SMN2

Survival of motor neuron 2 (SMN2) is a gene that encodes the SMN protein (full and truncated) in humans. ^[1]

4 relations: Gene, SMN1, Spinal muscular atrophy, Survival of motor neuron.

Gene

In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.

SMN1

Survival of motor neuron 1 (SMN1), also known as component of gems 1 or GEMIN1, is a gene that encodes the SMN protein in humans.

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Spinal muscular atrophy

Spinal muscular atrophy (SMA) is a rare neuromuscular disorder characterised by loss of motor neurons and progressive muscle wasting, often leading to early death.

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Survival of motor neuron

Survival of motor neuron or survival motor neuron (SMN) is a protein that in humans is encoded by the SMN1 and SMN2 genes.

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SMN2 (gene).

References

[1] https://en.wikipedia.org/wiki/SMN2

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