chr11:64570982:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr11:64,570,982-64,578,766
hg38 chr11:64,803,510-64,811,294 

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
<0.001 Cardiovascular Diseases NA BeFree Detail
<0.001 celiac disease NA BeFree Detail
<0.001 Malignant tumor of cervix NA BeFree Detail
<0.001 Congenital chromosomal disease NA BeFree Detail
0.080 Colonic Neoplasms NA RGD Detail
<0.001 colorectal carcinoma NA BeFree Detail
<0.001 Coronary heart disease NA BeFree Detail
<0.001 Cushing syndrome NA BeFree Detail
0.001 Diabetes NA BeFree Detail
0.001 diabetes mellitus NA BeFree Detail
<0.001 Diabetes Mellitus, Non-Insulin-Dependent NA BeFree Detail
<0.001 diarrhea NA BeFree Detail
0.120 VIPoma NA BeFree,CTD_human Detail
0.004 Endocrine System Diseases NA BeFree Detail
0.006 Endocrine Gland Neoplasms Menin, encoded by the MEN1 gene, was initially identified as a tumor suppressor ... BeFree 25962847 Detail
0.006 Endocrine Gland Neoplasms MEN1, which is secondary to the mutation of the MEN1 gene, is a rare autosomal-d... BeFree 26392472 Detail
0.001 Ependymoma NA BeFree Detail
<0.001 Fatty Liver Here, we further explore the role of Menin in liver steatosis. BeFree 25962847 Detail
0.134 gastrinoma NA BeFree,CTD_human,LHGDN Detail
<0.001 gastritis NA BeFree Detail
<0.001 Gastritis, Atrophic NA BeFree Detail
<0.001 Gigantism NA BeFree Detail
0.121 Glucagonoma NA BeFree,CTD_human Detail
<0.001 Von Hippel-Lindau syndrome NA BeFree Detail
<0.001 HIV Infections NA BeFree Detail
0.003 Hyperaldosteronism NA BeFree,LHGDN Detail
0.080 Hyperalgesia NA RGD Detail
0.004 hypercalcemia NA BeFree,LHGDN Detail
<0.001 hyperglycemia Recently, Menin has been proven to negatively regulate β-cell proliferation in s... BeFree 25753880 Detail
0.003 hyperinsulinism Suppression of β-catenin signalling by genetic ablation or a molecular antagonis... BeFree,GAD 25517963 Detail
0.032 hyperparathyroidism NA BeFree,GAD,LHGDN Detail
<0.001 Hyperparathyroidism, Secondary NA BeFree Detail
0.003 Hyperplasia NA LHGDN Detail
<0.001 Hypertensive disease NA BeFree Detail
0.003 hyperthyroidism NA LHGDN Detail
0.003 hypoglycemia Suppression of β-catenin signalling by genetic ablation or a molecular antagonis... BeFree,GAD 25517963 Detail
<0.001 hypogonadism NA BeFree Detail
0.132 insulinoma Menin, encoded by the Men1 gene, is responsible for β-cell tumor formation in pa... BeFree,CTD_human,GAD,LHGDN 25753880 Detail
<0.001 Kidney Failure, Chronic NA BeFree Detail
<0.001 Lentigo NA BeFree Detail
0.007 leukemia Pharmacologic inhibition of the Menin-MLL interaction blocks progression of MLL ... BeFree,LHGDN 25817203 Detail
<0.001 Leukemia, T-Cell NA BeFree Detail
<0.001 Adult T-Cell Lymphoma/Leukemia NA BeFree Detail
0.002 lipoma NA BeFree Detail
<0.001 lipomatosis NA BeFree Detail
<0.001 Lung Neoplasms NA BeFree Detail
<0.001 lymphoma NA BeFree Detail
<0.001 Malignant Carcinoid Syndrome NA BeFree Detail
0.001 melanoma NA BeFree Detail
0.687 multiple endocrine neoplasia type 1 Intriguingly, those neuroendocrine tissues affected in Cdk4(-/-) mice are the pr... BeFree,CLINVAR,CTD_human,GAD,LHGDN,MGD,ORPHANET,UNIPROT 24531709 Detail
0.687 multiple endocrine neoplasia type 1 Multiple Endocrine Neoplasia Type 1 (MEN1) is an autosomal dominant inherited sy... BeFree,CLINVAR,CTD_human,GAD,LHGDN,MGD,ORPHANET,UNIPROT 24997771 Detail
0.687 multiple endocrine neoplasia type 1 The menin protein is certainly known to have a role in regulating oestrogen rece... BeFree,CLINVAR,CTD_human,GAD,LHGDN,MGD,ORPHANET,UNIPROT 25279812 Detail
0.687 multiple endocrine neoplasia type 1 Germline mutations in MEN1 (encoding menin) result in multiple endocrine neoplas... BeFree,CLINVAR,CTD_human,GAD,LHGDN,MGD,ORPHANET,UNIPROT 25350067 Detail
0.687 multiple endocrine neoplasia type 1 The tumor suppressor gene MEN1 is frequently mutated in sporadic pancreatic neur... BeFree,CLINVAR,CTD_human,GAD,LHGDN,MGD,ORPHANET,UNIPROT 25537453 Detail
0.687 multiple endocrine neoplasia type 1 To examine the in vivo function of menin in bone, we conditionally inactivated M... BeFree,CLINVAR,CTD_human,GAD,LHGDN,MGD,ORPHANET,UNIPROT 25538250 Detail
0.687 multiple endocrine neoplasia type 1 Menin, encoded by the Men1 gene, is responsible for β-cell tumor formation in pa... BeFree,CLINVAR,CTD_human,GAD,LHGDN,MGD,ORPHANET,UNIPROT 25753880 Detail
0.006 multiple endocrine neoplasia type 2A NA BeFree Detail
0.001 meningioma We found that these Pak inhibitors suppressed the proliferation and motility of ... BeFree 25596744 Detail
0.004 Neoplasm Metastasis NA BeFree Detail
0.021 multiple endocrine neoplasia While most cases (95%) occur sporadically, about 5% are associated with a heredi... BeFree,GAD,LHGDN 26163537 Detail
<0.001 neuroblastoma NA BeFree Detail
<0.001 Melanocytic nevus NA BeFree Detail
<0.001 osteosarcoma NA BeFree Detail
<0.001 Pancreatic Diseases NA BeFree Detail
<0.001 paraganglioma NA BeFree Detail
<0.001 Parathyroid Diseases NA BeFree Detail
0.015 Parathyroid Neoplasms NA BeFree,GAD,LHGDN Detail
<0.001 Peptic Ulcer NA BeFree Detail
0.002 pheochromocytoma Tumor tissue analysis identified LOH at the SDHB locus in three pituitary adenom... BeFree 25494863 Detail
0.011 pituitary adenoma In this Review, we describe the clinical features of patients with sporadic pitu... BeFree 25350067 Detail
0.013 Pituitary Diseases These data suggest that CDK4 is a critical downstream target of MEN1-dependent t... BeFree 24531709 Detail
0.013 Pituitary Diseases Germline mutations in MEN1 (encoding menin) result in multiple endocrine neoplas... BeFree 25350067 Detail
0.017 Pituitary Neoplasms NA BeFree,GAD,LHGDN Detail
<0.001 Adenomatous Polyposis Coli NA BeFree Detail
0.084 prolactinoma NA BeFree,MGD Detail
<0.001 Prostatic Neoplasms NA BeFree Detail
<0.001 kidney failure NA BeFree Detail
<0.001 Skin Neoplasms NA BeFree Detail
<0.001 Thyroid Neoplasm NA BeFree Detail
<0.001 tuberculosis The results revealed that increasing numbers of young patients were infected wit... BeFree 25297330 Detail
<0.001 tuberous sclerosis NA BeFree Detail
0.001 uremia NA BeFree Detail
<0.001 urinary tract infection NA BeFree Detail
<0.001 Uterine Fibroids NA BeFree Detail
0.002 Zollinger-Ellison syndrome NA BeFree Detail
<0.001 Central Nervous System Neoplasms NA BeFree Detail
<0.001 acute leukemia NA BeFree Detail
0.001 Atrophic condition of skin NA BeFree Detail
<0.001 Adenocarcinoma of lung (disorder) NA BeFree Detail
0.001 Malignant tumor of parathyroid gland NA BeFree Detail
<0.001 Neurofibromatoses NA BeFree Detail
<0.001 Tumor Progression NA BeFree Detail
<0.001 Hibernoma NA BeFree Detail
<0.001 angiomyolipoma NA BeFree Detail
<0.001 smooth muscle tumor NA BeFree Detail
<0.001 Neuroectodermal Tumor, Primitive NA BeFree Detail
0.001 adrenal cortical adenoma NA BeFree Detail
0.121 adrenocortical carcinoma NA BeFree,CTD_human Detail
<0.001 Carcinoma, Neuroendocrine NA BeFree Detail
0.001 Angiofibroma NA BeFree Detail
0.138 Neuroendocrine Tumors Targeting β-catenin signaling for therapeutic intervention in MEN1-deficient pan... BeFree,CTD_human,GAD,LHGDN 25517963 Detail
0.021 Hyperparathyroidism, Primary NA BeFree,GAD,LHGDN Detail
0.005 pituitary-dependent Cushing's disease NA GAD Detail
<0.001 pancreatic carcinoma NA BeFree Detail
<0.001 Leiomyoma of esophagus NA BeFree Detail
<0.001 Gastrointestinal Stromal Tumors A role of the MEN1 gene in the pathogenesis of GISTs could be hypothesized. BeFree 25022420 Detail
<0.001 Medullary carcinoma of thyroid NA BeFree Detail
<0.001 Papillary thyroid carcinoma NA BeFree Detail
<0.001 Angiomyolipoma of kidney NA BeFree Detail
0.001 McCune-Albright syndrome NA BeFree Detail
0.003 islet cell tumor NA BeFree Detail
<0.001 Malignant neoplasm of lung NA BeFree Detail
0.003 Breast Neoplasms, Male NA LHGDN Detail
0.001 Multiple tumors NA BeFree Detail
0.008 parathyroid adenoma NA BeFree Detail
<0.001 Fibrous skin tumor of tuberous sclerosis NA BeFree Detail
0.001 Autosomal dominant hereditary disorder NA BeFree Detail
0.003 Parathyroid hyperplasia NA BeFree Detail
0.004 Familial hyperparathyroidism While most cases (95%) occur sporadically, about 5% are associated with a heredi... BeFree 26163537 Detail
<0.001 Tertiary hyperparathyroidism NA BeFree Detail
0.121 Carcinoid tumor of lung NA BeFree,CLINVAR Detail
<0.001 diffuse astrocytoma NA BeFree Detail
<0.001 anaplastic ependymoma NA BeFree Detail
<0.001 Adenocarcinoma of pancreas NA BeFree Detail
<0.001 benign meningioma NA BeFree Detail
<0.001 cervix carcinoma NA BeFree Detail
0.002 Carcinoid tumor no ICD-O subtype NA BeFree Detail
<0.001 Adrenal hypertrophy or hyperplasia NA BeFree Detail
<0.001 Adrenocortical hyperplasia NA BeFree Detail
0.001 Hypocalciuric hypercalcemia, familial, type 1 NA BeFree Detail
<0.001 Macroprolactinoma Patients aged younger than 20 years at macroprolactinoma diagnosis and seen in t... BeFree 25532043 Detail
0.005 pituitary carcinoma NA GAD Detail
<0.001 Pituitary microadenoma NA BeFree Detail
<0.001 Pituitary macroadenoma NA BeFree Detail
<0.001 Malignant neoplasm of pancreas NA BeFree Detail
<0.001 Gastric Carcinoid Tumor NA BeFree Detail
<0.001 Malignant neoplasm of prostate NA BeFree Detail
<0.001 Hematopoietic Neoplasms NA BeFree Detail
0.004 Carney complex NA BeFree Detail
<0.001 urolithiasis NA BeFree Detail
0.001 Secondary malignant neoplasm of liver NA BeFree Detail
<0.001 Thyroid carcinoma MEN1 mutations in Hürthle cell (oncocytic) thyroid carcinoma. BeFree 25625803 Detail
<0.001 Osteosarcoma of bone NA BeFree Detail
0.023 Carcinogenesis These data suggest that CDK4 is a critical downstream target of MEN1-dependent t... BeFree 24531709 Detail
0.023 Carcinogenesis In this Review, we describe the clinical features of patients with sporadic pitu... BeFree 25350067 Detail
0.023 Carcinogenesis Conditional knockout of β-catenin suppresses the tumorigenesis and growth of Men... BeFree 25517963 Detail
0.023 Carcinogenesis Epigenetic profiling and gene expression analysis in Men1-deficient pancreatic i... BeFree 25537453 Detail
0.002 Leukemogenesis NA BeFree Detail
<0.001 prostate carcinoma NA BeFree Detail
0.001 breast carcinoma Breast cancer risk in MEN1 - a cancer genetics perspective. BeFree 25279812 Detail
0.002 Carcinoma of lung Therefore, these results suggest a previously unknown miR‑802/menin molecular ne... BeFree 24994111 Detail
0.004 Parathyroid Gland Adenocarcinoma NA BeFree,GAD Detail
<0.001 Carcinoma of bladder NA BeFree Detail
<0.001 Central neuroblastoma NA BeFree Detail
<0.001 hyperparathyroid NA BeFree Detail
<0.001 Adrenal Cancer NA BeFree Detail
<0.001 Intraepithelial Neoplasia NA BeFree Detail
0.003 ovarian neoplasm NA LHGDN Detail
<0.001 Hurthle Cell Tumor Subsequently, 72 oncocytic thyroid carcinomas, one cell line, and five Hürthle c... BeFree 25625803 Detail
<0.001 Enterochromaffin-like cell carcinoid NA BeFree Detail
<0.001 Atypical carcinoid tumor NA BeFree Detail
<0.001 Single tumor NA BeFree Detail
<0.001 Esophageal Gastrointestinal Stromal Tumor An esophageal gastrointestinal stromal tumor in a patient with MEN1-related panc... BeFree 25022420 Detail
0.004 Hereditary Malignant Neoplasm NA BeFree Detail
<0.001 Liver Neuroendocrine Tumor NA BeFree Detail
0.001 Thymic Carcinoid Tumor NA BeFree Detail
<0.001 Thyroid Gland Oncocytic Adenoma Subsequently, 72 oncocytic thyroid carcinomas, one cell line, and five Hürthle c... BeFree 25625803 Detail
<0.001 Well Differentiated Pancreatic Endocrine Tumor To elucidate the role of methylation of histone H3 at lysine 4 (H3K4) mediated b... BeFree 25537453 Detail
<0.001 pancreatic gastrinoma An esophageal gastrointestinal stromal tumor in a patient with MEN1-related panc... BeFree 25022420 Detail
<0.001 Primary Lesion NA BeFree Detail
<0.001 Benign melanocytic nevus NA BeFree Detail
<0.001 Adrenal hyperplasia NA BeFree Detail
0.002 Hyperparathyroidism-Jaw Tumor Syndrome NA BeFree Detail
<0.001 Non-Neoplastic Disorder NA BeFree Detail
<0.001 Meningioma, benign, no ICD-O subtype We found that these Pak inhibitors suppressed the proliferation and motility of ... BeFree 25596744 Detail
0.120 Parathyroid Adenoma, Familial NA ORPHANET Detail
<0.001 PITUITARY ADENOMA PREDISPOSITION (disorder) NA BeFree Detail
0.007 HYPERPARATHYROIDISM 3 NA BeFree Detail
<0.001 Malignant Vipoma NA BeFree Detail
0.001 Multiple endocrine neoplasia (MEN) Syndrome NA BeFree Detail
0.002 liver carcinoma The functional and mechanistic relatedness of EZH2 and menin in hepatocellular c... BeFree 24845612 Detail
0.001 PITUITARY ADENOMA, FAMILIAL ISOLATED (disorder) NA BeFree Detail
<0.001 Steatohepatitis Here, we further explore the role of Menin in liver steatosis. BeFree 25962847 Detail
<0.001 Pancreatic islet cell tumors NA BeFree Detail
<0.001 Benign symmetrical lipomatosis NA BeFree Detail
0.001 Lipomatosis, Multiple NA BeFree Detail
<0.001 Somatotrophinoma, Familial NA BeFree Detail
0.004 acromegaly NA BeFree Detail
0.004 adenocarcinoma A subgroup analysis indicates that women had longer RTL compared with men (1.12 ... BeFree,LHGDN 25299235 Detail
0.008 adenoma NA BeFree,GAD Detail
0.002 adrenal gland hyperfunction NA GAD Detail
0.005 Adrenal Gland Neoplasms NA BeFree,GAD Detail
<0.001 congenital adrenal hyperplasia NA BeFree Detail
<0.001 Anxiety Disorders NA BeFree Detail
<0.001 Malignant neoplasm of urinary bladder NA BeFree Detail
<0.001 Bone Diseases NA BeFree Detail
0.001 Malignant neoplasm of breast Breast cancer risk in MEN1 - a cancer genetics perspective. BeFree 25279812 Detail
0.014 Carcinoid Tumor NA BeFree,LHGDN Detail
<0.001 Non-small cell lung carcinoma NA BeFree Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
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Menin, encoded by the MEN1 gene, was initially identified as a tumor suppressor for endocrine neopla... DisGeNET Detail
MEN1, which is secondary to the mutation of the MEN1 gene, is a rare autosomal-dominant disease that... DisGeNET Detail
NA DisGeNET Detail
Here, we further explore the role of Menin in liver steatosis. DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
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NA DisGeNET Detail
Recently, Menin has been proven to negatively regulate β-cell proliferation in several mouse models,... DisGeNET Detail
Suppression of β-catenin signalling by genetic ablation or a molecular antagonist inhibits the expre... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Suppression of β-catenin signalling by genetic ablation or a molecular antagonist inhibits the expre... DisGeNET Detail
NA DisGeNET Detail
Menin, encoded by the Men1 gene, is responsible for β-cell tumor formation in patients with multiple... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Pharmacologic inhibition of the Menin-MLL interaction blocks progression of MLL leukemia in vivo. DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Intriguingly, those neuroendocrine tissues affected in Cdk4(-/-) mice are the primary targets of tum... DisGeNET Detail
Multiple Endocrine Neoplasia Type 1 (MEN1) is an autosomal dominant inherited syndrome, related to m... DisGeNET Detail
The menin protein is certainly known to have a role in regulating oestrogen receptor activity; but h... DisGeNET Detail
Germline mutations in MEN1 (encoding menin) result in multiple endocrine neoplasia type 1 and are fo... DisGeNET Detail
The tumor suppressor gene MEN1 is frequently mutated in sporadic pancreatic neuroendocrine tumors (P... DisGeNET Detail
To examine the in vivo function of menin in bone, we conditionally inactivated Men1 in mature osteob... DisGeNET Detail
Menin, encoded by the Men1 gene, is responsible for β-cell tumor formation in patients with multiple... DisGeNET Detail
NA DisGeNET Detail
We found that these Pak inhibitors suppressed the proliferation and motility of both benign (Ben-Men... DisGeNET Detail
NA DisGeNET Detail
While most cases (95%) occur sporadically, about 5% are associated with a hereditary syndrome: multi... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Tumor tissue analysis identified LOH at the SDHB locus in three pituitary adenomas and loss of heter... DisGeNET Detail
In this Review, we describe the clinical features of patients with sporadic pituitary adenomas that ... DisGeNET Detail
These data suggest that CDK4 is a critical downstream target of MEN1-dependent tumor suppression and... DisGeNET Detail
Germline mutations in MEN1 (encoding menin) result in multiple endocrine neoplasia type 1 and are fo... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
The results revealed that increasing numbers of young patients were infected with M. tuberculosis SC... DisGeNET Detail
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NA DisGeNET Detail
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Targeting β-catenin signaling for therapeutic intervention in MEN1-deficient pancreatic neuroendocri... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
A role of the MEN1 gene in the pathogenesis of GISTs could be hypothesized. DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
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While most cases (95%) occur sporadically, about 5% are associated with a hereditary syndrome: multi... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Patients aged younger than 20 years at macroprolactinoma diagnosis and seen in three tertiary referr... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
MEN1 mutations in Hürthle cell (oncocytic) thyroid carcinoma. DisGeNET Detail
NA DisGeNET Detail
These data suggest that CDK4 is a critical downstream target of MEN1-dependent tumor suppression and... DisGeNET Detail
In this Review, we describe the clinical features of patients with sporadic pituitary adenomas that ... DisGeNET Detail
Conditional knockout of β-catenin suppresses the tumorigenesis and growth of Men1-deficient PNETs, a... DisGeNET Detail
Epigenetic profiling and gene expression analysis in Men1-deficient pancreatic islet cells reveals v... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Breast cancer risk in MEN1 - a cancer genetics perspective. DisGeNET Detail
Therefore, these results suggest a previously unknown miR‑802/menin molecular network controlling lu... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Subsequently, 72 oncocytic thyroid carcinomas, one cell line, and five Hürthle cell adenomas were ex... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
An esophageal gastrointestinal stromal tumor in a patient with MEN1-related pancreatic gastrinoma: a... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Subsequently, 72 oncocytic thyroid carcinomas, one cell line, and five Hürthle cell adenomas were ex... DisGeNET Detail
To elucidate the role of methylation of histone H3 at lysine 4 (H3K4) mediated by menin-HMT complexe... DisGeNET Detail
An esophageal gastrointestinal stromal tumor in a patient with MEN1-related pancreatic gastrinoma: a... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
We found that these Pak inhibitors suppressed the proliferation and motility of both benign (Ben-Men... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
The functional and mechanistic relatedness of EZH2 and menin in hepatocellular carcinoma. DisGeNET Detail
NA DisGeNET Detail
Here, we further explore the role of Menin in liver steatosis. DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
A subgroup analysis indicates that women had longer RTL compared with men (1.12 versus 1.06, p = 0.0... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Breast cancer risk in MEN1 - a cancer genetics perspective. DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
Genome
hg19
Position
chr11:64,570,982-64,578,766
Variant Type
snv
Genome browser