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Symbol Name ID |
Tgfbr2
transforming growth factor, beta receptor II MGI:98729 |
| Darker colors indicate more annotations |
| Human Phenotypes | Adenoma sebaceum |
Breast carcinoma |
Jaundice |
Striae distensae |
Soft skin |
Axillary freckling |
Multiple cafe-au-lait spots |
Hypopigmentation of the skin |
Dermal translucency |
Reduced subcutaneous adipose tissue |
Neoplasm of the skin |
Basal cell carcinoma |
Plexiform neurofibroma |
| Disease(s) Associated with TGFBR2 | |||||||||||||
| Loeys-Dietz syndrome 2 | |||||||||||||
| Lynch syndrome | |||||||||||||
| Marfan syndrome | |||||||||||||
| mismatch repair cancer syndrome | |||||||||||||
| pancreatic cancer |
| Mouse Phenotypes | abnormal coat/hair pigmentation |
abnormal hair follicle melanocyte morphology |
ectopic hair follicle melanin granules |
pigment incontinence |
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| Availability | Mouse Genotype | ||||
| Dcttm1(cre)Bee/Dcttm1(cre)Bee Tgfbr2tm1Roes/Tgfbr2tm1Roes Tg(Dct-lacZ)A12Jkn/0 (conditional) |
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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 04/23/2024 MGI 6.23 |
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