synaptotagmin-2 [Homo sapiens]

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Dominant and recessive congenital myasthenic syndromes caused by SYT2 mutations. [Muscle Nerve. 2021]
Dominant and recessive congenital myasthenic syndromes caused by SYT2 mutations.
Maselli RA, Wei DT, Hodgson TS, Sampson JB, Vazquez J, Smith HL, Pytel P, Ferns M. Muscle Nerve. 2021 Aug; 64(2):219-224. Epub 2021 Jun 12.
New recessive mutations in SYT2 causing severe presynaptic congenital myasthenic syndromes. [Neurol Genet. 2020]
New recessive mutations in SYT2 causing severe presynaptic congenital myasthenic syndromes.
Bauché S, Sureau A, Sternberg D, Rendu J, Buon C, Messéant J, Boëx M, Furling D, Fauré J, Latypova X, et al. Neurol Genet. 2020 Dec; 6(6):e534. Epub 2020 Dec 3.
A new de novo SYT2 mutation presenting as distal weakness. Neuropathy or neuromuscular junction dysfunction? [J Peripher Nerv Syst. 2021]
A new de novo SYT2 mutation presenting as distal weakness. Neuropathy or neuromuscular junction dysfunction?
Fionda L, Turon-Sans J, Fuentes Prior P, Bernal Noguera S, Cortés-Vicente E, López-Pérez MA, Gallardo E, Rojas-García R. J Peripher Nerv Syst. 2021 Mar; 26(1):113-117. Epub 2020 Dec 22.

RefSeq genomic sequence
See the genomic reference sequence for the SYT2 gene (NG_041776.1).
RefSeq mRNA
See reference mRNA sequence for the SYT2 gene (NM_001136504.1).
RefSeq protein isoforms
See 14 reference sequence protein isoforms for the SYT2 gene.

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NP_001129976 [Domain Mapping of Disease Mut...]
NP_001129976
Domain Mapping of Disease Mutations
Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
OncoMX cancer biomarker resource [OncoMX cancer biomarker resou...]
OncoMX cancer biomarker resource
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome
reagent reviews [ExactAntigen/Labome]
reagent reviews
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