Symbol Name ID |
Ret
ret proto-oncogene MGI:97902 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Elevated circulating calcitonin concentration |
Increased circulating cortisol level |
Parathyroid adenoma |
Parathyroid hyperplasia |
Hyperparathyroidism |
Nodular goiter |
Neoplasm of the thyroid gland |
Medullary thyroid carcinoma |
Thyroid C cell hyperplasia |
Thyroid nodule |
Pheochromocytoma |
Disease(s) Associated with RET | |||||||||||
familial medullary thyroid carcinoma | |||||||||||
Hirschsprung's disease | |||||||||||
multiple endocrine neoplasia type 2A | |||||||||||
multiple endocrine neoplasia type 2B | |||||||||||
pheochromocytoma |
Mouse Phenotypes | abnormal submandibular gland morphology |
endocrine/exocrine gland phenotype |
abnormal adrenal gland morphology |
adrenal cortical hyperplasia |
abnormal adrenal medulla morphology |
adrenergic chromaffin cell hyperplasia |
abnormal thyroid gland morphology |
thyroid gland hyperplasia |
ectopic ovary |
seminiferous tubule degeneration |
cryptorchism |
ectopic testis |
increased pheochromocytoma incidence |
increased thyroid adenoma incidence |
|
Availability | Mouse Genotype | ||||||||||||||
Rettm1Cos/Rettm1Cos | * | ||||||||||||||
Rettm1Jmi/Rettm1Jmi | |||||||||||||||
Rettm2.1Cos/Rettm2.1Cos | |||||||||||||||
Rettm8(RET)Jmi/Rettm8(RET)Jmi | |||||||||||||||
Rettm11(RET)Jmi/Rettm11(RET)Jmi | |||||||||||||||
Rettm1Cos/Rettm2.1Cos | * | ||||||||||||||
Rettm1Giro/Ret+ | |||||||||||||||
Rettm2.1Cos/Ret+ | |||||||||||||||
Rettm3.1(RET)Jmi/Ret+ |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 08/02/2024 MGI 6.24 |
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