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Search references for SEPSECS. Phrases containing SEPSECS
See searches and references containing SEPSECS!SEPSECS
Protein-coding gene in the species Homo sapiens
selenium transferase is an enzyme that in humans is encoded by the SEPSECS gene. GRCh38: Ensembl release 89: ENSG00000109618 – Ensembl, May 2017 GRCm38:
SEPSECS
Group of neurodegenerative disorders
Pontocerebellar hypoplasia is caused by mutations in genes including Sepsecs gene, VRK1 (PCH1); TSEN2, TSEN34 (PCH2); RARS2 (PCH6); and TSEN54 (PCH2
Pontocerebellar_hypoplasia
Episodes of sustained upward deviation of the eyes
been associated with mutations in the following genes: CACNA1A, GRID2 and SEPSECS. Because of the rarity of this condition there are few reports of successful
Paroxysmal_tonic_upgaze
O-phospho-L-seryl-tRNASec:L-selenocysteinyl-tRNA synthase (EC 2.9.1.2, MMPSepSecS, SepSecS, SLA/LP, O-phosphoseryl-tRNA:selenocysteinyl-tRNA synthase,
O-phospho-L-seryl-tRNASec:L-selenocysteinyl-tRNA synthase
O-phospho-L-seryl-tRNASec:L-selenocysteinyl-tRNA_synthase
14541 SEPHS1 HGNC:19685; P49903 14542 SEPHS2 HGNC:19686; Q99611 14543 SEPSECS HGNC:30605; Q9HD40 14544 SEPTIN1 HGNC:2879; Q8WYJ6 14545 SEPTIN2 HGNC:7729;
List of human protein-coding genes 7
List_of_human_protein-coding_genes_7
Israeli physician and scientist
FRMD4A mutation. PCCA – Progressive Cerebello-Cerebral Atrophy: due to SEPSECS mutation, precluding selenium incorporation. 1:40 Iraqi Jews and 1:40 Moroccan
Ohad_Birk
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