GTP-binding subunit ERF3B is an enzyme that in humans is encoded by the GSPT2 gene. GSPT2 is closely related to GSPT1 (MIM 139259), a GTP-binding protein that...
4 KB (589 words) - 16:46, 17 July 2025
Initiation factor Elongation factor Release factor Class 1 eRF1 Class 2/RF3 GSPT1 GSPT2 Ribosomal Proteins...
35 KB (4,225 words) - 17:44, 27 July 2025
essential for maintaining ATP levels in cells with a high energy demand. GSPT2 MAGED1 UBE2A OGT Xp11.2 Duplication "Fragile X Syndrome - X-linked Mental...
19 KB (2,025 words) - 18:52, 17 July 2025
PABPC1 has been shown to interact with: ANAPC5, CNOT7, EIF4G3, EIF4G1, GSPT2, PAIP1, and PAIP2. GRCh38: Ensembl release 89: ENSG00000070756 – Ensembl...
14 KB (1,663 words) - 17:47, 17 July 2025
HGNC:20343 Q9P0R6 6691 GSN HGNC:4620 P06396 6692 GSPT1 HGNC:4621 P15170 6693 GSPT2 HGNC:4622 Q8IYD1 6694 GSR HGNC:4623 P00390 6695 GSS HGNC:4624 P48637 6696...
277 KB (17 words) - 09:51, 23 June 2025
MTRF1, MTRF1L, MRPL58 (ICT1), MTRFR (C12orf65) eRF1: ETF1 eRF3: GSPT1, GSPT2 Crystal structures have been solved for bacterial 70S ribosome bound to...
14 KB (1,728 words) - 05:04, 23 May 2025
(2017-04-17). "Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability". PLOS ONE. 12...
27 KB (3,280 words) - 07:54, 19 July 2025
et al. (2017). "Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability". PLOS ONE. 12...
11 KB (1,248 words) - 17:19, 17 July 2025
secondary structure. The following genes have interactions with FAM63A: GSPT2, NAA38, RNMT, CSNIK1G2, ACOX1, PSMC1, SLC25A37, MMS19, DIAPH1, ME1, GAPDH...
14 KB (1,257 words) - 10:28, 17 July 2025