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Proteintech
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Immunogen sequence: MDPSDFPSP FDPLTLPEKP LAGDLPVDME FGEDLLESQT APTRGWAPPG PSPSSGALDL LDTPAGLEKD PGVLDGATEL LGLGGLLYKA PSPPEVDHGP EGTLAWDAGD QTLEPGPGGQ TPEVVPPDPG AGANSCSPEG LLEPLAPDSP ITLQSPHIEE EETTSIATAR RGSPGQEEEL PQGQPQSPNA PPSPSVGETL GDGINSSQTK PGGSSPPAHP SLPGDGLTAK ASEKPPERKR SERVRRAEPP KPEVVDSTES IPVSDEDSDA MVDDPNDEDF VPFRPRRSPR MSLRSSVSQR AGRSAVGTKM TCAHCRTP (1-317 aa encoded by BC013009)
This gene is located on the X chromosome and is subject to X inactivation. It is highly conserved in vertebrates and most abundantly expressed in the brain. The encoded protein is a component of histone deacetylase-containing multiprotein complexes that function through modifying chromatin structure to keep genes silent. A chromosomal translocation (X;13) involving this gene is associated with X-linked cognitive disability. Several alternatively spliced transcript variants have been found for this gene.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: DXHXS6673E protein; Zinc finger MYM-type protein 3; Zinc finger protein 261; zinc finger, MYM-type 3
基因别名: 9030216B10Rik; AW122925; DXS6673E; DXS6673El; KIAA0385; MYM; XFIM; Zfp261; ZMYM3; ZNF198L2; ZNF261
UniProt ID: (Human) Q14202, (Mouse) Q9JLM4
Entrez Gene ID: (Human) 9203, (Mouse) 56364