CAV1 (caveolin 1) - Rat Genome Database
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Gene: CAV1 (caveolin 1) Homo sapiens
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Symbol: CAV1
Name: caveolin 1
RGD ID: 619568
HGNC Page HGNC
Description: Exhibits several functions, including enzyme binding activity; inward rectifier potassium channel inhibitor activity; and ion channel binding activity. Involved in several processes, including endocytosis; regulation of cellular protein metabolic process; and regulation of signal transduction. Localizes to several cellular components, including apical plasma membrane; basolateral plasma membrane; and caveola. Colocalizes with focal adhesion. Implicated in several diseases, including breast cancer (multiple); lipodystrophy (multiple); primary open angle glaucoma; primary pulmonary hypertension; and systemic scleroderma (multiple). Biomarker of several diseases, including acoustic neuroma; breast cancer (multiple); carcinoma (multiple); pulmonary hypertension; and systemic scleroderma.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: BSCL3; CAV; caveolin 1, caveolae protein, 22kDa; caveolin-1; cell growth-inhibiting protein 32; CGL3; LCCNS; MSTP085; PPH3; VIP21
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 Ensembl7116,524,994 - 116,561,179 (+)EnsemblGRCh38hg38GRCh38
GRCh38.p13 Ensembl7116,525,001 - 116,561,184 (+)EnsemblGRCh38hg38GRCh38
GRCh387116,525,009 - 116,561,185 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh377116,165,063 - 116,201,239 (+)NCBIGRCh37GRCh37hg19GRCh37
GRCh377116,164,839 - 116,201,239 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 367115,952,075 - 115,988,466 (+)NCBINCBI36hg18NCBI36
Build 347115,758,789 - 115,795,181NCBI
Celera7110,972,249 - 111,008,654 (+)NCBI
Cytogenetic Map7q31.2NCBI
HuRef7110,530,835 - 110,566,784 (+)NCBIHuRef
CHM1_17116,098,482 - 116,134,827 (+)NCBICHM1_1
CRA_TCAGchr7v27115,560,275 - 115,596,679 (+)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View
abdominal aortic aneurysm  (ISO)
acoustic neuroma  (IEP)
Acute Lung Injury  (ISO)
Alcoholic Liver Diseases  (ISO)
Alzheimer's disease  (ISS)
atherosclerosis  (ISO)
atrial fibrillation  (EXP)
brain ischemia  (ISO)
breast cancer  (IAGP,IDA,IEP,ISS)
breast carcinoma  (IAGP,IEP)
Breast Neoplasms  (EXP)
Carcinogenesis  (EXP)
Cardiomegaly  (EXP,ISO)
congenital generalized lipodystrophy type 3  (IAGP)
Dermal Fibrosis  (ISO)
diabetes mellitus  (IAGP)
diabetic neuropathy  (ISO)
diffuse scleroderma  (IAGP)
exfoliation syndrome  (IAGP)
Experimental Autoimmune Myocarditis  (ISO)
Experimental Autoimmune Neuritis  (ISO)
Experimental Diabetes Mellitus  (EXP,ISO)
Experimental Liver Cirrhosis  (EXP)
familial partial lipodystrophy  (EXP)
genetic disease  (IAGP)
Hemorrhage  (ISO)
high grade glioma  (ISO)
Hyperplasia  (ISO)
hypertension  (EXP,ISO)
hypertrophic cardiomyopathy  (ISS)
hypothyroidism  (ISO)
invasive ductal carcinoma  (IAGP)
leiomyoma  (IEP)
limited scleroderma  (IAGP)
Lipodystrophy with Congenital Cataracts and Neurodegeneration  (IAGP)
low tension glaucoma  (IAGP)
Lung Neoplasms  (EXP)
Lymphatic Metastasis  (IEP)
Mammary Neoplasms, Experimental  (IMP,ISO)
melanoma  (IEP)
multiple sclerosis  (IAGP)
Neoplasm Metastasis  (EXP,IMP,ISO)
Nephrogenic Fibrosing Dermopathy  (IAGP)
obesity  (ISO)
open-angle glaucoma  (EXP)
osteoarthritis  (ISO)
ovarian carcinoma  (IEP)
Ovarian Neoplasms  (EXP)
pleomorphic xanthoastrocytoma  (IAGP)
primary open angle glaucoma  (IAGP)
primary pulmonary hypertension  (EXP)
Primary Pulmonary Hypertension, 3  (IAGP)
prostate cancer  (IAGP,IDA,IEP)
Prostatic Neoplasms  (EXP,ISO)
psoriasis  (IEP)
Pulmonary Arterial Hypertension  (IAGP)
pulmonary fibrosis  (ISO)
pulmonary hypertension  (IEP,ISO)
renal cell carcinoma  (IEP)
Reperfusion Injury  (ISO)
Sarcopenia  (IAGP)
sciatic neuropathy  (ISO)
Spinal Cord Injuries  (ISO)
squamous cell carcinoma  (ISO)
Stevens-Johnson syndrome  (EXP)
Stomach Neoplasms  (EXP)
systemic scleroderma  (IAGP,IEP)
transient cerebral ischemia  (ISO)
transitional cell carcinoma  (IEP)
urinary bladder cancer  (IEP)
Weight Gain  (EXP)

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-alpha-tocopherol  (EXP)
(-)-anisomycin  (EXP)
1,1-bis(2-aminoethyl)-2-hydroxy-3-oxotriazane  (EXP)
1,2-dimethylhydrazine  (ISO)
13-HPODE  (EXP)
17beta-estradiol  (EXP,ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2-ethoxyethanol  (ISO)
2-methoxyethanol  (ISO)
22-Hydroxycholesterol  (EXP)
3,3',4,4',5-pentachlorobiphenyl  (EXP,ISO)
3,3',4,4'-tetrachlorobiphenyl  (ISO)
3,3',5,5'-tetrabromobisphenol A  (ISO)
3-isobutyl-1-methyl-7H-xanthine  (ISO)
4,4'-diaminodiphenylmethane  (ISO)
4,4'-sulfonyldiphenol  (ISO)
5-aza-2'-deoxycytidine  (EXP)
5-fluorouracil  (EXP)
6-propyl-2-thiouracil  (ISO)
acetylcholine  (ISO)
acetylsalicylic acid  (ISO)
acrolein  (EXP)
actinomycin D  (EXP)
aflatoxin B1  (EXP)
aldehydo-D-glucose  (EXP)
all-trans-retinoic acid  (EXP)
alpha-pinene  (EXP)
aminoguanidine  (EXP)
ammonium chloride  (ISO)
amphetamine  (ISO)
amphibole asbestos  (ISO)
antirheumatic drug  (EXP)
Aroclor 1254  (ISO)
arsenite(3-)  (EXP,ISO)
arsenous acid  (EXP)
atrazine  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP)
benzo[b]fluoranthene  (ISO)
beta-carotene  (EXP)
beta-naphthoflavone  (ISO)
bis(2-ethylhexyl) phthalate  (EXP)
bisphenol A  (ISO)
Bisphenol A diglycidyl ether  (EXP)
bisphenol F  (ISO)
bleomycin A2  (ISO)
butan-1-ol  (EXP)
butyric acid  (ISO)
cadmium atom  (ISO)
cadmium dichloride  (EXP)
cadmium nitrate  (EXP)
caffeine  (EXP)
calcitriol  (EXP)
calcium atom  (ISO)
calcium(0)  (ISO)
camptothecin  (EXP)
captan  (ISO)
carbamazepine  (EXP)
carbon nanotube  (ISO)
carboxy-PTIO  (EXP)
celecoxib  (EXP)
chlorohydrocarbon  (ISO)
chloropicrin  (EXP)
cholesterol  (EXP,ISO)
chromium atom  (ISO)
chrysene  (ISO)
ciprofloxacin  (EXP)
cisplatin  (EXP,ISO)
clofibrate  (EXP)
cobalt dichloride  (EXP)
coumestrol  (EXP)
crocidolite asbestos  (ISO)
cumene  (ISO)
cycloheximide  (EXP)
cyclosporin A  (EXP)
cylindrospermopsin  (EXP)
cyproconazole  (EXP)
D-glucose  (EXP)
depsipeptide  (EXP)
desferrioxamine B  (EXP)
dexamethasone  (EXP,ISO)
diallyl disulfide  (EXP)
diallyl trisulfide  (EXP)
diarsenic trioxide  (EXP)
dibutyl phthalate  (ISO)
diethylstilbestrol  (ISO)
dioxygen  (EXP,ISO)
diuron  (ISO)
dorsomorphin  (EXP)
doxorubicin  (EXP,ISO)
equol  (EXP)
ethanol  (EXP,ISO)
ethyl methanesulfonate  (EXP)
fenofibrate  (EXP)
folic acid  (ISO)
folpet  (ISO)
formaldehyde  (EXP)
fulvestrant  (ISO)
furan  (ISO)
gefitinib  (EXP)
genistein  (EXP)
geranylgeraniol  (EXP)
glucose  (EXP)
hexadecanoic acid  (EXP)
hydrogen peroxide  (EXP,ISO)
iron atom  (ISO)
iron(0)  (ISO)
iron(2+) sulfate (anhydrous)  (ISO)
isoprenaline  (ISO)
lead diacetate  (ISO)
lipopolysaccharide  (EXP,ISO)
lithocholic acid  (EXP)
lysophosphatidylcholine  (EXP)
manganese atom  (ISO)
manganese(0)  (ISO)
mercury dibromide  (EXP)
methamphetamine  (ISO)
methotrexate  (EXP)
methoxychlor  (ISO)
methyl beta-cyclodextrin  (ISO)
methyl methanesulfonate  (EXP)
methylisothiazolinone  (EXP)
methylmercury chloride  (ISO)
mifepristone  (EXP)
miquelianin  (EXP)
monocrotaline  (ISO)
N-[3-(aminomethyl)benzyl]acetamidine  (EXP)
N-acetyl-L-cysteine  (EXP)
N-acetylsphingosine  (EXP)
N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal  (EXP,ISO)
N-nitrosodiethylamine  (EXP,ISO)
N-nitrosodimethylamine  (ISO)
nicotinic acid  (ISO)
nimesulide  (EXP)
nitric oxide  (EXP)
nitrofen  (ISO)
nitroprusside  (EXP)
NS-398  (EXP)
nystatin  (EXP)
octanoic acid  (ISO)
ouabain  (EXP)
oxaliplatin  (ISO)
ozone  (EXP,ISO)
p-menthan-3-ol  (EXP)
paclitaxel  (EXP)
paracetamol  (EXP,ISO)
paraquat  (ISO)
phenethyl isothiocyanate  (EXP)
phenobarbital  (ISO)
phenylephrine  (ISO)
phenylmercury acetate  (EXP)
pioglitazone  (EXP)
pirinixic acid  (EXP,ISO)
piroxicam  (EXP)
poly(I:C)  (ISO)
potassium chloride  (ISO)
progesterone  (EXP)
quercetin  (EXP,ISO)
raloxifene  (EXP,ISO)
reactive oxygen species  (ISO)
rebaudioside A  (EXP)
resveratrol  (EXP,ISO)
rimonabant  (ISO)
SB 203580  (EXP,ISO)
SB 431542  (EXP)
silicon dioxide  (EXP,ISO)
simvastatin  (EXP,ISO)
sodium arsenite  (EXP,ISO)
Soman  (ISO)
streptozocin  (ISO)
sulfasalazine  (ISO)
tamoxifen  (EXP)
taurocholic acid  (EXP)
tert-butyl hydroperoxide  (EXP)
testosterone  (EXP)
tetrachloromethane  (ISO)
tetraphene  (ISO)
theophylline  (EXP)
thioacetamide  (ISO)
titanium dioxide  (EXP,ISO)
tolfenamic acid  (EXP)
toluene 2,4-diisocyanate  (EXP,ISO)
topotecan  (ISO)
tremolite asbestos  (ISO)
triadimefon  (EXP)
trichostatin A  (EXP)
triclosan  (EXP)
trimellitic anhydride  (ISO)
Triptolide  (ISO)
troglitazone  (ISO)
tyrphostin AG 1478  (EXP)
valproic acid  (EXP)
vinclozolin  (ISO)
vitamin E  (EXP,ISO)
vorinostat  (EXP)
wogonin  (EXP)
wortmannin  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
angiogenesis  (IEA,ISO)
angiotensin-activated signaling pathway involved in heart process  (ISO,ISS)
animal organ regeneration  (ISO)
apoptotic signaling pathway  (IMP)
basement membrane organization  (IEA,ISO)
beta-catenin destruction complex disassembly  (TAS)
calcium ion homeostasis  (ISO,ISS)
calcium ion transport  (ISO,ISS)
caveola assembly  (IBA,IEA,IGI,IMP,ISO,ISS)
caveolin-mediated endocytosis  (IDA,ISO)
cell differentiation  (IBA)
cellular calcium ion homeostasis  (ISO,ISS)
cellular response to exogenous dsRNA  (IMP)
cellular response to hyperoxia  (IMP)
cellular response to mechanical stimulus  (ISO)
cellular response to peptide hormone stimulus  (ISO,ISS)
cellular response to starvation  (IEP)
cellular response to transforming growth factor beta stimulus  (IEA,ISO)
cellular senescence  (ISO)
cholesterol efflux  (ISO)
cholesterol homeostasis  (ISO,ISS,TAS)
cholesterol transport  (TAS)
inactivation of MAPK activity  (ISO,ISS)
insulin receptor internalization  (IEA,ISO)
lactation  (IEA,ISO)
leukocyte migration  (TAS)
lipid storage  (ISO,ISS)
maintenance of protein location in cell  (ISO,ISS)
mammary gland development  (ISO,ISS)
mammary gland involution  (ISO,ISS)
membrane depolarization  (ISO,ISS)
microtubule polymerization  (ISO)
negative regulation of anoikis  (IMP,ISO)
negative regulation of BMP signaling pathway  (IDA)
negative regulation of canonical Wnt signaling pathway  (ISO,ISS)
negative regulation of cation channel activity  (ISO)
negative regulation of cell population proliferation  (ISO)
negative regulation of cytokine-mediated signaling pathway  (IEA,ISO)
negative regulation of endothelial cell proliferation  (IBA,ISO,ISS)
negative regulation of epithelial cell differentiation  (ISO,ISS)
negative regulation of ERK1 and ERK2 cascade  (ISO)
negative regulation of inward rectifier potassium channel activity  (IMP)
negative regulation of MAP kinase activity  (ISO)
negative regulation of MAPK cascade  (ISO,ISS)
negative regulation of muscle cell apoptotic process  (ISO)
negative regulation of necroptotic process  (IEA,ISO)
negative regulation of neuron differentiation  (ISO)
negative regulation of nitric oxide biosynthetic process  (ISO,ISS)
negative regulation of nitric-oxide synthase activity  (IEA,ISO)
negative regulation of peptidyl-serine phosphorylation  (IDA)
negative regulation of peptidyl-tyrosine autophosphorylation  (IMP,ISO)
negative regulation of pinocytosis  (IMP)
negative regulation of potassium ion transmembrane transport  (IMP)
negative regulation of protein binding  (IDA)
negative regulation of protein tyrosine kinase activity  (IBA,IMP,ISO)
negative regulation of protein ubiquitination  (IMP,ISO)
negative regulation of receptor signaling pathway via JAK-STAT  (ISO,ISS)
negative regulation of signal transduction  (ISO)
negative regulation of smooth muscle cell proliferation  (ISO)
negative regulation of transcription by RNA polymerase II  (ISO,ISS)
negative regulation of transforming growth factor beta receptor signaling pathway  (IDA)
negative regulation of tyrosine phosphorylation of STAT protein  (IEA,ISO)
nitric oxide homeostasis  (ISO,ISS)
positive regulation of calcium ion transport into cytosol  (ISO,ISS)
positive regulation of canonical Wnt signaling pathway  (IMP)
positive regulation of catalytic activity  (ISO,ISS)
positive regulation of cell adhesion molecule production  (IMP)
positive regulation of cell migration  (IMP)
positive regulation of cholesterol efflux  (IDA)
positive regulation of cold-induced thermogenesis  (ISO,ISS)
positive regulation of endocytosis  (ISO)
positive regulation of endothelial cell proliferation  (ISO)
positive regulation of ER-associated ubiquitin-dependent protein catabolic process  (IMP)
positive regulation of extrinsic apoptotic signaling pathway  (IMP)
positive regulation of gap junction assembly  (ISO,ISS)
positive regulation of gene expression  (IEA,ISO)
positive regulation of intrinsic apoptotic signaling pathway  (IMP)
positive regulation of microtubule polymerization  (ISO)
positive regulation of NF-kappaB transcription factor activity  (IMP)
positive regulation of peptidase activity  (IEA)
positive regulation of peptidyl-serine phosphorylation  (IDA)
positive regulation of protein binding  (IMP)
positive regulation of protein ubiquitination  (IMP)
positive regulation of signal transduction  (ISO)
positive regulation of toll-like receptor 3 signaling pathway  (IMP)
positive regulation of vasoconstriction  (ISO,ISS)
posttranscriptional regulation of gene expression  (IEA,ISO)
protein localization  (ISO,ISS)
protein localization to basolateral plasma membrane  (ISS)
protein localization to plasma membrane raft  (ISS)
protein transport  (IEA,ISO)
receptor internalization  (IDA)
receptor internalization involved in canonical Wnt signaling pathway  (IMP)
receptor-mediated endocytosis of virus by host cell  (IGI)
regulation of blood coagulation  (IMP)
regulation of cardiac muscle cell action potential involved in regulation of contraction  (IC)
regulation of cell communication by electrical coupling involved in cardiac conduction  (ISO,ISS)
regulation of cytosolic calcium ion concentration  (IBA,IDA)
regulation of entry of bacterium into host cell  (IDA)
regulation of fatty acid metabolic process  (ISO,ISS)
regulation of heart rate by cardiac conduction  (ISO,ISS)
regulation of membrane repolarization during action potential  (IMP)
regulation of nitric-oxide synthase activity  (TAS)
regulation of peptidase activity  (ISO,ISS)
regulation of ruffle assembly  (IDA)
regulation of smooth muscle contraction  (ISO,ISS)
regulation of the force of heart contraction  (ISO)
regulation of the force of heart contraction by chemical signal  (IEA,ISO)
regulation of ventricular cardiac muscle cell action potential  (ISO,ISS)
response to bacterium  (IDA)
response to calcium ion  (ISO,ISS)
response to drug  (ISO)
response to estrogen  (IDA,ISO)
response to gamma radiation  (ISO)
response to glucocorticoid  (ISO)
response to hypoxia  (ISO,ISS)
response to ischemia  (IEA,ISO)
response to mechanical stimulus  (ISO)
response to nutrient  (ISO)
response to progesterone  (IDA)
skeletal muscle tissue development  (ISO,ISS)
T cell costimulation  (IDA)
triglyceride metabolic process  (ISO,ISS)
vasculogenesis  (ISO,ISS)
vasoconstriction  (IEA,ISO)
vesicle organization  (ISS)
wound healing  (ISO)

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Abnormal bowel sounds  (IAGP)
Abnormal facial shape  (IAGP)
Abnormality of the face  (IAGP)
Absence of subcutaneous fat  (IAGP)
Acanthosis nigricans  (IAGP)
Accelerated skeletal maturation  (IAGP)
Adipose tissue loss  (IAGP)
Amenorrhea  (IAGP)
Arthralgia  (IAGP)
Arthritis  (IAGP)
Autoimmunity  (IAGP)
Autosomal dominant inheritance  (IAGP)
Autosomal recessive inheritance  (IAGP)
Babinski sign  (IAGP)
Bone cyst  (IAGP)
Carious teeth  (IAGP)
Cirrhosis  (IAGP)
Clitoral hypertrophy  (IAGP)
Clonus  (IAGP)
Congestive heart failure  (IAGP)
Contractures involving the joints of the feet  (IAGP)
Decreased adipose tissue around neck  (IAGP)
Decreased body mass index  (IAGP)
Decreased muscle mass  (IAGP)
Developmental cataract  (IAGP)
Diabetes mellitus  (IAGP)
Distal sensory impairment  (IAGP)
Dysmetria  (IAGP)
Dyspareunia  (IAGP)
Dysphagia  (IAGP)
Dyspnea  (IAGP)
Elevated pulmonary artery pressure  (IAGP)
Elevated serum creatinine  (IAGP)
Failure to thrive  (IAGP)
Flexion contracture  (IAGP)
Gait ataxia  (IAGP)
Gastroesophageal reflux  (IAGP)
Generalized lipodystrophy  (IAGP)
Global developmental delay  (IAGP)
Hepatic steatosis  (IAGP)
Hepatomegaly  (IAGP)
Hepatosplenomegaly  (IAGP)
Hirsutism  (IAGP)
Hypercholesterolemia  (IAGP)
Hyperinsulinemia  (IAGP)
Hypertensive crisis  (IAGP)
Hypertrichosis  (IAGP)
Hypertriglyceridemia  (IAGP)
Hypertrophic cardiomyopathy  (IAGP)
Hypocalcemia  (IAGP)
Hypopigmented skin patches  (IAGP)
Impaired glucose tolerance  (IAGP)
Incomplete penetrance  (IAGP)
Increased C-peptide level  (IAGP)
Increased pulmonary vascular resistance  (IAGP)
Infantile onset  (IAGP)
Insulin resistance  (IAGP)
Intellectual disability  (IAGP)
Joint contracture of the hand  (IAGP)
Lack of facial subcutaneous fat  (IAGP)
Large hands  (IAGP)
Lipodystrophy  (IAGP)
Long foot  (IAGP)
Loss of subcutaneous adipose tissue in limbs  (IAGP)
Low anterior hairline  (IAGP)
Low posterior hairline  (IAGP)
Lower limb muscle weakness  (IAGP)
Macroglossia  (IAGP)
Malabsorption  (IAGP)
Mandibular prognathia  (IAGP)
Mucosal telangiectasiae  (IAGP)
Muscle weakness  (IAGP)
Narrow foramen obturatorium  (IAGP)
Nausea and vomiting  (IAGP)
Nystagmus  (IAGP)
Oligomenorrhea  (IAGP)
Oliguria  (IAGP)
Orthostatic hypotension  (IAGP)
Osteolysis  (IAGP)
Overgrowth of external genitalia  (IAGP)
Pancreatitis  (IAGP)
Pigmentary retinopathy  (IAGP)
Polycystic ovaries  (IAGP)
Precocious puberty in females  (IAGP)
Primary amenorrhea  (IAGP)
Prominent superficial veins  (IAGP)
Prominent supraorbital ridges  (IAGP)
Proportionate tall stature  (IAGP)
Psychomotor retardation  (IAGP)
Pulmonary arterial hypertension  (IAGP)
Pulmonary fibrosis  (IAGP)
Pulmonary infiltrates  (IAGP)
Reduced subcutaneous adipose tissue  (IAGP)
Renal insufficiency  (IAGP)
Scleroderma  (IAGP)
Short stature  (IAGP)
Skin ulcer  (IAGP)
Splenomegaly  (IAGP)
Telangiectasia of the skin  (IAGP)
Variable expressivity  (IAGP)
Xerostomia  (IAGP)
References

References - curated
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PMID:28498397   PMID:28499918   PMID:28514055   PMID:28514442   PMID:28515480   PMID:28542134   PMID:28554768   PMID:28560511   PMID:28592633   PMID:28625953   PMID:28684115   PMID:28698382  
PMID:28734243   PMID:28735300   PMID:28741517   PMID:28753840   PMID:28760776   PMID:28778116   PMID:28857238   PMID:28899682   PMID:28904206   PMID:28923854   PMID:28966723   PMID:28971726  
PMID:28988699   PMID:29022911   PMID:29049173   PMID:29111166   PMID:29111846   PMID:29118431   PMID:29137977   PMID:29141593   PMID:29169152   PMID:29180619   PMID:29270591   PMID:29288243  
PMID:29301501   PMID:29309750   PMID:29323707   PMID:29331414   PMID:29358576   PMID:29374556   PMID:29395067   PMID:29402961   PMID:29458077   PMID:29479989   PMID:29507755   PMID:29509190  
PMID:29525429   PMID:29563255   PMID:29568061   PMID:29599191   PMID:29662258   PMID:29720121   PMID:29746866   PMID:29752441   PMID:29760379   PMID:29762069   PMID:29847075   PMID:29850392  
PMID:29877208   PMID:29896915   PMID:29986880   PMID:30015970   PMID:30086884   PMID:30088837   PMID:30097533   PMID:30098223   PMID:30144070   PMID:30158247   PMID:30171601   PMID:30209302  
PMID:30249137   PMID:30262154   PMID:30297114   PMID:30338706   PMID:30348118   PMID:30355208   PMID:30415776   PMID:30424755   PMID:30446170   PMID:30463805   PMID:30483772   PMID:30510281  
PMID:30583072   PMID:30593761   PMID:30604627   PMID:30644419   PMID:30673589   PMID:30686114   PMID:30745168   PMID:30746562   PMID:30768959   PMID:30771426   PMID:30786746   PMID:30805811  
PMID:30899070   PMID:30916825   PMID:30943774   PMID:30944060   PMID:30949900   PMID:30981205   PMID:30986357   PMID:31048545   PMID:31081050   PMID:31116089   PMID:31180492   PMID:31199921  
PMID:31235510   PMID:31256294   PMID:31257611   PMID:31284269   PMID:31285524   PMID:31303379   PMID:31362353   PMID:31382626   PMID:31386584   PMID:31485620   PMID:31493519   PMID:31534543  
PMID:31541456   PMID:31583475   PMID:31586073   PMID:31629729   PMID:31635212   PMID:31664124   PMID:31673241   PMID:31676327   PMID:31678930   PMID:31685812   PMID:31740664   PMID:31753913  
PMID:31810383   PMID:31877626   PMID:31884607   PMID:31889028   PMID:31911435   PMID:31919341   PMID:31926991   PMID:31980649   PMID:32109845   PMID:32141441   PMID:32377291   PMID:32401768  
PMID:32415943   PMID:32416067   PMID:32428234   PMID:32668406   PMID:32780723   PMID:32814053   PMID:32855410   PMID:32877691  


Genomics

Comparative Map Data
CAV1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl7116,524,994 - 116,561,179 (+)EnsemblGRCh38hg38GRCh38
GRCh38.p13 Ensembl7116,525,001 - 116,561,184 (+)EnsemblGRCh38hg38GRCh38
GRCh387116,525,009 - 116,561,185 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh377116,165,063 - 116,201,239 (+)NCBIGRCh37GRCh37hg19GRCh37
GRCh377116,164,839 - 116,201,239 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 367115,952,075 - 115,988,466 (+)NCBINCBI36hg18NCBI36
Build 347115,758,789 - 115,795,181NCBI
Celera7110,972,249 - 111,008,654 (+)NCBI
Cytogenetic Map7q31.2NCBI
HuRef7110,530,835 - 110,566,784 (+)NCBIHuRef
CHM1_17116,098,482 - 116,134,827 (+)NCBICHM1_1
CRA_TCAGchr7v27115,560,275 - 115,596,679 (+)NCBI
Cav1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39617,306,287 - 17,341,327 (+)NCBIGRCm39mm39
GRCm38617,306,335 - 17,341,328 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl617,306,335 - 17,341,452 (+)EnsemblGRCm38mm10GRCm38
MGSCv37617,256,370 - 17,291,324 (+)NCBIGRCm37mm9NCBIm37
MGSCv36617,256,370 - 17,291,324 (+)NCBImm8
Celera617,378,835 - 17,414,670 (+)NCBICelera
Cytogenetic Map6A2NCBI
Cav1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2445,640,624 - 45,673,708 (+)NCBI
Rnor_6.0 Ensembl444,597,123 - 44,630,200 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0444,597,123 - 44,630,206 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.0445,203,494 - 45,236,461 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4442,956,102 - 42,989,057 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.1443,098,177 - 43,130,873 (+)NCBI
Celera440,918,628 - 40,949,677 (+)NCBICelera
Cytogenetic Map4q21NCBI
Cav1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495543222,258,250 - 22,292,403 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495543222,258,262 - 22,292,403 (+)NCBIChiLan1.0ChiLan1.0
CAV1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.17121,193,678 - 121,229,655 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl7121,193,424 - 121,229,655 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v07108,497,125 - 108,533,090 (+)NCBIMhudiblu_PPA_v0panPan3
CAV1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1 Ensembl1455,461,048 - 55,492,935 (+)EnsemblCanFam3.1canFam3CanFam3.1
CanFam3.11455,458,934 - 55,494,563 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Cav1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
SpeTri2.0NW_0049365892,504,235 - 2,536,778 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CAV1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1829,649,992 - 29,682,465 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11829,648,120 - 29,682,451 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21831,745,664 - 31,778,987 (-)NCBISscrofa10.2Sscrofa10.2susScr3
CAV1
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12185,222,724 - 85,258,562 (+)NCBI
ChlSab1.1 Ensembl2185,222,879 - 85,258,627 (+)Ensembl
Cav1
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046248272,844,855 - 2,878,367 (-)NCBI

Position Markers
D7S2756  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,200,904 - 116,201,059UniSTSGRCh37
Build 367115,988,140 - 115,988,295RGDNCBI36
Celera7111,008,319 - 111,008,474RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,566,449 - 110,566,604UniSTS
CRA_TCAGchr7v27115,596,344 - 115,596,499UniSTS
TNG Radiation Hybrid Map751957.0UniSTS
Stanford-G3 RH Map75722.0UniSTS
NCBI RH Map71114.5UniSTS
GeneMap99-G3 RH Map75722.0UniSTS
RH91504  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,200,904 - 116,201,049UniSTSGRCh37
Build 367115,988,140 - 115,988,285RGDNCBI36
Celera7111,008,319 - 111,008,464RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,566,449 - 110,566,594UniSTS
CRA_TCAGchr7v27115,596,344 - 115,596,489UniSTS
GeneMap99-GB4 RH Map7547.79UniSTS
ECD00439  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,166,881 - 116,167,787UniSTSGRCh37
Build 367115,954,117 - 115,955,023RGDNCBI36
Celera7110,974,291 - 110,975,197RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,532,877 - 110,533,783UniSTS
CRA_TCAGchr7v27115,562,317 - 115,563,223UniSTS
ECD01055  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,172,171 - 116,173,050UniSTSGRCh37
Build 367115,959,407 - 115,960,286RGDNCBI36
Celera7110,979,585 - 110,980,464RGD
Cytogenetic Map7q31.1UniSTS
CRA_TCAGchr7v27115,567,611 - 115,568,490UniSTS
ECD01546  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,167,942 - 116,168,803UniSTSGRCh37
Build 367115,955,178 - 115,956,039RGDNCBI36
Celera7110,975,352 - 110,976,214RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,533,938 - 110,534,800UniSTS
CRA_TCAGchr7v27115,563,378 - 115,564,240UniSTS
ECD02409  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,197,527 - 116,198,357UniSTSGRCh37
Build 367115,984,763 - 115,985,593RGDNCBI36
Celera7111,004,942 - 111,005,772RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,563,071 - 110,563,901UniSTS
CRA_TCAGchr7v27115,592,967 - 115,593,797UniSTS
ECD02781  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,196,676 - 116,197,493UniSTSGRCh37
Build 367115,983,912 - 115,984,729RGDNCBI36
Celera7111,004,089 - 111,004,908RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,562,218 - 110,563,037UniSTS
CRA_TCAGchr7v27115,592,114 - 115,592,933UniSTS
ECD04428  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,179,106 - 116,179,870UniSTSGRCh37
Build 367115,966,342 - 115,967,106RGDNCBI36
Celera7110,986,520 - 110,987,284RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,544,680 - 110,545,444UniSTS
CRA_TCAGchr7v27115,574,545 - 115,575,309UniSTS
ECD05019  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,174,870 - 116,175,617UniSTSGRCh37
Build 367115,962,106 - 115,962,853RGDNCBI36
Celera7110,982,284 - 110,983,031RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,540,444 - 110,541,191UniSTS
CRA_TCAGchr7v27115,570,309 - 115,571,056UniSTS
ECD05091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,163,640 - 116,164,385UniSTSGRCh37
Build 367115,950,876 - 115,951,621RGDNCBI36
Celera7110,971,049 - 110,971,795RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,529,634 - 110,530,381UniSTS
CRA_TCAGchr7v27115,559,074 - 115,559,821UniSTS
ECD05195  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,198,869 - 116,199,611UniSTSGRCh37
Build 367115,986,105 - 115,986,847RGDNCBI36
Celera7111,006,284 - 111,007,026RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,564,414 - 110,565,156UniSTS
CRA_TCAGchr7v27115,594,309 - 115,595,051UniSTS
ECD05272  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,179,933 - 116,180,673UniSTSGRCh37
Build 367115,967,169 - 115,967,909RGDNCBI36
Celera7110,987,347 - 110,988,087RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,545,507 - 110,546,247UniSTS
CRA_TCAGchr7v27115,575,372 - 115,576,112UniSTS
ECD05273  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,199,691 - 116,200,431UniSTSGRCh37
Build 367115,986,927 - 115,987,667RGDNCBI36
Celera7111,007,106 - 111,007,846RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,565,236 - 110,565,976UniSTS
CRA_TCAGchr7v27115,595,131 - 115,595,871UniSTS
ECD05303  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,164,465 - 116,165,204UniSTSGRCh37
Build 367115,951,701 - 115,952,440RGDNCBI36
Celera7110,971,875 - 110,972,614RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,530,461 - 110,531,200UniSTS
CRA_TCAGchr7v27115,559,901 - 115,560,640UniSTS
ECD05342  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,166,088 - 116,166,826UniSTSGRCh37
Build 367115,953,324 - 115,954,062RGDNCBI36
Celera7110,973,498 - 110,974,236RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,532,084 - 110,532,822UniSTS
CRA_TCAGchr7v27115,561,524 - 115,562,262UniSTS
ECD05380  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,175,627 - 116,176,364UniSTSGRCh37
Build 367115,962,863 - 115,963,600RGDNCBI36
Celera7110,983,041 - 110,983,778RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,541,201 - 110,541,938UniSTS
CRA_TCAGchr7v27115,571,066 - 115,571,803UniSTS
ECD05966  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,200,491 - 116,201,212UniSTSGRCh37
Build 367115,987,727 - 115,988,448RGDNCBI36
Celera7111,007,906 - 111,008,627RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,566,036 - 110,566,757UniSTS
CRA_TCAGchr7v27115,595,931 - 115,596,652UniSTS
ECD06677  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,190,429 - 116,191,131UniSTSGRCh37
Build 367115,977,665 - 115,978,367RGDNCBI36
Celera7110,997,842 - 110,998,544RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,556,001 - 110,556,703UniSTS
CRA_TCAGchr7v27115,585,867 - 115,586,569UniSTS
ECD06713  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,170,360 - 116,171,061UniSTSGRCh37
Build 367115,957,596 - 115,958,297RGDNCBI36
Celera7110,977,774 - 110,978,475RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,536,360 - 110,537,061UniSTS
CRA_TCAGchr7v27115,565,800 - 115,566,501UniSTS
ECD06753  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,169,600 - 116,170,300UniSTSGRCh37
Build 367115,956,836 - 115,957,536RGDNCBI36
Celera7110,977,011 - 110,977,714RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,535,597 - 110,536,300UniSTS
CRA_TCAGchr7v27115,565,037 - 115,565,740UniSTS
ECD06962  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,165,246 - 116,165,940UniSTSGRCh37
Build 367115,952,482 - 115,953,176RGDNCBI36
Celera7110,972,656 - 110,973,350RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,531,242 - 110,531,936UniSTS
CRA_TCAGchr7v27115,560,682 - 115,561,376UniSTS
ECD07255  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,189,713 - 116,190,399UniSTSGRCh37
Build 367115,976,949 - 115,977,635RGDNCBI36
Celera7110,997,126 - 110,997,812RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,555,285 - 110,555,971UniSTS
CRA_TCAGchr7v27115,585,151 - 115,585,837UniSTS
ECD08231  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,195,878 - 116,196,538UniSTSGRCh37
Build 367115,983,114 - 115,983,774RGDNCBI36
Celera7111,003,291 - 111,003,951RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,561,420 - 110,562,080UniSTS
CRA_TCAGchr7v27115,591,316 - 115,591,976UniSTS
ECD08445  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,180,843 - 116,181,497UniSTSGRCh37
Build 367115,968,079 - 115,968,733RGDNCBI36
Celera7110,988,257 - 110,988,911RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,546,417 - 110,547,071UniSTS
CRA_TCAGchr7v27115,576,282 - 115,576,936UniSTS
ECD08482  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,183,703 - 116,184,356UniSTSGRCh37
Build 367115,970,939 - 115,971,592RGDNCBI36
Celera7110,991,116 - 110,991,769RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,549,276 - 110,549,929UniSTS
CRA_TCAGchr7v27115,579,141 - 115,579,794UniSTS
ECD12784  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,178,213 - 116,178,747UniSTSGRCh37
Build 367115,965,449 - 115,965,983RGDNCBI36
Celera7110,985,627 - 110,986,161RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,543,787 - 110,544,321UniSTS
CRA_TCAGchr7v27115,573,652 - 115,574,186UniSTS
ECD13448  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,182,558 - 116,183,075UniSTSGRCh37
Build 367115,969,794 - 115,970,311RGDNCBI36
Celera7110,989,971 - 110,990,488RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,548,131 - 110,548,648UniSTS
CRA_TCAGchr7v27115,577,996 - 115,578,513UniSTS
ECD13690  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,177,678 - 116,178,189UniSTSGRCh37
Build 367115,964,914 - 115,965,425RGDNCBI36
Celera7110,985,092 - 110,985,603RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,543,252 - 110,543,763UniSTS
CRA_TCAGchr7v27115,573,117 - 115,573,628UniSTS
ECD14093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,185,409 - 116,185,910UniSTSGRCh37
Build 367115,972,645 - 115,973,146RGDNCBI36
Celera7110,992,822 - 110,993,323RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,550,982 - 110,551,483UniSTS
CRA_TCAGchr7v27115,580,847 - 115,581,348UniSTS
ECD14440  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,192,947 - 116,193,440UniSTSGRCh37
Build 367115,980,183 - 115,980,676RGDNCBI36
Celera7111,000,360 - 111,000,853RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,558,519 - 110,559,012UniSTS
CRA_TCAGchr7v27115,588,385 - 115,588,878UniSTS
ECD14441  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,193,487 - 116,193,980UniSTSGRCh37
Build 367115,980,723 - 115,981,216RGDNCBI36
Celera7111,000,900 - 111,001,393RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,559,059 - 110,559,552UniSTS
CRA_TCAGchr7v27115,588,925 - 115,589,418UniSTS
ECD14493  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,187,313 - 116,187,805UniSTSGRCh37
Build 367115,974,549 - 115,975,041RGDNCBI36
Celera7110,994,726 - 110,995,218RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,552,885 - 110,553,377UniSTS
CRA_TCAGchr7v27115,582,751 - 115,583,243UniSTS
ECD14844  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,185,958 - 116,186,442UniSTSGRCh37
Build 367115,973,194 - 115,973,678RGDNCBI36
Celera7110,993,371 - 110,993,855RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,551,531 - 110,552,015UniSTS
CRA_TCAGchr7v27115,581,396 - 115,581,880UniSTS
ECD15500  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,181,873 - 116,182,341UniSTSGRCh37
Build 367115,969,109 - 115,969,577RGDNCBI36
Celera7110,989,286 - 110,989,754RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,547,446 - 110,547,914UniSTS
CRA_TCAGchr7v27115,577,311 - 115,577,779UniSTS
ECD17066  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,188,361 - 116,188,775UniSTSGRCh37
Build 367115,975,597 - 115,976,011RGDNCBI36
Celera7110,995,774 - 110,996,188RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,553,933 - 110,554,347UniSTS
CRA_TCAGchr7v27115,583,799 - 115,584,213UniSTS
ECD18009  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,191,301 - 116,191,677UniSTSGRCh37
Build 367115,978,537 - 115,978,913RGDNCBI36
Celera7110,998,714 - 110,999,090RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,556,873 - 110,557,249UniSTS
CRA_TCAGchr7v27115,586,739 - 115,587,115UniSTS
ECD18414  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,171,207 - 116,171,567UniSTSGRCh37
Build 367115,958,443 - 115,958,803RGDNCBI36
Celera7110,978,621 - 110,978,981RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,537,207 - 110,537,567UniSTS
CRA_TCAGchr7v27115,566,647 - 115,567,007UniSTS
ECD18449  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,183,304 - 116,183,663UniSTSGRCh37
Build 367115,970,540 - 115,970,899RGDNCBI36
Celera7110,990,717 - 110,991,076RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,548,877 - 110,549,236UniSTS
CRA_TCAGchr7v27115,578,742 - 115,579,101UniSTS
ECD18532  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,189,204 - 116,189,560UniSTSGRCh37
Build 367115,976,440 - 115,976,796RGDNCBI36
Celera7110,996,617 - 110,996,973RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,554,776 - 110,555,132UniSTS
CRA_TCAGchr7v27115,584,642 - 115,584,998UniSTS
ECD18777  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,177,098 - 116,177,445UniSTSGRCh37
Build 367115,964,334 - 115,964,681RGDNCBI36
Celera7110,984,512 - 110,984,859RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,542,672 - 110,543,019UniSTS
CRA_TCAGchr7v27115,572,537 - 115,572,884UniSTS
ECD18959  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,171,773 - 116,172,113UniSTSGRCh37
Build 367115,959,009 - 115,959,349RGDNCBI36
Celera7110,979,187 - 110,979,527RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,537,773 - 110,538,113UniSTS
CRA_TCAGchr7v27115,567,213 - 115,567,553UniSTS
ECD19567  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,173,681 - 116,173,998UniSTSGRCh37
Build 367115,960,917 - 115,961,234RGDNCBI36
Celera7110,981,095 - 110,981,412RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,539,224 - 110,539,541UniSTS
CRA_TCAGchr7v27115,569,120 - 115,569,437UniSTS
ECD20013  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,194,202 - 116,194,502UniSTSGRCh37
Build 367115,981,438 - 115,981,738RGDNCBI36
Celera7111,001,615 - 111,001,915RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,559,774 - 110,560,074UniSTS
CRA_TCAGchr7v27115,589,640 - 115,589,940UniSTS
ECD21441  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,188,878 - 116,189,127UniSTSGRCh37
Build 367115,976,114 - 115,976,363RGDNCBI36
Celera7110,996,291 - 110,996,540RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,554,450 - 110,554,699UniSTS
CRA_TCAGchr7v27115,584,316 - 115,584,565UniSTS
ECD21690  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,184,865 - 116,185,107UniSTSGRCh37
Build 367115,972,101 - 115,972,343RGDNCBI36
Celera7110,992,278 - 110,992,520RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,550,438 - 110,550,680UniSTS
CRA_TCAGchr7v27115,580,303 - 115,580,545UniSTS
ECD22214  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,194,717 - 116,194,942UniSTSGRCh37
Build 367115,981,953 - 115,982,178RGDNCBI36
Celera7111,002,130 - 111,002,355RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,560,289 - 110,560,514UniSTS
CRA_TCAGchr7v27115,590,155 - 115,590,380UniSTS
ECD22774  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,192,294 - 116,192,502UniSTSGRCh37
Build 367115,979,530 - 115,979,738RGDNCBI36
Celera7110,999,707 - 110,999,915RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,557,866 - 110,558,074UniSTS
CRA_TCAGchr7v27115,587,732 - 115,587,940UniSTS
REN66695  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,201,308 - 116,201,572UniSTSGRCh37
Build 367115,988,544 - 115,988,808RGDNCBI36
Celera7111,008,723 - 111,008,987RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,566,853 - 110,567,117UniSTS
CRA_TCAGchr7v27115,596,748 - 115,597,012UniSTS
REN66696  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,201,035 - 116,201,287UniSTSGRCh37
Build 367115,988,271 - 115,988,523RGDNCBI36
Celera7111,008,450 - 111,008,702RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,566,580 - 110,566,832UniSTS
CRA_TCAGchr7v27115,596,475 - 115,596,727UniSTS
REN66697  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,200,773 - 116,201,046UniSTSGRCh37
Build 367115,988,009 - 115,988,282RGDNCBI36
Celera7111,008,188 - 111,008,461RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,566,318 - 110,566,591UniSTS
CRA_TCAGchr7v27115,596,213 - 115,596,486UniSTS
REN66698  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,200,563 - 116,200,792UniSTSGRCh37
Build 367115,987,799 - 115,988,028RGDNCBI36
Celera7111,007,978 - 111,008,207RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,566,108 - 110,566,337UniSTS
CRA_TCAGchr7v27115,596,003 - 115,596,232UniSTS
REN66699  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,200,294 - 116,200,544UniSTSGRCh37
Build 367115,987,530 - 115,987,780RGDNCBI36
Celera7111,007,709 - 111,007,959RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,565,839 - 110,566,089UniSTS
CRA_TCAGchr7v27115,595,734 - 115,595,984UniSTS
REN66700  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,200,037 - 116,200,298UniSTSGRCh37
Build 367115,987,273 - 115,987,534RGDNCBI36
Celera7111,007,452 - 111,007,713RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,565,582 - 110,565,843UniSTS
CRA_TCAGchr7v27115,595,477 - 115,595,738UniSTS
REN66701  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,199,832 - 116,200,056UniSTSGRCh37
Build 367115,987,068 - 115,987,292RGDNCBI36
Celera7111,007,247 - 111,007,471RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,565,377 - 110,565,601UniSTS
CRA_TCAGchr7v27115,595,272 - 115,595,496UniSTS
REN66702  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,199,596 - 116,199,842UniSTSGRCh37
Build 367115,986,832 - 115,987,078RGDNCBI36
Celera7111,007,011 - 111,007,257RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,565,141 - 110,565,387UniSTS
CRA_TCAGchr7v27115,595,036 - 115,595,282UniSTS
REN66703  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,199,383 - 116,199,609UniSTSGRCh37
Build 367115,986,619 - 115,986,845RGDNCBI36
Celera7111,006,798 - 111,007,024RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,564,928 - 110,565,154UniSTS
CRA_TCAGchr7v27115,594,823 - 115,595,049UniSTS
REN66704  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,199,072 - 116,199,302UniSTSGRCh37
Build 367115,986,308 - 115,986,538RGDNCBI36
Celera7111,006,487 - 111,006,717RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,564,617 - 110,564,847UniSTS
CRA_TCAGchr7v27115,594,512 - 115,594,742UniSTS
REN66705  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,198,826 - 116,199,050UniSTSGRCh37
Build 367115,986,062 - 115,986,286RGDNCBI36
Celera7111,006,241 - 111,006,465RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,564,371 - 110,564,595UniSTS
CRA_TCAGchr7v27115,594,266 - 115,594,490UniSTS
REN66706  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,198,402 - 116,198,636UniSTSGRCh37
Build 367115,985,638 - 115,985,872RGDNCBI36
Celera7111,005,817 - 111,006,051RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,563,946 - 110,564,180UniSTS
CRA_TCAGchr7v27115,593,842 - 115,594,076UniSTS
REN66707  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,198,171 - 116,198,403UniSTSGRCh37
Build 367115,985,407 - 115,985,639RGDNCBI36
Celera7111,005,586 - 111,005,818RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,563,715 - 110,563,947UniSTS
CRA_TCAGchr7v27115,593,611 - 115,593,843UniSTS
REN66708  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,197,895 - 116,198,149UniSTSGRCh37
Build 367115,985,131 - 115,985,385RGDNCBI36
Celera7111,005,310 - 111,005,564RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,563,439 - 110,563,693UniSTS
CRA_TCAGchr7v27115,593,335 - 115,593,589UniSTS
REN66709  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,197,648 - 116,197,895UniSTSGRCh37
Build 367115,984,884 - 115,985,131RGDNCBI36
Celera7111,005,063 - 111,005,310RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,563,192 - 110,563,439UniSTS
CRA_TCAGchr7v27115,593,088 - 115,593,335UniSTS
REN66710  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,197,418 - 116,197,646UniSTSGRCh37
Build 367115,984,654 - 115,984,882RGDNCBI36
Celera7111,004,833 - 111,005,061RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,562,962 - 110,563,190UniSTS
CRA_TCAGchr7v27115,592,858 - 115,593,086UniSTS
REN66711  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,197,131 - 116,197,391UniSTSGRCh37
Build 367115,984,367 - 115,984,627RGDNCBI36
Celera7111,004,546 - 111,004,806RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,562,675 - 110,562,935UniSTS
CRA_TCAGchr7v27115,592,571 - 115,592,831UniSTS
REN66712  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,196,889 - 116,197,146UniSTSGRCh37
Build 367115,984,125 - 115,984,382RGDNCBI36
Celera7111,004,304 - 111,004,561RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,562,433 - 110,562,690UniSTS
CRA_TCAGchr7v27115,592,329 - 115,592,586UniSTS
REN66713  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,196,666 - 116,196,907UniSTSGRCh37
Build 367115,983,902 - 115,984,143RGDNCBI36
Celera7111,004,079 - 111,004,322RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,562,208 - 110,562,451UniSTS
CRA_TCAGchr7v27115,592,104 - 115,592,347UniSTS
REN66714  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,196,426 - 116,196,661UniSTSGRCh37
Build 367115,983,662 - 115,983,897RGDNCBI36
Celera7111,003,839 - 111,004,074RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,561,968 - 110,562,203UniSTS
CRA_TCAGchr7v27115,591,864 - 115,592,099UniSTS
REN66715  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,196,170 - 116,196,411UniSTSGRCh37
Build 367115,983,406 - 115,983,647RGDNCBI36
Celera7111,003,583 - 111,003,824RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,561,712 - 110,561,953UniSTS
CRA_TCAGchr7v27115,591,608 - 115,591,849UniSTS
REN66716  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,195,962 - 116,196,189UniSTSGRCh37
Build 367115,983,198 - 115,983,425RGDNCBI36
Celera7111,003,375 - 111,003,602RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,561,504 - 110,561,731UniSTS
CRA_TCAGchr7v27115,591,400 - 115,591,627UniSTS
REN66717  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,195,728 - 116,195,957UniSTSGRCh37
Build 367115,982,964 - 115,983,193RGDNCBI36
Celera7111,003,141 - 111,003,370RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,561,270 - 110,561,499UniSTS
CRA_TCAGchr7v27115,591,166 - 115,591,395UniSTS
REN66718  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,195,064 - 116,195,302UniSTSGRCh37
Build 367115,982,300 - 115,982,538RGDNCBI36
Celera7111,002,477 - 111,002,715RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,560,636 - 110,560,874UniSTS
CRA_TCAGchr7v27115,590,502 - 115,590,740UniSTS
REN66719  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,194,773 - 116,195,007UniSTSGRCh37
Build 367115,982,009 - 115,982,243RGDNCBI36
Celera7111,002,186 - 111,002,420RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,560,345 - 110,560,579UniSTS
CRA_TCAGchr7v27115,590,211 - 115,590,445UniSTS
REN66720  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,194,493 - 116,194,738UniSTSGRCh37
Build 367115,981,729 - 115,981,974RGDNCBI36
Celera7111,001,906 - 111,002,151RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,560,065 - 110,560,310UniSTS
CRA_TCAGchr7v27115,589,931 - 115,590,176UniSTS
REN66721  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,194,256 - 116,194,509UniSTSGRCh37
Build 367115,981,492 - 115,981,745RGDNCBI36
Celera7111,001,669 - 111,001,922RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,559,828 - 110,560,081UniSTS
CRA_TCAGchr7v27115,589,694 - 115,589,947UniSTS
REN66722  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,194,011 - 116,194,271UniSTSGRCh37
Build 367115,981,247 - 115,981,507RGDNCBI36
Celera7111,001,424 - 111,001,684RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,559,583 - 110,559,843UniSTS
CRA_TCAGchr7v27115,589,449 - 115,589,709UniSTS
REN66723  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,193,774 - 116,194,016UniSTSGRCh37
Build 367115,981,010 - 115,981,252RGDNCBI36
Celera7111,001,187 - 111,001,429RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,559,346 - 110,559,588UniSTS
CRA_TCAGchr7v27115,589,212 - 115,589,454UniSTS
REN66724  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,193,523 - 116,193,766UniSTSGRCh37
Build 367115,980,759 - 115,981,002RGDNCBI36
Celera7111,000,936 - 111,001,179RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,559,095 - 110,559,338UniSTS
CRA_TCAGchr7v27115,588,961 - 115,589,204UniSTS
REN66725  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,193,267 - 116,193,506UniSTSGRCh37
Build 367115,980,503 - 115,980,742RGDNCBI36
Celera7111,000,680 - 111,000,919RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,558,839 - 110,559,078UniSTS
CRA_TCAGchr7v27115,588,705 - 115,588,944UniSTS
REN66726  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,193,007 - 116,193,231UniSTSGRCh37
Build 367115,980,243 - 115,980,467RGDNCBI36
Celera7111,000,420 - 111,000,644RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,558,579 - 110,558,803UniSTS
CRA_TCAGchr7v27115,588,445 - 115,588,669UniSTS
REN66727  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,192,799 - 116,193,026UniSTSGRCh37
Build 367115,980,035 - 115,980,262RGDNCBI36
Celera7111,000,212 - 111,000,439RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,558,371 - 110,558,598UniSTS
CRA_TCAGchr7v27115,588,237 - 115,588,464UniSTS
REN66728  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,192,572 - 116,192,798UniSTSGRCh37
Build 367115,979,808 - 115,980,034RGDNCBI36
Celera7110,999,985 - 111,000,211RGD
Cytogenetic Map7q31.1UniSTS
HuRef7110,558,144 - 110,558,370UniSTS
CRA_TCAGchr7v27115,588,010 - 115,588,236UniSTS
REN66729  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377116,192,334 - 116,192,562UniSTS