2_5
Description:insulin like growth factor 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15398  EPDNEW_H15399  EPDNEW_H15400  EPDNEW_H15402  EPDNEW_H15404  EPDNEW_H15403  EPDNEW_H15406  EPDNEW_H15405  EPDNEW_H15408  EPDNEW_H15407  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,132,381 - 2,132,441EPDNEW
RGD ID:7219313
Promoter ID:EPDNEW_H15402
Type:initiation region
Name:IGF2_7
Description:insulin like growth factor 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15398  EPDNEW_H15399  EPDNEW_H15400  EPDNEW_H15401  EPDNEW_H15404  EPDNEW_H15403  EPDNEW_H15406  EPDNEW_H15405  EPDNEW_H15408  EPDNEW_H15407  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,132,871 - 2,132,931EPDNEW
RGD ID:7219317
Promoter ID:EPDNEW_H15403
Type:initiation region
Name:IGF2_6
Description:insulin like growth factor 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15398  EPDNEW_H15399  EPDNEW_H15400  EPDNEW_H15401  EPDNEW_H15402  EPDNEW_H15404  EPDNEW_H15406  EPDNEW_H15405  EPDNEW_H15408  EPDNEW_H15407  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,133,647 - 2,133,707EPDNEW
RGD ID:6850048
Promoter ID:EP17071
Type:single initiation site
Name:HS_IGF2_1
Description:Insulin-like growth factor II, IGF2 gene.
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:alternative promoter #1 of 4; 5' exon 1; site 1.; see alsoEP28010  EP17072  EP28009  
Tissues & Cell Lines:adult, liver
Experiment Methods:Primer extension
Position:
Human AssemblyChrPosition (strand)Source
Build 36112,136,189 - 2,136,249EPD
RGD ID:7219315
Promoter ID:EPDNEW_H15404
Type:multiple initiation site
Name:IGF2_2
Description:insulin like growth factor 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15398  EPDNEW_H15399  EPDNEW_H15400  EPDNEW_H15401  EPDNEW_H15402  EPDNEW_H15403  EPDNEW_H15406  EPDNEW_H15405  EPDNEW_H15408  EPDNEW_H15407  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,137,288 - 2,137,348EPDNEW
RGD ID:7219321
Promoter ID:EPDNEW_H15405
Type:initiation region
Name:IGF2_4
Description:insulin like growth factor 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15398  EPDNEW_H15399  EPDNEW_H15400  EPDNEW_H15401  EPDNEW_H15402  EPDNEW_H15404  EPDNEW_H15403  EPDNEW_H15406  EPDNEW_H15408  EPDNEW_H15407  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,138,352 - 2,138,412EPDNEW
RGD ID:7219319
Promoter ID:EPDNEW_H15406
Type:initiation region
Name:IGF2_9
Description:insulin like growth factor 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15398  EPDNEW_H15399  EPDNEW_H15400  EPDNEW_H15401  EPDNEW_H15402  EPDNEW_H15404  EPDNEW_H15403  EPDNEW_H15405  EPDNEW_H15408  EPDNEW_H15407  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,138,642 - 2,138,702EPDNEW
RGD ID:7219325
Promoter ID:EPDNEW_H15407
Type:initiation region
Name:IGF2_1
Description:insulin like growth factor 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15398  EPDNEW_H15399  EPDNEW_H15400  EPDNEW_H15401  EPDNEW_H15402  EPDNEW_H15404  EPDNEW_H15403  EPDNEW_H15406  EPDNEW_H15405  EPDNEW_H15408  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,139,389 - 2,139,449EPDNEW
RGD ID:7219323
Promoter ID:EPDNEW_H15408
Type:initiation region
Name:IGF2_11
Description:insulin like growth factor 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15398  EPDNEW_H15399  EPDNEW_H15400  EPDNEW_H15401  EPDNEW_H15402  EPDNEW_H15404  EPDNEW_H15403  EPDNEW_H15406  EPDNEW_H15405  EPDNEW_H15407  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38112,141,246 - 2,141,306EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
IGF2, 6815A-T single nucleotide variant INSULIN-LIKE GROWTH FACTOR II POLYMORPHISM [RCV000015869] Chr11:11p15.5 benign
IGF2, 1156C-T single nucleotide variant INSULIN-LIKE GROWTH FACTOR II POLYMORPHISM [RCV000015870] Chr11:11p15.5 benign
IGF2, 1926C-G single nucleotide variant INSULIN-LIKE GROWTH FACTOR II POLYMORPHISM [RCV000015871] Chr11:11p15.5 benign
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(chr11:196966-4435344)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(chr11:218365-3377077)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
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 11p15.5-15.4(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(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(chr11:1975511-3624139)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_000612.6(IGF2):c.23C>A (p.Ser8Ter) single nucleotide variant Growth restriction, severe, with distinctive facies [RCV000186560] Chr11:2135501 [GRCh38]
Chr11:2156731 [GRCh37]
Chr11:11p15.5
pathogenic|likely pathogenic
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.518dup (p.Glu174fs) duplication not provided [RCV000520721] Chr11:2133011..2133012 [GRCh38]
Chr11:2154241..2154242 [GRCh37]
Chr11:11p15.5
uncertain significance
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_000612.6(IGF2):c.78C>G (p.Tyr26Ter) single nucleotide variant Russell-Silver syndrome [RCV000491853]|not provided [RCV000479354] Chr11:2135446 [GRCh38]
Chr11:2156676 [GRCh37]
Chr11:11p15.5
pathogenic
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 Russell-Silver syndrome [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 11p15.5-15.3(chr11:193146-12643136) copy number gain Russell-Silver syndrome [RCV000767567] Chr11:193146..12643136 [GRCh37]
Chr11:11p15.5-15.3
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 11p15.5-15.4(chr11:230615-9704511)x3 copy number gain not provided [RCV000683369] Chr11:230615..9704511 [GRCh37]
Chr11:11p15.5-15.4
pathogenic
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-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.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.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 not provided [RCV000903609] Chr11:2133149 [GRCh38]
Chr11:2154379 [GRCh37]
Chr11:11p15.5
benign
NM_000612.6(IGF2):c.480T>C (p.Ala160=) single nucleotide variant not provided [RCV000948858] Chr11:2133050 [GRCh38]
Chr11:2154280 [GRCh37]
Chr11:11p15.5
likely benign
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 not provided [RCV000882263] Chr11:2140200 [GRCh38]
Chr11:2161430 [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_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
GRCh37/hg19 11p15.5-13(chr11:235934-33826995)x3 copy number gain not provided [RCV001006372] Chr11:235934..33826995 [GRCh37]
Chr11:11p15.5-13
pathogenic
NC_000011.9:g.(?_532616)_(2906985_?)dup duplication Neuronal ceroid lipofuscinosis [RCV001032557] Chr11:532616..2906985 [GRCh37]
Chr11:11p15.5-15.4
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
NC_000011.9:g.(?_612625)_(2193840_?)dup duplication Immunodeficiency 39 [RCV001033372] Chr11:612625..2193840 [GRCh37]
Chr11:11p15.5
uncertain significance
NM_000612.6(IGF2):c.157+3A>C single nucleotide variant Growth restriction, severe, with distinctive facies [RCV001174515] Chr11:2135364 [GRCh38]
Chr11:2156594 [GRCh37]
Chr11:11p15.5
pathogenic
NM_000612.6(IGF2):c.101G>A (p.Gly34Asp) single nucleotide variant Growth restriction, severe, with distinctive facies [RCV001174514] Chr11:2135423 [GRCh38]
Chr11:2156653 [GRCh37]
Chr11:11p15.5
pathogenic
NM_000612.6(IGF2):c.195del (p.Ile66fs) deletion Growth restriction, severe, with distinctive facies [RCV001174516] Chr11:2133628 [GRCh38]
Chr11:2154858 [GRCh37]
Chr11:11p15.5
pathogenic
NM_000612.6(IGF2):c.110_117delinsAGGTAA (p.Leu37fs) indel Growth restriction, severe, with distinctive facies [RCV001174513] Chr11:2135407..2135414 [GRCh38]
Chr11:2156637..2156644 [GRCh37]
Chr11:11p15.5
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.27del (p.Met9fs) deletion Growth restriction, severe, with distinctive facies [RCV001253454] Chr11:2135497 [GRCh38]
Chr11:2156727 [GRCh37]
Chr11:11p15.5
uncertain significance
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.100G>T (p.Gly34Cys) single nucleotide variant Growth restriction, severe, with distinctive facies [RCV001253240] Chr11:2135424 [GRCh38]
Chr11:2156654 [GRCh37]
Chr11:11p15.5
likely pathogenic
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(chr11:210300-8664358)x3 copy number gain Russell-Silver syndrome [RCV001263222] Chr11:210300..8664358 [GRCh37]
Chr11:11p15.5-15.4
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:5466 AgrOrtholog
COSMIC IGF2 COSMIC
Ensembl Genes ENSG00000167244 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Protein ENSP00000370796 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000370799 UniProtKB/Swiss-Prot
  ENSP00000370802 UniProtKB/Swiss-Prot
  ENSP00000370813 UniProtKB/Swiss-Prot
  ENSP00000391826 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000402047 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000414497 ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000381389 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000381392 UniProtKB/Swiss-Prot
  ENST00000381395 UniProtKB/Swiss-Prot
  ENST00000381406 UniProtKB/Swiss-Prot
  ENST00000416167 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000418738 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000434045 ENTREZGENE, UniProtKB/Swiss-Prot
GTEx ENSG00000167244 GTEx
HGNC ID HGNC:5466 ENTREZGENE
Human Proteome Map IGF2 Human Proteome Map
InterPro IGF2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  IGF2_C UniProtKB/Swiss-Prot
  Insulin-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Insulin-like_growth_factor UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Insulin-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Insulin_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Insulin_family UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:3481 UniProtKB/Swiss-Prot
NCBI Gene 3481 ENTREZGENE
OMIM 147470 OMIM
  616489 OMIM
Pfam IGF2_C UniProtKB/Swiss-Prot
  Insulin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA29699 PharmGKB
PRINTS INSLNLIKEGF UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  INSLNLIKEGF2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  INSULINFAMLY UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE INSULIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART IlGF UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF56994 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A024RCE6_HUMAN UniProtKB/TrEMBL
  B2MUX6_HUMAN UniProtKB/TrEMBL
  E3UN46 ENTREZGENE, UniProtKB/TrEMBL
  IGF2_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
UniProt Secondary B3KX48 UniProtKB/Swiss-Prot
  B7WP08 UniProtKB/Swiss-Prot
  C9JAF2 UniProtKB/Swiss-Prot
  E3UN45 UniProtKB/Swiss-Prot
  P78449 UniProtKB/Swiss-Prot
  Q14299 UniProtKB/Swiss-Prot
  Q1WM26 UniProtKB/Swiss-Prot
  Q9UC68 UniProtKB/Swiss-Prot
  Q9UC69 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-01 IGF2  insulin like growth factor 2    insulin-like growth factor 2  Symbol and/or name change 5135510 APPROVED
2014-09-24 IGF2  insulin-like growth factor 2    insulin-like growth factor 2 (somatomedin A)  Symbol and/or name change 5135510 APPROVED