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Immunogen sequence: MKGTDSGSCC RRRCDFGCCC RASRRAHYTP YRSGDATRTP QSPRQTPSRE RRRPEPAGSW AAAAEEEEAA AAATPWMRDY FAEDDGEMVP RTSHTAAFLS DTKDRGPPVQ SQIWRSGEKV PFVQTYSLRA FEKPPQVQTQ ALRDFEKHLN DLKKENFSLK LRIYFLEERM QQKYEASRED IYKRNIELKV EVESLKRELQ DKKQHLDKTW ADVENLNSQN EAELRRQFEE RQQETEHVYE LLENKIQLLQ EESRLAKNEA ARMAALVEAE KECNLELSEK LKGVTKNWED VPGDQVKPDQ YTEALAQRDK; Positive Samples: Mouse skeletal muscle; Cellular Location: Cytoplasm, Golgi apparatus, Nucleus, centrosome, cytoskeleton, microtubule organizing center
The protein encoded by this gene serves to anchor phosphodiesterase 4D to the Golgi/centrosome region of the cell. Defects in this gene may be a cause of myeloproliferative disorder (MBD) associated with eosinophilia. Several transcript variants encoding different isoforms have been found for this gene.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Cardiomyopathy-associated protein 2; Myomegalin; myomegalin/phosphodiesterase 4D interacting protein variant 8; Phosphodiesterase 4D-interacting protein; Phosphodiesterase-binding protein clone 46; upregulated during skeletal muscle growth 4
Gene Aliases: 4732458A06Rik; 9430063L05Rik; C87016; CMYA2; D130016K21Rik; D3Bwg1078e; KIAA0454; KIAA0477; mKIAA0454; MMGL; Pbp46; PDE4DIP; Usmg4
UniProt ID: (Human) Q5VU43, (Rat) Q9WUJ3, (Mouse) Q80YT7
Entrez Gene ID: (Human) 9659, (Rat) 64183, (Mouse) 83679
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