Homo sapiens calcium dependent secretion activator (CADPS), transcript - Nucleotide

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Fibril treatment changes protein interactions of tau and α-synuclein in human neurons. [J Biol Chem. 2023]
Fibril treatment changes protein interactions of tau and α-synuclein in human neurons.
Griffin TA, Schnier PD, Cleveland EM, Newberry RW, Becker J, Carlson GA. J Biol Chem. 2023 Mar; 299(3):102888. Epub 2023 Jan 10.
Chr21 protein-protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer's disease. [Life Sci Alliance. 2022]
Chr21 protein-protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer's disease.
Viard J, Loe-Mie Y, Daudin R, Khelfaoui M, Plancon C, Boland A, Tejedor F, Huganir RL, Kim E, Kinoshita M, et al. Life Sci Alliance. 2022 Aug 1; 5(12). Epub 2022 Aug 1.
OpenCell: Endogenous tagging for the cartography of human cellular organization. [Science. 2022]
OpenCell: Endogenous tagging for the cartography of human cellular organization.
Cho NH, Cheveralls KC, Brunner AD, Kim K, Michaelis AC, Raghavan P, Kobayashi H, Savy L, Li JY, Canaj H, et al. Science. 2022 Mar 11; 375(6585):eabi6983. Epub 2022 Mar 11.

RefSeq alternative splicing
See 99 reference mRNA sequence splice variants for the CADPS gene.
RefSeq protein product
See the reference protein sequence for calcium-dependent secretion activator 1 isoform 3 (NP_899630.1).

Protein
Protein sequence from Nucleotide coding region
PubMed
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Taxonomy
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CCDS
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Functional Class
Functional class of the sequence domain architecture
Gene
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OMIM
OMIM records associated with Nucleotide sequence
PubMed (RefSeq)
Link to RefSeq PubMed articles
PubMed (Weighted)
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Ensembl [Ensembl]
Ensembl
GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
GenScript latest version of gene cDNA ORF Clone
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Homo sapiens calcium dependent secretion activator (CADPS), transcript variant 3...
Homo sapiens calcium dependent secretion activator (CADPS), transcript variant 3, mRNA
gi|1676318114|ref|NM_183393.3|

Nucleotide
Mucopolysaccharidosis IV
Mucopolysaccharidosis IV
Genetic disorder of mucopolysaccharide metabolism characterized by skeletal abnormalities, joint instability, development of cervical myelopathy, and excessive urinary keratan...<br/>Year introduced: 1992

MeSH
Mannosidase Deficiency Diseases
Mannosidase Deficiency Diseases
Diseases caused by the loss of one or more enzymes involved in the hydrolysis of mannoside linkages (MANNOSIDASES). The defects in enzyme activity are primarily associated wit...<br/>Year introduced: 2004

MeSH

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Nucleotide