-
selenium transferase is an
enzyme that in
humans is
encoded by the
SEPSECS gene. GRCh38:
Ensembl release 89: ENSG00000109618 – Ensembl, May 2017 GRCm38:...
- been ****ociated with
mutations in the
following genes: CACNA1A, GRID2 and
SEPSECS.
Because of the
rarity of this
condition there are few
reports of successful...
- Q96LD8 14534 SEPHS1 HGNC:19685 P49903 14535 SEPHS2 HGNC:19686 Q99611 14536
SEPSECS HGNC:30605 Q9HD40 14537 SEPTIN1 HGNC:2879 Q8WYJ6 14538 SEPTIN2 HGNC:7729...
- O-phospho-L-seryl-tRNASec:L-selenocysteinyl-tRNA
synthase (EC 2.9.1.2, MMPSepSecS,
SepSecS, SLA/LP, O-phosphoseryl-tRNA:selenocysteinyl-tRNA synthase,...
-
Pontocerebellar hypoplasia is
caused by
mutations in
genes including Sepsecs gene, VRK1 (PCH1); TSEN2, TSEN34 (PCH2); RARS2 (PCH6); and TSEN54 (PCH2...
- FRMD4A mutation. PCCA –
Progressive Cerebello-Cerebral Atrophy: due to
SEPSECS mutation,
precluding selenium incorporation. 1:40
Iraqi Jews and 1:40 Moroccan...
