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Proteintech
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Immunogen sequence: ESDTGLWLH NKLGATDELW APPSIASLLT AAVIDNIRLC FHGLSSAVKL KLLLGTLHLP RRTVDEMKGA LMEIIQLASL DSDPWVLMVA DILKSFPDTG SLNLELEEQN PNVQDILGEL REKVGECEAS AMLPLECQYL NKNALTTLAG PLTPPVKHFQ LKRKPKSATL RAELLQKSTE TAQQLKRSAG VPFHAKGRGL LRKMDTTTPL KGIPKQAPFR SPTAPSVFSP TGNRTPIPPS RTLLRKERGV KLLDISELDM VGAGREAKRR RKTLDAEVVE KPAKEETVVE NATPDYAAGL VSTQKLGSLN (6-314 aa encoded by BC002764)
This gene is expressed ubiquitously with higher levels in fetal than in adult tissues. It encodes a protein sharing 93% sequence identity with the mouse protein. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene is mapped to the 165 kb WHS critical region, and may play a role in the phenotype of the WHS or Pitt-Rogers-Danks syndrome. The encoded protein is found to be capable of reacting with HLA-A2-restricted and tumor-specific cytotoxic T lymphocytes, suggesting a target for use in specific immunotherapy for a large number of cancer patients. This protein has also been shown to be a member of the NELF (negative elongation factor) protein complex that participates in the regulation of RNA polymerase II transcription elongation.
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: FLJ10442; FLJ25112; mWHSC2; Negative elongation factor A; NELF-A; Wolf-Hirschhorn syndrome candidate 2 homolog; Wolf-Hirschhorn syndrome candidate 2 protein
基因别名: NELF-A; NELFA; P/OKcl.15; WHSC2; Whsc2h
UniProt ID: (Human) Q9H3P2, (Mouse) Q8BG30
Entrez Gene ID: (Human) 7469, (Mouse) 24116