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Proteintech
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Immunogen sequence: MSQVKSSYS YDAPSDFINF SSLDDEGDTQ NIDSWFEEKA NLENKLLGKN GTGGLFQGKT PLRKANLQQA IVTPLKPVDN TYYKEAEKEN LVEQSIPSNA CSSLEVEAAI SRKTPAQPQR RSLRLSAQKD LEQKEKHHVK MKAKRCATPV IIDEILPSKK MKVSNNKKKP EEEGSAHQDT AEKNASSPEK AKGRHTVPCM PPAKQKFLKS TEEQELEKSM KMQQEVVEMR KKNEEFKKLA LAGIGQPVKK SVSQVTKSVD FHFRTDERIK QHPKNQEEYK EVNFTSELRK HPSSPARVTK GCTIVKPFNL SQGKKRTFDE TVSTYVPLAQ QVEDFHKRTP NRYHLRSKKD DINLLPSKSS VTKICRDPQT PVLQTKHRAR AVTCKSTAEL EAEELE
The protein encoded by this gene is found in the nucleolus and is similar to that of a family of genes on the Y-chromosome. This gene is intronless. Defects in this gene are a cause of sudden infant death with dysgenesis of the testes syndrome (SIDDT).
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Differentially expressed in cancerous and non-cancerous lung cells 2; differentially expressed in lung cells; DIL-2; GD: HCA519; Hepatocellular carcinoma-associated antigen 519; Hepatocellular carcinoma-associated antigen 90; p100; preferentially expressed in colorectal cancer; Protein fls353; restricted expression proliferation associated protein 100; Restricted expression proliferation-associated protein 100; Targeting protein for Xklp2; TPX 2; TPX2, microtubule-associated protein homolog; TPX2, microtubule-associated, homolog
Gene Aliases: 2610005B21Rik; C20orf1; C20orf2; DIL-2; DIL2; FLS353; GD:C20orf1; HCA519; HCTP4; p100; REPP86; TPX2
UniProt ID: (Human) Q9ULW0, (Mouse) A2APB8
Entrez Gene ID: (Human) 22974, (Rat) 311546, (Mouse) 72119
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