WBSCR22
Williams Beuren syndrome chromosome region 22
HASJ4442, HUSSY-3, MERM1, PP3381, WBMT
Human WBSCR22 (114049), Mouse Wbscr22 (66138), Rat Wbscr22 (368084), Zebrafish wbscr22 (572367), chicken WBSCR22 (431053), dog WBSCR22 (479717), domestic cat WBSCR22 (101093160), naked mole-rat Wbscr22 (101702132), domestic guinea pig Wbscr22 (100725388), cow WBSCR22 (513878)
- Human(114049) Summary: 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. Alternatively spliced transcript variants have been found. [provided by RefSeq, Feb 2011]
- Mouse(66138) Williams Beuren syndrome chromosome region 22
- Rat(368084) Williams Beuren syndrome chromosome region 22
- Zebrafish(572367) Williams Beuren syndrome chromosome region 22
- chicken(431053) Williams Beuren syndrome chromosome region 22
- dog(479717) Williams Beuren syndrome chromosome region 22
- domestic cat(101093160) Williams Beuren syndrome chromosome region 22
- naked mole-rat(101702132) Williams Beuren syndrome chromosome region 22
- domestic guinea pig(100725388) Williams Beuren syndrome chromosome region 22
- cow(513878) Williams Beuren syndrome chromosome region 22
- sheep(101112944) Williams Beuren syndrome chromosome region 22
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Antibodies
Anti-WBSCR22 antibody produced in rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution,
human
immunofluorescence
immunohistochemistry
immunohistochemistry
Anti-WBSCR22 antibody produced in rabbit, purified immunoglobulin, buffered aqueous solution,
human
western blot