Danio rerio clone RZ151A4E06 calcium binding protein P22 (CHP) mRNA, c - Nucleotide

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CHP1 reduction ameliorates spinal muscular atrophy pathology by restoring calcineurin activity and endocytosis. [Brain. 2018]
CHP1 reduction ameliorates spinal muscular atrophy pathology by restoring calcineurin activity and endocytosis.
Janzen E, Mendoza-Ferreira N, Hosseinibarkooie S, Schneider S, Hupperich K, Tschanz T, Grysko V, Riessland M, Hammerschmidt M, Rigo F, et al. Brain. 2018 Aug 1; 141(8):2343-2361.
Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 function. [Neurol Genet. 2018]
Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 function.
Mendoza-Ferreira N, Coutelier M, Janzen E, Hosseinibarkooie S, Löhr H, Schneider S, Milbradt J, Karakaya M, Riessland M, Pichlo C, et al. Neurol Genet. 2018 Feb; 4(1):e209. Epub 2018 Jan 19.
Evolutionary and Expression Analyses Show Co-option of khdrbs Genes for Origin of Vertebrate Brain. [Front Genet. 2017]
Evolutionary and Expression Analyses Show Co-option of khdrbs Genes for Origin of Vertebrate Brain.
Wang S, Yang Q, Wang Z, Feng S, Li H, Ji D, Zhang S. Front Genet. 2017; 8:225. Epub 2018 Jan 4.

p4 [Allamanda chlorotic virus A]
p4 [Allamanda chlorotic virus A]
gi|2664215582|gb|WVH15867.1|

Protein
Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome
Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome

MedGen
C5681321[conceptid] (1)
MedGen
NADH dehydrogenase subunit 2 (mitochondrion) [Percis japonica]
NADH dehydrogenase subunit 2 (mitochondrion) [Percis japonica]
gi|2580315464|gb|WNH37424.1|

Protein
Artedius corallinus voucher #01-124 small subunit ribosomal RNA gene, partial se...
Artedius corallinus voucher #01-124 small subunit ribosomal RNA gene, partial sequence; mitochondrial
gi|2491777080|gb|OQ846275.1|

Nucleotide

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Nucleotide