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Williams Beuren syndrome chromosome region 22
This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq]
Normal tissues
|
|
||
|---|---|---|---|
| Substantia nigra par… |
100
|
||
| Medial globus pallid… |
99
|
||
| Substantia nigra par… |
94
|
||
| Lateral globus palli… |
93
|
||
| Lateral nuclear grou… |
92
|
||
| Subthalamic nucleus |
92
|
Compounds
|
|
||
|---|---|---|---|
| Nsc102773 |
100
|
||
| N-formylmethionine L… |
99
|
||
| Meptazinol |
98
|
||
| Oxybenzone |
90
|
||
| SID 7980107 |
90
|
||
| Bevacizumab |
87
|
Diseases
|
|
||
|---|---|---|---|
| Chronic granulomatou… |
100
|
||
| Papilloma of skin |
94
|
||
| Carcinoma in situ of… |
85
|
||
| Blunt injury |
84
|
||
| Septic shock |
83
|
||
| Renal failure |
80
|
 Individual Studies |
|
|---|---|
|
|
Mus musculus
|
RNA Expression
-
Structural insights into mechanisms of the small RNA methyltransferase HEN1.
Authors: Ying Huang, Lijuan Ji, Qichen Huang, Dmitry G Vassylyev, Xuemei Chen, Jin-Biao Ma
Nature 2009 Oct 8 -
Eukaryotic cytosine methyltransferases.
Authors: Mary Grace Goll, Timothy H Bestor
Annual review of biochemistry 2005
Thought leaders and organizations working on research involving WBSCR22.
- Janusz M Bujnicki
- Stewart Shuman
- Joanna Wysocka
- Mark T Bedford
- Katarzyna H Kaminska
- Rockefeller University
- Harvard Medical School
- University of Alabama - Birmingham
- College of Physicians and Surgeons of Columbia University
- Martin Luther University Halle
Community
PhD
Rutgers the State University of New Jersey, UMDNJ
Mikael Huss
Post-doctoral fellow
Genome Institute of Singapore
-
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